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"Wei Cong"

Brief Communications
Seroprevalence of Encephalitozoon cuniculi and Toxoplasma gondii in domestic rabbits (Oryctolagus cuniculus) in China
Qing-Feng Meng, Wei-Lin Wang, Xiao-Ting Ni, Hai-Bin Li, Gui-Zhe Yao, Xiao-Lin Sun, Wei-Li Wang, Wei Cong
Korean J Parasitol 2015;53(6):759-763.
Published online December 31, 2015
DOI: https://doi.org/10.3347/kjp.2015.53.6.759
The breeding of domestic rabbits (Oryctolagus cuniculus) for human consumption has a long tradition in China. Infections that can affect the production of meat or even be transmitted from animals to humans are important to monitor, especially for public health reasons as well as for their impact on animal health. Thus, a total of 1,132 domestic rabbit sera from 4 regions in China were collected for serological screening for Encephalitozoon cuniculi and for Toxoplasma gondii by ELISA and modified agglutination test (MAT), respectively. Antibodies to E. cuniculi were detected in 248/1,132 (21.9%) sera tested while antibodies against T. gondii revealed a seroprevalence of 51/1,132 (4.5%). We believe that the present results are of epidemiological implications and public health importance due to the acknowledged susceptibility of humans to E. cuniculi and T. gondii infections. Therefore, routine screening tests of domestic rabbits are proposed considering the zoonotic potential of these parasites.

Citations

Citations to this article as recorded by  Crossref logo
  • The Prevalence of Encephalitozoon cuniculi in Domestic Rabbits (Oryctolagus cuniculus) in the North-Western Region of Romania Using Serological Diagnosis: A Preliminary Study
    Anca-Alexandra Doboși, Anamaria Ioana Paștiu, Lucia-Victoria Bel, Dana Liana Pusta
    Microorganisms.2024; 12(7): 1440.     CrossRef
  • Serological survey for antibodies to Encephalitozoon cuniculi and Toxoplasma gondii in pet rabbits in eastern coastal areas of China
    Yong WANG, Xuling QIN, Xiuguo DIAO, Yongxia LIU, Jianzhu LIU
    Journal of Veterinary Medical Science.2022; 84(6): 777.     CrossRef
  • Epidemiological and Public Health Significance of Toxoplasma gondii Infection in Wild Rabbits and Hares: 2010–2020
    Sonia Almeria, Fernando H. A. Murata, Camila K. Cerqueira-Cézar, Oliver C. H. Kwok, Alicia Shipley, Jitender P. Dubey
    Microorganisms.2021; 9(3): 597.     CrossRef
  • Comparison of Seroprevalence and PCR Results in the Detection of Toxoplasma gondii in Pet Rabbits in Poland
    Anna Woźniak-Biel, Aleksandra Podolak
    Vector-Borne and Zoonotic Diseases.2020; 20(4): 281.     CrossRef
  • Surveillance of Microsporidia and Protozoan Pathogens in Pensacola Florida: A One‐year Study
    Joseph A. Moss, Richard A. Snyder
    Journal of Eukaryotic Microbiology.2019; 66(4): 617.     CrossRef
  • Relationship between seropositivity of Encephalitozoon cuniculi and renal biochemical markers in clinically healthy rabbits
    Özcan ÖZKAN, Banuçiçek YÜCESAN, Selçuk PEKKAYA, Mehmet Eray ALÇIĞIR, İsmayil Safa GÜRCAN
    Ankara Üniversitesi Veteriner Fakültesi Dergisi.2019; 66(2): 197.     CrossRef
  • Occurrence and genetic characterization of Toxoplasma gondii and Neospora caninum in slaughtered domestic rabbits in central China
    Weifeng Qian, Wenchao Yan, Chaochao Lv, Rongzhen Bai, Tianqi Wang
    Parasite.2019; 26: 36.     CrossRef
  • Seroprevalence and risk factors of Toxoplasma gondii infection in rabbit of local Algerian population
    Mina Henneb, Khaled Harhoura, Mohamed Amine Bekara, Safia Zenia, Miriem Aissi
    Veterinary World.2019; 12(6): 855.     CrossRef
  • Seroprevalence of Toxoplasma gondii and Encephalitozoon cuniculi among domestic rabbits in central China
    Shuai Wang, Zhijun Yao, Lingjuan Li, Yaoqian Pan, Pengju Li, Xiaoxu Nan, Qing Xie, Zhenchao Zhang
    Parasite.2018; 25: 9.     CrossRef
  • Rapid detection of three rabbit pathogens by use of the Luminex x-TAG assay
    Miaoli Wu, Yujun Zhu, Feng Cong, Dan Rao, Wen Yuan, Jing Wang, Bihong Huang, Yuexiao Lian, Yu Zhang, Ren Huang, Pengju Guo
    BMC Veterinary Research.2018;[Epub]     CrossRef
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  • 10 Web of Science
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Prevalence of Toxoplasma gondii in Dogs in Zhanjiang, Southern China
Hai-Hai Jiang, Ming-Wei Li, Min-Jun Xu, Wei Cong, Xing-Quan Zhu
Korean J Parasitol 2015;53(4):493-496.
Published online August 25, 2015
DOI: https://doi.org/10.3347/kjp.2015.53.4.493
Toxoplasmosis, caused by Toxoplasma gondii, is a parasitic zoonosis with worldwide distribution. The present study investigated the prevalence of T. gondii in dogs in Zhanjiang city, southern China, using both serological and molecular detection. A total of 364 serum samples and 432 liver tissue samples were collected from the slaughter house between December 2012 and January 2013 and were examined for T. gondii IgG antibody by ELISA and T. gondii DNA by semi-nested PCR based on B1 gene, respectively. The overall seroprevalence of T. gondii IgG antibody was 51.9%, and T. gondii DNA was detected in 37 of 432 (8.6%) liver tissue samples. These positive DNA samples were analyzed by PCR-RFLP at 3'- and 5'-SAG2. Only 8 samples gave the PCR-RFLP data, and they were all classified as type I, which may suggest that the T. gondii isolates from dogs in Zhanjiang city may represent type I or type I variant. This study revealed the high prevalence of T. gondii infection in dogs in Zhanjiang city, southern China. Integrated measures should be taken to prevent and control toxoplasmosis in dogs in this area for public health concern.

Citations

Citations to this article as recorded by  Crossref logo
  • An investigation into Toxoplasma gondii at the human-livestock-wildlife interface, South Africa
    Refilwe P. Bokaba, Veronique Dermauw, Darshana Morar-Leather, Pierre Dorny, Louis van Schalkwyk, Luis Neves
    Onderstepoort Journal of Veterinary Research.2024;[Epub]     CrossRef
  • Seropositivity of toxoplasmosis in pregnant women living with HIV/AIDS worldwide: A systematic review and meta-analysis
    Eden Woldegerima, Mulugeta Aemiro, Getnet Fetene, Nega Birhanie
    Parasitology International.2024; 102: 102922.     CrossRef
  • Exploring similarities and differences between Toxoplasma gondii and Neospora caninum infections in dogs
    Giulia Morganti, Giulia Rigamonti, Leonardo Brustenga, Valentina Calgaro, Giovanni Angeli, Iolanda Moretta, Manuela Diaferia, Fabrizia Veronesi
    Veterinary Research Communications.2024; 48(6): 3563.     CrossRef
  • Seroprevalence and B1 gene Phylogeny of Toxoplasma gondii of Dogs and Cats in Republic of Korea
    Yeojin Park, Jinhyeong Noh, Hyun-Ji Seo, Keun-Ho Kim, Subin Min, Mi-Sun Yoo, Bo-Ram Yun, Jong-Ho Kim, Eun-Jin Choi, Doo-Sung Cheon, Sung-Jong Hong, Soon-Seek Yoon, Yun Sang Cho
    The Korean Journal of Parasitology.2020; 58(3): 257.     CrossRef
  • Toxoplasma gondii infections in dogs: 2009-2020
    Jitender P. Dubey, Fernando H.A. Murata, Camila K. Cerqueira-Cézar, Oliver C.H. Kwok, Yurong Yang, Chunlei Su
    Veterinary Parasitology.2020; 287: 109223.     CrossRef
  • Toxoplasma gondii Triggers Neutrophil Extracellular Traps Release in Dogs
    Zhengkai Wei, Zedong Wang, Xiao Liu, Chaoqun Wang, Zhen Han, Di Wu, Yong Zhang, Xichen Zhang, Zhengtao Yang, Quan Liu
    Frontiers in Cellular and Infection Microbiology.2020;[Epub]     CrossRef
  • Prevalence of Toxoplasma gondii Antibodies in Stray Dogs from Various Locations in West and East Malaysia
    Malaika Watanabe, Mohammed Babatunde Sadiq, Nazrul Iqbal Abdul Mulop, Konto Mohammed, Puteri Azaziah Megat Rani, Lau Seng Fong, Nor Azlina Aziz, Juriah Kamaludeen, Siti Zubaidah Ramanoon, Rozaihan Mansor, Tan Li Ping, Sharifah Salmah Syed-Hussain
    The Korean Journal of Parasitology.2020; 58(5): 487.     CrossRef
  • Prevalence, risk factors and genetic characterization of Toxoplasma gondii in sick pigs and stray cats in Jiangsu Province, eastern China
    Zhao-feng Hou, Shi-jie Su, Dan-dan Liu, Le-le Wang, Chuan-li Jia, Zhen-xing Zhao, Yi-fei Ma, Qiao-qiao Li, Jin-jun Xu, Jian-ping Tao
    Infection, Genetics and Evolution.2018; 60: 17.     CrossRef
  • Prevalence and genetic characterization of Toxoplasma gondii in badgers ( Melogale moschata ) in southern China by PCR-RFLP
    Kai Chen, Si-Yang Huang, Jin-Lei Wang, Rong-Liang Hu, Qiu-Xia Yao, Shou-Feng Zhang, Xing-Quan Zhu, Quan Liu
    Infection, Genetics and Evolution.2017; 52: 30.     CrossRef
  • 10,089 View
  • 100 Download
  • 10 Web of Science
  • Crossref
Prevalence and Genetic Characterization of Toxoplasma gondii in House Sparrows (Passer domesticus) in Lanzhou, China
Wei Cong, Si-Yang Huang, Dong-Hui Zhou, Xiao-Xuan Zhang, Nian-Zhang Zhang, Quan Zhao, Xing-Quan Zhu
Korean J Parasitol 2013;51(3):363-367.
Published online June 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.3.363

The prevalence of Toxoplasma gondii infection in birds has epidemiological significance because birds are indeed considered as a good indicator of environmental contamination by T. gondii oocysts. In this study, the prevalence of T. gondii in 313 house sparrows in Lanzhou, northwestern China was assayed by the modified agglutination test (MAT). Antibodies to T. gondii were positive in 39 (12.46%) of 313 samples (MAT titer ≥ 1:5). Tissues of heart, brain, and lung from the 39 seropositive house sparrows were tested for T. gondii DNA, 11 of which were found to be positive for the T. gondii B1 gene by PCR amplification. These positive DNA samples were typed at 9 genetic markers, including 8 nuclear loci, i.e., SAG1, 5'- and 3'-SAG2, alternative SAG2, SAG3, GRA6, L358, PK1, c22-8 and an apicoplast locus Apico. Of them, 4 isolates were genotyped with complete data for all loci, and 2 genotypes (Type II variants; ToxoDB #3 and a new genotype) were identified. These results showed that there is a potential risk for human infection with T. gondii in this region. To our knowledge, this is the first report of T. gondii seroprevalence in house sparrows in China.

Citations

Citations to this article as recorded by  Crossref logo
  • Global prevalence and risk factors associated with Toxoplasma gondii infection in wild birds: A systematic review and meta-analysis
    Chao Chen, Si-Yuan Qin, Xing Yang, Xiao-Man Li, Yanan Cai, Cong-Cong Lei, Quan Zhao, Hany M. Elsheikha, Hongwei Cao
    Preventive Veterinary Medicine.2024; 226: 106187.     CrossRef
  • Molecular detection of Toxoplasma gondii (Chromista: Apicomplexa) in the blood of passerines (Aves: Passeriformes) in south-eastern Armenia
    Sargis A. Aghayan, Manan Asikyan, Marko Raković, Daliborka Stanković, Igor V. Fadeev, Hasmik Gevorgyan, Oleg Shcherbakov, Marine Arakelyan, Karen Aghababyan, Abdol Sattar Pagheh, Mehdi Sharif, Ahmad Daryani
    Zoologia (Curitiba).2024;[Epub]     CrossRef
  • Two viable Toxoplasma gondii isolates from red-necked wallaby (Macropus rufogriseus) and red kangaroo (M. rufus)
    Liulu Yang, Shilin Xin, Niuping Zhu, Junbao Li, Chunlei Su, Yurong Yang
    Parasitology International.2023; 92: 102687.     CrossRef
  • Epidemiology and isolation of viable Toxoplasma gondii strain from macropods
    Liulu Yang, Hongjie Ren, Niuping Zhu, Gaohui Mao, Junbao Li, Chunlei Su, Yibao Jiang, Yurong Yang
    Heliyon.2023; 9(3): e13960.     CrossRef
  • Genetic diversity of Toxoplasma gondii isolates from birds in the world: A systematic review
    Tahereh Mikaeili Galeh, Shahabeddin Sarvi, Alireza Khalilian, Seyed Abdollah Hosseini, Ahmad Daryani
    Experimental Parasitology.2023; 248: 108480.     CrossRef
  • Metagenomic insights into the composition and function of the gut microbiota of mice infected with Toxoplasma gondii
    Jin-Xin Meng, Xin-Yu Wei, Huanping Guo, Yu Chen, Wei Wang, Hong-Li Geng, Xing Yang, Jiang Jiang, Xiao-Xuan Zhang
    Frontiers in Immunology.2023;[Epub]     CrossRef
  • Low Prevalence of Toxoplasma gondii in Sheep and Isolation of a Viable Strain from Edible Mutton from Central China
    Yibao Jiang, Shilin Xin, Yiheng Ma, Heng Zhang, Xu Yang, Yurong Yang
    Pathogens.2023; 12(6): 827.     CrossRef
  • Abundance of Non-Native Birds in the City: Spatial Variation and Relationship with Socioeconomics in a South American City
    Macarena Silva-Ortega, Catalina B. Muñoz-Pacheco, Nélida R. Villaseñor
    Animals.2023; 13(11): 1737.     CrossRef
  • Investigation of Toxoplasma gondii in wastewater and surface water in the Qinghai-Tibet Plateau, China using real-time PCR and multilocus genotyping
    Anna Lass, Ioannis Kontogeorgos, Liqing Ma, Xueyong Zhang, Xiuping Li, Panagiotis Karanis
    Scientific Reports.2022;[Epub]     CrossRef
  • Epidemiologic significance of Toxoplasma gondii infections in turkeys, ducks, ratites and other wild birds: 2009–2020
    J. P. Dubey, F. H. A. Murata, C. K. Cerqueira-Cézar, O. C. H. Kwok, C. Su
    Parasitology.2021; 148(1): 1.     CrossRef
  • Molecular Prevalence and Genetic Characterization of Toxoplasma gondii in Wild Birds in Hunan Province, China
    Meng-Ting Liu, Wei-Xing Jiang, Bin-Ze Gui, Yuan-Chun Jin, Jia-Ning Yi, Fen Li, Wen-Bin Zheng, Guo-Hua Liu
    Vector-Borne and Zoonotic Diseases.2019; 19(5): 378.     CrossRef
  • Seroprevalence and risk assessment of Toxoplasma gondii in Java sparrows (Lonchura oryzivora) in China
    Si-Yang Huang, Yi-Min Fan, Kai Chen, Qiu-Xia Yao, Bin Yang
    BMC Veterinary Research.2019;[Epub]     CrossRef
  • Prevalence, risk factors and genetic characterization of Toxoplasma gondii in sick pigs and stray cats in Jiangsu Province, eastern China
    Zhao-feng Hou, Shi-jie Su, Dan-dan Liu, Le-le Wang, Chuan-li Jia, Zhen-xing Zhao, Yi-fei Ma, Qiao-qiao Li, Jin-jun Xu, Jian-ping Tao
    Infection, Genetics and Evolution.2018; 60: 17.     CrossRef
  • First genetic characterization of Toxoplasma gondii infection in common quails (Coturnix coturnix) intended for human consumption in China
    Wei Cong, Hong-Liang Ju, Xiao-Xuan Zhang, Qing-Feng Meng, Jian-Gang Ma, Ai-Dong Qian, Xing-Quan Zhu
    Infection, Genetics and Evolution.2017; 49: 14.     CrossRef
  • Prevalence and genetic characterization of Toxoplasma gondii in badgers ( Melogale moschata ) in southern China by PCR-RFLP
    Kai Chen, Si-Yang Huang, Jin-Lei Wang, Rong-Liang Hu, Qiu-Xia Yao, Shou-Feng Zhang, Xing-Quan Zhu, Quan Liu
    Infection, Genetics and Evolution.2017; 52: 30.     CrossRef
  • Geographical distribution of Toxoplasma gondii genotypes in Asia: A link with neighboring continents
    P. Chaichan, A. Mercier, L. Galal, A. Mahittikorn, F. Ariey, S. Morand, F. Boumédiène, R. Udonsom, A. Hamidovic, J.B. Murat, Y. Sukthana, M.L. Dardé
    Infection, Genetics and Evolution.2017; 53: 227.     CrossRef
  • Sixty Years (1957–2017) of Research on Toxoplasmosis in China—An Overview
    Ming Pan, Congcong Lyu, Junlong Zhao, Bang Shen
    Frontiers in Microbiology.2017;[Epub]     CrossRef
  • Molecular detection of Toxoplasma gondii in house sparrow (Passer domesticus) by LAMP and PCR methods in Tehran, Iran
    Amir Abdoli, Abdolhossein Dalimi, Haleh Soltanghoraee, Fatemeh Ghaffarifar
    Journal of Parasitic Diseases.2016; 40(4): 1317.     CrossRef
  • Seroprevalence and genotypes of Toxoplasma gondii isolated from pigs intended for human consumption in Liaoning province, northeastern China
    Dawei Wang, Yan Liu, Tiantian Jiang, Guoxin Zhang, Gaoming Yuan, Jianbin He, Chunlei Su, Na Yang
    Parasites & Vectors.2016;[Epub]     CrossRef
  • Multi-scale occupancy approach to estimate Toxoplasma gondii prevalence and detection probability in tissues: an application and guide for field sampling
    Stacey A. Elmore, Kathryn P. Huyvaert, Larissa L. Bailey, Asma Iqbal, Chunlei Su, Brent R. Dixon, Ray T. Alisauskas, Alvin A. Gajadhar, Emily J. Jenkins
    International Journal for Parasitology.2016; 46(9): 563.     CrossRef
  • Molecular Detection and Genetic Characterization of Toxoplasma gondii in Farmed Minks (Neovison vison) in Northern China by PCR-RFLP
    Wen-Bin Zheng, Xiao-Xuan Zhang, Jian-Gang Ma, Fa-Cai Li, Quan Zhao, Si-Yang Huang, Xing-Quan Zhu, Gordon Langsley
    PLOS ONE.2016; 11(11): e0165308.     CrossRef
  • Toxoplasma gondii infection in cancer patients: Prevalence, risk factors, genotypes and association with clinical diagnosis
    Wei Cong, Guo-Hua Liu, Qing-Feng Meng, Wei Dong, Si-Yuan Qin, Fu-Kai Zhang, Xiang-Yan Zhang, Xiang-Yang Wang, Ai-Dong Qian, Xing-Quan Zhu
    Cancer Letters.2015; 359(2): 307.     CrossRef
  • Prevalence of <i>Toxoplasma gondii</i> in Dogs in Zhanjiang, Southern China
    Hai-Hai Jiang, Ming-Wei Li, Min-Jun Xu, Wei Cong, Xing-Quan Zhu
    The Korean Journal of Parasitology.2015; 53(4): 493.     CrossRef
  • Prevalence of Antibody toToxoplasma gondiiin Black-headed Gulls (Chroicocephalus ridibundus), Dianchi Lake, China
    Qiang Miao, Jiang-qiang Han, Xun Xiang, Fei-Zhou Yuan, Yong-zhang Liu, Gang Duan, Xing-quan Zhu, Feng-cai Zou
    Journal of Wildlife Diseases.2014; 50(3): 717.     CrossRef
  • Seroprevalence and genetic characterization of Toxoplasma gondii in three species of pet birds in China
    Wei Cong, Qing-Feng Meng, Hui-Qun Song, Dong-Hui Zhou, Si-Yang Huang, Ai-Dong Qian, Chunlei Su, Xing-Quan Zhu
    Parasites & Vectors.2014;[Epub]     CrossRef
  • First Report of Genotyping ofToxoplasma gondiiin Free-LivingMicrotus fortisin Northeastern China
    Xiao-Xuan Zhang, Si-Yang Huang, Ying-Guang Zhang, Yuan Zhang, Xing-Quan Zhu, Quan Liu
    Journal of Parasitology.2014; 100(5): 692.     CrossRef
  • Genetic characterization of Toxoplasma gondii from cats in Yunnan Province, Southwestern China
    Yi-Ming Tian, Si-Yang Huang, Qiang Miao, Hai-Hai Jiang, Jian-Fa Yang, Chunlei Su, Xing-Quan Zhu, Feng-Cai Zou
    Parasites & Vectors.2014;[Epub]     CrossRef
  • Genetic characterization of Toxoplasma gondii from pigs from different localities in China by PCR-RFLP
    Hai-Hai Jiang, Si-Yang Huang, Dong-Hui Zhou, Xiao-Xuan Zhang, Chunlei Su, Shun-Zhou Deng, Xing-Quan Zhu
    Parasites & Vectors.2013;[Epub]     CrossRef
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