Parasites, Hosts and Diseases

"cattle"

Brief Communication

Molecular detection of Borrelia theileri in cattle in Korea: Hyeon-Ji Hyung, Yun-Sil Choi, Jinho Park, Kwang-Jun Lee, Jun-Gu Kang; Parasites Hosts Dis 2024;62(1):151-156.
Published online February 23, 2024; DOI: https://doi.org/10.3347/PHD.23105

Abstract
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Bovine borreliosis, caused by Borrelia theileri which is transmitted via hard tick bites, is associated with mild clinical symptoms, such as fever, lethargy, hemoglobinuria, anorexia, and anemia. Borrelia theileri infects various animals, such as cattle, deer, horses, goats, sheep, and wild ruminants, in Africa, Australia, and South America. Notably, no case of B. theileri infection has been reported in Korean cattle to date. In this study, 101 blood samples were collected from a Korean indigenous cattle breed, among which 1.98% tested positive for B. theileri via nested PCR. The obtained sequences exhibited high homology with B. theileri strains identified in other regions. Phylogenetic analysis of 16S rRNA confirmed the B. theileri group affiliation; however, flagellin B sequences exhibited divergence, potentially due to regional evolutionary differences. This study provides the first molecular confirmation of B. theileri infection in Korean livestock. Further isolation and nucleotide sequence analyses are necessary to better understand the presence of B. theileri strains in cows in Korea.

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Nationwide Geographical and Temporal Distribution of Tick-Borne Diseases in Korean Water Deer (Hydropotes inermis argyropus)
Beoul Kim, Su-Jin Chae, You-Jeong Lee, Haksub Shin, Sunmin Kwak, Hyesung Jeong, Suwoong Lee, Dongmi Kwak, Min-Goo Seo
Animals.2025; 15(10): 1499. CrossRef
Circulation of tick-borne pathogens in wildlife of the Republic of Korea
Hye-ryung Byun, Seong-Ryeong Ji, Jun-Gu Kang, Chang-Yong Choi, Ki-Jeong Na, Jong-Taek Kim, Joon-Seok Chae
One Health.2024; 19: 100913. CrossRef

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Original Article

Latitude and seasons influence the prevalence of Theileria orientalis and affect the hematology of non-grazed dairy cows in Korea: Hector Espiritu, Hee-Woon Lee, Md Shohel Al Faruk, Su-Jeong Jin, Sang-Suk Lee, Yong-Il Cho; Parasites Hosts Dis 2024;62(1):64-74.
Published online February 23, 2024; DOI: https://doi.org/10.3347/PHD.23087

Abstract
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This pilot study aimed to investigate the effects of regional and seasonal variations on the prevalence of Theileria orientalis and the hematological profile of non-grazed dairy cows in Korea. A total of 365 clinically healthy lactating Holstein Friesian cows from 26 dairy farms in 7 provinces that were categorized into northern, central, and southern regions were sampled during the warm period from July to August and the cold period from October to December. The detection of T. orientalis major piroplasm surface protein gene and the hematology non-grazed dairy cows were analyzed using peripheral blood samples. The T. orientalis prevalence was 20.0% (73/365). The prevalence in the southern region was 35.9%, which was significantly higher than that in the central (21.6%) and northern (12.9%) regions (P < 0.05). The prevalence during warm period was higher (43.0%) than that during the cold season (13.5%). The infected cows showed significantly lower erythrocyte counts in the southern region (5.8 ± 0.6 M/µl) and during the warm period (5.8 ± 0.7 M/µl) compared with those in the central and northern regions and during the cold season, which affected the extended RBC parameters, including hematocrit and hemoglobin concentrations. Our findings revealed the prevalence of T. orientalis in Korea, highlighting its high occurrence during warm periods and in certain geographical regions. Climatic factors could contribute to the health and productivity of cattle, as evidenced by the prevalence of T. orientalis and its negative impact on animals.

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Characterization and identification of novel polymorphisms in the OR51H1 gene associated with resistance/tolerance to natural Theileria infection in Vechur (Bos indicus) and crossbred (B. taurus × B. indicus) cattle in a Theileria-endemic region
K. Kalaiyarasi, Muhammed Elayadeth-Meethal
Veterinary Parasitology: Regional Studies and Reports.2025; 60: 101242. CrossRef
Molecular characterization of tick genera Haemaphysalis, Ixodes, and Amblyomma in Korea
Subin Lee, Badriah Alkathiri, Kyu-Sung Ahn, Jiwon Kim, So Youn Youn, Mi-Sun Yoo, Hyang-Sim Lee, Jae-Myung Kim, Dongmi Kwak, Sung Shik Shin, Seung-Hun Lee
Parasites, Hosts and Diseases.2025; 63(3): 272. CrossRef

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Brief Communication

Molecular epidemiology of Toxoplasma gondii in cattle in Korea: Kyoo-Tae Kim, Min-Goo Seo; Parasites Hosts Dis 2023;61(2):210-215.
Published online May 23, 2023; DOI: https://doi.org/10.3347/PHD.23016

Abstract
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Toxoplasmosis is a major public health concern, with raw or undercooked meat being the primary source of human infection. Knowledge regarding the molecular epidemiology of Toxoplasma gondii in cattle destined for human consumption in Korea is lacking. The present study aimed to genetically characterize the infectious strains of T. gondii. Overall, 455 cattle blood samples from 84 farms in the Gyeongnam-do (Province) were randomly collected in 2017. Nested PCR analysis revealed that only 3 (0.7%) samples were infected with T. gondii. The B1 gene sequence of T. gondii was observed to be similar (97.3–99.6%) to that of other T. gondii isolates. This is the first study to perform the molecular detection of T. gondii in cattle in Korea. Although the prevalence of infection was low, our findings suggest that cattle present a potential public health issue. It may be crucial to recognize the importance of T. gondii infection in cattle meat.

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Molecular detection of Toxoplasma gondii in ticks and their respective host dogs
Min-Goo Seo, Dongmi Kwak
Parasites, Hosts and Diseases.2025; 63(1): 66. CrossRef
Prevalence and molecular characterization of intestinal parasites in shelter dogs from South Korea
You-Jeong Lee, Beoul Kim, Gyeonghyeon Lee, Yong-Myung Kang, Dongmi Kwak, Min-Goo Seo
Research in Veterinary Science.2025; 188: 105620. CrossRef
Antileishmanial and Antitoxoplasmal Activities of 1,4-Dihydropyridines
Thaís A. S. Oliveira, Yan R. Robles, Ibrahim S. Al Nasr, Waleed S. Koko, Tariq A. Khan, Ismail Daoud, Seyfeddine Rahali, Noureddine Amdouni, Ridha B. Said, Antônio E. M. Crotti
ACS Omega.2025; 10(28): 31066. CrossRef
Tick-borne pathogens in Mongolian ticks: The high prevalence of Rickettsia raoultii and its public health implications
You-Jeong Lee, Beoul Kim, Dongmi Kwak, Ochirkhuu Nyamsuren, Nyamdavaa Guugandaa, Min-Goo Seo
Acta Tropica.2024; 260: 107412. CrossRef

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Original Articles

Molecular epidemiological survey of pathogenic trypanosomes in naturally infected cattle in northern Côte d’ivoire: Jean-Yves Ekra, Edouard K. N’Goran, Leonard E.G. Mboera, Biégo Guillaume Gragnon, Koco Rita Nadège Assovié, Eliakunda Michael Mafie; Parasites Hosts Dis 2023;61(2):127-137.
Published online May 23, 2023; DOI: https://doi.org/10.3347/PHD.22170

Bovine trypanosomiasis is a significant health concern for livestock intensification in Côte d’Ivoire. This study aimed to determine the prevalence and distribution of pathogenic trypanosomes and identify the most infected cattle breed in northern Côte d'Ivoire. We examined 700 cattle and found that polymerase chain reaction (PCR) was more sensitive (12.3%) than microscopic observation (5.6%). Among the trypanosome species detected in naturally infected cattle, Trypanosoma vivax was 7.3%, Trypanosoma simiae tsavo was 6.7%, and Trypanosoma congolense was 0.4%. The overall prevalence of trypanosome infection in all cattle breeds was 12.3%, while the prevalence in individual breeds was 14.8%, 7.3%, 10.6%, and 12.3% for N’Dama, Baoule, Zebu, and Mere breed, respectively. The infected animals had low packed cell volume, influencing the prevalence. Our findings indicate that bovine trypanosomes are prevalent in Côte d’Ivoire, and their prevalence varies by region and breed. These pathogens include T. vivax, T. simiae tsavo, and T. congolense.

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Prediction of the molecular action of Trypanosoma vivax on bovine reproductive parameters and risk factors associated with trypanosomiasis in northern Minas Gerais, Brazil
Amanda Cristielly Nunes De Lima, Joely Ferreira Figueiredo Bittar, Otaviano de Souza Pires Neto, Eliane Macedo Sobrinho Santos, Priscilla Elias Ferreira da Silva, Hércules Otacílio Santos, Cintya Neves de Souza, Franciane Gabrielle dos Santos, Anna Christ
Veterinary World.2025; : 837. CrossRef
Genetic Diversity of Trypanosomes Infesting Cattle from Savannah District in North of Côte d’Ivoire Using Conserved Genomic Signatures: rRNA, ITS1 and gGAPDH
Jean-Yves Ekra, Eliakunda Michael Mafie, Edouard K. N’Goran, Dramane Kaba, Biégo Guillaume Gragnon, Jagan Srinivasan
Pathogens.2024; 13(3): 262. CrossRef
Trypanocide Use and Molecular Characterization of Trypanosomes Resistant to Diminazene Aceturate in Cattle in Northern Côte D’Ivoire
Jean-Yves Ekra, Eliakunda Michael Mafie, Henri Sonan, Michael Kanh, Biégo Guillaume Gragnon, Edouard K. N’Goran, Jagan Srinivasan
Tropical Medicine and Infectious Disease.2024; 9(9): 192. CrossRef

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Genotypes of Echinococcus Species from Cattle in Tanzania: Mohammed Mebarek Bia, Seongjun Choe, Barakaeli Abdieli Ndosi, Hansol Park, Yeseul Kang, Chatanun Eamudomkarn, Tilak Chandra Nath, Sunmin Kim, Hyeong-Kyu Jeon, Dongmin Lee, Keeseon S. Eom; Korean J Parasitol 2021;59(5):457-464.
Published online October 22, 2021; DOI: https://doi.org/10.3347/kjp.2021.59.5.457

Cystic echinococcosis is a zoonotic parasitic disease caused by Echinococcus species. Tanzania is one of the endemic countries with cystic echinococcosis. This study focussed on identifying genotypes of Echinococcus spp. in Tanzania. We collected 7 cysts from cattle in Mwanza municipal (n=4) and Loliondo district (n=3). The cysts from Mwanza were all E. ortleppi and fertile. In contrast, the cysts from Loliondo were all E. granulosus sensu stricto and sterile. Two from the 4 cysts were a new haplotype of E. ortleppi (G5). These results can improve the preventive and control programs for humans and livestock in Tanzania. To our knowledge, this study is considered the first to identify the genotype and haplotype of Echinococcus spp. in Tanzania.

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Occurrence of Echinococcus felidis in Apex Predators and Warthogs in Tanzania: First Molecular Evidence of Leopards as a New, Definitive Host and Implications for Ecosystem Health
Barakaeli Abdieli Ndossi, Eblate Ernest Mjingo, Mary Wokusima Zebedayo, Seongjun Choe, Hansol Park, Lee Dongmin, Keeseon S. Eom, Mohammed Mebarek Bia
Pathogens.2025; 14(5): 443. CrossRef

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Brief Communications

Prevalence and Multilocus Genotyping of Giardia lamblia in Cattle in Jiangxi Province, China: Novel Assemblage E Subtypes Identified: Sen Li, Yang Zou, Xue-Liang Zhang, Ping Wang, Xiao-Qing Chen, Xing-Quan Zhu; Korean J Parasitol 2020;58(6):681-687.
Published online December 29, 2020; DOI: https://doi.org/10.3347/kjp.2020.58.6.681

Giardia lamblia is a common enteric pathogen associated with diarrheal diseases. There are some reports of G. lamblia infection among different breeds of cattle in recent years worldwide. However, it is yet to know whether cattle in Jiangxi province, southeastern China is infected with G. lamblia. The
objective
s of the present study were to investigate the prevalence and examine the multilocus genotypes of G. lamblia in cattle in Jiangxi province. A total of 556 fecal samples were collected from 3 cattle breeds (dairy cattle, beef cattle, and buffalo) in Jiangxi province, and the prevalence and genotypes of G. lamblia were determined by the nested PCR amplification of the beta-giardin (bg) gene. A total of 52 samples (9.2%) were positive for G. lamblia. The highest prevalence of G. lamblia was detected in dairy cattle (20.0%), followed by that in beef cattle (6.4%), and meat buffalo (0.9%). Multilocus sequence typing of G. lamblia was performed based on sequences of the bg, triose phosphate isomerase and glutamate dehydrogenase loci, and 22, 42, and 52 samples were amplifiable, respectively, forming 15 MLGs. Moreover, one mixed G. lamblia infection (assemblages A and E) was found in the present study. Altogether, 6 novel assemblage E subtypes (E41*-E46*) were identified for the first time. These results not only provided baseline data for the control of G. lamblia infection in cattle in this southeastern province of China, but also enriched the molecular epidemiological data and genetic diversity of G. lamblia in cattle.

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Kareem Hatam-Nahavandi, Ehsan Ahmadpour, Milad Badri, Aida Vafae Eslahi, Davood Anvari, David Carmena, Lihua Xiao, Aysegul Taylan Ozkan
PLOS Neglected Tropical Diseases.2025; 19(4): e0013021. CrossRef
Investigation of Infection of Enterocytozoon bieneusi and Giardia duodenalis in Beef Cattle in Yunnan, China
Fan Yang, Wenjie Cheng, Jianfa Yang, Junjun He, Liujia Li, Fengcai Zou, Fanfan Shu
Veterinary Sciences.2025; 12(6): 552. CrossRef
An Epidemiology Study on Distribution of Giardia lamblia in Incheon City
Su Jin Park, Ju Hee Kim, Hyeon-Jeong Go, Nam Yee Kim, Sung Suck Oh, Young Woo Gong, MunJu Kwon, Jeong-An Gim, Soo-Son Lim
Biomedical Science Letters.2025; 31(2): 218. CrossRef
Genetic Characterization and Zoonotic Potential of Cryptosporidium spp. and Giardia duodenalis in Cattle From Northeast China
Qile Yu, Sining Chen, Xichen Zhang, Qi Zhao, Mengfei Xu, Jianhua Li, Pengtao Gong, Xiaocen Wang, Xin Li, Xu Zhang, Nan Zhang, Xiangrui Li
Transboundary and Emerging Diseases.2025;[Epub] CrossRef
Molecular Epidemiology of Cryptosporidium spp., Giardia duodenalis, and Enterocytozoon bieneusi in Guizhou Angus Calves: Dominance of Angus Cattle-Adapted Genotypes and Zoonotic Potential of E. bieneusi
Peixi Qin, Zhuolin Tao, Kaizhi Shi, Jiaxian Zhao, Bingyan Huang, Hui Liu, Chunqun Wang, Jigang Yin, Guan Zhu, Simone M. Cacciò, Min Hu
Microorganisms.2025; 13(8): 1735. CrossRef
First report of Giardia duodenalis in dairy cattle and beef cattle in Shanxi, China
Li Zhao, Yan Wang, Mingyuan Wang, Shan Zhang, Lifeng Wang, Zhansheng Zhang, Hailiang Chai, Chao Yi, Wenjun Fan, Yonghong Liu
Molecular Biology Reports.2024;[Epub] CrossRef
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Li Zhao, Zhan-Sheng Zhang, Wen-Xiong Han, Bo Yang, Hai-Liang Chai, Ming-Yuan Wang, Yan Wang, Shan Zhang, Wei-Hong Zhao, Yi-Min Ma, Yong-Jie Zhan, Li-Feng Wang, Yu-Lin Ding, Jin-Ling Wang, Yong-Hong Liu
Scientific Reports.2023;[Epub] CrossRef
Meta-Analysis of the Prevalence of Giardia duodenalis in Cattle in China
Xiang-Zhu Meng, Chao Kang, Jiaqi Wei, He Ma, Gang Liu, Jin-Ping Zhao, Hong-Shun Zhang, Xin-Bo Yang, Xiang-Yu Wang, Li-Hua Yang, Hong-Li Geng, Hongwei Cao
Foodborne Pathogens and Disease.2023; 20(1): 17. CrossRef
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Qianming Zhao, Chenyang Lu, Zhiyang Pei, Pihong Gong, Junqiang Li, Fuchun Jian, Bo Jing, Meng Qi, Changshen Ning
Parasite.2023; 30: 2. CrossRef
Prevalence and Molecular Characterization of Cryptosporidium spp., Giardia duodenalis, and Enterocytozoon bieneusi in Diarrheic and Non-Diarrheic Calves from Ningxia, Northwestern China
Haihui Gao, Gaoxing Liang, Na Su, Qirui Li, Dong Wang, Jiandong Wang, Long Zhao, Xiaodong Kang, Kangkang Guo
Animals.2023; 13(12): 1983. CrossRef
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Rashidin Abdugheni, Li Li, Zhen-Ni Yang, Yin Huang, Bao-Zhu Fang, Vyacheslav Shurigin, Osama Abdalla Abdelshafy Mohamad, Yong-Hong Liu, Wen-Jun Li
Microorganisms.2023; 11(8): 1897. CrossRef
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Sang-Ik Oh, Suk-Han Jung, Han-Kyoung Lee, Changyong Choe, Tai-Young Hur, Kyoung-Min So
Veterinary Sciences.2021; 8(7): 118. CrossRef

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Molecular Detection of Coxiella burnetii in Cattle on Ulleung Island, Korea: A Population-based Study with Four Years of Follow Up: Min-Goo Seo, Oh-Deog Kwon, Dongmi Kwak; Korean J Parasitol 2019;57(1):69-73.
Published online February 26, 2019; DOI: https://doi.org/10.3347/kjp.2019.57.1.69

Abstract
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In a population-based study with 4 years of follow up, we evaluated the prevalence of Coxiella burnetii in cattle on Ulleung Island, Korea. In this study, the rates of C. burnetii infection in cattle on Ulleung Island were determined by PCR and were found to be 0.3-1.0% in the period 2011-2014. All 17 C. burnetii partial 16S rRNA gene sequences from PCR-positive cattle were identical and 2 geographic representatives were included in our analysis. The nucleotide sequences of the 2 samples showed high (98.4-100%) identity with C. burnetii sequences obtained from the GenBank. In this long-term tracking study, the number of cattle positive for C. burnetii on Ulleung Island was low. To prevent the transmission of C. burnetii on Ulleung Island, control strategy should include biosecurity improvement in surveillance, livestock management, administering suitable tests before purchasing animals to detect C. burnetii shedders, and restricting movements between herds.

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Comprehensive Analysis of SPL Genes in Cucurbitaceae Species: Evolutionary Insights, Functional Diversity and Regulatory Mechanisms
PavanKalyan Neelam, Balakishore Lalam, Jaswanth Manavi, Ghanishtha Prusty, Suman Polaki, Pushpalatha Ganesh
Iranian Journal of Science.2025; 49(5): 1209. CrossRef

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Anaplasma marginale and A. platys Characterized from Dairy and Indigenous Cattle and Dogs in Northern Vietnam: Nguyen Thi Hong Chien, Thi Lan Nguyen, Khanh Linh Bui, Tho Van Nguyen, Thanh Hoa Le; Korean J Parasitol 2019;57(1):43-47.
Published online February 26, 2019; DOI: https://doi.org/10.3347/kjp.2019.57.1.43

Abstract
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Anaplasma marginale and A. platys were detected and characterized (16S rDNA sequence analysis) from dairy and indigenous cattle, and the latter in domestic dogs in Vietnam. A phylogenetic tree was inferred from 26 representative strains/species of Anaplasma spp. including 10 new sequences from Vietnam. Seven of our Vietnamese sequences fell into the clade of A. marginale and 3 into A. platys, with strong nodal support of 99 and 90%, respectively. Low genetic distances (0.2-0.4%) within each species supported the identification. Anaplasma platys is able to infect humans. Our discovery of this species in cattle and domestic dogs raises considerable concern about zoonotic transmission in Vietnam. Further systematic investigations are needed to gain data for Anaplasma spp. and members of Anaplasmataceae in animal hosts, vectors and humans across Vietnam.

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Bongekile L. Khoza, Charles Byaruhanga, S. Marcus Makgabo, Nkululeko Nyangiwe, Themba Mnisi, Samukelo Nxumalo, Marinda C. Oosthuizen, Zamantungwa T. H. Mnisi
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Madina Kadyrova, Alexandr Ostrovskii, Kassym Mukanov, Amirkhan Kassen, Elena Shevtsova, Maxat Berdikulov, Gilles Vergnaud, Alexandr Shevtsov
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Barbara A. Qurollo, Brett A. Stillman, Melissa J. Beall, Paulette Foster, Barbara C. Hegarty, Edward B. Breitschwerdt, Ramaswamy Chandrashekar
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Viet-Linh Nguyen, Filipe Dantas-Torres, Domenico Otranto
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Benedicto Byamukama, Patrick Vudriko, Maria Agnes Tumwebaze, Dickson Stuart Tayebwa, Joseph Byaruhanga, Martin Kamilo Angwe, Jixu Li, Eloiza May Galon, Aaron Ringo, Mingming Liu, Yongchang Li, Shengwei Ji, Mohamed Abdo Rizk, Paul Frank Adjou Moumouni, Seu
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Ly Na Huynh, Adama Zan Diarra, Quang Luan Pham, Nhiem Le-Viet, Jean-Michel Berenger, Van Hoang Ho, Xuan Quang Nguyen, Philippe Parola, Lynn Soong
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Marcos Rogério André, Ana Cláudia Calchi, Heitor Miraglia Herrera, Diego Carlos de Souza Zanatto, Bruna de Carvalho Le Senéchal Horta, Júlia Banhareli Tasso, Inalda Angélica de Souza Ramos, Victória Valente Califre de Mello, Rosangela Zacarias Machado
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BMC Veterinary Research.2020;[Epub] CrossRef

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Original Article

Analysis of Five Arboviruses and Culicoides Distribution on Cattle Farms in Jeollabuk-do, Korea: Daram Yang, Myeon-Sik Yang, Haerin Rhim, Jae-Ik Han, Jae-Ku Oem, Yeon-Hee Kim, Kyoung-Ki Lee, Chae-Woong Lim, Bumseok Kim; Korean J Parasitol 2018;56(5):477-485.
Published online October 31, 2018; DOI: https://doi.org/10.3347/kjp.2018.56.5.477

Arthropod-borne viruses (Arboviruses) are transmitted by arthropods such as Culicoides biting midges and cause abortion, stillbirth, and congenital malformation in ruminants, apparently leading to economic losses to farmers. To monitor the distribution of Culicoides and to determine their relationship with different environmental conditions (temperature, humidity, wind speed, and altitude of the farms) on 5 cattle farms, Culicoides were collected during summer season (May-September) in 2016 and 2017, and analyzed for identification of species and detection of arboviruses. About 35% of the Culicoides were collected in July and the collection rate increased with increase in temperature and humidity. The higher altitude where the farms were located, the more Culicoides were collected on inside than outside. In antigen test of Culicoides against 5 arboviruses, only Chuzan virus (CHUV) (2.63%) was detected in 2016. The Akabane virus (AKAV), CHUV, Ibaraki virus and Bovine ephemeral fever virus (BEFV) had a positive rate of less than 1.8% in 2017. In antigen test of bovine whole blood, AKAV (12.96%) and BEFV (0.96%) were positive in only one of the farms. As a result of serum neutralization test, antibodies against AKAV were generally measured in all the farms. These results suggest that vaccination before the season in which the Culicoides are active is probably best to prevent arbovirus infections.

Citations

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Isolation and identification of an AKAV strain in dairy cattle in China
Miaomiao Zhang, Menghua Deng, Sisi Zhao, Dengshuai Zhao, Yajie Zheng, Limei Qin, Han Gao, Mengmeng Zhao, Keshan Zhang
Frontiers in Veterinary Science.2025;[Epub] CrossRef
The Role of Hematophagous Arthropods, Other than Mosquitoes and Ticks, in Arbovirus Transmission
Bradley J. Blitvich
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Brief Communication

Prevalence of Tick-Borne Pathogens from Ticks Collected from Cattle and Wild Animals in Tanzania in 2012: Tae Yun Kim, You Shine Kwak, Ju Yeong Kim, Sung-Hyun Nam, In-Yong Lee, Simon Mduma, Julius Keyyu, Robert Fyumagwa, Tai-Soon Yong; Korean J Parasitol 2018;56(3):305-308.
Published online June 30, 2018; DOI: https://doi.org/10.3347/kjp.2018.56.3.305

Abstract
PDF

This study was aimed to disclose the prevalence rate of tick-borne pathogens from ticks collected from cattle and wild animals in Tanzania in 2012. Ticks were collected from slaughtered cattle and dead wild animals from November 5 to December 23, 2012 and identified. PCR for detecting Anaplasmataceae, Piroplamidae, Rickettsiaceae, Borrelia spp., and Coxiella spp. were done. Among those tested, Rickettsiaceae, Piroplasmidae, and Anaplasmataceae, were detected in ticks from the 2 regions. Rickettsiaceae represented the major tick-borne pathogens of the 2 regions. Ticks from animals in Maswa were associated with a higher pathogen detection rate compared to that in ticks from Iringa. In addition, a higher pathogen detection rate was observed in ticks infesting cattle than in ticks infesting wild animals. All examined ticks of the genus Amblyomma were infected with diverse pathogens. Ticks of the genera Rhipicephalus and Hyalomma were infected with 1 or 2 pathogens. Collectively, this study provides important information regarding differences in pathogen status among various regions, hosts, and tick species in Tanzania. Results in this study will affect the programs to prevent tick-borne diseases (TBD) of humans and livestock in Tanzania.

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Original Articles

First Molecular Characterization of Hypoderma actaeon in Cattle and Red Deer (Cervus elaphus) in Portugal: Haroon Ahmed, S?rgio Ramalho Sousa, Sami Simsek, Sofia Anast?cio, Seyma Gunyakti Kilinc; Korean J Parasitol 2017;55(6):653-658.
Published online December 31, 2017; DOI: https://doi.org/10.3347/kjp.2017.55.6.653

Abstract
PDF

Hypoderma spp. larvae cause subcutaneous myiasis in several animal species. The
objective
of the present investigation was to identify and characterize morphologically and molecularly the larvae of Hypoderma spp. collected from cattle (Bos taurus taurus) and red deer (Cervus elaphus) in the district of Castelo Branco, Portugal. For this purpose, a total of 8 larvae were collected from cattle (n=2) and red deer (n=6). After morphological identification of Hypoderma spp. larvae, molecular characterization was based on PCR-RFLP and mitochondrial CO1 gene sequence analysis. All larvae were morphologically characterized as the third instar larvae (L3) of H. actaeon. Two restriction enzymes were used for molecular identification of the larvae. TaqI restriction enzyme was not able to cut H. actaeon. However, MboII restriction enzyme differentiated Hypoderma species showing 210 and 450 bp bands in H. actaeon. Furthermore, according to the alignment of the mt-CO1 gene sequences of Hypoderma species and to PCR-RFLP findings, all the identified Hypoderma larvae were confirmed as H. actaeon. This is the first report of identification of Hypoderma spp. (Diptera; Oestridae) from cattle and red deer in Portugal, based on morphological and molecular analyses.

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Ema Gagović, Daria Jurković Žilić, Krunoslav Pintur, Adnan Hodžić, Šimun Naletilić, Relja Beck
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Microscopy Research and Technique.2023; 86(1): 3. CrossRef
Temporal and spatial spread of Hypoderma actaeon infection in roe deer from peninsular Spain determined by an indirect enzyme‐linked immunosorbent assay
R. Panadero, C. M. López, S. Remesar, E. Cabanelas, G. Varas, F. Markina, P. Díaz, D. García‐Dios, A. Prieto, G. Fernández, P. Díez‐Baños, P. Morrondo
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Hematological Changes Associated with Theileria orientalis Infection in Korean Indigenous Cattle: Suhee Kim, Do-Hyeon Yu, Sung-Woo Kang, Jeong-Byoung Chae, Kyoung-Seong Choi, Hyeon-Cheol Kim, Bae-Keun Park, Joon-Seok Chae, Jinho Park; Korean J Parasitol 2017;55(5):481-489.
Published online October 31, 2017; DOI: https://doi.org/10.3347/kjp.2017.55.5.481

Tick-borne pathogens can cause serious problems in grazing cattle. However, little information is available on tick-mediated diseases in cattle grazing on mountains. Thus, this study aimed to understand the potential problems related to tick-borne diseases in grazing cattle through the investigation of prevalent tick-transmitted infections, and their associated hematological changes, in terms of season and grazing type in Korean indigenous cattle (=Hanwoo). Hanwoo cattle from 3 regions of the Republic of Korea (=Korea) were either maintained indoors or placed on grassy mountains from spring to fall of 2014 and 2015. Cattle that grazed in mountainous areas showed a greater prevalence of tick-borne infections with an increased Theileria orientalis infection rate (54.7%) compared to that in non-grazing cattle (16.3%) (P<0.001). Accordingly, the red blood cell (RBC) count and hematocrit (HCT) values of grazing cattle were significantly lower than those of non-grazing cattle throughout the season (P<0.05). Moreover, RBC, hemoglobin (Hb), and HCT of T. orientalis-positive group were significantly lower than those of T. orientalis-negative group (P<0.05). T. orientalis is a widespread tick-borne pathogen in Korea. Grazing of cattle in mountainous areas is closely associated with an increase in T. orientalis infection (RR=3.4, P<0.001), and with consequent decreases in RBC count and HCT. Thus, these findings suggest that the Hanwoo cattle in mountainous areas of Korea are at a high risk of infection by T. orientalis, which can lead to hematological alterations. This study highlights the necessity of preventive strategies that target T. orientalis infection.

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Brief Communication

First Record of Paramphistomes Fischoederius cobboldi and Paramphistomum epiclitum Detected in Bovine Rumen from a Local Market of Savannakhet Province, Lao PDR: Surapol Sanguankiat, Marcello Otake Sato, Megumi Sato, Wanna Maipanich, Tippayarat Yoonuan, Tiengkham Pongvongsa, Boungnong Boupha, Yuichi Chigusa, Kazuhiko Moji, Jitra Waikagul; Korean J Parasitol 2016;54(4):543-547.
Published online August 31, 2016; DOI: https://doi.org/10.3347/kjp.2016.54.4.543

Abstract
PDF

In the present study, we report on the occurrence of paramphistomes, Fischoederius cobboldi and Paramphistomum epiclitum, in Lao PDR with the basis of molecular data. Parasite materials were collected from bovines bred in Ban Lahanam area, Savannakhet Province, Lao PDR at Lahanam public market. Morphological observations indicated 2 different species of paramphistomes. The mitochondrial gene cox1 of the specimens was successfully amplified by PCR and DNA sequencing was carried out for diagnosis of 11 specimens. Pairwise alignment of cox1 sequences were performed and confirmed F. cobboldi and P. epiclitum infecting bovines in Laos. Although there were many limiting points, as the small number of worm samples, and the restricted access of the animal host materials, we confirmed for the first time that 2 species of paramphistomes, F. cobboldi and P. epiclitum, are distributed in Lao PDR. More studies are needed to confirm the paramphistome species present in Savannakhet and its hosts to clear the natural history of these parasites of ruminants in the region and measure the impact of this parasite infection in the life and health of the local people.

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Sirapat Nak-on, Thapana Chontananarth
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Original Articles

Two Echinostome Species, Pegosomum bubulcum and Nephrostomum ramosum (Digenea: Echinostomatidae), from an Eastern Cattle Egret, Bubulcus ibis coromandus, in Republic of Korea: Seongjun Choe, Dongmin Lee, Hansol Park, Hyeong-Kyu Jeon, Youngsun Lee, Eunju Kim, Ki-Jeong Na, Keeseon S. Eom; Korean J Parasitol 2016;54(4):485-496.
Published online August 31, 2016; DOI: https://doi.org/10.3347/kjp.2016.54.4.485

Abstract
PDF

We describe 2 echinostome species recovered from an Eastern cattle egret, Bubulcus ibis coromandus, from Cheongju-si (city), Chungcheongbuk-do (province), Korea. Total 72 Pegosomum bubulcum specimens were recovered from the bile duct. They were 7,566×2,938 μm in average size and had 27 collar spines with vitelline extension from anterior 1/3 level of the esophagus to mid-level of the posterior testis as characteristic features. Total 9 specimens of Nephrostomum ramosum were recovered in the small intestines of the bird. They were ribbon-shaped, 11,378×2,124 μm in average size, and morphologically variable in some organs, i.e., the number of collar spines (47-50), the shape of ovary and testes, and the extension of vitelline follicles. These morphological variations observed in a single host indicated that these features are not critical for the classification of Nephrostomum species and thus were reconsidered taxonomically as synonym of N. ramosum. This study is the first report documenting and describing both flukes and their associated genera in Korea.

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Seongjun Choe, Ki-Jeong Na, Youngjun Kim, Dong-Hyuk Jeong, Jeong-Jin Yang, Keeseon S. Eom
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The Korean Journal of Parasitology.2017; 55(5): 541. CrossRef

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Biological Parameters of Rhipicephalus (Boophilus) microplus (Acari: Ixodidae) Fed on Rabbits, Sheep, and Cattle: Miling Ma, Ze Chen, Aihong Liu, Qiaoyun Ren, Junlong Liu, Zhijie Liu, Youquan Li, Hong Yin, Guiquan Guan, Jianxun Luo; Korean J Parasitol 2016;54(3):301-305.
Published online June 30, 2016; DOI: https://doi.org/10.3347/kjp.2016.54.3.301

Abstract
PDF

In order to determine the effect of various hosts on feeding performance of Rhipicephalus (Boophilus) microplus, we used 3 mammalian species as hosts, cattle (Qinchuan), sheep (T an), and rabbits (Japanese white rabbit) for infest-ing ticks. Five hundreds of R. microplus larvae were exposed to each animal (3 animals/host species). Tick recoveries were 11.0%, 0.47%, and 5.5% from cattle, sheep, and rabbits, respectively. The averages of tick feeding periods were not significantly different on cattle, sheep, and rabbits, 28.8, 25.3, and 26.7 days, respectively. The average weights of individual engorged female from cattle, sheep, and rabbits were 312.5, 219.1, and 130.2 mg, respectively and those of egg mass weights each to 85.0, 96.6, and 17.8 mg. The highest egg hatching rate was in the ticks from cattle (96.0%), fol-lowed by those from rabbits (83.0%) and sheep (19.2%). These data suggest that rabbits could be as an alternative host to cultivate R. microplus for evaluating vaccines and chemical and biological medicines against the tick in the laboratory, although the biological parameters of ticks were less than those from cattle.

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Brief Communication

Identification of Cryptosporidium from Dairy Cattle in Pahang, Malaysia: Nur Hazirah Hisamuddin, Najat Hashim, Sharmeen Nellisa Soffian, Mohd Hishammfariz Mohd Amin, Ridhwan Abdul Wahab, Mardhiah Mohammad, Muhammad Lokman Md Isa, Afzan Mat Yusof; Korean J Parasitol 2016;54(2):197-200.
Published online April 30, 2016; DOI: https://doi.org/10.3347/kjp.2016.54.2.197

Abstract
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Cryptosporidium, a protozoan parasite, can cause cryptosporidiosis which is a gastrointestinal disease that can infect humans and livestock. Cattle are the most common livestock that can be infected with this protozoan. This study was carried out to determine the prevalence of Cryptosporidium infection in cattle in Kuantan, Pahang, Malaysia and to find out the association between the occurrence of infection and 3 different ages of cattle (calves less than 1 year, yearling, and adult cattle). The samples were processed by using formol-ether concentration technique and stained by modified Ziehl Neelsen. The results showed that 15.9% (24/151) of cattle were positive for Cryptosporidium oocysts. The occurrence of Cryptosporidium in calves less than 1 year was the highest with the percentage of 20.0% (11/55) followed by yearling and adult cattle, with the percentage occurrence of 15.6 % (7/45) and 11.8% (6/51), respectively. There was no significant association between the occurrence and age of cattle and presence of diarrhea. Good management practices and proper hygiene management must be taken in order to reduce the infection. It is highly important to control the infection since infected cattle may serve as potential reservoirs of the infection to other animals and humans, especially animal handlers.

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Mircea Jifcu, Diana Hoffman , Ioan-Cristian Dreghiciu , Alesia Cioacă , Tiana Florea , Anamaria Plesko , Ion Oprescu , Sorin Morariu , Marius Stelian Ilie
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Acta Parasitologica.2017;[Epub] CrossRef

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Original Article

Prevalence and Associated Risk Factors of Toxocara vitulorum Infections in Buffalo and Cattle Calves in Three Provinces of Central Cambodia: Pierre Dorny, Brecht Devleesschauwer, Val?rie Stoliaroff, Meas Sothy, Rortana Chea, Bunthon Chea, Hor Sourloing, Sum Samuth, Seth Kong, Koemseang Nguong, San Sorn, Davun Holl, Jozef Vercruysse; Korean J Parasitol 2015;53(2):197-200.
Published online April 22, 2015; DOI: https://doi.org/10.3347/kjp.2015.53.2.197

Abstract
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The prevalence and associated risk factors of Toxocara vitulorum infection in buffalo and cattle calves was studied in 3 provinces in central Cambodia. Fecal samples were collected from 517 calves between the age of 1-15 weeks and processed for nematode egg counts by a modified McMaster method. A total of 64 calves were found to excrete T. vitulorum eggs in their feces (12.4%; 95% exact CI: 9.7-15.5). The mean fecal egg count was 2,798 EPG (SD=16,351; range=0-224,400). A multivariable generalized linear mixed model showed higher odds of T. vitulorum infection for buffalo versus cattle, for animals aged 4-8 weeks versus younger and older ones, and for animals with strongyle infection. There was no association with fecal consistency. Farmers should be aware of the potential impact of T. vitulorum, and treat their calves at the age of 2-3 weeks with anthelmintics such as benzimidazoles or pyrantel.

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Brief Communication

Ixodid Tick Infestation in Cattle and Wild Animals in Maswa and Iringa, Tanzania: You Shine Kwak, Tae Yun Kim, Sung-Hyun Nam, In-Yong Lee, Hyung-Pyo Kim, Simon Mduma, Julius Keyyu, Robert Fyumagwa, Tai-Soon Yong; Korean J Parasitol 2014;52(5):565-568.
Published online October 22, 2014; DOI: https://doi.org/10.3347/kjp.2014.52.5.565

Abstract
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Ticks and tick-borne diseases are important in human and livestock health worldwide. In November 2012, ixodid ticks were collected and identified morphologically from cattle and wild animals in the Maswa district and Iringa urban, Tanzania. Amblyomma gemma, A. lepidum, and A. variegatum were identified from Maswa cattle, and A. variegatum was the predominant species. A. marmoreum, Hyalomma impeltatum, and Rhipicephalus pulchellus were identified from Iringa cattle in addition to the above 3 Amblyomma species, and A. gemma was the most abundant species. Total 4 Amblyomma and 6 Rhipicephalus species were identified from wild animals of the 2 areas. A. lepidum was predominant in Maswa buffaloes, whereas A. gemma was predominant in Iringa buffaloes. Overall, A. variegatum in cattle was predominant in the Maswa district and A. gemma was predominant in Iringa, Tanzania.

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Original Article

Phylogenetic Analysis of Ruminant Theileria spp. from China Based on 28S Ribosomal RNA Gene: Huitian Gou, Guiquan Guan, Miling Ma, Aihong Liu, Zhijie Liu, Zongke Xu, Qiaoyun Ren, Youquan Li, Jifei Yang, Ze Chen, Hong Yin, Jianxun Luo; Korean J Parasitol 2013;51(5):511-517.
Published online October 31, 2013; DOI: https://doi.org/10.3347/kjp.2013.51.5.511

Abstract
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Species identification using DNA sequences is the basis for DNA taxonomy. In this study, we sequenced the ribosomal large-subunit RNA gene sequences (3,037-3,061 bp) in length of 13 Chinese Theileria stocks that were infective to cattle and sheep. The complete 28S rRNA gene is relatively difficult to amplify and its conserved region is not important for phylogenetic study. Therefore, we selected the D2-D3 region from the complete 28S rRNA sequences for phylogenetic analysis. Our analyses of 28S rRNA gene sequences showed that the 28S rRNA was useful as a phylogenetic marker for analyzing the relationships among Theileria spp. in ruminants. In addition, the D2-D3 region was a short segment that could be used instead of the whole 28S rRNA sequence during the phylogenetic analysis of Theileria, and it may be an ideal DNA barcode.

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An insight into misidentification of the small-subunit ribosomal RNA (18S rRNA) gene sequences of Theileria spp. as Theileria annulata
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DNA-based molecular identification of Urnula mediterranea (Ascomycota, Pezizales) collected in Central Serbia
Dejan Arsenijević, Stefan Blagojević, Nevena Planojević, Aleksandra Nikezić, Dejan Vidanović, Nenad Milosavljević, Snežana Marković
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Brief Communications

Development of a Disperse Dye Immunoassay Technique for Detection of Antibodies against Neospora caninum in Cattle: Fatemeh Selahi, Mehdi Namavari, Mohammad Hossein Hosseini, Maryam Mansourian, Yahya Tahamtan; Korean J Parasitol 2013;51(1):129-132.
Published online February 18, 2013; DOI: https://doi.org/10.3347/kjp.2013.51.1.129

Abstract
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In this study a disperse dye immunoassay method was standardized and evaluated for detection of antibodies against Neospora caninum in cattle. Sera from 150 cattle with a recent history of abortion were collected and tested by commercial ELISA kit and a standardized in-house dye immunoassay system. The positivity rate for the sera used in this study was 34.6% for the disperse dye immunoassay (DDIA) compared to 32% obtained by ELISA kit. This study showed no significant difference between DDIA and ELISA. The results indicated that the DDIA provide an economic, simple, rapid and robust test for detection of N. caninum infection in cattle.

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Jing Liu, Qiongqiong Yu, Guangying Zhao, Wenchao Dou
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Francine Alves Sinnott, Leonardo Garcia Monte, Thaís Farias Collares, Roberta Maraninchi Silveira, Sibele Borsuk
Veterinary Parasitology.2017; 239: 19. CrossRef
Markers related to the diagnosis and to the risk of abortion in bovine neosporosis
Sonia Almería, Fernando López-Gatius
Research in Veterinary Science.2015; 100: 169. CrossRef

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Intestinal Parasite Infections in Pigs and Beef Cattle in Rural Areas of Chungcheongnam-do, Korea: Hassan Ahmed Hassan Ahmed Ismail, Hyung-Kyu Jeon, Yong-Man Yu, Changhee Do, Young-Ha Lee; Korean J Parasitol 2010;48(4):347-349.
Published online December 16, 2010; DOI: https://doi.org/10.3347/kjp.2010.48.4.347

Abstract
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The present study was performed to investigate the infection status of intestinal parasites in pigs and beef cattle in rural areas of Chungcheongnam-do, Korea. From November 2009 to April 2010, a total of 241 fecal samples of pigs and beef cattle (136 and 105, respectively) were examined by direct smear and centrifugal sedimentation methods. The overall positive rates of intestinal parasites among pigs and beef cattle were 73.5% and 4.8%, respectively, and the double-infection rate was 10.3% in pigs. Of 136 specimens from pigs, Balantidium coli, Ascaris suum, and Entamoeba spp. infections were found in 88 (64.7%), 24 (17.6%), and 5 cases (3.7%), respectively. Of 105 beef cattle, Entamoeba spp. infections were detected in 5 cases (4.8%). From these results, it is shown that pigs raised on rural farms in Chungcheongnam-do had a high B. coli infection rate and a moderate A. suum infection rate. These results demonstrate that environmentally resistant cysts or eggs could be widespread on the farms examined, and thus an effective hygienic management system is needed to prevent them from serving as the source of infection for human beings.

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Case Report

The First Outbreak of Chorioptes texanus (Acari: Psoroptidae) Infestation in a Cattle Farm in Korea: Guk-Hyun Suh, Tai-Young Hur, Sun Lim, Sang-Min Shin, Jungkee Kwon, Shin-Hyeong Cho, Chai-Yong Lee, Sung-Shik Shin; Korean J Parasitol 2008;46(4):273-278.
Published online December 20, 2008; DOI: https://doi.org/10.3347/kjp.2008.46.4.273

Abstract
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Mites in the genus Chorioptes cause a mild form of skin disease in both domestic and wild ruminants. In July 2006, dermatitis characterized by alopecia, marked lichenification, accumulation of crust, and fissuring was recognized in 14 out of 200 Holstein dairy cattle raised in the cattle farm of the National Institute of Animal Science in Cheonan, Republic of Korea. Skin lesions were distributed mainly over the tail base, and sacral and perineal regions. Microscopic examinations of skin scraping samples from severely affected areas revealed numerous mites of all developmental stages. Morphologically, pedicels of the mites were short and unjointed. The tarsal suckers occurred on the pedicels of all the legs in the male worm and on the first, second, and fourth pair of legs in the adult female worm. A single long seta at the tarsus of legs III and the length of legs II being about twice as long as legs IV in adult male mites were observed. Arising anterior to the inner-most spatulate seta was a short seta with an average of 26.4 ± 5.8 ?m in length. Also, the length of setae #4 on the opisthosomal lobes was relatively short. Based on these observations, the mites were identified as Choriptes texanus. Although the chorioptic mange may not influence the mortality rate in the affected farm, reports indicate that a decline in milk production can be observed. This is the first report of chorioptic infestation in a cattle farm from Korea.

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Andre V. Bochkov, Pavel B. Klimov, Gete Hestvik, Alexander P. Saveljev
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Xiang Nong, Shu-Hua Li, Jia-Hai Wang, Yue Xie, Feng-Zheng Chen, Tian-Fei Liu, Ran He, Xiao-Bin Gu, Xue-Rong Peng, Guang-You Yang
Parasitology Research.2014; 113(3): 1201. CrossRef
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Brief Communication

Prevalence of ixodid ticks on cattle in Mazandaran province, Iran: Gholam Reza Razmi, Meisam Glinsharifodini, Shaboddin Sarvi; Korean J Parasitol 2007;45(4):307-310.
Published online December 20, 2007; DOI: https://doi.org/10.3347/kjp.2007.45.4.307

Abstract
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A survey was carried out to investigate the prevalence of hard tick species (Acari: Ixodidae) on cattle in Mazandaran province, Iran. A total of 953 ticks were collected from 86 infested cattle during activating seasons of ticks during 2004-2005. Nine species were identified: Boophilus annulatus (51.3%), Rhipicephalus bursa (16.8%), Haemaphysalis punctata (6.3%), Ixodes ricinus (6.8%), Hyalomma marginatum (12.5%), Hyalomma anatolicum excavatum (5.2%), Hyalomma asiaticum (0.6%), Hyalomma detritum (0.2 %), and Dermacentor spp. (0.1%). The results show that Boophilus annulatus, Rhipicephalus bursa, and Hyalomma species are dominant tick species in the surveyed area.

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Hassan Nasirian
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M. Dehuri, M. R. Panda, B. N. Mohanty, N. Sahoo, P C Behera, A. K. Kundu, S. K. Panda
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Hassan Nasirian
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Hassan Nasirian
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Zubaria Iqbal, Amjad Rashid Kayani, Ali Akhter, Mazhar Qayyum
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Saied Reza Naddaf, Ahmad Mahmoudi, Ahmad Ghasemi, Mahdi Rohani, Ali Mohammadi, Seyyed Payman Ziapour, Amir Hesam Nemati, Ehsan Mostafavi
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R. Balasubramanian, Pragya D. Yadav, S. Sahina, V. Arathy Nadh
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Afyonkarahisar Yöresindeki Koyun, Keçi ve Sığırlarda Kene (Ixodoidea) İnfestasyonu Üzerine Araştırmalar
mustafa eser, Hatice ÇİÇEK
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Seyyed Payman Ziapour, Sadegh Kheiri, Mahmoud Fazeli-Dinan, Farzaneh Sahraei-Rostami, Reza Ali Mohammadpour, Mohsen Aarabi, Seyed Hassan Nikookar, Mohammad Sarafrazi, Fatemeh Asgarian, Ahmadali Enayati, Janet Hemingway
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Moslem Sarani, Zakkyeh Telmadarraiy, Abdolreza Salahi Moghaddam, Kamal Azam, Mohammad Mehdi Sedaghat
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Ahmad Jafarbekloo, Hassan Vatandoost, Alireza Davari, Faezeh Faghihi, Hasan Bakhshi, Maryam Roya Ramzgouyan, Mohammad Nasrabadi, Zakkyeh Telmadarraiy
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Ehsan Mostafavi, Sadegh Chinikar, Saber Esmaeili, Fahimeh Bagheri Amiri, Amir Mohammad Ali Tabrizi, Sahar KhakiFirouz
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Asian Pacific Journal of Tropical Biomedicine.2012; 2(6): 489. CrossRef
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Mohammad Yakhchali, Kia Bahramnejad, Omid Almasi
International Journal of Acarology.2012; 38(4): 353. CrossRef
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Mahdieh Zaeemi, Hamidreza Haddadzadeh, Parvaneh Khazraiinia, Bahram Kazemi, M. Bandehpour
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Asian Pacific Journal of Tropical Medicine.2010; 3(10): 804. CrossRef

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Original Articles

Treatment of natural tropical theileriosis with the extract of the plant Peganum harmala: Mohammad Mirzaei; Korean J Parasitol 2007;45(4):267-271.
Published online December 20, 2007; DOI: https://doi.org/10.3347/kjp.2007.45.4.267

Abstract
PDF

Theileria annulata, a protozoan parasite of cattle and domestic buffaloes, is transmitted by ticks of the genus Hyalomma, and causes a disease named Mediterranean or tropical theileriosis. In this research 50 cattle naturally infected with Theileria annulata were treated with the extract of the plant Peganum harmala. The treatment was continued for 5 days, the dose of the extract being 5 mg/kg per day. After the treatment, 39 cattle responded to the treatment and recovered, but 11 did not respond to the treatment and died. The recovery rate of animals treated with the extract of the plant Peganum harmala was 78%.

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Barbara Huber, Marta Luciani, Ahmed M. Abualhassan, Daniel Giddings Vassão, Ricardo Fernandes, Thibaut Devièse
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Genotype analysis of Cryptosporidium spp. prevalent in a rural village in Hwasun-gun, Republic of Korea: Jae-Hwan Park, Sang-Mee Guk, Eun-Taek Han, Eun-Hee Shin, Jae-Lip Kim, Jong-Yil Chai; Korean J Parasitol 2006;44(1):27-33.
Published online March 20, 2006; DOI: https://doi.org/10.3347/kjp.2006.44.1.27

Abstract
PDF

Two species of Cryptosporidium are known to infect man; C. hominis which shows anthroponotic transmission between humans, and C. parvum which shows zoonotic transmission between animals or between animals and man. In this study, we focused on identifying genotypes of Cryptosporidium prevalent among inhabitants and domestic animals (cattle and goats), to elucidate transmittal routes in a known endemic area in Hwasun-gun, Jeollanam-do, Republic of Korea. The existence of Cryptosporidium oocysts was confirmed using a modified Ziehl-Neelsen stain. Human infections were found in 7 (25.9%) of 27 people examined. Cattle cryptosporidiosis cases constituted 7 (41.2%) of 17 examined, and goat cases 3 (42.9%) of 7 examined. Species characterizations were performed on the small subunit of the rRNA gene using both PCR-RFLP and sequence analysis. Most of the human isolates were mixtures of C. hominis and C. parvum genotypes and similar PCR-RFLP patterns were observed in cattle and goat isolates. However, sequence analyses identified only C. hominis in all isolates examined. The natural infection of cattle and goats with C. hominis is a new and unique finding in the present study. It is suggested that human cryptosporidiosis in the studied area is caused by mixtures of C. hominis and C. parvum oocysts originating from both inhabitants and domestic animals.

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Brief Communication

ELISA detection of IgG antibody against a recombinant major surface antigen (Nc-p43) fragment of Neospora caninum in bovine sera: Hye-Jin Ahn, Sera Kim, Dae-Yong Kim, Ho-Woo Nam; Korean J Parasitol 2003;41(3):175-177.
Published online September 20, 2003; DOI: https://doi.org/10.3347/kjp.2003.41.3.175

Abstract
PDF

An ELISA was established to measure bovine IgG directed against the recombinant antigenic determinant of Nc-p43, a major surface antigen of Neospora caninum. In a previous study, two thirds of the C-terminal of the molecule was expressed as a 6 × His tagged protein (Ncp43P) for ELISA using 2/3 of the N-terminal of SAG1 from Toxoplasma gondii as a control (TgSAG1A). Among 852 cattle sera collected from stock farms scattered nation-wide, 103 sera (12.1%) were found to react with Ncp43P positively, but no positive reaction was observed with TgSAG1A. This study shows that Ncp43P could be available as an efficient antigen for the diagnosis of neosporosis in cattle. Furthermore, it together with TgSAG1A, could be useful for the differential diagnosis of N. caninum and T. gondii infections in other mammals.

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Original Article

Prevalence of Theileria sergenti infection in Korean native cattle by polymerase chain reaction: Kun-Ho Song, Byung-Chan Sang; Korean J Parasitol 2003;41(3):141-145.
Published online September 20, 2003; DOI: https://doi.org/10.3347/kjp.2003.41.3.141

Abstract
PDF

This study was performed to investigate the prevalence of theileriosis and to compare the prevalence of this disease in Korean native cattle reared under different environmental conditions, namely, in a grazing area and a non-grazing area by polymerase chain reaction. Three hundred and one Korean native cattle (276 cows and 25 bulls) that had not received prior treatment or been vaccinated to prevent theileriosis were examined by PCR for Theileria sergenti infection from 2001 to 2002. In our study, the parasitemia range in T. sergenti-positive cattle by microscopy were from 0.1 to 3% (mean 0.8%). In terms of mean prevalence, 204 of the 301 Korean native cattle (67.8%) were positive reaction by PCR. Our results also revealed that the infection rate among cows (70.3%) was significantly higher than that among bulls (40.0%) (p < 0.01). T. sergenti infection among the over 3 year-old-group (75%) had a significant higher prevalence than that among the less than 3 year-old-group (61.8%) (p < 0.05). Our data also showed that grazing areas (76.1%) had the significant higher prevalence than non-grazing areas (51%) (p < 0.001). In conclusion, this study demonstrates that the prevalence of T. sergenti infection is high and that its prevalence in grazing cattle is higher than that in non-grazing cattle. Therefore, life-long treatment and the development of an optimal vaccine are needed to reduce the numbers of bovine theileriosis in both grazing and non-grazing areas.

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Mini Review

Review of Neospora caninum and neosporosis in animals: J.P. Dubey; Korean J Parasitol 2003;41(1):1-16.
Published online March 20, 2003; DOI: https://doi.org/10.3347/kjp.2003.41.1.1

Abstract
PDF

Neospora caninum is a coccidian parasite of animals. It is a major pathogen for cattle and dogs and it occasionally causes clinical infections in horses, goats, sheep, and deer. Domestic dogs are the only known definitive hosts for N. caninum. It is one of the most efficiently transmitted parasite of cattle and up to 90% of cattle in some herds are infected. Transplacental transmission is considered the major route of transmission of N. caninum in cattle. Neospora caninum is a major cause of abortion in cattle in many countries. To elicit protective immunity against abortion in cows that already harbor a latent infection is a major problem. This paper reviews information on biology, diagnosis, epidemiology and control of neosporosis in animals.

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The seasonality as a relevant aspect to be considered for differential diagnosis of Trypanosoma vivax infection and co-infections in female cattle
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Acta Veterinaria.2024; 74(4): 573. CrossRef
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Cynthia Maria Morais de Queiroz Galvão, Pollyanne Raysa Fernandes de Oliveira, André Luiz de Aguiar Cavalcanti, Denise Batista Nogueira, Sérgio Santos de Azevedo, Rafael Antônio do Nascimento Ramos, Rinaldo Aparecido Mota
Revista Brasileira de Parasitologia Veterinária.2023;[Epub] CrossRef
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mBio.2023;[Epub] CrossRef
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Parasites & Vectors.2023;[Epub] CrossRef
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Ciência Rural.2023;[Epub] CrossRef
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Herd and animal level prevalences and risk factors for Neospora caninum infection in cattle in the state of Paraíba, northeastern Brazil
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Veterinary Parasitology: Regional Studies and Reports.2023; 40: 100866. CrossRef
Seroepidemiological Survey of Anti-Toxoplasma gondii and Anti-Neospora caninum Antibodies in Domestic Cats (Felis catus) in Rolim de Moura, State of Rondônia, North Brazil
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Luca Villa, Carolina Allievi, Alessia Libera Gazzonis, Giordano Ventura, Matteo Gradassi, Sergio Aurelio Zanzani, Maria Teresa Manfredi
Animals.2023; 13(11): 1730. CrossRef
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European Journal of Wildlife Research.2023;[Epub] CrossRef
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Journal of Parasitic Diseases.2023; 47(3): 677. CrossRef
Prevalence of intestinal parasites in street dogs (Canis lupus familiaris) with highlights on zoonosis in Lalitpur, Nepal
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Veterinary Medicine and Science.2023; 9(6): 2513. CrossRef
Evidence of Australian wild deer exposure to N. caninum infection and potential implications for the maintenance of N. caninum sylvatic cycle
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BMC Veterinary Research.2023;[Epub] CrossRef
Neospora caninum infection in dairy cattle in Egypt: a serosurvey and associated risk factors
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Scientific Reports.2023;[Epub] CrossRef
Molecular detection and phylogenic characterization of Neospora caninum in naturally infected sheep in Alborz and Qazvin provinces, the north of the central region of Iran
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Identification of IMC43, a novel IMC protein that collaborates with IMC32 to form an essential daughter bud assembly complex in Toxoplasma gondii
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Serosurvey of selected reproductive pathogens in domestic ruminants from Upper Egypt
Shimaa Ismail Farag, David Cano-Terriza, Moisés Gonzálvez, Doaa Salman, Nasr-Eldin M. Aref, Murad A. Mubaraki, Débora Jiménez-Martín, Ignacio García-Bocanegra, Ehab Kotb Elmahallawy
Frontiers in Veterinary Science.2023;[Epub] CrossRef
Transcriptome profiling of Madin-Darby bovine kidney cells uncover differences in the susceptibility of cattle to Toxoplasma gondii and Neospora caninum
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Veterinary Parasitology.2023; 324: 110072. CrossRef
Seroprevalence and risk factors for Neospora spp. infection in equine in Egypt
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Gestational monitoring in buffalo females: detection of Neospora caninum by PCR
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Active shedding of Neospora caninum detected in Australian wild canids in a nonexperimental context
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Neospora caninum, a cause of abortion in donkeys (Equus asinus) in Iran
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Molecular detection and phylogenetic analysis of Neospora caninum in various hosts from Iran
Jamal Gharekhani, Mohammad Yakhchali, Reza Heidari
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Matheus M. Bitencourt, Alexandra M. R. Bezerra
Mammalia.2022; 86(2): 105. CrossRef
Stability analysis and optimal control of production-limiting disease in farm with two vaccines
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Discrete & Continuous Dynamical Systems - B.2022; 27(2): 619. CrossRef
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Ana Elisa Del’Arco, Deivison Silva Argolo, Gilles Guillemin, Maria de Fátima Dias Costa, Silvia Lima Costa, Alexandre Moraes Pinheiro
Frontiers in Immunology.2022;[Epub] CrossRef
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Parasitology Research.2022; 121(3): 1033. CrossRef
Prevalence and associated risk factors of Neospora caninum infection among cattle in mainland China: A systematic review and meta-analysis
Zhu Ying, Zi-Fu Zhu, Xu Yang, Jing Liu, Qun Liu
Preventive Veterinary Medicine.2022; 201: 105593. CrossRef
Multivalent Interactions Drive the Toxoplasma AC9:AC10:ERK7 Complex To Concentrate ERK7 in the Apical Cap
Peter S. Back, William J. O’Shaughnessy, Andy S. Moon, Pravin S. Dewangan, Michael L. Reese, Peter J. Bradley, Jon P. Boyle
mBio.2022;[Epub] CrossRef
Detection of Anti-Neospora caninum Antibodies on Dairy Cattle Farms in Southern Italy
Raffaella Manca, Giuseppina Ciccarese, Domenico Scaltrito, Daniela Chirizzi
Veterinary Sciences.2022; 9(2): 87. CrossRef
The Utility of Serological Analysis for Neospora caninum Infection in Dairy Cattle Farms Management: Serological Investigation and Evaluation of the Effects on Reproductive and Productive Performances in Two Study Herds in Northern Italy
Luca Villa, Alessia Libera Gazzonis, Emanuele Fumagalli, Sergio Aurelio Zanzani, Maria Teresa Manfredi
Animals.2022; 12(6): 786. CrossRef
Determination of B and T Cell Epitopes in Neospora caninum Immune Mapped Protein‐1 (IMP‐1): Implications in Vaccine Design against Neosporosis
Naser Nazari, Bahareh Kordi, Bahman Maleki, Morteza Shams, Esfandiar Azizi, Hamidreza Majidiani, Razi Naserifar, Adam Reich
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Neospora caninum SRS2 Protein: Essential Vaccination Targets and Biochemical Features for Next‐Generation Vaccine Design
Ali Asghari, Bahareh Kordi, Bahman Maleki, Hamidreza Majidiani, Morteza Shams, Razi Naserifar, Jane Hanrahan
BioMed Research International.2022;[Epub] CrossRef
The Global Prevalence of Neospora caninum Infection in Sheep and Goats That Had an Abortion and Aborted Fetuses: A Systematic Review and Meta-Analysis
Tooran Nayeri, Shahabeddin Sarvi, Mahmood Moosazadeh, Ahmad Daryani
Frontiers in Veterinary Science.2022;[Epub] CrossRef
Neospora caninum infection in aborting bovines and lost fetuses: A systematic review and meta-analysis
Tooran Nayeri, Mahmood Moosazadeh, Shahabeddin Sarvi, Ahmad Daryani, Benjamin M. Rosenthal
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Investigation of Toxoplasma gondii and Neospora caninum as cause of ovine abortion in affected flocks of Urmia, northwest of Iran
A. Khodadadi, F. Malekifard, R. A. Batavani
BULGARIAN JOURNAL OF VETERINARY MEDICINE.2022; 25(2): 308. CrossRef
Towards the First Multiepitope Vaccine Candidate against Neospora caninum in Mouse Model: Immunoinformatic Standpoint
Morteza Shams, Bahman Maleki, Bahareh Kordi, Hamidreza Majidiani, Naser Nazari, Hamid Irannejad, Ali Asghari, Abdelwahab Omri
BioMed Research International.2022;[Epub] CrossRef
Ovine Neosporosis: The Current Global Situation
Julio Benavides, Marta González-Warleta, Noive Arteche-Villasol, Valentín Pérez, Mercedes Mezo, Daniel Gutiérrez-Expósito
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First molecular detection of Neospora caninum from naturally infected slaughtered camels in Tunisia
Yosra Amdouni, Imen abedennebi, Safa Amairia, Amara Abdelkader, Walid Chandoul, Mohamed Gharbi
Veterinary Medicine and Science.2022; 8(5): 2241. CrossRef
Seroprevalence and Risk Factors for Toxoplasma gondii and Neospora caninum in Cattle in Portugal
Helga Waap, Andrea Bärwald, Telmo Nunes, Gereon Schares
Animals.2022; 12(16): 2080. CrossRef
Investigation of Toxoplasma gondii, Neospora caninum and Tritrichomonas foetus in abortions of cattle, sheep and goats in Turkey: Analysis by real-time PCR, conventional PCR and histopathological methods
Bunyamin Irehan, Ayse Sonmez, Muge Metin Atalay, Aysel Itik Ekinci, Figen Celik, Nalan Durmus, Ayse Turkan Ciftci, Sami Simsek
Comparative Immunology, Microbiology and Infectious Diseases.2022; 89: 101867. CrossRef
Seroprevalence of Neospora caninum in Goats from Korkuteli District of Antalya
Mübeccel Atelge, Mustafa Karatepe, Alparslan Yıldırım
Turkish Journal of Parasitology.2022; 46(3): 180. CrossRef
Microcephaly and hydrocephalus in a sheep fetus infected with Neospora caninum in Southern Brazil – Short communication
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Acta Veterinaria Hungarica.2022; 70(3): 226. CrossRef
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Frontiers in Veterinary Science.2022;[Epub] CrossRef
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Frontiers in Veterinary Science.2022;[Epub] CrossRef
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Pathogens.2022; 11(11): 1305. CrossRef
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Frontiers in Cellular and Infection Microbiology.2022;[Epub] CrossRef
Retrospective Molecular Survey on Bacterial and Protozoan Abortive Agents in Roe Deer (Capreolus capreolus) from Central Italy
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Animals.2022; 12(22): 3202. CrossRef
Exploiting the Macrophage Production of IL-12 in Improvement of Vaccine Development against Toxoplasma gondii and Neospora caninum Infections
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Frontiers in Veterinary Science.2022;[Epub] CrossRef
Soroprevalência de Toxoplasma gondii, Neospora caninum e Brucella abortus em ovinos de Toledo, Paraná, Brasil
Cristian André Bertuzzi, Evaldo Alan Weschenfelder, Douglas Adriano Webber, Thais Agostinho Martins, Beatriz Souza Lima Nino, Tiago André Frigotto, João Luis Garcia, Dauton Luiz Zulpo
Semina: Ciências Agrárias.2022; 43(6): 2657. CrossRef
Neospora caninum in Aborted Bovine Fetuses in Trakya Region, Turkey - Histopathological, Immunohistochemical and Molecular Detection
Ozge Erdogan Bamac, Damla Haktanir, Handan Çetinkaya, Gülay Yuzbasioglu Özturk, Aydın Gurel, Aslı Mete
Acta Scientiae Veterinariae.2022;[Epub] CrossRef
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Parasite Immunology.2021;[Epub] CrossRef
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Apicomplexan Protozoa Responsible for Reproductive Disorders: Occurrence of DNA in Blood and Milk of Donkeys (Equus asinus) and Minireview of the Related Literature
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Pathogens.2021; 10(2): 111. CrossRef
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Tooran Nayeri, Shahabeddin Sarvi, Mahmood Moosazadeh, Ahmad Daryani
Veterinary Parasitology.2021; 290: 109370. CrossRef
Toxoplasma gondii induced abortions in a goat herd in Rio de Janeiro, Brazil
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Ciência Rural.2021;[Epub] CrossRef
Vaccination with Neospora GRA6 Interrupts the Vertical Transmission and Partially Protects Dams and Offspring against Neospora caninum Infection in Mice
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Vaccines.2021; 9(2): 155. CrossRef
Microneme Protein 6 Is Involved in Invasion and Egress by Neospora caninum
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Seroprevalence of Neospora caninum and Toxoplasma gondii IgG and IgM antibodies among buffaloes and cattle from Menoufia Province, Egypt
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Journal of Parasitic Diseases.2021; 45(4): 952. CrossRef
Reevaluation of the Toxoplasma gondii and Neospora caninum genomes reveals misassembly, karyotype differences, and chromosomal rearrangements
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Modelling and Analyzing the Potential Controls for Neospora caninum Infection in Dairy Cattle Using an Epidemic Approach
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Complexity.2021;[Epub] CrossRef
Serological Survey on the Occurrence of Rickettsia spp., Neospora caninum, Bartonella henselae and Toxoplasma gondii in Cats from Tuscany (Central Italy)
Valentina Virginia Ebani, Simona Nardoni, Michela Maestrini, Stefania Perrucci, Francesca Mancianti
Animals.2021; 11(6): 1842. CrossRef
A recent update about seroprevalence of ovine neosporosis in Northern Egypt and its associated risk factors
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Prevalence of Neospora caninum Exposure in Wild Pigs (Sus scrofa) from Oklahoma with Implications of Testing Method on Detection
Katelyn M. Haydett, Steven T. Peper, Cynthia Reinoso Webb, Hannah S. Tiffin, Alexander N. Wilson-Fallon, Yava L. Jones-Hall, Stephen L. Webb, Steven M. Presley
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Equine Protozoal Myeloencephalitis associated with Neospora caninum in a USA captive bred zebra (Equus zebra)
Stephani Ruppert, Jung Keun Lee, Antoinette E. Marsh
Veterinary Parasitology: Regional Studies and Reports.2021; 26: 100620. CrossRef
Congenital Transmission of Apicomplexan Parasites: A Review
Maura Rojas-Pirela, Lisvaneth Medina, Maria Verónica Rojas, Ana Isabel Liempi, Christian Castillo, Elizabeth Pérez-Pérez, Jesús Guerrero-Muñoz, Sebastian Araneda, Ulrike Kemmerling
Frontiers in Microbiology.2021;[Epub] CrossRef
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Thiosemicarbazone Copper Chelator BLT-1 Blocks Apicomplexan Parasite Replication by Selective Inhibition of Scavenger Receptor B Type 1 (SR-BI)
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In Silico Investigation of Conserved miRNAs and Their Targets From the Expressed Sequence Tags in Neospora Caninum Genome
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Neospora caninum Infection in Cattle in the Province of Kohgiluyeh and Boyer Ahmad, Southwest of Iran: Seroprevalence and Molecular Assessment
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Experimental infection by Neospora caninum in gerbil reduces activity of enzymes involved in energy metabolism
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M. Lefkaditis, R. Mpairamoglou, A. Sossidou, K. Spanoudis, M. Tsakiroglou
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Contribution of introns to the species diversity associated with the apicomplexan parasite, Neospora caninum
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Diagnostic studies of abortion in Danish cattle 2015–2017
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Species-specific differences in Toxoplasma gondii, Neospora caninum and Besnoitia besnoiti seroprevalence in Namibian wildlife
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Seroprevalence of canine neosporosis and bovine viral diarrhoea in dairy cattle in selected regions of Kenya
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Serological survey of Neospora spp. and Besnoitia spp. in horses in Portugal
Helga Waap, Uillians Volkart de Oliveira, Telmo Nunes, Jacinto Gomes, Tiago Gomes, Andrea Bärwald, Alexandre Dias Munhoz, Gereon Schares
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Preventive Veterinary Medicine.2020; 179: 105022. CrossRef
Planning and Animal Welfare Law: Considering Why Planning Authorities in the Republic of Ireland Should have Regard to Animal Welfare Laws as Part of the Planning Process
Michelle Strauss
Liverpool Law Review.2020; 41(2): 129. CrossRef
From Signaling Pathways to Distinct Immune Responses: Key Factors for Establishing or Combating Neospora caninum Infection in Different Susceptible Hosts
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The evaluation of attenuated Neospora caninum by long-term passages on murine macrophage cell line in prevention of vertical transmission in mice
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Estimating the total economic costs of Neospora caninum infections in dairy cows in Turkey
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Tropical Animal Health and Production.2020; 52(6): 3251. CrossRef
Performance of the Dot-blot test method for detecting antibodies to Sarcocystis spp. in cattle
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Pesquisa Veterinária Brasileira.2020; 40(5): 385. CrossRef
Aborto infeccioso por Neospora spp. em equino ˗ relato de caso
J.I. Octaviano, F.P. Carneiro, M.A. Redoan, M.A. Alonso, C.B. Fernandes
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Impact of Neospora caninum Infection on the Bioenergetics and Transcriptome of Cerebrovascular Endothelial Cells
Hany M. Elsheikha, Mamdowh Alkurashi, Suzy Palfreman, Marcos Castellanos, Kenny Kong, Evita Ning, Nashwa A. Elsaied, Kalotina Geraki, William MacNaughtan
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Neospora caninum infection in Iran (2004–2020): A review
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Seroprevalence and incidence of Toxoplasma gondii and Neospora caninum infection in naturally exposed domestic dogs from a rural area of São Paulo state, Brazil
Anaiá da Paixão Sevá, Daniela Pontes Chiebao, Ana Perola Drulla Brandão, Silvia Neri Godoy, Tatiana Jimenez-Villegas, Hilda Fátima Jesus Pena, Fernando Ferreira
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Global seroprevalence of Neospora spp. in horses and donkeys: A systematic review and meta-analysis
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Prevalence and Risk Factors Associated to Neospora caninum (Apicomplexa: Toxoplasmatidae) in Pet Dogs From Hamadan, West of Iran, 2016
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Avicenna Journal of Clinical Microbiology and Infection.2020; 7(1): 22. CrossRef
Serological evaluation of Neospora caninum in pregnant women treated at referral center for prenatal screening in Mato Grosso do Sul, Brazil
Pâmella Oliveira Duarte, Bárbara Guimarães Csordas, Leandra Marla Oshiro, Leandro de Oliveira Souza Higa, Namor Pinheiro Zimmermann, Kauê Rodriguez Martins, Jacqueline Cavalcante Barros, Renato Andreotti
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Investigation of anti-Neospora caninum Antibodies in Goats in Mesudiye District of Ordu using ELISA
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Kocatepe Veterinary Journal.2020;[Epub] CrossRef
Etymologia: Neospora caninum
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Emerging Infectious Diseases.2019; 25(6): 1228. CrossRef
Prevalence and Risk Factors of Brucellosis, Toxoplasmosis, and Neosporosis Among Yanbian Yellow Cattle in Jilin Province, China
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Annotating the ‘hypothetical’ in hypothetical proteins: In-silico analysis of uncharacterised proteins for the Apicomplexan parasite, Neospora caninum
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The state of art of neutrophil extracellular traps in protozoan and helminthic infections
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Gregory A. Ballash, Mark C. Jenkins, O. C. H. Kwok, J. P. Dubey, Abigail B. Shoben, Terry L. Robison, Tom Kraft, Erik E. Shaffer, Patricia M. Dennis
EcoHealth.2019; 16(1): 109. CrossRef
14-3-3 Protein of Neospora caninum Modulates Host Cell Innate Immunity Through the Activation of MAPK and NF-κB Pathways
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Frontiers in Microbiology.2019;[Epub] CrossRef
Neospora GRA6 possesses immune-stimulating activity and confers efficient protection against Neospora caninum infection in mice
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Veterinary Parasitology.2019; 267: 61. CrossRef
Pinniped- and Cetacean-Derived ETosis Contributes to Combating Emerging Apicomplexan Parasites (Toxoplasma gondii, Neospora caninum) Circulating in Marine Environments
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Biology.2019; 8(1): 12. CrossRef
Seroprevalence of Neospora caninum infection and associated risk factors in dairy cattle in Serbia
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Serological response to Neospora caninum infection in goats and agreement between three diagnostic techniques to detect caprine neosporosis
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Seroprevalence of Neospora caninum and Toxoplasma gondii in dogs from an urban area of North-eastern Brazil: a spatial approach
Islanne Barbosa de Souza, Pollyanne Raysa Fernandes, Tatiene Rossana Móta Silva, Cleber Vinicius Brito Santos, Naiara Mirelly Marinho da Silva, Carlos Roberto Cruz Ubirajara Filho, Gílcia Aparecida de Carvalho, Leucio Câmara Alves, Rinaldo Aparecido Mota,
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Detection of Neospora caninum DNA in cases of bovine and ovine abortion in the South-West of Scotland
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Who let the cats out? A global meta-analysis on risk of parasitic infection in indoor versus outdoor domestic cats (Felis catus)
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Biology Letters.2019; 15(4): 20180840. CrossRef
Evaluation of abortions spontaneously induced by Neospora caninum and risk factors in dairy cattle from Lima, Peru
Marcos Enrique Serrano-Martínez, Cesar Abel Burga Cisterna, Roberto Carlos Evaristo Romero, Marco Antonio Quispe Huacho, Alessandra Matienzo Bermabé, Luis Antonio Llanco Albornoz
Revista Brasileira de Parasitologia Veterinária.2019; 28(2): 215. CrossRef
Canine encephalitis — inflammation of the brain
Ellen Andrews
The Veterinary Nurse.2019; 10(5): 257. CrossRef
Atık yapan sığırlarda Anti-Neospora caninum antikorlarının yaygınlığının araştırılması
Ufuk EROL, Erdem DANYER, Selim TUNCER, Çağla KORKMAZ, Ahmet DENİZ
Etlik Veteriner Mikrobiyoloji Dergisi.2019; 30(1): 78. CrossRef
Neospora caninum infection in dairy farms with history of abortion in West of Iran
Jamal Gharekhani, Mohammad Yakhchali
Veterinary and Animal Science.2019; 8: 100071. CrossRef
A photoactivatable crosslinking system reveals protein interactions in the Toxoplasma gondii inner membrane complex
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Seroprevalence of Neospora caninum and Toxoplasma gondii Infections in Stray Dogs of Hamadan Suburb, West of Iran, 2018
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Avicenna Journal of Clinical Microbiology and Infection.2019; 6(2): 57. CrossRef
Neospora caninum: soroepidemiologia de vacas e cães de propriedades leiteiras de Cunha, São Paulo, Brasil
Sintia Barboza Bastos, Thais Agostinho Martins, Ana Sue Sammi, Felippe Danyel Cardoso Martins, Ivo Alexandre Leme da Cunha, Luiz Daniel de Barros, Dauton Luiz Zulpo, João Luis Garcia
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Effect of natural neosporosis on bull sperm quality
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Tropical Animal Health and Production.2018; 50(1): 85. CrossRef
Characteristic pro-inflammatory cytokines and host defence cathelicidin peptide produced by human monocyte-derived macrophages infected withNeospora caninum
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Prevalence of Bovine Viral Diarrhoea Virus (BVDV), Bovine Herpes Virus 1 (BHV 1), Leptospirosis and Neosporosis, and associated risk factors in 161 Irish beef herds
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BMC Veterinary Research.2018;[Epub] CrossRef
The serostatus of Brucella spp., Chlamydia abortus, Coxiella burnetii and Neospora caninum in cattle in three cantons in Bosnia and Herzegovina
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First detection and molecular identification ofNeospora caninumfrom naturally infected cattle and sheep in North Africa
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Seroprevalence of Neospora caninum-specific antibodies in German breeding bitches
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A clinical case of neosporosis in a 4-week-old holstein friesian calf which developed hindlimb paresis postnatally
Karin UESAKA, Kenji KOYAMA, Noriyuki HORIUCHI, Yoshiyasu KOBAYASHI, Yoshifumi NISHIKAWA, Hisashi INOKUMA
Journal of Veterinary Medical Science.2018; 80(2): 280. CrossRef
Risk factors and anti-Toxoplasma gondii and Neospora caninum antibody occurrence in dogs in João Pessoa, Paraíba state, Northeastern Brazil
Arthur Willian de Lima Brasil, Roberta Nunes Parentoni, José Givanildo da Silva, Carolina de Sousa Américo Batista Santos, Rinaldo Aparecido Mota, Sérgio Santos de Azevedo
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Prevalence of Neospora spp. in donkeys in China
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Parasite.2018; 25: 16. CrossRef
Neospora caninum in birds: A review
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Parasitology International.2018; 67(4): 397. CrossRef
Coinfecções por Leishmania infantum, Neospora caninum e Toxoplasma gondii em cães necropsiados da região central do Rio Grande do Sul, Brasil
F.R. Ratzlaff, A.M. Engelmann, F.S. Luz, P. Bräunig, C.M. Andrade, R.A. Fighera, S.A. Botton, F.S. F. Vogel, L. Pötter, L.A. Sangioni
Arquivo Brasileiro de Medicina Veterinária e Zootecnia.2018; 70(1): 109. CrossRef
Bovine macrophage-derived extracellular traps act as early effectors against the abortive parasite Neospora caninum
Zhengkai Wei, Yanan Wang, Xu Zhang, Xiaocen Wang, Pengtao Gong, Jianhua Li, Anja Taubert, Carlos Hermosilla, Xichen Zhang, Zhengtao Yang
Veterinary Parasitology.2018; 258: 1. CrossRef
Placental lesions associated with abortion and stillbirth in goats naturally infected by Neospora caninum
Leonardo P. Mesquita, Rafael C. Costa, Clayton I. Nogueira, Camila C. Abreu, Débora R. Orlando, Ivan Ascari Junior, Ana Paula Peconick, Mary S. Varaschin
Pesquisa Veterinária Brasileira.2018; 38(3): 444. CrossRef
Caprine Monocytes Release Extracellular Traps against Neospora caninum In Vitro
Zhengtao Yang, Zhengkai Wei, Carlos Hermosilla, Anja Taubert, Xuexiu He, Xiaocen Wang, Pengtao Gong, Jianhua Li, Xichen Zhang
Frontiers in Immunology.2018;[Epub] CrossRef
Identification of the antigenic region of Neospora caninum dense granule protein 7 using ELISA
Hanan H. Abdelbaky, Ragab M. Fereig, Yoshifumi Nishikawa
Parasitology International.2018; 67(6): 675. CrossRef
Seroprevalence of Neospora caninum in local Bali dog
I Made Dwinata, Ida Bagus Made Oka, Kadek Karang Agustina, I Made Damriyasa
Veterinary World.2018; 11(7): 926. CrossRef
Detecção molecular de Neospora caninum em macaco-da-noite (Aotus azarae) de vida livre no estado do Mato Grosso: relato de caso
T.L.C. Costa, G.A. Iglesias, J.M.A. Rosa, H.J. Bento, L.A.S. Rondelli, F. Furlan, T.O. Morgado, V. Dutra, S.H.R. Corrêa
Arquivo Brasileiro de Medicina Veterinária e Zootecnia.2018; 70(4): 1227. CrossRef
Seroprevalence of Cryptosporidium parvum and Neospora caninum in cattle in the southern Kyushu region of Japan
Tatsunori Masatani, Ragab M. Fereig, Konosuke Otomaru, Shingo Ishikawa, Isshu Kojima, Seiji Hobo, Yoshifumi Nishikawa
Parasitology International.2018; 67(6): 763. CrossRef
Seroprevalence of anti-Neospora caninum antibodies in sheep from the rapidly expanding flock of Rio de Janeiro, Brazil
R.I.J. Cosendey, F.C.R. de Oliveira, E. Frazão-Teixeira, G.N. de Souza, F.Z. Brandão, A.M.R. Ferreira, W. Lilenbaum
Veterinary Parasitology: Regional Studies and Reports.2018; 14: 59. CrossRef
Genome Wide Identification of Mutational Hotspots in the Apicomplexan Parasite Neospora caninum and the Implications for Virulence
Larissa Calarco, Joel Barratt, John Ellis, Geoff McFadden
Genome Biology and Evolution.2018; 10(9): 2417. CrossRef
Retracted: Prevalence of Toxoplasma gondii and Neospora caninum in different types of raw milk and traditional dairy product samples
Mahtab Alipour, Ebrahim Rahimi, Amir Shakerian
Journal of Food Safety.2018;[Epub] CrossRef
Toxoplasmatinae Parasites in Bats from Bahia State, Brazil
Rogério Fernando de Jesus, Gabriel Menezes Rodrigues, Evandro Moraes Silva, Aroldo José Borges Carneiro, Carlos Roberto Franke, Rogério de Magalhães Cunha, Luís Fernando Pita Gondim
Journal of Wildlife Diseases.2017; 53(1): 144. CrossRef
Serological survey of antibodies to Toxoplasma gondii and Neospora caninium in goat population in Canary Islands (Macaronesia Archipelago, Spain)
E. Rodríguez-Ponce, M. Conde, J.A. Corbera, J.R. Jaber, M.R. Ventura, C. Gutiérrez
Small Ruminant Research.2017; 147: 73. CrossRef
Extended-spectrum antiprotozoal bumped kinase inhibitors: A review
Wesley C. Van Voorhis, J. Stone Doggett, Marilyn Parsons, Matthew A. Hulverson, Ryan Choi, Samuel L.M. Arnold, Michael W. Riggs, Andrew Hemphill, Daniel K. Howe, Robert H. Mealey, Audrey O.T. Lau, Ethan A. Merritt, Dustin J. Maly, Erkang Fan, Kayode K. Oj
Experimental Parasitology.2017; 180: 71. CrossRef
Toxoplasmosis in cats in northeastern Brazil: Frequency, associated factors and coinfection with Neospora caninum , feline immunodeficiency virus and feline leukemia virus
Alexandre Dias Munhoz, Samir Batista Hage, Rebeca Dalety Santos Cruz, Ana Paula Fernandes Calazans, Fabiana Lessa Silva, George Rêgo Albuquerque, Luciana Carvalho Lacerda
Veterinary Parasitology: Regional Studies and Reports.2017; 8: 35. CrossRef
Effects of Thai piperaceae plant extracts on Neospora caninum infection
Arpron Leesombun, Sookruetai Boonmasawai, Yoshifumi Nishikawa
Parasitology International.2017; 66(3): 219. CrossRef
Molecular analyses on Neospora caninum -triggered NETosis in the caprine system
R. Villagra-Blanco, L.M.R. Silva, U. Gärtner, H. Wagner, K. Failing, A. Wehrend, A. Taubert, C. Hermosilla
Developmental & Comparative Immunology.2017; 72: 119. CrossRef
Serological study of Neospora caninum in dogs and wildlife in a nature conservation area in southern Portugal
H. WAAP, T. NUNES, Y. VAZ, A. LEITÃO
Parasitology Open.2017;[Epub] CrossRef
Peroxisome proliferator-activated receptor-γ-mediated polarization of macrophages in Neospora caninum infection
Xuexiu He, Pengtao Gong, Zhengkai Wei, Weijian Liu, Weili Wang, Jianhua Li, Zhengtao Yang, Xichen Zhang
Experimental Parasitology.2017; 178: 37. CrossRef
Bovine Polymorphonuclear Neutrophils Cast Neutrophil Extracellular Traps against the Abortive Parasite Neospora caninum
Rodolfo Villagra-Blanco, Liliana M. R. Silva, Tamara Muñoz-Caro, Zhengtao Yang, Jianhua Li, Ulrich Gärtner, Anja Taubert, Xichen Zhang, Carlos Hermosilla
Frontiers in Immunology.2017;[Epub] CrossRef
Immunization with inactivated antigens of Neospora caninum induces toll-like receptors 3, 7, 8 and 9 in maternal-fetal interface of infected pregnant heifers
M.S. Marin, Y.P. Hecker, S. Quintana, S.E. Pérez, M.R. Leunda, G.J. Cantón, E.R. Cobo, D.P. Moore, A.C. Odeón
Veterinary Parasitology.2017; 243: 12. CrossRef
PCR-based identification of Neospora caninum in the umbilical cord of a newborn calf in Brazil
Nilton Azevedo da Cunha Filho, Plínio Aguiar de Oliveira, Fernando Caetano de Oliveira, Felipe Geraldo Pappen, Cintia Lidiane Guidotti Aguiar, Alceu Gonçalves dos Santos Junior, André Luis Costa-da-Silva, Fabio Pereira Leivas Leite, Nara Amélia da Rosa Fa
Ciência Rural.2017;[Epub] CrossRef
In vitro screening of the open source Pathogen Box identifies novel compounds with profound activities against Neospora caninum
Joachim Müller, Adriana Aguado, Benoît Laleu, Vreni Balmer, Dominic Ritler, Andrew Hemphill
International Journal for Parasitology.2017; 47(12): 801. CrossRef
Activation of ERK Signaling via TLR11 Induces IL-12p40 Production in Peritoneal Macrophages Challenged by Neospora caninum
Xiaoxia Jin, Pengtao Gong, Xichen Zhang, Guojiang Li, Tao Zhu, Mengge Zhang, Jianhua Li
Frontiers in Microbiology.2017;[Epub] CrossRef
Toxoplasma gondii and Neospora caninum induce different host cell responses at proteome-wide phosphorylation events; a step forward for uncovering the biological differences between these closely related parasites
Mariwan M. M. Al-Bajalan, Dong Xia, Stuart Armstrong, Nadine Randle, Jonathan M. Wastling
Parasitology Research.2017; 116(10): 2707. CrossRef
Development of a loop-mediated isothermal amplification technique and comparison with quantitative real-time PCR for the rapid visual detection of canine neosporosis
Aongart Mahittikorn, Nipa Thammasonthijarern, Amonrattana Roobthaisong, Ruenruetai Udonsom, Supaluk Popruk, Sukhontha Siri, Hirotake Mori, Yaowalark Sukthana
Parasites & Vectors.2017;[Epub] CrossRef
Advances in the diagnosis of bovine besnoitiosis: current options and applications for control
Daniel Gutiérrez-Expósito, Ignacio Ferre, Luis M. Ortega-Mora, Gema Álvarez-García
International Journal for Parasitology.2017; 47(12): 737. CrossRef
Bottlenose dolphins (Tursiops truncatus) do also cast neutrophil extracellular traps against the apicomplexan parasite Neospora caninum
R. Villagra-Blanco, L.M.R. Silva, A. Aguilella-Segura, I. Arcenillas-Hernández, C. Martínez-Carrasco, A. Seipp, U. Gärtner, R. Ruiz de Ybañez, A. Taubert, C. Hermosilla
International Journal for Parasitology: Parasites and Wildlife.2017; 6(3): 287. CrossRef
Occurrence of abortions induced by Neospora caninum in dairy cattle from Santa Catarina, southern Brazil
Cesar Augusto Barbosa de Macedo, Madlaine Frigo Silveira Barbosa de Macedo, Ana Carolina Miura, Alessandra Taroda, Sergio Tosi Cardim, Elisabeth Ann Innes, Frank Katzer, German Jose Cantón, Francesca Chianini, Selwyn Arlington Headley, João Luis Garcia
Revista Brasileira de Parasitologia Veterinária.2017; 26(3): 292. CrossRef
Activation of a Neospora caninum EGFR-Like Kinase Facilitates Intracellular Parasite Proliferation
Xiaoxia Jin, Guojiang Li, Xichen Zhang, Pengtao Gong, Yanhui Yu, Jianhua Li
Frontiers in Microbiology.2017;[Epub] CrossRef
A novel loop-mediated isothermal amplification-based test for detecting Neospora caninum DNA
Andrea Estefanía Ramos, Marina Muñoz, Jesús Alfredo Cortés-Vecino, Paola Barato, Manuel Alfonso Patarroyo
Parasites & Vectors.2017;[Epub] CrossRef
Association of Rubella, Cytomegalovirus, and Toxoplasma Infections with Recurrent Miscarriages in Bonab-Iran: A Case-Control Study
Hesam Nasirpour, Yashar Azari Key, Nasrin Kazemipur, Mehdi Majidpour, Saman Mahdavi, Saba Hajazimian, Alireza Issazadeh, Sina Taefehshokr
Gene, Cell and Tissue.2017;[Epub] CrossRef
Approaches for the vaccination and treatment ofNeospora caninuminfections in mice and ruminant models
ANDREW HEMPHILL, ADRIANA AGUADO-MARTÍNEZ, JOACHIM MÜLLER
Parasitology.2016; 143(3): 245. CrossRef
Relation between Neospora caninum and abortion in dairy cows: Risk factors and pathogenesis of disease
Vanderlei Klauck, Gustavo Machado, Rafael Pazinato, Willian M. Radavelli, Daiane S. Santos, Jean Carlo Berwaguer, Patricia Braunig, Fernanda F. Vogel, Aleksandro S. Da Silva
Microbial Pathogenesis.2016; 92: 46. CrossRef
EstimatingNeospora caninumprevalence in wildlife populations using Bayesian inference
Karla Moreno‐Torres, Barbara Wolfe, William Saville, Rebecca Garabed
Ecology and Evolution.2016; 6(7): 2216. CrossRef
EFFECT OF DIFFERENT ECOSYSTEMS AND MANAGEMENT PRACTICES ONTOXOPLASMA GONDIIANDNEOSPORA CANINUMINFECTIONS IN WILD RUMINANTS IN SPAIN
José M. San Miguel, Daniel Gutiérrez-Expósito, Adriana Aguado-Martínez, Elena González-Zotes, Juana Pereira-Bueno, Mercedes Gómez-Bautista, Pedro Rubio, Luis M. Ortega-Mora, Esther Collantes-Fernández, Gema Álvarez-García
Journal of Wildlife Diseases.2016; 52(2): 293. CrossRef
Changes in neurotransmitter levels and expression of immediate early genes in brain of mice infected with Neospora caninum
Fumiaki Ihara, Maki Nishimura, Yoshikage Muroi, Hidefumi Furuoka, Naoaki Yokoyama, Yoshifumi Nishikawa
Scientific Reports.2016;[Epub] CrossRef
Maternal and foetal cytokine production in dams naturally and experimentally infected with Neospora caninum on gestation day 110
L. Darwich, Y. Li, B. Serrano-Pérez, R. Mur-Novales, I. Garcia-Ispierto, O. Cabezón, F. López-Gatius, S. Almería
Research in Veterinary Science.2016; 107: 55. CrossRef
PREVALENCE OF ANTIBODIES FOR SELECTED CANINE PATHOGENS AMONG WOLVES (CANIS LUPUS) FROM THE ALASKA PENINSULA, USA
Dominique E. Watts, Anna-Marie Benson
Journal of Wildlife Diseases.2016; 52(3): 506. CrossRef
Serological study ofNeospora caninuminfection in dogs in central China
Shuai Wang, Zhijun Yao, Nian Zhang, Dong Wang, Jingbo Ma, Shiguo Liu, Bin Zheng, Bin Zhang, Kuo Liu, Haizhu Zhang
Parasite.2016; 23: 25. CrossRef
Nucleotide-binding oligomerization domain-containing protein 2 prompts potent inflammatory stimuli during Neospora caninum infection
Marcela Davoli-Ferreira, Denise M. Fonseca, Caroline M. Mota, Murilo S. Dias, Djalma S. Lima-Junior, Murilo V. da Silva, Gustavo F. S. Quirino, Dario S. Zamboni, João S. Silva, Tiago W. P. Mineo
Scientific Reports.2016;[Epub] CrossRef
Seroprevalence and risk factors of two abortive diseases, toxoplasmosis and neosporosis, in small ruminants of the Mongo County, southern Gabon
Gael Darren Maganga, Andre Lea Abessolo, Clency Sylde Mikala Okouyi, Ingrid Labouba, Antoine Mitte Mbeang Beyeme, Jacques François Mavoungou, Ernest Agossou, Brieuc Cossic, Jean-Paul Akue
Small Ruminant Research.2016; 144: 56. CrossRef
Seroprevalence of anti-Toxoplasma gondii and anti-Neospora caninum antibodies in domestic mammals from two distinct regions in the semi-arid region of Northeastern Brazil
Ana Isabel Arraes-Santos, Andreina C. Araújo, Maíra F. Guimarães, Josenilton R. Santos, Hilda F.J. Pena, Solange M. Gennari, Sérgio S. Azevedo, Marcelo B. Labruna, Maurício C. Horta
Veterinary Parasitology: Regional Studies and Reports.2016; 5: 14. CrossRef
Molecular assessment of the transplacental transmission of Toxoplasma gondii , Neospora caninum , Brucella canis and Ehrlichia canis in dogs
Isis Indaiara Gonçalves Granjeiro Taques, Tatiane Rodrigues Barbosa, Andresa de Cássia Martini, Letícia Camara Pitchenin, Ísis Assis Braga, Andréia Lima Tomé de Melo, Luciano Nakazato, Valéria Dutra, Daniel Moura de Aguiar
Comparative Immunology, Microbiology and Infectious Diseases.2016; 49: 47. CrossRef
Canine Neutrophil Extracellular Traps Release Induced by the Apicomplexan Parasite Neospora caninum In Vitro
Zhengkai Wei, Carlos Hermosilla, Anja Taubert, Xuexiu He, Xiaocen Wang, Pengtao Gong, Jianhua Li, Zhengtao Yang, Xichen Zhang
Frontiers in Immunology.2016;[Epub] CrossRef
Enzyme-linked immunosorbent assays using recombinant TgSAG2 and NcSAG1 to detect Toxoplasma gondii and Neospora caninum-specific antibodies in domestic animals in Turkey
Mo ZHOU, Shinuo CAO, Ferda SEVINC, Mutlu SEVINC, Onur CEYLAN, Mingming LIU, Guanbo WANG, Paul Franck Adjou MOUMOUNI, Charoonluk JIRAPATTHARASATE, Hiroshi SUZUKI, Yoshifumi NISHIKAWA, Xuenan XUAN
Journal of Veterinary Medical Science.2016; 78(12): 1877. CrossRef
Antibodies against Neospora caninum, Sarcocystis spp. and Toxoplasma gondii detected in buffaloes from Rio Grande do Sul, Brazil
Luiza P. Portella, Gustavo C. Cadore, Marcelo de Lima, Luís A. Sangioni, Geferson Fischer, Fernanda S.F. Vogel
Pesquisa Veterinária Brasileira.2016; 36(10): 947. CrossRef
Molecular detection of protozoa of the Sarcocystidae family in sheep from the State of Rio Grande do Sul, Brazil
Luiza Pires Portella, Gustavo Cauduro Cadore, Luis Antonio Sangioni, Marta Elena Machado Alves, Raiza Chemeris, Larissa Picada Brum, Fernanda Silveira Flores Vogel
Ciência Rural.2016; 46(9): 1613. CrossRef
Intra-uterine exposure of horses to Sarcocystis spp. antigens
A.M. Antonello, G.C. Cadore, F.L. Pivoto, G. Camillo, P. Braunig, L.A. Sangioni, E. Pompermayer, L.F.P. Gondim, F.S.F. Vogel
Arquivo Brasileiro de Medicina Veterinária e Zootecnia.2016; 68(2): 271. CrossRef
Wild boar (Sus scrofa) – reservoir host of Toxoplasma gondii, Neospora caninum and Anaplasma phagocytophilum in Slovakia
Katarína Reiterová, Silvia Špilovská, Lucia Blaňarová, Markéta Derdáková, Andrea Čobádiová, Vladimír Hisira
Acta Parasitologica.2016;[Epub] CrossRef
Prevalence of Toxoplasma gondii and Neospora caninum in red foxes in Slovakia
Katarína Reiterová, Silvia Špilovská, Andrea Čobádiová, Zuzana Hurníková
Acta Parasitologica.2016;[Epub] CrossRef
Transcriptome and Histopathological Changes in Mouse Brain Infected with Neospora caninum
Maki Nishimura, Sachi Tanaka, Fumiaki Ihara, Yoshikage Muroi, Junya Yamagishi, Hidefumi Furuoka, Yutaka Suzuki, Yoshifumi Nishikawa
Scientific Reports.2015;[Epub] CrossRef
Blocking ELISA Using Recombinant NcSRS2 Protein for Diagnosing Bovine Neosporosis
Francine A. Sinnott, Leonardo G. Monte, Thais F. Collares, Bruno M. De Matos, Diene B. Pacheco, Sibele Borsuk, Renato Andreotti, Cláudia P. Hartleben
Current Microbiology.2015; 70(3): 429. CrossRef
Role of the chemokine receptor CCR5-dependent host defense system in Neospora caninum infections
Chisa Abe, Sachi Tanaka, Maki Nishimura, Fumiaki Ihara, Xuenan Xuan, Yoshifumi Nishikawa
Parasites & Vectors.2015;[Epub] CrossRef
Buparvaquone is active against Neospora caninum in vitro and in experimentally infected mice
Joachim Müller, Adriana Aguado-Martinez, Vera Manser, Vreni Balmer, Pablo Winzer, Dominic Ritler, Isabel Hostettler, David Arranz-Solís, Luis Ortega-Mora, Andrew Hemphill
International Journal for Parasitology: Drugs and Drug Resistance.2015; 5(1): 16. CrossRef
Vertical transmission in experimentally infected sheep despite previous inoculation with Neospora caninum NcNZ1 isolate
S.S. Syed-Hussain, L. Howe, W.E. Pomroy, D.M. West, M. Hardcastle, N.B. Williamson
Veterinary Parasitology.2015; 208(3-4): 150. CrossRef
The first report of Neospora caninum prevalence in aborted and healthy sheep from west of Iran
Behrouz Ezatpour, Masoud Alirezaei, Ali Hassanvand, Mohammad Zibaei, Mojgan Azadpour, Farzad Ebrahimzadeh
Comparative Clinical Pathology.2015; 24(1): 19. CrossRef
Abortion and foetal lesions induced by Neospora caninum in experimentally infected water buffalos (Bubalus bubalis)
Andreas L. Chryssafidis, Germán Cantón, Francesca Chianini, Elisabeth A. Innes, Ed H. Madureira, Rodrigo M. Soares, Solange M. Gennari
Parasitology Research.2015; 114(1): 193. CrossRef
Seroprevalence of Toxoplasma gondii and Neospora spp. Infections in Arab Horses, Southwest of Iran
Mehdi Tavalla, Mohammad Sabaghan, Rahman Abdizadeh, Shahram khademvatan, Abdollah Rafiei
Jundishapur Journal of Microbiology.2015;[Epub] CrossRef
A review of neosporosis and pathologic findings of Neospora caninum infection in wildlife
Shannon L. Donahoe, Scott A. Lindsay, Mark Krockenberger, David Phalen, Jan Šlapeta
International Journal for Parasitology: Parasites and Wildlife.2015; 4(2): 216. CrossRef
Identification and characterization of a microneme protein (NcMIC6) in Neospora caninum
Wensheng Li, Jing Liu, Jing Wang, Yong Fu, Huizhu Nan, Qun Liu
Parasitology Research.2015; 114(8): 2893. CrossRef
Neospora caninum: the First Demonstration of the Enteroepithelial Stages in the Intestines of a Naturally Infected Dog
O. Kul, H.T. Atmaca, T. Anteplioglu, N. Ocal, S. Canpolat
Journal of Comparative Pathology.2015; 153(1): 9. CrossRef
Genetic diversity of bovine Neospora caninum determined by microsatellite markers
N. Salehi, B. Gottstein, H.R. Haddadzadeh
Parasitology International.2015; 64(5): 357. CrossRef
Serum levels of nitric oxide and protein oxidation in goats seropositive for Toxoplasma gondii and Neospora caninum
A.A. Tonin, A. Weber, A. Ribeiro, G. Camillo, F.F. Vogel, A.B. Moura, G.V. Bochi, R.N. Moresco, A.S. Da Silva
Comparative Immunology, Microbiology and Infectious Diseases.2015; 41: 55. CrossRef
Neospora caninum immune mapped protein 1 (NcIMP1) is a novel vaccine candidate against neosporosis
Xia CUI, Daoyu YANG, Tao LEI, Hui WANG, Pan HAO, Qun LIU
Frontiers of Agricultural Science and Engineering.2015; 2(1): 66. CrossRef
Evaluation of Neospora caninum truncated dense granule protein 2 for serodiagnosis by enzyme-linked immunosorbent assay in dogs
Chunmei Jin, Longzheng Yu, Yinan Wang, Shiyue Hu, Shoufa Zhang
Experimental Parasitology.2015; 157: 88. CrossRef
Herd-level prevalence and associated risk factors for Toxoplasma gondii, Neospora caninum, Chlamydia abortus and bovine viral diarrhoea virus in commercial dairy and beef cattle in eastern, northern and northeastern China
Wu-Wen Sun, Qing-Feng Meng, Wei Cong, Xiao-Feng Shan, Chun-Feng Wang, Ai-Dong Qian
Parasitology Research.2015; 114(11): 4211. CrossRef
Risk Factors for Occurrence of Anti-Neospora spp. Antibodies in Horses From Alagoas, Brazil
Sandra Regina Fonseca de Araújo Valença, Rômulo Menna Barreto Valença, José Wilton Pinheiro Junior, Pedro Paulo Feitosa de Albuquerque, Orestes Luiz Souza Neto, Rinaldo Aparecido Mota
Journal of Equine Veterinary Science.2015; 35(11-12): 917. CrossRef
Neospora caninum in crows from Israel
H. Salant, M.L. Mazuz, I. Savitsky, A. Nasereddin, E. Blinder, G. Baneth
Veterinary Parasitology.2015; 212(3-4): 375. CrossRef
Detection of Neospora caninum-DNA in brain tissues from pigeons in Changchun, Jilin (China)
Ling Du, Dongsheng Yang, Tao Zhai, Pengtao Gong, Xichen Zhang, Jianhua Li
Veterinary Parasitology.2015; 214(1-2): 171. CrossRef
Anti-Neospora caninum and anti-Sarcocystis spp. specific antibodies cross-react with Besnoitia besnoiti and influence the serological diagnosis of bovine besnoitiosis
P. García-Lunar, G. Moré, L. Campero, L.M. Ortega-Mora, G. Álvarez-García
Veterinary Parasitology.2015; 214(1-2): 49. CrossRef
Seroprevalence of <i>Neospora caninum</i> in Sheep and Goats from Grenada, West Indies
Ravindra Nath Sharma, Jehna Bush, Keshaw Tiwari, Alfred Chikweto, Muhammad Iqbal Bhaiyat
Open Journal of Veterinary Medicine.2015; 05(11): 219. CrossRef
Prevalence of Toxoplasma and Neospora Antibodies in Clinically Healthy Household Dogs in Some Parts of the Kinki and Shikoku Regions
Takehisa SOMA, Shigeki IMAMOTO, Takashi HASE, Akira KATO, Kazuhiro SUNAGAWA, Masakazu OHARA, Xuenan XUAN
Journal of the Japan Veterinary Medical Association.2015; 68(9): 581. CrossRef
Antibodies to Neospora caninum in sheep from slaughterhouses in the state of São Paulo, Brazil
Laís Moraes Paiz, Rodrigo Costa da Silva, Benedito Donizete Menozzi, Helio Langoni
Revista Brasileira de Parasitologia Veterinária.2015; 24(1): 95. CrossRef
Verificação da transmissão vertical de Neospora spp. em equinos
Pedro S. Quevedo, Luciana F.C. Avila, Andréia Saggin, Tony R. Silveira, Lorena S. Feijó, Friedrich Frey Jr, Bruna R. Curcio, Nara Amélia R. Farias
Pesquisa Veterinária Brasileira.2015; 35(1): 29. CrossRef
Neospora caninum and Toxoplasma gondii serodiagnosis in human immunodeficiency virus carriers
Leandra Marla Oshiro, Ana Rita Coimbra Motta-Castro, Solange Zacalusni Freitas, Rodrigo Casquero Cunha, Rosangela Locatelli Dittrich, Andréa Christine Ferreira Meirelles, Renato Andreotti
Revista da Sociedade Brasileira de Medicina Tropical.2015; 48(5): 568. CrossRef
Risk factors for Toxoplasma gondii and Neospora caninum seropositivity in buffaloes in Paraiba State, Brazil
Arthur Willian de Lima Brasil, Roberta Nunes Parentoni, Thais Ferreira Feitosa, Camila de Sousa Bezerra, Vinicius Longo Ribeiro Vilela, Hilda Fátima de Jesus Pena, Sergio Santos de Azevedo
Revista Brasileira de Parasitologia Veterinária.2015; 24(4): 459. CrossRef
Pathogenicity of Nc-Bahia and Nc-1 strains of Neospora caninum in experimentally infected cows and buffaloes in early pregnancy
Andreas Lazaros Chryssafidis, Germán Cantón, Francesca Chianini, Elisabeth A. Innes, Ed Hoffmann Madureira, Solange Maria Gennari
Parasitology Research.2014; 113(4): 1521. CrossRef
Clinical outcome and vertical transmission variability among canine Neospora caninum isolates in a pregnant mouse model of infection
ANDREA DELLARUPE, JAVIER REGIDOR-CERRILLO, ELENA JIMÉNEZ-RUIZ, GEREON SCHARES, JUAN MANUEL UNZAGA, MARÍA CECILIA VENTURINI, LUIS M. ORTEGA-MORA
Parasitology.2014; 141(3): 356. CrossRef
Adaptation of a commercial ELISA to determine the IgG avidity in sheep experimentally and naturally infected with Neospora caninum
S.S. Syed-Hussain, L. Howe, W.E. Pomroy, D.M. West, S.L. Smith, N.B. Williamson
Veterinary Parasitology.2014; 203(1-2): 21. CrossRef
Transmission paths of Neospora caninum in a dairy herd of crossbred cattle in the northeast of Brazil
Vanessa Carvalho Sampaio de Magalhães, Uillians Volkart de Oliveira, Sonia Carmen Lopo Costa, Ivanildo dos Anjos Santos, Maria Julia Salim Pereira, Alexandre Dias Munhoz
Veterinary Parasitology.2014; 202(3-4): 257. CrossRef
PCR detection of Neospora caninum in water buffalo foetal tissues
Clementina Auriemma, Maria Lucibelli, Giorgia Borriello, Esterina Carlo, Alessandra Martucciello, Lorena Schiavo, Amalia Gallo, Francesca Bove, Federica Corrado, Santa Girardi, Maria Amoroso, Barbara ?egli Uberti, Giorgio Galiero
Acta Parasitologica.2014; 59(1): 1. CrossRef
Toxoplasma gondii and Neospora caninum infections in goat abortions from Argentina
J.M. Unzaga, G. Moré, D. Bacigalupe, M. Rambeaud, L. Pardini, A. Dellarupe, L. De Felice, M.L. Gos, M.C. Venturini
Parasitology International.2014; 63(6): 865. CrossRef
Neospora caninum DNA detection by TaqMan real-time PCR assay in experimentally infected pregnant heifers
Gabriel Ribas Pereira, Fernanda Silveira Flores Vogel, Rodrigo Camponogara Bohrer, Janduí Escarião da Nóbrega, Gustavo Freitas Ilha, Paulo Roberto Antunes da Rosa, Werner Giehl Glanzner, Giovana Camillo, Patricia Braunig, João Francisco Coelho de Oliveira
Veterinary Parasitology.2014; 199(3-4): 129. CrossRef
Fluorescent ester dye-based assays for the in vitro measurement of Neospora caninum proliferation
Caroline M. Mota, Marcela D. Ferreira, Lourenço F. Costa, Patrício S.C. Barros, Murilo V. Silva, Fernanda M. Santiago, José R. Mineo, Tiago W.P. Mineo
Veterinary Parasitology.2014; 205(1-2): 14. CrossRef
Gallus gallus domesticus are resistant to infection with Neospora caninum tachyzoites of the NC-1 strain
Alexandre Dias Munhoz, Tatiane Fernanda do Amaral, Luiz Ricardo Gonçalves, Vera Maria Barbosa de Moraes, Rosangela Zacarias Machado
Veterinary Parasitology.2014; 206(3-4): 123. CrossRef
Tracking Neospora caninum parasites using chimera monoclonal antibodies against its surface antigen-related sequences (rNcSRS2)
Jinhua Dong, Takahiro Otsuki, Tatsuya Kato, Enoch Y. Park
Journal of Bioscience and Bioengineering.2014; 117(3): 351. CrossRef
Histological and immunohistochemical characterization of the inflammatory and glial cells in the central nervous system of goat fetuses and adult male goats naturally infected with Neospora caninum
Rafael Carneiro Costa, Débora Ribeiro Orlando, Camila Costa Abreu, Karen Yumi Ribeiro Nakagaki, Leonardo Pereira Mesquita, Lismara Castro Nascimento, Aline Costa Silva, Paulo César Maiorka, Ana Paula Peconick, Djeison Lutier Raymundo, Mary Suzan Varaschin
BMC Veterinary Research.2014;[Epub] CrossRef
Cloning and expression of Neospora caninum dense-granule 7 in E. coli
Marziye Kefayat, Hossein Hamidinejat, Masoud Reza Seifiabadshapoori, Mohammad Mehdi Namavari, Parviz Shayan, Saad Gooraninejad
Journal of Parasitic Diseases.2014; 38(2): 196. CrossRef
Oxidative Stress in Brain Tissue of Gerbils Experimentally Infected withNeospora caninum
Alexandre A Tonin, Aleksandro S. da Silva, Gustavo R. Thomé, Guilherme V. Bochi, Maria R. C. Schetinger, Rafael N. Moresco, Giovana Camillo, Gustavo Toscan, Fernanda F. Vogel, Sonia T. A. Lopes
Journal of Parasitology.2014; 100(1): 154. CrossRef
Detection of Neospora caninum-DNA in feces collected from dogs in Shenyang (China) and ITS1 phylogenetic analysis
Jianhua Li, Pengfei He, Yanhui Yu, Ling Du, Pengtao Gong, Guocai Zhang, Xichen Zhang
Veterinary Parasitology.2014; 205(1-2): 361. CrossRef
Comparison of different serological methods to detect antibodies specific to Neospora caninum in bovine and canine sera
Farida Ghalmi, Bernard China, Mark Jenkins, Naouelle Azzag, Bertand Losson
Journal of Veterinary Diagnostic Investigation.2014; 26(1): 136. CrossRef
Seroprevalence and risk factors for Neospora caninum in goats in Santa Catarina state, Brazil
Josué Pires Topazio, Augusto Weber, Giovana Camillo, Fernanda Flores Vogel, Gustavo Machado, André Ribeiro, Anderson Barbosa Moura, Leandro Sâmia Lopes, Alexandre Alberto Tonin, Natan Marcos Soldá, Patrícia Bräunig, Aleksandro Schafer da Silva
Revista Brasileira de Parasitologia Veterinária.2014; 23(3): 360. CrossRef
Occurrences of anti-Toxoplasma gondiiand anti-Neospora caninum antibodies in Barbary sheep at Curitiba zoo, southern Brazil
Vivien Midori Morikawa, Cristina Kraemer Zimpel, Igor Adolfo Dexheimer Paploski, Maria do Carmo Custódio de Souza Hunold Lara, Eliana Monteforte Cassaro Villalobos, Adriana Hellmeister de Campos Nogueira Romaldini, Liria Hiromi Okuda, Alexander Welker Bio
Revista Brasileira de Parasitologia Veterinária.2014; 23(2): 255. CrossRef
Seroprevalences of Toxoplasma gondii and Neospora caninum in Pet Rabbits in Japan
Doaa SALMAN, Eiji OOHASHI, Adel Elsayed Ahmed MOHAMED, Abd El-Raheem ABD EL-MOTTELIB, Tadashi OKADA, Makoto IGARASHI
Journal of Veterinary Medical Science.2014; 76(6): 855. CrossRef
Effects of Neospora caninum on reproductive performance and the efficacy of treatment with a combination of sulphadiazine-trimethoprim and toltrazuril: a longitudinal field study
H.E. Canatan, I.M. Polat, R. Bayramoglu, S. Kuplulu, M.R. Vural, E. Aktug
Veterinární medicína.2014; 59(1): 22. CrossRef
Detection of Neospora caninum DNA in semen of experimental infected rams with no evidence of horizontal transmission in ewes
S.S. Syed-Hussain, L. Howe, W.E. Pomroy, D.M. West, S.L. Smith, N.B. Williamson
Veterinary Parasitology.2013; 197(3-4): 534. CrossRef
Neospora caninum: Infection induces high lysosomal activity
Alexandre M. Pinheiro, Cláudia Valle Cabral D. Santos, Luiz Erlon A. Rodrigues
Experimental Parasitology.2013; 134(4): 409. CrossRef
Comparative study of protective activities of Neospora caninum bradyzoite antigens, NcBAG1, NcBSR4, NcMAG1, and NcSAG4, in a mouse model of acute parasitic infection
Masaki Uchida, Kotomi Nagashima, Yui Akatsuka, Takashi Murakami, Akira Ito, Soichi Imai, Kazunori Ike
Parasitology Research.2013; 112(2): 655. CrossRef
Neospora caninum as causative agent of ovine encephalitis in Iran
Farhang Sasani, Javad Javanbakht, Parvaneh Seifori, Saeid Fathi, Mehdi Aghamohammad Hassan
Pathology Discovery.2013; 1(1): 5. CrossRef
Risk factors associated with seroprevalence of Neospora caninum in dogs from urban and rural areas of milk and coffee production in Minas Gerais state, Brazil
C. I. NOGUEIRA, L. P. MESQUITA, C. C. ABREU, K. Y. R. NAKAGAKI, J. N. SEIXAS, P. S. BEZERRA, C. M. B. M. ROCHA, A. M. GUIMARAES, A. P. PECONICK, M. S. VARASCHIN
Epidemiology and Infection.2013; 141(11): 2286. CrossRef
Comparison of use of Vero cell line and suspension culture of murine macrophage to attenuation of virulence of Neospora caninum
Monireh Khordadmehr, Mehdi Namavari, Azizollah Khodakaram-Tafti, Maryam Mansourian, Abdollah Rahimian, Yahya Daneshbod
Research in Veterinary Science.2013; 95(2): 515. CrossRef
First molecular detection of Neospora caninum in European brown bear (Ursus arctos)
A. Čobádiová, B. Víchová, V. Majláthová, K. Reiterová
Veterinary Parasitology.2013; 197(1-2): 346. CrossRef
Flock-level risk factors associated with Neospora caninum seroprevalence in dairy goats in a semiarid region of Northeastern Brazil
C.S.A.B. Santos, S.S. Azevedo, H.S. Soares, S.S.S. Higino, F.A. Santos, M.L.C.R. Silva, H.F.J. Pena, C.J. Alves, S.M. Gennari
Small Ruminant Research.2013; 112(1-3): 239. CrossRef
Study on outbreak of Neospora caninum-associated abortion in dairy cows in Tabriz (Northwest Iran) by serological, molecular and histopathologic methods
A. Nematollahi, G.H. Moghaddam, R. Jaafari, J. Ashrafi Helan, M. Norouzi
Asian Pacific Journal of Tropical Medicine.2013; 6(12): 942. CrossRef
Neospora caninum NC-6 Argentina induces fetopathy in both serologically positive and negative experimentally inoculated pregnant dams
D. Bacigalupe, W. Basso, S. G. Caspe, G. Moré, L. Lischinsky, M. L. Gos, M. Leunda, L. Campero, D. P. Moore, G. Schares, C. M. Campero, M. C. Venturini
Parasitology Research.2013; 112(7): 2585. CrossRef
Dose-dependent immunogenicity of a soluble Neospora caninum tachyzoite-extract vaccine formulated with a soy lecithin/β-glucan adjuvant in cattle
F.C. Mansilla, W. Czepluch, D.A. Malacari, Y.P. Hecker, D. Bucafusco, O.L. Franco-Mahecha, D.P. Moore, A.V. Capozzo
Veterinary Parasitology.2013; 197(1-2): 13. CrossRef
Gene Cloning and Characterization of the Protein Encoded by theNeospora caninumBradyzoite-Specific Antigen GeneBag1
T. Kobayashi, S. Narabu, Y. Yanai, Y. Hatano, A. Ito, S. Imai, K. Ike
Journal of Parasitology.2013; 99(3): 453. CrossRef
Plasma Concentrations of Pregnancy‐Associated Glycoproteins Measured Using Anti‐Bovine PAG‐2 Antibodies on Day 120 of Gestation Predict Abortion in Dairy Cows Naturally Infected withNeospora caninum
I García‐Ispierto, S Almería, B Serrano, NM de Sousa, JF Beckers, F López‐Gatius
Reproduction in Domestic Animals.2013; 48(4): 613. CrossRef
A Review of Some Protozoan Parasites Causing Infertility in Farm Animals
B. Y. Kaltungo, I. W. Musa
ISRN Tropical Medicine.2013; 2013: 1. CrossRef
Seroprevalence and risk factors of Neospora spp. in donkeys from Southern Italy
T. Machačová, E. Bártová, A. Di Loria, K. Sedlák, J. Guccione, D. Fulgione, V. Veneziano
Veterinary Parasitology.2013; 198(1-2): 201. CrossRef
Screening for Toxoplasma gondii in aborted bovine fetuses in Brazil
A.D. Cabral, C.N. Camargo, N.T.C. Galleti, L.H. Okuda, E.M. Pituco, C. Del Fava
Arquivos do Instituto Biológico.2013; 80(1): 103. CrossRef
Abortos por Neosporacaninum em bovinos do sul de Minas Gerais
Débora R. Orlando, Rafael C. Costa, Bruno A. Soares, Natália S.C. Oliveira, Lismara C. Nascimento, Ana P. Peconick, Djeison L. Raymundo, Mary S. Varaschin
Pesquisa Veterinária Brasileira.2013; 33(11): 1332. CrossRef
First report of Neospora caninum infection in cattle in Sudan
Amira Mohamed Elhassan Ibrahim, Abdelghafar Mohamed Elfahal, Abdel Rahim Mohamed El Hussein
Tropical Animal Health and Production.2012; 44(4): 769. CrossRef
Seroprevalence and risk factors for Neospora caninum in sheep in the state Minas Gerais, southeastern Brazil
Gislaine da Silva Andrade, Fábio Raphael Pascoti Bruhn, Christiane Maria Barcellos Magalhãe Rocha, Alessandro de Sá Guimarães, Aurora Maria Guimarães Gouveia, Antônio Marcos Guimarães
Veterinary Parasitology.2012; 188(1-2): 168. CrossRef
Occurrence of Neospora caninum and Toxoplasma gondii infections in ovine and caprine abortions
B. Moreno, E. Collantes-Fernández, A. Villa, A. Navarro, J. Regidor-Cerrillo, L.M. Ortega-Mora
Veterinary Parasitology.2012; 187(1-2): 312. CrossRef
Seroprevalence of Neospora caninum in Stray Dogs of Tabriz, Iran
Garedaghi Yagoob
Journal of Animal and Veterinary Advances.2012; 11(6): 723. CrossRef
Seroprevalence of Toxoplasma gondii and Neospora caninum in dairy goats from Romania
Anamaria Iovu, Adriana Györke, Viorica Mircean, Raluca Gavrea, Vasile Cozma
Veterinary Parasitology.2012; 186(3-4): 470. CrossRef
Factors associated with infection by Neospora caninum in dogs in Brazil
Patrícia Mara Lopes Sicupira, Vanessa Carvalho Sampaio de Magalhães, Gideão da Silva Galvão, Maria Julia Salim Pereira, Luís Fernando Pita Gondim, Alexandre Dias Munhoz
Veterinary Parasitology.2012; 185(2-4): 305. CrossRef
Seroprevalence of Neospora caninum Infection on Dairy Cattle in Farms from Southern Romania
Ioan Liviu Mitrea, Violeta Enachescu, Ruxandra Radulescu, Mariana Ionita
Journal of Parasitology.2012; 98(1): 69. CrossRef
Potential involvement of Neospora caninum in naturally occurring ovine abortions in New Zealand
L. Howe, M.G. Collett, R.S. Pattison, J. Marshall, D.M. West, W.E. Pomroy
Veterinary Parasitology.2012; 185(2-4): 64. CrossRef
Seroprevalence of Toxoplasma gondii and Neospora caninum infection in dairy cows in subtropical southern China
M. J. XU, Q. Y. LIU, J. H. FU, A. J. NISBET, D. S. SHI, X. H. HE, Y. PAN, D. H. ZHOU, H. Q. SONG, X. Q. ZHU
Parasitology.2012; 139(11): 1425. CrossRef
Development of latex agglutination test with recombinant NcSAG1 for the rapid detection of antibodies to Neospora caninum in cattle
Marjan Moraveji, Arsalan Hosseini, Nasrin Moghaddar, Mohammad Mehdi Namavari, Mohammad Hadi Eskandari
Veterinary Parasitology.2012; 189(2-4): 211. CrossRef
Congenital Neosporosis in Goats from the State of Minas Gerais, Brazil
Mary S. Varaschin, Christian Hirsch, Flademir Wouters, Karen Y. Nakagaki, Antônio M. Guimarães, Domingos S. Santos, Pedro S. Bezerra, Rafael C. Costa, Ana P. Peconick, Ingeborg M. Langohr
The Korean Journal of Parasitology.2012; 50(1): 63. CrossRef
Characterization of Neospora caninum microneme protein 10 (NcMIC10) and its potential use as a diagnostic marker for neosporosis
Jigang Yin, Guanggang Qu, Lili Cao, Qichang Li, Raymond Fetterer, Xiaosheng Feng, Quan Liu, Guiping Wang, Dongmei Qi, Xichen Zhang, Eliseo Miramontes, Mark Jenkins, Naisheng Zhang, Wenbin Tuo
Veterinary Parasitology.2012; 187(1-2): 28. CrossRef
Immunohistochemical and polymerase chain reaction studies in Neospora caninum experimentally infected broiler chicken embryonated eggs
Azizollah Khodakaram-Tafti, Maryam Mansourian, Mehdi Namavari, Arsalan Hosseini
Veterinary Parasitology.2012; 188(1-2): 10. CrossRef
Neospora caninum in Estonian dairy herds in relation to herd size, reproduction parameters, bovine virus diarrhoea virus, and bovine herpes virus 1
Brian Lassen, Toomas Orro, Annely Aleksejev, Kerli Raaperi, Toivo Järvis, Arvo Viltrop
Veterinary Parasitology.2012; 190(1-2): 43. CrossRef
Seroprevalence of Toxoplasma gondii and Neospora caninum in dogs from Korea
Thuy Nguyen, Se-Eun Choe, Jae-Won Byun, Hong-Bum Koh, Hee-Soo Lee, Seung-Won Kang
Acta Parasitologica.2012;[Epub] CrossRef
Increased incidence of DNA amplification in follicular than in uterine and blood samples indicates possible tropism of Neospora caninum to the ovarian follicle
Andressa F. Silva, Lucia Rangel, Carlos Garcia Ortiz, Elizabeth Morales, Eraldo L. Zanella, Uziel Castillo-Velázquez, Carlos G. Gutierrez
Veterinary Parasitology.2012; 188(1-2): 175. CrossRef
Detection of Nesopora caninum-Specific DNA from Cerebrospinal Fluid by Polymerase Chain Reaction in a Dog with Confirmed Neosporosis
Kyohei ISHIGAKI, Masahiko NOYA, Yumiko KAGAWA, Kazunori IKE, Hiromitsu ORIMA, Soichi IMAI
Journal of Veterinary Medical Science.2012; 74(8): 1051. CrossRef
Molecular detection of Coxiella burnetii and Neospora caninum in equine aborted foetuses and neonates
Albertine Leon, Eric Richard, Christine Fortier, Claire Laugier, Guillaume Fortier, Stéphane Pronost
Preventive Veterinary Medicine.2012; 104(1-2): 179. CrossRef
Detection of specific antibodies anti-Neospora caninum in the fallow deer (Dama dama)
Justyna Bień, Bożena Moskwa, Marek Bogdaszewski, Władyslaw Cabaj
Research in Veterinary Science.2012; 92(1): 96. CrossRef
The importance of vertical transmission of Neospora sp. in naturally infected horses
Ana Maria Antonello, Felipe Lamberti Pivoto, Giovana Camillo, Patricia Braunig, Luis Antonio Sangioni, Endrigo Pompermayer, Fernanda Silveira Flores Vogel
Veterinary Parasitology.2012; 187(3-4): 367. CrossRef
Study of the risk factors associated with Neospora caninum seroprevalence in Algerian cattle populations
Farida Ghalmi, Bernard China, Asma Ghalmi, Darifa Hammitouche, Bertrand Losson
Research in Veterinary Science.2012; 93(2): 655. CrossRef
The immune enhancement of a novel soy lecithin/β-glucans based adjuvant on native Neospora caninum tachyzoite extract vaccine in mice
Florencia Celeste Mansilla, Olga Lucía Franco-Mahecha, María Ángeles Lavoria, Dadín Prando Moore, Adrián Nicolás Giraldez, Marcela Elvira Iglesias, Maximiliano Wilda, Alejandra Victoria Capozzo
Vaccine.2012; 30(6): 1124. CrossRef
Neospora caninum: A successful testing and eradication program in a dairy goat herd
Jennifer A. Altbuch, Michael J. Schofield, Catherine A. Porter, William G. Gavin
Small Ruminant Research.2012; 105(1-3): 341. CrossRef
Serological screening for Coxiella burnetii infection and related reproductive performance in high producing dairy cows
F. López-Gatius, S. Almeria, I. Garcia-Ispierto
Research in Veterinary Science.2012; 93(1): 67. CrossRef
Detection of Neospora sp. antibodies in cart horses from urban areas of Curitiba, Southern Brazil
Eliana Monteforte Cassaro Villalobos, Keiko Endo Furman, Maria do Carmo Custódio de Souza Hunold Lara, Elenice Maria Sequetin Cunha, Mariane Angélica Finger, Ana Paula Brenner Busch, Ivan Roque de Barros Filho, Ivan Deconto, Peterson Triches Dornbusch, Al
Revista Brasileira de Parasitologia Veterinária.2012; 21(1): 68. CrossRef
Detection and molecular analysis of Toxoplasma gondii and Neospora caninum from dogs with neurological disorders
Helio Langoni, Guilherme Matteucci, Bruno Medici, Lucilene Granuzio Camossi, Virgínia Bodelão Richini-Pereira, Rodrigo Costa da Silva
Revista da Sociedade Brasileira de Medicina Tropical.2012; 45(3): 365. CrossRef
Sheep abortion associated with Neospora caninum in Mato Grosso do Sul, Brazil
Ana Paula Pinto, Flávia B. Bacha, Bethania S. Santos, David Driemeier, Nadia A.B. Antoniassi, Nickolly L.K. de Sá Ribas, Ricardo A.A. Lemos
Pesquisa Veterinária Brasileira.2012; 32(8): 739. CrossRef
Seroprevalence of antibodies to Neospora caninum in dogs in the state of Alagoas, Brazil
Maria Evódia de Sousa, Wagnner José Nascimento Porto, Pedro Paulo Feitosa de Albuquerque, Orestes Luiz de Souza Neto, José Wilton Pinheiro Júnior, Rinaldo Aparecido Mota
Revista Brasileira de Parasitologia Veterinária.2012; 21(3): 287. CrossRef
Quantification of vertical transmission of Neospora caninum in dairy cows in Minas Gerais, Brazil
Raquel Ribeiro Dias Santos, Christiane Maria Barcellos Magalhães da Rocha, Tarcísio de Morais Gonçalves, Antônio Marcos Guimarães
Revista Brasileira de Parasitologia Veterinária.2012; 21(3): 294. CrossRef
Neospora caninum em bovinos em matadouros de Pernambuco e Alagoas
Rodolfo L.G. Amaral, Leonildo B.G. Silva, José W. Pinheiro Júnior, Orestes L. Souza Neto, Carlos A.S. Leal, Wagnner J.N. Porto, José M.P. Barbosa, Rinaldo A. Mota
Pesquisa Veterinária Brasileira.2012; 32(10): 953. CrossRef
Toxoplasma gondii and Neospora caninum antibodies in goats in the Czech Republic
E. Bartova, K. Sedlak
Veterinární medicína.2012; 57(3): 111. CrossRef
Vaccines against a Major Cause of Abortion in Cattle, Neospora caninum Infection
Thierry Monney, Karim Debache, Andrew Hemphill
Animals.2011; 1(3): 306. CrossRef
Identification of a gene cluster for cell-surface genes of the SRS superfamily inNeospora caninumand characterization of the novelSRS9gene
V. RISCO-CASTILLO, V. MARUGÁN-HERNÁNDEZ, A. FERNÁNDEZ-GARCÍA, A. AGUADO-MARTÍNEZ, E. JIMÉNEZ-RUIZ, S. RODRÍGUEZ-MARCO, G. ÁLVAREZ-GARCÍA, L. M. ORTEGA-MORA
Parasitology.2011; 138(14): 1832. CrossRef
Transplacental transmission in cattle: is Toxoplasma gondii less potent than Neospora caninum?
Jitbanjong Wiengcharoen, R. C. Andrew Thompson, Chawalit Nakthong, Parntep Rattanakorn, Yaowalark Sukthana
Parasitology Research.2011; 108(5): 1235. CrossRef
First in vitro isolation of Neospora caninum from a naturally infected adult dairy cow in Slovakia
Katar?na Reiterov?, Silvia ?pilovsk?, Andrea ?ob?diov?, Rastislav Mucha
Acta Parasitologica.2011;[Epub] CrossRef
Seroprevalence of Neospora caninum Infection in Dairy Cattle of Southern China
Hui-Yan Xia, Dong-Hui Zhou, Kun Jia, Xian-Bin Zeng, Dun-Wei Zhang, Li-Xuan She, Rui-Qing Lin, Zi-Guo Yuan, Shou-Jun Li, Xing-Quan Zhu
Journal of Parasitology.2011; 97(1): 172. CrossRef
Transgenic Neospora caninum strains constitutively expressing the bradyzoite NcSAG4 protein proved to be safe and conferred significant levels of protection against vertical transmission when used as live vaccines in mice
V. Marugán-Hernández, L.M. Ortega-Mora, A. Aguado-Martínez, E. Jiménez-Ruíz, G. Álvarez-García
Vaccine.2011; 29(44): 7867. CrossRef
Seroprevalence and risk factors associated with neosporosis in sheep and dogs from farms
Gustavo Puglia Machado, Mariana Kikuti, Helio Langoni, Antonio Carlos Paes
Veterinary Parasitology.2011; 182(2-4): 356. CrossRef
Prevalence of antibodies against Neospora caninum in dogs from urban areas in Central Poland
Katarzyna Goździk, Robert Wrzesień, Adrianna Wielgosz-Ostolska, Justyna Bień, Monika Kozak-Ljunggren, Władysław Cabaj
Parasitology Research.2011; 108(4): 991. CrossRef
Toxoplasma gondii and Neospora caninum in wildlife: Common parasites in Belgian foxes and Cervidae?
S. De Craeye, N. Speybroeck, D. Ajzenberg, M.L. Dardé, F. Collinet, P. Tavernier, S. Van Gucht, P. Dorny, K. Dierick
Veterinary Parasitology.2011; 178(1-2): 64. CrossRef
Evaluation of Toxoplasma gondii and Neospora caninum infections in sheep from Uberlândia, Minas Gerais State, Brazil, by different serological methods
G.F. Rossi, D.D. Cabral, D.P. Ribeiro, A.C.A.M. Pajuaba, R.R. Corrêa, R.Q. Moreira, T.W.P. Mineo, J.R. Mineo, D.A.O. Silva
Veterinary Parasitology.2011; 175(3-4): 252. CrossRef
A mixture model for the detection ofNeosporosiswithout a gold standard
Andrés Farall, Ricardo Maronna, Tomás Tetzlaff
Journal of Applied Statistics.2011; 38(5): 913. CrossRef
What is your diagnosis? Fine‐needle aspirate of ulcerative skin lesions in a dog
Aradhana Gupta, Shannon Stroup, Andrea Dedeaux, Rudy W. Bauer, Stephen D. Gaunt
Veterinary Clinical Pathology.2011; 40(3): 401. CrossRef
Endogenous Transplacental Transmission of Neospora hughesi in Naturally Infected Horses
N. Pusterla, P. A. Conrad, A. E. Packham, S. M. Mapes, C. J. Finno, I. A. Gardner, B. C. Barr, G. L. Ferraro, W. D. Wilson
Journal of Parasitology.2011; 97(2): 281. CrossRef
Serological profile of Toxoplasma gondii and Neospora caninum infection in commercial sheep from São Paulo State, Brazil
Helio Langoni, Haroldo Greca, Felipe F. Guimarães, Leila S. Ullmann, Fernanda C. Gaio, Robson S. Uehara, Eric P. Rosa, Rogério M. Amorim, Rodrigo C. Da Silva
Veterinary Parasitology.2011; 177(1-2): 50. CrossRef
Seroprevalence of antibodies to Neospora caninum in cattle at Seoul slaughtering center
Jee-Eun Kim, Jang-Won Son, Yun-Mo Yang, Hae-Chang Jeon, Kyung-Sun Jin, Kyu-Hyun Kim, Bang-Woo Shin, Jung-Hark Lee
Korean Journal of Veterinary Service.2011; 34(2): 179. CrossRef
Seroprevalence of Toxoplasma gondii and Neospora caninum infections in goats in Poland
Michał Czopowicz, Jarosław Kaba, Olga Szaluś-Jordanow, Mariusz Nowicki, Lucjan Witkowski, Tadeusz Frymus
Veterinary Parasitology.2011; 178(3-4): 339. CrossRef
Evidence of congenital transmission of Neospora caninum in naturally infected water buffalo (Bubalus bubalis) fetus from Brazil
Andreas L. Chryssafidis, Rodrigo M. Soares, Aline A. R. Rodrigues, Nelcio A. T. Carvalho, Solange Maria Gennari
Parasitology Research.2011; 108(3): 741. CrossRef
Prevalence of infectious agents in cattle reared in Ulleung island
Min-Goo Seo, Jae-Cheul Do, In-Ohk Ouh, Min-Hee Coh, Joong-Kew Kim, Young-Hoan Kim, No-Chan Park, Dong-Mi Kwak
Korean Journal of Veterinary Service.2011; 34(4): 303. CrossRef
Neosporosis in animals—The last five years
J.P. Dubey, G. Schares
Veterinary Parasitology.2011; 180(1-2): 90. CrossRef
Identification of Novel Proteins in Neospora caninum Using an Organelle Purification and Monoclonal Antibody Approach
Catherine S. Sohn, Tim T. Cheng, Michael L. Drummond, Eric D. Peng, Sarah J. Vermont, Dong Xia, Stephen J. Cheng, Jonathan M. Wastling, Peter J. Bradley, Gordon Langsley
PLoS ONE.2011; 6(4): e18383. CrossRef
Fatores associados a soroprevalência de Neospora caninum e Toxoplasma gondii em rebanhos caprinos na região sul de Minas Gerais
Mary S. Varaschin, Antônio M. Guimarães, Christian Hirsch, Leonardo P. Mesquita, Camila C. Abreu, Christiane M.B.M. Rocha, Flademir Wouters, Moisés C. Moreira
Pesquisa Veterinária Brasileira.2011; 31(1): 53. CrossRef
Pesquisa de anticorpos anti-Neospora spp. e anti-herpersvírus equino em cavalos de tração no município de Santa Maria, RS, Brasil
Luís Antonio Sangioni, Sônia de Avila Botton, Juliana Felipetto Cargnelutti, Gustavo Cauduro Cadore, Alfredo Skrebsky Cezar, Rudi Weiblen, Sonia Terezinha Anjos Lopes, Fernanda Silveira Flores Vogel
Ciência Rural.2011; 41(2): 321. CrossRef
Neospora caninum in bovine fetuses of Minas Gerais, Brazil: genetic characteristics of rDNA
Domingos Sávio dos Santos, Michele Placedino Andrade, Mary Suzan Varaschin, Antônio Marcos Guimarães, Christian Hirsch
Revista Brasileira de Parasitologia Veterinária.2011; 20(4): 281. CrossRef
Occurrence of anti-Neospora caninum and anti-Toxoplasma gondii IgG antibodies in goats and sheep in western Maranhão, Brazil
Larissa Martins de Brito Moraes, Juliana Macedo Raimundo, Andresa Guimarães, Huarrisson Azevedo Santos, Gilberto de Lima Macedo Junior, Carlos Luiz Massard, Rosangela Zacarias Machado, Cristiane Divan Baldani
Revista Brasileira de Parasitologia Veterinária.2011; 20(4): 312. CrossRef
Reação de imunofluorescência indireta para detecção de anticorpos anti-Neospora caninum em amostras coletivas de leite
Giovana Camillo, Ana Maria Antonello, Gabriel Ribas Pereira, Paulo Bayard Dias Gonçalves, Luís Antônio Sangioni, Lilian Muller, Fernanda Silveira Flores Vogel
Ciência Rural.2011; 41(9): 1600. CrossRef
Detecção de anticorpos anti-Neospora caninum em amostras individuais e coletivas de leite de bovinos pela reação de imunofluorescência indireta
Giovana Camillo, Alfredo Skrebsky Cezar, Ana Maria Antonello, Luís Antônio Sangioni, Eduardo Furtado Flores, Gabriel Ribas Pereira, Paulo Bayard Dias Gonçalves, Fernanda Silveira Flôres Vogel
Pesquisa Veterinária Brasileira.2011; 31(6): 482. CrossRef
Occurrence of antibodies against Neospora caninum and/or Toxoplasma gondii in dogs with neurological signs
Nicolle Fridlund Plugge, Fabiano Montiani Ferreira, Rosária Regina Tesoni de Barros Richartz, Adriana de Siqueira, Rosangela Locatelli Dittrich
Revista Brasileira de Parasitologia Veterinária.2011; 20(3): 202. CrossRef
Serological survey of Neospora caninum in small ruminants from Pernambuco State, Brazil
Antonio Amélia Santos Mucalane Tembue, Rafael Antonio de Nascimento Ramos, Thais Rabelo de Sousa, Alessandra Ribeiro Albuquerque, Alvimar José da Costa, Isabelle Maria Jaqueline Meunier, Maria Aparecida da Gloria Faustino, Leucio Câmara Alves
Revista Brasileira de Parasitologia Veterinária.2011; 20(3): 246. CrossRef
CONSTRUÇÃO DE UM INDICADOR QUANTITATIVO (STATUS DE SAÚDE) PARA AVALIAÇÃO DA QUALIDADE DE SAÚDE ANIMAL DE PROPRIEDADES RURAIS
C.R. Padovani, A.V.M Stachissini, H.F. da Costa, F.F. Aragon, J.R. Modolo
Arquivos do Instituto Biológico.2011; 78(3): 359. CrossRef
SEROPREVALENCE AND RISK FACTORS ASSOCIATED TO NEOSPORA CANINUM IN FEMALE BOVINES FROM THE WESTERN SÃO PAULO STATE, BRAZIL
D.M. Aguiar, D.P Lacerda, R.C. Orlandelli, A.O. Medina, S.S Azevedo, L.H. Okuda, V. Castro, M.E. Genovez, E.M. Pituco
Arquivos do Instituto Biológico.2011; 78(2): 183. CrossRef
Histopathologic Observation of the Aborted Fetus from Pregnant Dairy Cows Naturally Infected with Neospora caninum
Jeong-Hoon Son, Sung-Whan Cho
Journal of Life Science.2010; 20(10): 1556. CrossRef
Prevalence of antibodies to Neospora caninum in stray dogs of Urmia, Iran
Mohammad Yakhchali, Shahram Javadi, Ahmad Morshedi
Parasitology Research.2010; 106(6): 1455. CrossRef
First identification of Neospora caninum by PCR in aborted bovine foetuses in Romania
Ovidiu Şuteu, Adriana Titilincu, David Modrý, Andrei Mihalca, Viorica Mircean, Vasile Cozma
Parasitology Research.2010; 106(3): 719. CrossRef
Clinical neosporosis in three dogs in Shahrekord, Iran
Morteza Hosseininejad, Abdolali Malmasi
Comparative Clinical Pathology.2010; 19(3): 315. CrossRef
In vitro isolation and identification of the first Neospora caninum isolate from European bison (Bison bonasus bonasus L.)
Justyna Bień, Bożena Moskwa, Władysław Cabaj
Veterinary Parasitology.2010; 173(3-4): 200. CrossRef
Detection of Toxoplasma gondii, Neospora caninum, and Encephalitozoon cuniculi in the brains of common voles (Microtus arvalis) and water voles (Arvicola terrestris) by gene amplification techniques in western Austria (Vorarlberg)
Hans-Peter Fuehrer, Ingrid Blöschl, Christian Siehs, Andreas Hassl
Parasitology Research.2010; 107(2): 469. CrossRef
CASE REPORT: Detection of Neospora caninum tachyzoites in cerebrospinal fluid of a dog following prednisone and cyclosporine therapy
Bradley I. Galgut, Kyathanahalli S. Janardhan, Tanya M. Grondin, Kenneth R. Harkin, Mary T. Wight-Carter
Veterinary Clinical Pathology.2010; 39(3): 386. CrossRef
The first report of ovine cerebral neosporosis and evaluation of Neospora caninum prevalence in sheep in New South Wales
Stephanie Bishop, Jessica King, Peter Windsor, Michael P. Reichel, John Ellis, Jan Šlapeta
Veterinary Parasitology.2010; 170(1-2): 137. CrossRef
The prevalence and spatial clustering of Neospora caninum in dairy herds in Norway
S. Klevar, M. Norström, J. Tharaldsen, T. Clausen, C. Björkman
Veterinary Parasitology.2010; 170(1-2): 153. CrossRef
Investigation of Neospora caninum, Hammondia sp., and Toxoplasma gondii in tissues from slaughtered beef cattle in Bahia, Brazil
Sara Lima Santos, Kattyanne de Souza Costa, Leane Queiroz Gondim, Mariana Sampaio Anares da Silva, Rosângela Soares Uzêda, Kiyoko Abe-Sandes, Luís Fernando Pita Gondim
Parasitology Research.2010; 106(2): 457. CrossRef
A second generation multiplex PCR for typing strains of Neospora caninum using six DNA targets
Sarwat Al-Qassab, Michael P. Reichel, John Ellis
Molecular and Cellular Probes.2010; 24(1): 20. CrossRef
Neospora caninum and coxiella burnetii seropositivity are related to endocrine pattern changes during gestation in lactating dairy cows
I. García-Ispierto, C. Nogareda, J.L. Yániz, S. Almería, D. Martínez-Bello, N.M. de Sousa, J.F. Beckers, F. López-Gatius
Theriogenology.2010; 74(2): 212. CrossRef
Neospora caninum: In vitro culture of tachyzoites in MCF-7 human breast carcinoma cells
Qiang Lv, Jianhua Li, Pengtao Gong, Shenyang Xing, Xichen Zhang
Experimental Parasitology.2010; 126(4): 536. CrossRef
Roles of CD122+ Cells in Resistance against Neospora caninum Infection in a Murine Model
Yoshifumi NISHIKAWA, Houshuang ZHANG, Hany M. IBRAHIM, Kyoko YAMADA, Hideyuki NAGASAWA, Xuenan XUAN
Journal of Veterinary Medical Science.2010; 72(10): 1275. CrossRef
Neospora caninum: Early immune response of rat mixed glial cultures after tachyzoites infection
A.M. Pinheiro, S.L. Costa, S.M. Freire, C.S.O. Ribeiro, M. Tardy, R.S. El-Bachá, M.F.D. Costa
Experimental Parasitology.2010; 124(4): 442. CrossRef
Plasmacytoid and conventional dendritic cells are early producers of IL‐12 inNeospora caninum‐infected mice
Luzia Teixeira, Ana Sofia Botelho, Sandro Dá Mesquita, Alexandra Correia, Filipe Cerca, Renata Costa, Paula Sampaio, António Gil Castro, Manuel Vilanova
Immunology & Cell Biology.2010; 88(1): 79. CrossRef
Neospora caninum and Toxoplasma gondii antibodies in European brown hares in the Czech Republic, Slovakia and Austria
Eva Bártová, Kamil Sedlák, František Treml, Ivan Holko, Ivan Literák
Veterinary Parasitology.2010; 171(1-2): 155. CrossRef
Neospora caninum: Application of apical membrane antigen 1 encapsulated in the oligomannose-coated liposomes for reduction of offspring mortality from infection in BALB/c mice
Houshuang Zhang, Yoshifumi Nishikawa, Junya Yamagishi, Jinlin Zhou, Yuzuru Ikehara, Naoya Kojima, Naoaki Yokoyama, Xuenan Xuan
Experimental Parasitology.2010; 125(2): 130. CrossRef
Seroprevalence of Neospora caninum infection in dogs in Chaharmahal-va-Bakhtiari Province, Iran
M. Hosseininejad, F. Hosseini, M. Mahzounieh, A. Raisi Nafchi, M. Mosharraf
Comparative Clinical Pathology.2010; 19(3): 269. CrossRef
Abortions in bovines and Neospora caninum transmission in an embryo transfer center
Vanessa Silvestre Ferreira de Oliveira, Gema Álvarez-Garcia, Luis Miguel Ortega-Mora, Lígia Miranda Ferreira Borges, Andréa Caetano da Silva
Veterinary Parasitology.2010; 173(3-4): 206. CrossRef
A survey of Neospora caninum-associated bovine abortion in large dairy farms of Mashhad, Iran
G R Razmi, H Zarea, Z Naseri
Parasitology Research.2010; 106(6): 1419. CrossRef
Flock-level seroprevalence of, and risk factors for, Neospora caninum among sheep and goats in northern Jordan
Mahmoud N. Abo-Shehada, Marwan M. Abu-Halaweh
Preventive Veterinary Medicine.2010; 93(1): 25. CrossRef
Neospora spp. and Toxoplasma gondii antibodies in horses in the Czech Republic
Eva Bártová, Kamil Sedlák, Michaela Syrová, Ivan Literák
Parasitology Research.2010; 107(4): 783. CrossRef
On the Biological and Genetic Diversity in Neospora caninum
Sarwat E. Al-Qassab, Michael P. Reichel, John T. Ellis
Diversity.2010; 2(3): 411. CrossRef
Anticorpos anti-Neospora caninum em bovinos de leite do sudoeste do estado do Paraná
G Camillo, G Cadore, A.S Cezar, G Toscan, P Bräunig, L.A Sangioni, F.S.F Vogel
Arquivo Brasileiro de Medicina Veterinária e Zootecnia.2010; 62(6): 1511. CrossRef
IgM e IgG como marcadores da infecção transplacentária por Neospora caninum em fetos bovinos
Gustavo C. Cadore, Fernanda S.F. Vogel, Luis Antonio Sangioni, Hilda F.J. Pena, Solange M. Gennari
Pesquisa Veterinária Brasileira.2010; 30(7): 551. CrossRef
Prevalência de anticorpos anti-Neospora caninum (Apicomplexa: Sarcocystidae) em bovinos leiteiros de propriedades rurais em três microrregiões no estado do Maranhão
Whaubtyfran C. Teixeira, Rosângela S. Uzêda, Luís F.P. Gondim, Maria I.S. Silva, Helder M. Pereira, Leucio C. Alves, Maria A.G. Faustino
Pesquisa Veterinária Brasileira.2010; 30(9): 729. CrossRef
Prevalence of Neospora caninum antibodies in sheep flocks of Uberlândia county, MG
Sandra Renata Sampaio Salaberry, Liria Hiromi Okuda, Alessandra Figueiredo de Castro Nassar, Jacqueline Ribeiro de Castro, Anna Monteiro Correia Lima-Ribeiro
Revista Brasileira de Parasitologia Veterinária.2010; 19(3): 148. CrossRef
Anticorpos IgG anti-Neospora caninum e Toxoplasma gondii em búfalas (Bubalus bubalis) criadas no estado do Pará
Sandro P. Silva, Rinaldo A. Mota, Eduardo B. Faria, Erika F.T.S. Fernandes, Orestes L.S. Neto, Pedro P.F. Albuquerque, Hilma L.T. Dias
Pesquisa Veterinária Brasileira.2010; 30(5): 443. CrossRef
Some Factors Affecting the Abortion Rate in Dairy Herds with High Incidence ofNeospora-Associated Abortions are Different in Cows and Heifers
JL Yániz, F López-Gatius, I García-Ispierto, G Bech-Sàbat, B Serrano, C Nogareda, JA Sanchez-Nadal, S Almeria, P Santolaria
Reproduction in Domestic Animals.2009;[Epub] CrossRef
Seroprevalence of Neospora caninum in dairy cattle ranches with high abortion rate: Special emphasis to serologic co-existence with Toxoplasma gondii, Brucella abortus and Listeria monocytogenes
Kader Yildiz, Oguz Kul, Cahit Babur, Selcuk Kılıc, Aycan N. Gazyagcı, Bekir Celebi, I. Safa Gurcan
Veterinary Parasitology.2009; 164(2-4): 306. CrossRef
Seroprevalence and spatial distribution of Neospora caninum in a population of beef cattle
Mélanie Loobuyck, Jenny Frössling, Ann Lindberg, Camilla Björkman
Preventive Veterinary Medicine.2009; 92(1-2): 116. CrossRef
Early postabortion recovery of Neospora-infected lactating dairy cows
P. Santolaria, F. López-Gatius, J. Yániz, I. García-Ispierto, C. Nogareda, G. Bech-Sàbat, B. Serrano, S. Almeria
Theriogenology.2009; 72(6): 798. CrossRef
Detection of Neospora caninum from Farm-Bred Young Blue Foxes (Alopex lagopus) in China
XiuLing YU, NanHua CHEN, DongMei HU, Wei ZHANG, XiaoXia LI, BaoYue WANG, LiPing KANG, XiangDong LI, Qun LIU, KeGong TIAN
Journal of Veterinary Medical Science.2009; 71(1): 113. CrossRef
Genetic diversity amongst isolates of Neospora caninum, and the development of a multiplex assay for the detection of distinct strains
S. Al-Qassab, M.P. Reichel, A. Ivens, J.T. Ellis
Molecular and Cellular Probes.2009; 23(3-4): 132. CrossRef
Bibliometric Analysis of the Korean Journal of Parasitology: Measured from SCI, PubMed, Scopus, and Synapse Databases
Choon Shil Lee
The Korean Journal of Parasitology.2009; 47(Suppl): S155. CrossRef
Neospora caninum, potential cause of abortions in dairy cows: The current serological follow-up in Slovakia
K. Reiterová, S. Špilovská, D. Antolová, P. Dubinský
Veterinary Parasitology.2009; 159(1): 1. CrossRef
Infectious Neuromuscular Diseases of Dogs and Cats
Mark T. Troxel
Topics in Companion Animal Medicine.2009; 24(4): 209. CrossRef
The development of immune responses in Balb/c mice following inoculation with attenuated or virulentNeospora caninumtachyzoites
P. M. BARTLEY, S. E. WRIGHT, S. W. MALEY, D. BUXTON, M. NATH, E. A. INNES
Parasite Immunology.2009; 31(7): 392. CrossRef
Neospora caninum associated with epidemic abortions in dairy cattle: The first clinical neosporosis report in Turkey
Oğuz Kul, Nalan Kabakci, Kader Yildiz, Naci Öcal, Hakan Kalender, N. Aycan İlkme
Veterinary Parasitology.2009; 159(1): 69. CrossRef
Detection ofNeospora caninumin aborted bovine fetuses and dam blood samples by nested PCR and ELISA and seroprevalence in Beijing and Tianjin, China
L. YAO, N. YANG, Q. LIU, M. WANG, W. ZHANG, W. F. QIAN, Y. F. HU, J. DING
Parasitology.2009; 136(11): 1251. CrossRef
Effects of crossbreed pregnancies on the abortion risk of Neospora caninum-infected dairy cows
S. Almería, F. López-Gatius, I. García-Ispierto, C. Nogareda, G. Bech-Sàbat, B. Serrano, P. Santolaria, J.L. Yániz
Veterinary Parasitology.2009; 163(4): 323. CrossRef
Toltrazuril treatment of congenitally acquired Neospora caninum infection in newborn mice
M. Strohbusch, N. Müller, A. Hemphill, R. Krebber, G. Greif, B. Gottstein
Parasitology Research.2009; 104(6): 1335. CrossRef
Factors affecting plasma prolactin concentrations throughout gestation in high producing dairy cows
I. García-Ispierto, F. López-Gatius, S. Almería, J. Yániz, P. Santolaria, B. Serrano, G. Bech-Sàbat, C. Nogareda, J. Sulon, N.M. de Sousa, J.F. Beckers
Domestic Animal Endocrinology.2009; 36(2): 57. CrossRef
Toxoplasmosis and Other Intestinal Coccidial Infections in Cats and Dogs
J.P. Dubey, David S. Lindsay, Michael R. Lappin
Veterinary Clinics of North America: Small Animal Practice.2009; 39(6): 1009. CrossRef
Evaluation of a SRS2 Sandwich Commercial Enzyme-Linked Immunosorbent Assay for the Detection of Anti-Neospora Caninum Antibodies in Bovine and Canine Sera
Farida Ghalmi, Bernard China, Rachid Kaidi, Bertrand Losson
Journal of Veterinary Diagnostic Investigation.2009; 21(1): 108. CrossRef
Neospora caninum seropositivity in cattle breeds in the South Fluminense Paraíba Valley, state of Rio de Janeiro
Alexandre D. Munhoz, Maria Júlia S. Pereira, Walter Flausino, Carlos Wilson G. Lopes
Pesquisa Veterinária Brasileira.2009; 29(1): 29. CrossRef
Suscetibilidade de linhagens celulares e cultivos primários ao Neospora caninum
Gustavo Cauduro Cadore, Fernanda Silveira Flores Vogel, Eduardo Furtado Flores, Luis Antônio Sangioni, Giovana Camillo
Ciência Rural.2009; 39(5): 1581. CrossRef
Protozoal Hepatitis Associated with Immunosuppressive Therapy in a Dog
D.R. Fry, K.D. McSporran, J.T. Ellis, C. Harvey
Journal of Veterinary Internal Medicine.2009; 23(2): 366. CrossRef
Indoleamine 2,3-Dioxygenase Is Involved in Defense againstNeospora caninumin Human and Bovine Cells
Katrin Spekker, Markus Czesla, Vanessa Ince, Kathrin Heseler, Silvia K. Schmidt, Gereon Schares, Walter Däubener
Infection and Immunity.2009; 77(10): 4496. CrossRef
Seroprevalence of Neospora caninum in dogs in south-western Poland
Katarzyna Płoneczka, Michał Mazurkiewicz
Veterinary Parasitology.2008; 153(1-2): 168. CrossRef
Seroepidemiology of Neospora caninum and Toxoplasma gondii infection in yaks (Bos grunniens) in Qinghai, China
J. Liu, J.Z. Cai, W. Zhang, Q. Liu, D. Chen, J.P. Han, Q.R. Liu
Veterinary Parasitology.2008; 152(3-4): 330. CrossRef
The role of Neospora caninum in three cases of unexplained ewe abortions in the southern North Island of New Zealand
L. Howe, D.M. West, M.G. Collett, G. Tattersfield, R.S. Pattison, W.E. Pomroy, P.R. Kenyon, S.T. Morris, N.B. Williamson
Small Ruminant Research.2008; 75(2-3): 115. CrossRef
NcGRA2as a molecular target to assess the parasiticidal activity of toltrazuril againstNeospora caninum
M. STROHBUSCH, N. MÜLLER, A. HEMPHILL, G. GREIF, B. GOTTSTEIN
Parasitology.2008; 135(9): 1065. CrossRef
Seroepidemiological study of Neospora caninum infection in dogs found in dairy farms and urban areas of Aguascalientes, Mexico
C. Cruz-Vázquez, L. Medina-Esparza, A. Marentes, E. Morales-Salinas, Z. Garcia-Vázquez
Veterinary Parasitology.2008; 157(1-2): 139. CrossRef
Population Structure of Toxoplasma gondii: Clonal Expansion Driven by Infrequent Recombination and Selective Sweeps
L. David Sibley, James W. Ajioka
Annual Review of Microbiology.2008; 62(1): 329. CrossRef
Generation and infection of bovine PBMC-derived dendritic cells with Neospora caninum
G. Grandi, C. Genchi, C. Bazzocchi, M. Mortarino, P. Borghetti, E. De Angelis, L. H. Kramer
Veterinary Research Communications.2008; 32(S1): 207. CrossRef
Freqüência de anticorpos anti-Neospora caninum em soros de caprinos do estado de São Paulo e sua relação com o manejo dos animais
José R. Modolo, Anee V.M. Stachissini, Solange M. Gennari, Jitender P. Dubey, Helio Langoni, Carlos R. Padovani, Lígia V. Barrozo, Bárbara L.S. Leite
Pesquisa Veterinária Brasileira.2008; 28(12): 597. CrossRef
Frequency of antibodies against Neospora caninum in stray and domiciled dogs from urban, periurban and rural areas from Paraná State, Southern Brazil
Nicolle Fridlund-Plugge, Fabiano Montiani-Ferreira, Rosária R. T. B. Richartz, Juliano Dal Pizzol, Pedro C. Machado Jr, Lia F. L. Patrício, Adriana S. Rosinelli, Rosangela Locatelli-Dittrich
Revista Brasileira de Parasitologia Veterinária.2008; 17(4): 222. CrossRef
Serological Survey of Neospora caninum Infection among Dogs in Japan through Species-Specific ELISA
Naoki KUBOTA, Yoshimi SAKATA, Naomi MIYAZAKI, Kazuhito ITAMOTO, Hiroshi BANNAI, Yoshifumi NISHIKAWA, Xuenan XUAN, Hisashi INOKUMA
Journal of Veterinary Medical Science.2008; 70(8): 869. CrossRef
Serological evidence of Neospora caninum infections in goats from La Rioja Province, Argentina
D.P. Moore, M.G. de Yaniz, A.C. Odeón, D. Cano, M.R. Leunda, E.A.J. Späth, C.M. Campero
Small Ruminant Research.2007; 73(1-3): 256. CrossRef
Presence of Neospora caninum specific antibodies in three dairy farms in Georgia and two in Texas
Ynes R. Ortega, Maria P. Torres, Kristina D. Mena
Veterinary Parasitology.2007; 144(3-4): 353. CrossRef
Survey of Neospora caninum and bovine herpes virus 1 coinfection in cattle
L. Rinaldi, F. Pacelli, G. Iovane, U. Pagnini, V. Veneziano, G. Fusco, G. Cringoli
Parasitology Research.2007; 100(2): 359. CrossRef
From dog to man: The broad spectrum of inflammatory myopathies
G. Diane Shelton
Neuromuscular Disorders.2007; 17(9-10): 663. CrossRef
Histopathological and immunohistochemical aspects of Neospora caninum diagnosis in bovine aborted fetuses
C.A. Pescador, L.G. Corbellini, E.C. Oliveira, D.L. Raymundo, D. Driemeier
Veterinary Parasitology.2007; 150(1-2): 159. CrossRef
Isolation of Neospora caninum from dairy zero grazing cattle in Israel
L. Fish, M. Mazuz, T. Molad, I. Savitsky, V. Shkap
Veterinary Parasitology.2007; 149(3-4): 167. CrossRef
Loss of infectivity of Neospora caninum oocysts maintained for a prolonged time
Rosangela Soares Uzeda, Kattyanne De Souza Costa, Sara Lima Santos, Alexandre Moraes Pinheiro, Maria Angela Ornelas De Almeida, Milton M. McAllister, Luis Fernando Pita Gondim
The Korean Journal of Parasitology.2007; 45(4): 295. CrossRef
Seroprevalence of Neospora caninum infection in dogs from rural and urban environments in Tehran, Iran
H. R. Haddadzadeh, A. Sadrebazzaz, A. Malmasi, H. Talei Ardakani, P. Khazraii Nia, N. Sadreshirazi
Parasitology Research.2007; 101(6): 1563. CrossRef
Seroprevalence of Antibodies toNeospora caninumin Urban and Rural Dogs in north‐west Italy
E. Ferroglio, M. Pasino, F. Ronco, A. Benà, A. Trisciuoglio
Zoonoses and Public Health.2007; 54(3-4): 135. CrossRef
The host-parasite relationship in pregnant cattle infected withNeospora caninum
ELISABETH A. INNES
Parasitology.2007; 134(13): 1903. CrossRef
Neosporosis in Beagle dogs: Clinical signs, diagnosis, treatment, isolation and genetic characterization of Neospora caninum
J.P. Dubey, M.C.B. Vianna, O.C.H. Kwok, D.E. Hill, K.B. Miska, W. Tuo, G.V. Velmurugan, M. Conors, M.C. Jenkins
Veterinary Parasitology.2007; 149(3-4): 158. CrossRef
Evaluation of Neospora caninum and Toxoplasma gondii infections in alpaca (Vicugna pacos) and llama (Lama glama) aborted foetuses from Peru
E. Serrano-Martínez, E. Collantes-Fernández, A. Chávez-Velásquez, A. Rodríguez-Bertos, E. Casas-Astos, V. Risco-Castillo, R. Rosadio-Alcantara, L.M. Ortega-Mora
Veterinary Parasitology.2007; 150(1-2): 39. CrossRef
Dynamics of anti-Neospora caninum antibodies during gestation in chronically infected dairy cows
C. Nogareda, F. López-Gatius, P. Santolaria, I. García-Ispierto, G. Bech-Sàbat, M. Pabón, M. Mezo, M. Gonzalez-Warleta, J.A. Castro-Hermida, J. Yániz, S. Almeria
Veterinary Parasitology.2007; 148(3-4): 193. CrossRef
Neospora caninum detected in feral rodents
M.C. Jenkins, C. Parker, D. Hill, R.D. Pinckney, R. Dyer, J.P. Dubey
Veterinary Parasitology.2007; 143(2): 161. CrossRef
Evaluation of serological tests for the diagnosis of Neospora caninum infection in dogs: Optimization of cut off titers and inhibition studies of cross-reactivity with Toxoplasma gondii
Deise A.O. Silva, Janaína Lobato, Tiago W.P. Mineo, José R. Mineo
Veterinary Parasitology.2007; 143(3-4): 234. CrossRef
Plasma pregnancy-associated glycoprotein-1 (PAG-1) concentrations during gestation in Neospora-infected dairy cows
F. López-Gatius, J.M. Garbayo, P. Santolaria, J.L. Yániz, S. Almería, A. Ayad, N.M. de Sousa, J.F. Beckers
Theriogenology.2007; 67(3): 502. CrossRef
Prevalence of anti-Toxoplasma gondii and anti-Neospora caninum antibodies in goats slaughtered in the public slaughterhouse of Patos city, Paraíba State, Northeast region of Brazil
Eduardo B. Faria, Solange M. Gennari, Hilda F.J. Pena, Ana Célia R. Athayde, Maria Luana C.R. Silva, Sérgio S. Azevedo
Veterinary Parasitology.2007; 149(1-2): 126. CrossRef
Molecular characterisation of BSR4, a novel bradyzoite-specific gene from Neospora caninum
V. Risco-Castillo, A. Fernández-García, A. Zaballos, A. Aguado-Martínez, A. Hemphill, A. Rodríguez-Bertos, G. Álvarez-García, L.M. Ortega-Mora
International Journal for Parasitology.2007; 37(8-9): 887. CrossRef
Neosporosis and hammondiosis in dogs
M. P. Reichel, J. T. Ellis, J. P. Dubey
Journal of Small Animal Practice.2007; 48(6): 308. CrossRef
Serodiagnosis of Neospora caninum infection in cattle using a recombinant tNcSRS2 protein-based ELISA
Jing Liu, Jinshu Yu, Ming Wang, Qun Liu, Wei Zhang, Chong Deng, Jun Ding
Veterinary Parasitology.2007; 143(3-4): 358. CrossRef
Anti‐neosporal IgG and IgE antibodies in Canine Neosporosis
E. E. V. Jesus, M. A. O. Almeida, A. M. Atta
Zoonoses and Public Health.2007; 54(9-10): 387. CrossRef
Risk factors for canine neosporosis in farm and kennel dogs in southern Italy
Paola Paradies, Gioia Capelli, Gabriella Testini, Cinzia Cantacessi, Alexander J. Trees, Domenico Otranto
Veterinary Parasitology.2007; 145(3-4): 240. CrossRef
Characterization of the first Polish isolate of Neospora caninum from cattle
Katarzyna Goździk, Władysław Cabaj
Acta Parasitologica.2007;[Epub] CrossRef
Seroprevalence of Neospora caninum in non-carnivorous wildlife from Spain
S. Almería, D. Vidal, D. Ferrer, M. Pabón, M.I.G. Fernández-de-Mera, F. Ruiz-Fons, V. Alzaga, I. Marco, C. Calvete, S. Lavin, C. Gortazar, F. López-Gatius, J.P. Dubey
Veterinary Parasitology.2007; 143(1): 21. CrossRef
Experimental neosporosis in bulls: Parasite detection in semen and blood and specific antibody and interferon-gamma responses
E. Serrano-Martínez, I. Ferre, A. Martínez, K. Osoro, A. Mateos-Sanz, I. del-Pozo, G. Aduriz, C. Tamargo, C.O. Hidalgo, L.M. Ortega-Mora
Theriogenology.2007; 67(6): 1175. CrossRef
Neospora caninum: High susceptibility to the parasite in C57BL/10ScCr mice
A.S. Botelho, L. Teixeira, J.M. Correia-da-Costa, A.M.R. Faustino, A.G. Castro, M. Vilanova
Experimental Parasitology.2007; 115(1): 68. CrossRef
Seroprevalence of Neospora caninum in dairy goats from Bahia, Brazil
R.S. Uzêda, A.M. Pinheiro, S.Y. Fernández, M.C.C. Ayres, L.F.P. Gondim, M.A.O. Almeida
Small Ruminant Research.2007; 70(2-3): 257. CrossRef
The role of the colostrum and milk in Neospora caninum transmission
B. Moskwa, W. Cabaj
Helminthologia.2007; 44(3): 126. CrossRef
Intrauterine Neospora caninum inoculation of heifers and cows using contaminated semen with different numbers of tachyzoites
E. Serrano-Martínez, I. Ferre, K. Osoro, G. Aduriz, R.A. Mota, A. Martínez, I. del-Pozo, C.O. Hidalgo, L.M. Ortega-Mora
Theriogenology.2007; 67(4): 729. CrossRef
Analysis of the immune response to Neospora caninum in a model of intragastric infection in mice
L. TEIXEIRA, A. S. BOTELHO, A. R. BATISTA, C. S. MEIRELES, A. RIBEIRO, H. S. DOMINGUES, J. M. CORREIA DA COSTA, A. G. CASTRO, A. M. R. FAUSTINO, M. VILANOVA
Parasite Immunology.2007; 29(1): 23. CrossRef
First identification of Neospora caninum infection in aborted bovine foetuses in China
W. Zhang, C. Deng, Q. Liu, J. Liu, M. Wang, K.G. Tian, X.L. Yu, D.M. Hu
Veterinary Parasitology.2007; 149(1-2): 72. CrossRef
Protection against abortion linked to gamma interferon production in pregnant dairy cows naturally infected with Neospora caninum
F. López-Gatius, S. Almería, G. Donofrio, C. Nogareda, I. García-Ispierto, G. Bech-Sàbat, P. Santolaria, J.L. Yániz, M. Pabón, N.M. de Sousa, J.F. Beckers
Theriogenology.2007; 68(7): 1067. CrossRef
Natural killer cells act as early responders in an experimental infection with Neospora caninum in calves
Siv Klevar, Siri Kulberg, Preben Boysen, Anne K. Storset, Torfinn Moldal, Camilla Björkman, Ingrid Olsen
International Journal for Parasitology.2007; 37(3-4): 329. CrossRef
Immunogenicity and protective effect against murine cerebral neosporosis of recombinant NcSRS2 in different iscom formulations
Sunan Pinitkiatisakul, Mikaela Friedman, Maria Wikman, Jens G. Mattsson, Karin Lövgren-Bengtsson, Stefan Ståhl, Anna Lundén
Vaccine.2007; 25(18): 3658. CrossRef
Prevention of vertical transmission of Neospora caninum in C57BL/6 mice vaccinated with Brucella abortus strain RB51 expressing N. caninum protective antigens
Sheela Ramamoorthy, Neelima Sanakkayala, Ramesh Vemulapalli, Neeta Jain, David S. Lindsay, Gerhardt S. Schurig, Stephen M. Boyle, Nammalwar Sriranganathan
International Journal for Parasitology.2007; 37(13): 1531. CrossRef
Factors associated with variation in Neospora caninum bulk-milk S/P ratios in initially bulk-milk negative testing Dutch dairy herds
Chris J.M. Bartels, Gerdien van Schaik, Kees van Maanen, Willem Wouda, Thomas Dijkstra
Preventive Veterinary Medicine.2007; 81(4): 265. CrossRef
Prevalence of antibodies against Toxoplasma gondii and Neospora caninum in Hungarian red foxes (Vulpes vulpes)
Eva-Britt Jakubek, Robert Farkas, Vilmos Pálfi, Jens G. Mattsson
Veterinary Parasitology.2007; 144(1-2): 39. CrossRef
Isolation and molecular detection of Neospora caninum from naturally infected sheep from Brazil
H.F.J. Pena, R.M. Soares, A.M.A. Ragozo, R.M. Monteiro, L.E.O. Yai, S.M. Nishi, S.M. Gennari
Veterinary Parasitology.2007; 147(1-2): 61. CrossRef
Prevalence of anti-Neospora caninum antibodies in cattle from the state of Mato Grosso do Sul, Brazil
Leandra M. Oshiro, Maria de Fatima C. Matos, Jacqueline M. de Oliveira, Letícia A.R.C. Monteiro, Renato Andreotti
Revista Brasileira de Parasitologia Veterinária.2007; 16(3): 133. CrossRef
Aborto ovino associado com infecção por Sarcocystis sp
Caroline A. Pescador, Luís G. Corbellini, Eduardo C. de Oliveira, Paulo M. Bandarra, Juliano S. Leal, Pedro M.O. Pedroso, David Driemeier
Pesquisa Veterinária Brasileira.2007; 27(10): 393. CrossRef
VACCINATION WITH MICRONEME PROTEIN NCMIC4 INCREASES MORTALITY IN MICE INOCULATED WITH NEOSPORA CANINUM
Sangeetha Srinivasan, Joachim Mueller, Angela Suana, Andrew Hemphill
Journal of Parasitology.2007; 93(5): 1046. CrossRef
Prevalence of Neospora caninum and Toxoplasma gondii Antibodies in Wild Ruminants From the Countryside or Captivity in the Czech Republic
E. Bartova, K. Sedlak, I. Pavlik, I. Literak
Journal of Parasitology.2007; 93(5): 1216. CrossRef
Seroepidemiology of Toxoplasma gondii and Neospora caninum in Seals around Hokkaido, Japan
Kei FUJII, Chiharu KAKUMOTO, Mari KOBAYASHI, Sachiko SAITO, Tatsuya KARIYA, Yukiko WATANABE, Xuenan XUAN, Ikuo IGARASHI, Masatsugu SUZUKI
Journal of Veterinary Medical Science.2007; 69(4): 393. CrossRef
Dense-Granule Protein NcGRA7, a New Marker for the Serodiagnosis ofNeospora caninumInfection in Aborting Cows
Penglong Huang, Min Liao, Houshuang Zhang, Eung-goo Lee, Yoshifumi Nishikawa, Xuenan Xuan
Clinical and Vaccine Immunology.2007; 14(12): 1640. CrossRef
Epidemiology and Control of Neosporosis andNeospora caninum
J. P. Dubey, G. Schares, L. M. Ortega-Mora
Clinical Microbiology Reviews.2007; 20(2): 323. CrossRef
Humoral immune reaction of newborn calves congenitally infected with Neospora caninum and experimentally treated with toltrazuril
Corinne Haerdi, Michael Haessig, Heinz Sager, Gisela Greif, Daniela Staubli, Bruno Gottstein
Parasitology Research.2006; 99(5): 534. CrossRef
Pathogen exposure in endangered island fox (Urocyon littoralis) populations: Implications for conservation management
Deana L. Clifford, Jonna A.K. Mazet, Edward J. Dubovi, David K. Garcelon, Timothy J. Coonan, Patricia A. Conrad, Linda Munson
Biological Conservation.2006; 131(2): 230. CrossRef
Identification of a protein disulfide isomerase of Neospora caninum in excretory–secretory products and its IgA binding and enzymatic activities
Min Liao, Liqing Ma, Hiroshi Bannai, Eung-goo Lee, Zhixun Xie, Xiaofei Tang, Houshuang Zhang, Xuenan Xuan, Kozo Fujisaki
Veterinary Parasitology.2006; 139(1-3): 47. CrossRef
Neospora caninum antibodies in commercial fetal bovine serum
Maria P. Torres, Ynes R. Ortega
Veterinary Parasitology.2006; 140(3-4): 352. CrossRef
Vaccination with γ‐IrradiatedNeospora caninumTachyzoites Protects Mice Against Acute Challenge withN. caninum
S. RAMAMOORTHY, D. S. LINDSAY, G. G. SCHURIG, S. M. BOYLE, R. B. DUNCAN, R. VEMULAPALLI, N. SRIRANGANATHAN
Journal of Eukaryotic Microbiology.2006; 53(2): 151. CrossRef
Astroglial cells in primary culture: A valid model to study Neospora caninum infection in the CNS
A.M. Pinheiro, S.L. Costa, S.M. Freire, M.A.O. Almeida, M. Tardy, R. El Bachá, M.F.D. Costa
Veterinary Immunology and Immunopathology.2006; 113(1-2): 243. CrossRef
Neospora caninum: Antibodies directed against tachyzoite surface protein NcSRS2 inhibit parasite attachment and invasion of placental trophoblasts in vitro
Gary J. Haldorson, James B. Stanton, Bruce A. Mathison, Carlos E. Suarez, Tim V. Baszler
Experimental Parasitology.2006; 112(3): 172. CrossRef
PCR detection of Neospora caninum, Toxoplasma gondii and Encephalitozoon cuniculi in brains of wild carnivores
L Hůrková, D. Modrý
Veterinary Parasitology.2006; 137(1-2): 150. CrossRef
Pathogenesis of Bovine Neosporosis
J.P. Dubey, D. Buxton, W. Wouda
Journal of Comparative Pathology.2006; 134(4): 267. CrossRef
Neospora caninum and neosporosis — recent achievements in host and parasite cell biology and treatment
Andrew Hemphill, Bruno Gottstein
Acta Parasitologica.2006;[Epub] CrossRef
Prevalence of Neospora caninum infection in Sardinian dairy farms (Italy) detected by iscom ELISA on tank bulk milk
A. Varcasia, G. Capelli, A. Ruiu, M. Ladu, A. Scala, C. Bjorkman
Parasitology Research.2006; 98(3): 264. CrossRef
Seroprevalences of antibodies to Neospora caninum and Toxoplasma gondii in zoo animals
K. Sedlák, E. Bártová
Veterinary Parasitology.2006; 136(3-4): 223. CrossRef
Clinical Sarcocystis neurona, Sarcocystis canis, Toxoplasma gondii, and Neospora caninum infections in dogs
J.P. Dubey, Jennifer L. Chapman, Benjamin M. Rosenthal, M. Mense, Ronald L. Schueler
Veterinary Parasitology.2006; 137(1-2): 36. CrossRef
Neosporosis in dairy cattle: An update from an epidemiological perspective
John M. Gay
Theriogenology.2006; 66(3): 629. CrossRef
Investigation of Neospora sp. and Toxoplasma gondii antibodies in mares and in precolostral foals from Parana State, Southern Brazil
R. Locatelli-Dittrich, J.R. Dittrich, R.R.T.B. Richartz, M.E. Gasino Joineau, J. Antunes, R.D. Pinckney, I. Deconto, D.C.S. Hoffmann, V. Thomaz-Soccol
Veterinary Parasitology.2006; 135(3-4): 215. CrossRef
Detection ofNeospora caninumTachyzoites in Canine Cerebrospinal Fluid
Lluís Gaitero, Sònia Añor, Patrícia Montoliu, Ángeles Zamora, Martí Pumarol
Journal of Veterinary Internal Medicine.2006; 20(2): 410. CrossRef
A possible role for Neospora caninum in ovine abortion in New Zealand
D.M. West, W.E. Pomroy, M.G. Collett, F.I. Hill, A.L. Ridler, P.R. Kenyon, S.T. Morris, R.S. Pattison
Small Ruminant Research.2006; 62(1-2): 135. CrossRef
Occurrence of Neospora caninum in dogs and its correlation with visceral leishmaniasis in the urban area of Campo Grande, Mato Grosso do Sul, Brazil
Renato Andreotti, Jacqueline Marques Oliveira, Elaine Araujo e Silva, Leandra Marla Oshiro, Maria de Fatima Cepa Matos
Veterinary Parasitology.2006; 135(3-4): 375. CrossRef
Comparison of different methods for the solubilisation of Neospora caninum (Phylum Apicomplexa) antigen
Annetta Zintl, Stephen R. Pennington, Grace Mulcahy
Veterinary Parasitology.2006; 135(3-4): 205. CrossRef
Neosporosis, Toxoplasmosis, and Sarcocystosis in Ruminants
J.P. Dubey, David S. Lindsay
Veterinary Clinics of North America: Food Animal Practice.2006; 22(3): 645. CrossRef
Seroepidemiology of Neospora caninum infection in dairy cattle herds in Mashhad area, Iran
G.R. Razmi, G.R. Mohammadi, T. Garrosi, N. Farzaneh, A.H. Fallah, M. Maleki
Veterinary Parasitology.2006; 135(2): 187. CrossRef
Validation of a commercially available cELISA test for canine neosporosis against an indirect fluorescent antibody test (IFAT)
Gioia Capelli, Alda Natale, Stefano Nardelli, Antonio Frangipane di Regalbono, Mario Pietrobelli
Preventive Veterinary Medicine.2006; 73(4): 315. CrossRef
Cellular and immunological basis of the host-parasite relationship during infection withNeospora caninum
A. HEMPHILL, N. VONLAUFEN, A. NAGULESWARAN
Parasitology.2006; 133(3): 261. CrossRef
Application of repeated bulk milk testing for identification of infection dynamics of Neospora caninum in Thai dairy herds
Aran Chanlun, Ulf Emanuelson, Suthida Chanlun, Suneerat Aiumlamai, Camilla Björkman
Veterinary Parasitology.2006; 136(3-4): 243. CrossRef
Diagnosis of bovine neosporosis: Recent advances and perspectives
Luis Ortega-Mora, Aurora Fernández-García, Mercedes Gómez-Bautista
Acta Parasitologica.2006; 51(1): 1. CrossRef
Anticorpos anti-Neospora caninum em bovinos, ovinos e bubalinos no Estado do Rio Grande do Sul
Fernanda Silveira Flôres Vogel, Sandra Arenhart, Fernando Viçosa Bauermann
Ciência Rural.2006; 36(6): 1948. CrossRef
SEROLOGIC SURVEY FOR TOXOPLASMA GONDII AND NEOSPORA CANINUM IN THE COMMON BRUSHTAIL POSSUM (TRICHOSURUS VULPECULA) FROM URBAN SYDNEY, AUSTRALIA
Jutta Eymann, Catherine A. Herbert, Desmond W. Cooper, J. P. Dubey
Journal of Parasitology.2006; 92(2): 267. CrossRef
MULTILOCUS MICROSATELLITE ANALYSIS REVEALS EXTENSIVE GENETIC DIVERSITY IN NEOSPORA CANINUM
Javier Regidor-Cerrillo, Susana Pedraza-Díaz, Mercedes Gómez-Bautista, Luis M. Ortega-Mora
Journal of Parasitology.2006; 92(3): 517. CrossRef
First Report of Neospora Caninum Abortion in a Beef Cow–Calf Herd From Andorra, Europe
Ramon Armengol, Marcela Pabón, Carles Adelantado, Fernando López-Gatius, Sonia Almería
Journal of Parasitology.2006; 92(6): 1361. CrossRef
NEOSPORA CANINUM–LIKE OOCYSTS OBSERVED IN FECES OF FREE-RANGING RED FOXES (VULPES VULPES) AND COYOTES (CANIS LATRANS)
Wendela Wapenaar, Mark C. Jenkins, Ryan M. O'Handley, Herman W. Barkema
Journal of Parasitology.2006; 92(6): 1270. CrossRef
COMPARATIVE EFFECT OF NEOSPORA CANINUM INFECTION IN BALB/c MICE AT THREE DIFFERENT GESTATION PERIODS
Inmaculada C. López-Pérez, Verónica Risco-Castillo, Esther Collantes-Fernández, Luis Miguel Ortega-Mora
Journal of Parasitology.2006; 92(6): 1286. CrossRef
Seroprevalence of Neospora caninum and Toxoplasma gondii in camels (Camelus dromedarius) in Mashhad, Iran
A. Sadrebazzaz, H. Haddadzadeh, P. Shayan
Parasitology Research.2006; 98(6): 600. CrossRef
ESTUDO MORFOLÓGICO DE EMBRIÕES BOVINOS FERTILIZADOS IN VITRO EXPOSTOS EXPERIMENTALMENTE À NEOSPORA CANINUM
M. D’ Angelo, A.G. Galuppo, N.M.C. Zerio, G.M. Melo, E.M. Pituco, L.H. Okuda
Arquivos do Instituto Biológico.2006; 73(2): 211. CrossRef
The prevalence of Toxoplasma gondiiIgM and IgG antibodies in dogs and cats from the Czech Republic
K. Sedlak, E. Bartova
Veterinární medicína.2006; 51(12): 555. CrossRef
Neosporosis in Cattle
J.P. Dubey
Veterinary Clinics of North America: Food Animal Practice.2005; 21(2): 473. CrossRef
Prevalence of antibodies against Neospora caninum and Toxoplasma gondii in dogs and foxes in Austria
K. Wanha, R. Edelhofer, C. Gabler-Eduardo, H. Prosl
Veterinary Parasitology.2005; 128(3-4): 189. CrossRef
Seroprevalence of Neospora caninum in dairy and beef cattle with reproductive disorders in Japan
Masahiro Koiwai, Takahumi Hamaoka, Makoto Haritani, Shinya Shimizu, Toshiyuki Tsutsui, Mariko Eto, Itsuro Yamane
Veterinary Parasitology.2005; 130(1-2): 15. CrossRef
Neosporosis in a young dog presenting with dermatitis and neuromuscular signs
S. P. Boyd, P. A. Barr, H. W. Brooks, J. P. Orr
Journal of Small Animal Practice.2005; 46(2): 85. CrossRef
Serological responses to Neospora caninum in experimentally and naturally infected water buffaloes (Bubalus bubalis)
A.A.R. Rodrigues, S.M. Gennari, V.S.O. Paula, D.M. Aguiar, T.U. Fujii, W. Starke-Buzeti, R.Z. Machado, J.P. Dubey
Veterinary Parasitology.2005; 129(1-2): 21. CrossRef
Antibodies to Neospora caninum in the blood of European bison (Bison bonasus bonasus L.) living in Poland
W. Cabaj, B. Moskwa, K. Pastusiak, J. Gill
Veterinary Parasitology.2005; 128(1-2): 163. CrossRef
Comparison of proteome and antigenic proteome between two Neospora caninum isolates
Yong-Seung Shin, Gee-Wook Shin, Young-Rim Kim, Eun-Young Lee, Hyang-Hee Yang, K.J. Palaksha, Hee-Jeong Youn, Jae-Hoon Kim, Dae-Yong Kim, A.E. Marsh, J. Lakritz, Tae-Sung Jung
Veterinary Parasitology.2005; 134(1-2): 41. CrossRef
Immunization with native surface protein NcSRS2 induces a Th2 immune response and reduces congenital Neospora caninum transmission in mice
G.J. Haldorson, B.A. Mathison, K. Wenberg, P.A. Conrad, J.P. Dubey, A.J. Trees, I. Yamane, T.V. Baszler
International Journal for Parasitology.2005; 35(13): 1407. CrossRef
Seronegative conversion in four Neospora caninum-infected cows, with a low rate of transplacental transmission
T. Kyaw, J. Suwimonteerabutr, P. Virakul, C. Lohachit, W. Kalpravidh
Veterinary Parasitology.2005; 131(1-2): 145. CrossRef
Neosporosis in South America
D.P. Moore
Veterinary Parasitology.2005; 127(2): 87. CrossRef
Evaluation of three enzyme-linked immunosorbent assays for detection of antibodies to Neospora caninum in bulk milk
C.J.M. Bartels, C. van Maanen, A.M. van der Meulen, T. Dijkstra, W. Wouda
Veterinary Parasitology.2005; 131(3-4): 235. CrossRef
Serologic immunoreactivity to Neospora caninum antigens in dogs determined by indirect immunofluorescence, western blotting and dot-ELISA
A.M. Pinheiro, M.F. Costa, B. Paule, V. Vale, M. Ribeiro, I. Nascimento, R.E. Schaer, M.A.O. Almeida, R. Meyer, S.M. Freire
Veterinary Parasitology.2005; 130(1-2): 73. CrossRef
Confirmed clinical Neospora caninum infection in a boxer puppy from Argentina
W. Basso, M.C. Venturini, D. Bacigalupe, M. Kienast, J.M. Unzaga, A. Larsen, M. Machuca, L. Venturini
Veterinary Parasitology.2005; 131(3-4): 299. CrossRef
Neospora caninum in pastured cattle: determination of climatic, environmental, farm management and individual animal risk factors using remote sensing and geographical information systems
L. Rinaldi, G. Fusco, V. Musella, V. Veneziano, A. Guarino, R. Taddei, G. Cringoli
Veterinary Parasitology.2005; 128(3-4): 219. CrossRef
Protective efficacy of vaccination with Neospora caninum multiple recombinant antigens against experimental Neospora caninum infection
Jung-Hwa Cho, Woo-Suk Chung, Kyoung-Ju Song, Byoung-Kuk Na, Seung-Won Kang, Chul-Yong Song, Tong-Soo Kim
The Korean Journal of Parasitology.2005; 43(1): 19. CrossRef
Isolation of Neospora caninum from naturally infected white-tailed deer (Odocoileus virginianus)
M.C.B. Vianna, C. Sreekumar, K.B. Miska, D.E. Hill, J.P. Dubey
Veterinary Parasitology.2005; 129(3-4): 253. CrossRef
Prevalence of Antibodies to Neospora caninum in Wild Animals
J. P. Dubey, P. Thulliez*
Journal of Parasitology.2005; 91(5): 1217. CrossRef
Immunisation of mice against neosporosis with recombinant NcSRS2 iscoms
Sunan Pinitkiatisakul, Jens G. Mattsson, Maria Wikman, Mikaela Friedman, Karin Lövgren Bengtsson, Stefan Ståhl, Anna Lundén
Veterinary Parasitology.2005; 129(1-2): 25. CrossRef
Immune responses during pregnancy in heifers naturally infected with Neospora caninum with and without immunization
Aur�lie G. Andrianarivo, Mark L. Anderson, Joan D. Rowe, Ian A. Gardner, James P. Reynolds, Leszek Choromanski, Patricia A. Conrad
Parasitology Research.2005; 96(1): 24. CrossRef
Characterization of the B‐cell immune response elicited in BALB/c mice challenged with Neospora caninum tachyzoites
Luzia Teixeira, Andreia Marques, Carla Sofia Meireles, Ana Rita Seabra, Diana Rodrigues, Pedro Madureira, Augusto M. R. Faustino, Carolina Silva, Adília Ribeiro, Paula Ferreira, José Manuel Correia da Costa, Nuno Canada, Manuel Vilanova
Immunology.2005; 116(1): 38. CrossRef
ADAPTATION OF NEOSPORA CANINUM ISOLATES TO CELL-CULTURE CHANGES: AN ARGUMENT IN FAVOR OF ITS CLONAL POPULATION STRUCTURE
F. J. Pérez-Zaballos, L. M. Ortega-Mora, G. Álvarez-García, E. Collantes-Fernández, V. Navarro-Lozano, L. García-Villada, E. Costas
Journal of Parasitology.2005; 91(3): 507. CrossRef
Toltrazuril treatment to control diaplacentalNeospora caninumtransmission in experimentally infected pregnant mice
B. GOTTSTEIN, G. R. RAZMI, P. AMMANN, H. SAGER, N. MÜLLER
Parasitology.2005; 130(1): 41. CrossRef
Development of Rapid Immunochromatographic Test with Recombinant NcSAG1 for Detection of Antibodies toNeospora caninumin Cattle
Min Liao, Shoufa Zhang, Xuenan Xuan, Guohong Zhang, Xiaohong Huang, Ikuo Igarashi, Kozo Fujisaki
Clinical and Vaccine Immunology.2005; 12(7): 885. CrossRef
Identification of Vaccine Candidate Peptides in the NcSRS2 Surface Protein ofNeospora caninumby Using CD4+Cytotoxic T Lymphocytes and Gamma Interferon-Secreting T Lymphocytes of Infected Holstein Cattle
Lauren M. Staska, Christopher J. Davies, Wendy C. Brown, Travis C. McGuire, Carlos E. Suarez, Joo Youn Park, Bruce A. Mathison, Jeffrey R. Abbott, Timothy V. Baszler
Infection and Immunity.2005; 73(3): 1321. CrossRef
A GFP-based motif-trap reveals a novel mechanism of targeting for the Toxoplasma ROP4 protein
Peter J. Bradley, Nancy Li, John C. Boothroyd
Molecular and Biochemical Parasitology.2004; 137(1): 111. CrossRef
Coyotes (Canis latrans) are definitive hosts of Neospora caninum
Luis F.P Gondim, Milton M McAllister, William C Pitt, Doris E Zemlicka
International Journal for Parasitology.2004; 34(2): 159. CrossRef
Sero-epidemiological survey of Neospora caninum infection in dogs in north-eastern Italy
Gioia Capelli, Stefano Nardelli, Antonio Frangipane di Regalbono, Antonio Scala, Mario Pietrobelli
Veterinary Parasitology.2004; 123(3-4): 143. CrossRef
Biologic, morphologic, and molecular characterisation of Neospora caninum isolates from littermate dogs
J.P. Dubey, C. Sreekumar, E. Knickman, K.B. Miska, M.C.B. Vianna, O.C.H. Kwok, D.E. Hill, M.C. Jenkins, D.S. Lindsay, C.E. Greene
International Journal for Parasitology.2004; 34(10): 1157. CrossRef
First cases of animal diseases published since 2000 6. First update of dog diseases
Th.A.M. Elsinghorst
Veterinary Quarterly.2004; 26(1): 12. CrossRef
Detection of Neospora caninum in an aborted goat foetus
C. Eleni, S. Crotti, E. Manuali, S. Costarelli, G. Filippini, L. Moscati, S. Magnino
Veterinary Parasitology.2004; 123(3-4): 271. CrossRef
Meningoencephalomyelitis Caused byNeospora caninumin a Juvenile Fallow Deer (Dama dama)
S. Soldati, M. Kiupel, A. Wise, R. Maes, C. Botteron, N. Robert
Journal of Veterinary Medicine Series A.2004; 51(6): 280. CrossRef
Neospora caninum seroprevalence in dairy cattle in central Thailand
T Kyaw, P Virakul, M Muangyai, J Suwimonteerabutr
Veterinary Parasitology.2004; 121(3-4): 255. CrossRef
Detection of antibodies to Neospora caninum in two species of wild canids, Lycalopex gymnocercus and Cerdocyon thous from Brazil
W.A. Cañón-Franco, L.E.O. Yai, S.L.P. Souza, L.C. Santos, N.A.R. Farias, J. Ruas, F.W. Rossi, A.A.B. Gomes, J.P. Dubey, S.M. Gennari
Veterinary Parasitology.2004; 123(3-4): 275. CrossRef
Occasional detection of Neospora caninum DNA in frozen extended semen from naturally infected bulls
Andrea Caetano-da-Silva, Ignacio Ferre, Esther Collantes-Fernández, Vanesa Navarro, Gorka Aduriz, Carlos Ugarte-Garagalza, Luis Miguel Ortega-Mora
Theriogenology.2004; 62(7): 1329. CrossRef
Shedding of Neospora caninum oocysts by dogs fed tissues from naturally infected water buffaloes (Bubalus bubalis) from Brazil
A.A.R. Rodrigues, S.M. Gennari, D.M Aguiar, C. Sreekumar, D.E. Hill, K.B. Miska, M.C.B. Vianna, J.P. Dubey
Veterinary Parasitology.2004; 124(3-4): 139. CrossRef
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Original Articles

Experimental induction of the two-host life cycle of Sarcocystis cruzi between dogs and Korean native calves: Sung-Hwan Wee, Sung-Shik Shin; Korean J Parasitol 2001;39(3):227-232.
Published online September 30, 2001; DOI: https://doi.org/10.3347/kjp.2001.39.3.227

Abstract
PDF

Eight dogs were experimentally infected with Sarcocystis by oral inoculation of cardiac muscle from naturally infected cattle. The infected dogs commenced discharging of sporocysts in the feces after 10 to 12 days of inoculation, and continued until 20 and 35 days after inoculation. Three dogs were reinfected with cardiac muscle from the naturally infected cattle. Sporocysts reappeared in the feces on 12 to 13 days after reinfection. Sarcosystis sporocysts collected from the experimentally infected dogs were fed to each of the two 30-day-old Korean native calves. The infected calves remained clinically normal, except for the high fever (≥ 40℃) and decreased hematocrit values on day 30 to 40 post inoculation. Muscular cysts of Sarcocystis were found from infected calves on day 40 post inoculation. Proliferative forms of Sarcocystis were also observed in the muscle of infected calves. These results suggest that the Sarcocystis cruzi found in Korean native cattle has a 2-host life cycle with dogs as the definitive host and Korean native calves as the intermediate host.

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Detection of IgG antibody against Neospora caninum in cattle in Korea: Ji-Seon Bae, Dae-Yong Kim, Woo-Suk Hwang, Jae-Hoon Kim, Nam-Seok Lee, Ho-Woo Nam; Korean J Parasitol 2000;38(4):245-249.
Published online December 31, 2000; DOI: https://doi.org/10.3347/kjp.2000.38.4.245

Abstract
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A total of 492 cattle sera was screened by IgG-ELISA against Neospora caninum (Nc-1 strain and a Korean isolate, KBA-2) and Toxoplasma gondii. Out of 492, 113 sera (23.0%) reacted positively to either Nc-1 or KBA-2 strains of N. caninum. Among the 113 positive sera, 92 sera (81.4%) reacted with antigens of both strains, but 6 sera (5.3%) with Nc-1 and 15 sera (13.3%) with KBA-2 strain only. And with T. gondii antigen, 6 sera (1.2%) were positive but all reacted with N. caninum antigen also. Western blot revealed typical binding pattern according to ELISA values, such that high OD group reacted specifically to the major surface proteins including 43 kDa protein. Seroprevalence of 23.0% indicates that neosporosis seemed to be one of major causes of abortion in cattle. It is suggested here to establish more epidemiological researches nationwide systematically.

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