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Prevalence of Intestinal Helminth Infections in Dogs and Two Species of Wild Animals from Samarkand Region of Uzbekistan
Tai-Soon Yong, Kyu-Jae Lee, Myeong Heon Shin, Hak Sun Yu, Uktamjon Suvonkulov, Turycin Bladimir Sergeevich, Azamat Shamsiev, Gab-Man Park
Korean J Parasitol 2019;57(5):549-552.
Published online October 31, 2019
DOI: https://doi.org/10.3347/kjp.2019.57.5.549
This study aimed to determine the prevalence of intestinal helminth parasitic infections and associated risk factors for the human infection among the people of Samarkand, Uzbekistan. Infection status of helminths including Echinococcus granulosus was surveyed in domestic and wild animals from 4 sites in the Samarkand region, Uzbekistan during 2015-2018. Fecal samples of each animal were examined with the formalin-ether sedimentation technique and the recovery of intestinal helminths was performed with naked eyes and a stereomicroscope in total 1,761 animals (1,755 dogs, 1 golden jackal, and 5 Corsac foxes). Total 658 adult worms of E. granulosus were detected in 28 (1.6%) dogs and 1 (100%) golden jackal. More than 6 species of helminths, i.e., Taenia hydatigena, Dipylidium caninum, Diplopylidium nolleri, Mesocestoides lineatus, Toxocara canis, and Trichuris vulpis, were found from 18 (1.0%) dogs. Six (T. hydatigena, Toxascaris leonina, Alaria alata, Uncinaria stenocephala, D. caninum, and M. lineatus) and 2 (D. nolleri and M. lineatus) species of helminths were also detected from 5 Corsac foxes and 1 golden jackal, respectively. Taeniid eggs were found in 2 (20%) out of 10 soil samples. In the present study, it was confirmed that the prevalences of helminths including E. granulosus are not so high in domestic and wild animals. Nevertheless, the awareness on the zoonotic helminth infections should be continuously maintained in Uzbekistan for the prevention of human infection.

Citations

Citations to this article as recorded by  Crossref logo
  • Molecular identification and phylogenetic positioning of nematodes Toxocara canis, T. cati (Ascarididae) and Toxascaris leonina (Toxocaridae) from domestic and wild carnivores in the Fergana Valley, Uzbekistan
    A. E. Kuchboev, A. G. Sotiboldiyev, B. K. Ruziev, A. A. Safarov
    Biosystems Diversity.2025; 33(3): e2538.     CrossRef
  • High-Quality Chromosome-Level Genome Assembly of the Corsac Fox (Vulpes corsac) Reveals Adaptation to Semiarid and Harsh Environments
    Zhihao Zhang, Tian Xia, Shengyang Zhou, Xiufeng Yang, Tianshu Lyu, Lidong Wang, Jiaohui Fang, Qi Wang, Huashan Dou, Honghai Zhang
    International Journal of Molecular Sciences.2023; 24(11): 9599.     CrossRef
  • Time series modeling of animal bites
    Fatemeh Rostampour, Sima Masoudi
    Journal of Acute Disease.2023; 12(3): 121.     CrossRef
  • Diagnostic tools for the detection of taeniid eggs in different environmental matrices: A systematic review.
    Ganna Saelens, Lucy Robertson, Sarah Gabriël
    Food and Waterborne Parasitology.2022; 26: e00145.     CrossRef
  • Fleas from the Silk Road in Central Asia: identification of Ctenocephalides canis and Ctenocephalides orientis on owned dogs in Uzbekistan using molecular identification and geometric morphometrics
    Georgiana Deak, Alisher Safarov, Xi Carria Xie, Runting Wang, Andrei Daniel Mihalca, Jan Šlapeta
    Parasites & Vectors.2022;[Epub]     CrossRef
  • Control of cystic echinococcosis in the Middle Atlas, Morocco: Field evaluation of the EG95 vaccine in sheep and cesticide treatment in dogs
    Fatimaezzahra Amarir, Abdelkbir Rhalem, Abderrahim Sadak, Marianne Raes, Mohamed Oukessou, Aouatif Saadi, Mohammed Bouslikhane, Charles G. Gauci, Marshall W. Lightowlers, Nathalie Kirschvink, Tanguy Marcotty, María-Gloria Basáñez
    PLOS Neglected Tropical Diseases.2021; 15(3): e0009253.     CrossRef
  • Co-infection of Trichuris vulpis and Toxocara canis in different aged dogs: Influence on the haematological indices
    I. V. Saichenko, A. A. Antipov, T. I. Bakhur, L. V. Bezditko, S. S. Shmayun
    Biosystems Diversity.2021; 29(2): 129.     CrossRef
  • Spread and seasonal dynamics of dogs helminthiasis in BilaTserkva district
    I. Saichenko
    Naukovij vìsnik veterinarnoï medicini.2021; (1(165)): 119.     CrossRef
  • Monitoring of parasitic diseases of dogs
    Bogdan Morozov, Andrii Berezovskyi
    EUREKA: Health Sciences.2021; (4): 109.     CrossRef
  • An epizootic situation is in relation to the nematodosiss of gastroenteric channel of dogs
    I. Saichenko, A. Antipov
    Naukovij vìsnik veterinarnoï medicini.2020; (1(154)): 54.     CrossRef
  • 7,172 View
  • 140 Download
  • 8 Web of Science
  • Crossref
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
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.

Citations

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  • Tick Diversity and Distribution of Pathogen in Ticks Collected from Wild Animals and Vegetation in Africa
    Roland Eric Yessinou, Aldric Koumassou, Haruna Baba Galadima, Hospice Nanoukon-Ahigan, Souaïbou Farougou, Martin Pfeffer
    Pathogens.2025; 14(2): 116.     CrossRef
  • Molecular detection and prevalence of Anaplasma and Rickettsia species in rodents captured from wildlife-human interfaces in Iringa and Morogoro regions, Tanzania
    Venance T. Msoffe, Festo K. Mwombeki, Claus A. Thomas, Charles M. Lyimo, Abdul S. Katakweba, Moses I. Olotu, Gerald Misinzo, Erick V. Komba, Ladslaus L. Mnyone
    Mammalia.2025; 89(4): 437.     CrossRef
  • Climate-driven potential for tularemia in East Africa: skill testing and ecological consistency of a transferred risk model
    Komi Mensah Agboka, Allan Muohi Ngángá, Bonoukpoè Mawuko Sokame, Steve Soh Bernard Baleba, Tobias Landmann, Elfatih M. Abdel-Rahman, Chrysantus M. Tanga, Souleymane Diallo
    Spatial and Spatio-temporal Epidemiology.2025; 55: 100756.     CrossRef
  • Tick-Borne Diseases in Sub-Saharan Africa: A Systematic Review of Pathogens, Research Focus, and Implications for Public Health
    Tidjani A. Djiman, Abel S. Biguezoton, Claude Saegerman
    Pathogens.2024; 13(8): 697.     CrossRef
  • Review of Lyme Borreliosis in Africa—An Emerging Threat in Africa
    Nejib Doss, Aldo Morrone, Patrizia Forgione, Giusto Trevisan, Serena Bonin
    Biology.2024; 13(11): 897.     CrossRef
  • Prevalence and diversity of spotted fever group Rickettsia species in ixodid ticks from domestic dogs in Chad, Africa
    Stephanie Osip, Morgan Friedman, Ellen Haynes, Sarah M. Coker, John A. Bryan II, Metinou Sidouin, Philip Tchindebet Ouakou, Bongo Nare Richard Ngandolo, Christopher A. Cleveland, Michael J. Yabsley
    Ticks and Tick-borne Diseases.2024; 15(6): 102405.     CrossRef
  • Distribution and Prevalence of Anaplasmataceae, Rickettsiaceae and Coxiellaceae in African Ticks: A Systematic Review and Meta-Analysis
    Carlo Andrea Cossu, Nicola E. Collins, Marinda C. Oosthuizen, Maria Luisa Menandro, Raksha Vasantrai Bhoora, Ilse Vorster, Rudi Cassini, Hein Stoltsz, Melvyn Quan, Henriette van Heerden
    Microorganisms.2023; 11(3): 714.     CrossRef
  • Anaplasma Species in Africa—A Century of Discovery: A Review on Molecular Epidemiology, Genetic Diversity, and Control
    Agatha Kolo
    Pathogens.2023; 12(5): 702.     CrossRef
  • Ticks and Tick-Borne Pathogens in Domestic Animals, Wild Pigs, and Off-Host Environmental Sampling in Guam, USA
    Genevieve V. Weaver, Neil Anderson, Kayla Garrett, Alec T. Thompson, Michael J. Yabsley
    Frontiers in Veterinary Science.2022;[Epub]     CrossRef
  • Epidemiology of Ticks and Tick-Borne Pathogens in Domestic Ruminants across Southern African Development Community (SADC) Region from 1980 until 2021: A Systematic Review and Meta-Analysis
    Mpho Tawana, ThankGod E. Onyiche, Tsepo Ramatla, Sibusiso Mtshali, Oriel Thekisoe
    Pathogens.2022; 11(8): 929.     CrossRef
  • The diversity and evolutionary relationships of ticks and tick-borne bacteria collected in China
    JunHua Tian, Xin Hou, MiHong Ge, HongBin Xu, Bin Yu, Jing Liu, RenFu Shao, Edward C. Holmes, ChaoLiang Lei, Mang Shi
    Parasites & Vectors.2022;[Epub]     CrossRef
  • What do we know about the microbiome of I. ricinus?
    Richard Hodosi, Maria Kazimirova, Katarina Soltys
    Frontiers in Cellular and Infection Microbiology.2022;[Epub]     CrossRef
  • The molecular prevalence, distribution and risk factors associated with Babesia bigemina infection in Peninsular Malaysia
    Shola David Ola-Fadunsin, Reuben Sunil Kumar Sharma, Donea Abdurazak Abdullah, Fufa Ido Gimba, Faez Firdaus Jesse Abdullah, Rehana Abdullah Sani
    Ticks and Tick-borne Diseases.2021; 12(3): 101653.     CrossRef
  • Prioritizing smallholder animal health needs in East Africa, West Africa, and South Asia using three approaches: Literature review, expert workshops, and practitioner surveys
    Zoë Campbell, Paul Coleman, Andrea Guest, Peetambar Kushwaha, Thembinkosi Ramuthivheli, Tom Osebe, Brian Perry, Jeremy Salt
    Preventive Veterinary Medicine.2021; 189: 105279.     CrossRef
  • Comparative microbiomes of ticks collected from a black rhino and its surrounding environment
    Seogwon Lee, Ju Yeong Kim, Myung-hee Yi, In-Yong Lee, Robert Fyumagwa, Tai-Soon Yong
    International Journal for Parasitology: Parasites and Wildlife.2019; 9: 239.     CrossRef
  • 8,720 View
  • 212 Download
  • 14 Web of Science
  • Crossref
Serological and Molecular Detection of Toxoplasma gondii and Babesia microti in the Blood of Rescued Wild Animals in Gangwon-do (Province), Korea
Sung-Hee Hong, Hee-Jong Kim, Young-Il Jeong, Shin-Hyeong Cho, Won-Ja Lee, Jong-Tak Kim, Sang-Eun Lee
Korean J Parasitol 2017;55(2):207-212.
Published online April 30, 2017
DOI: https://doi.org/10.3347/kjp.2017.55.2.207
Infections of Toxoplasma gondii and Babesia microti are reported in many wild animals worldwide, but information on their incidence and molecular detection in Korean wild fields is limited. In this study, the prevalence of T. gondii and B. microti infection in blood samples of 5 animal species (37 Chinese water deer, 23 raccoon dogs, 6 roe deer, 1 wild boar, and 3 Eurasian badgers) was examined during 2008-2009 in Gangwon-do (Province), the Republic of Korea (=Korea) by using serological and molecular tests. The overall seropositivity of T. gondii was 8.6% (6/70); 10.8% in Chinese water deer, 4.3% in raccoon dogs, and 16.7% in roe deer. PCR revealed only 1 case of T. gondii infection in Chinese water deer, and phylogenic analysis showed that the positive isolate was practically identical to the highly pathogenetic strain type I. In B. microti PCR, the positive rate was 5.7% (4/70), including 2 Chinese water deer and 2 Eurasian badgers. Phylogenetic analysis results of 18S rRNA and the β-tubulin gene showed that all positive isolates were US-type B. microti. To our knowledge, this is the first report of B. microti detected in Chinese water deer and Eurasian badger from Korea. These results indicate a potentially high prevalence of T. gondii and B. microti in wild animals of Gangwon-do, Korea. Furthermore, Chinese water deer might act as a reservoir for parasite infections of domestic animals.

Citations

Citations to this article as recorded by  Crossref logo
  • Detection of US and Kobe‐type Babesia microti in ticks collected from small mammals of the Republic of Korea
    Tae Yun Kim, Seong Yoon Kim, Jiye Seo, Hee IL Lee, Wook‐Gyo Lee, Hyunwoo Kim
    Entomological Research.2024;[Epub]     CrossRef
  • Do Babesia microti Hosts Share a Blood Group System Gene Ortholog, Which Could Generate an Erythrocyte Antigen That Is Essential for Parasite Invasion?
    Ryan P. Jajosky, Audrey N. Jajosky, Philip G. Jajosky, Sean R. Stowell
    Tropical Medicine and Infectious Disease.2024; 9(9): 195.     CrossRef
  • Arthropod-Borne Pathogens in Wild Canids
    Valentina Virginia Ebani, Simona Nardoni, Francesca Mancianti
    Veterinary Sciences.2023; 10(2): 165.     CrossRef
  • Invasive raccoon (Procyon lotor) and raccoon dog (Nyctereutes procyonoides) as potential reservoirs of tick-borne pathogens: data review from native and introduced areas
    Izabella Myśliwy, Agnieszka Perec-Matysiak, Joanna Hildebrand
    Parasites & Vectors.2022;[Epub]     CrossRef
  • Evolutionary analysis of Babesia vulpes and Babesia microti-like parasites
    Sanghyun Lee, Yeonchul Hong, Dong-Il Chung, Hyung-Kwan Jang, Youn-Kyoung Goo, Xuenan Xuan
    Parasites & Vectors.2022;[Epub]     CrossRef
  • Recent epidemiologic and clinical Toxoplasma gondii infections in wild canids and other carnivores: 2009–2020
    Jitender P. Dubey, Fernando H.A. Murata, Camila K. Cerqueira-Cézar, Oliver C.H. Kwok
    Veterinary Parasitology.2021; 290: 109337.     CrossRef
  • Epidemiologic and Public Health Significance of Toxoplasma gondii Infections in Venison: 2009–2020
    J. P. Dubey, F. H. A. Murata, C. K. Cerqueira-Cézar, O. C. H. Kwok
    Journal of Parasitology.2021;[Epub]     CrossRef
  • Molecular investigation of tick-borne pathogens in ticks removed from tick-bitten humans in the southwestern region of the Republic of Korea
    Mi Seon Bang, Choon-Mee Kim, Sang-Hyun Pyun, Dong-Min Kim, Na Ra Yun, Martin Chtolongo Simuunza
    PLOS ONE.2021; 16(6): e0252992.     CrossRef
  • Animal reservoirs of zoonotic Babesia species: A global systematic review and meta-analysis of their prevalence, distribution and species diversity
    Solomon Ngutor Karshima, Magdalene Nguvan Karshima, Musa Isiyaka Ahmed
    Veterinary Parasitology.2021; 298: 109539.     CrossRef
  • Molecular evidence of zoonotic Babesia species, other than B. microti, in ixodid ticks collected from small mammals in the Republic of Korea
    Tae Yun Kim, Seong Yoon Kim, Tae‐Kyu Kim, Hee IL Lee, Shin‐Hyeong Cho, Wook‐Gyo Lee, Hyunwoo Kim
    Veterinary Medicine and Science.2021; 7(6): 2427.     CrossRef
  • A Review of Zoonotic Babesiosis as an Emerging Public Health Threat in Asia
    Sabir Hussain, Abrar Hussain, Muhammad Umair Aziz, Baolin Song, Jehan Zeb, David George, Jun Li, Olivier Sparagano
    Pathogens.2021; 11(1): 23.     CrossRef
  • The global seroprevalence of Toxoplasma gondii in deer from 1978 to 2019: A systematic review and meta-analysis
    Ao Zeng, Qing-Long Gong, Qi Wang, Chun-Ren Wang, Xiao-Xuan Zhang
    Acta Tropica.2020; 208: 105529.     CrossRef
  • Molecular Detection of Toxoplasma Gondii in Haemaphysalis Ticks in Korea
    Ju Yeong Kim, You Shine Kwak, In-Yong Lee, Tai-Soon Yong
    The Korean Journal of Parasitology.2020; 58(3): 327.     CrossRef
  • Molecular detection of Toxoplasma gondii in opossums from Southeastern, Brazil
    Marcos Antônio Bezerra-Santos, Bárbara Cristina Félix Nogueira, Ricardo Seiti Yamatogi, Artur Kanadani Campos
    Journal of Parasitic Diseases.2020; 44(3): 661.     CrossRef
  • Molecular Detection of Arthropod-Borne Pathogens in Eurasian Badgers (Meles meles) from the United Kingdom
    Lisa Guardone, Valentina Virginia Ebani, Ranieri Verin, Simona Nardoni, Antonio Consolazione, Malcolm Bennett, Francesca Mancianti
    Animals.2020; 10(3): 446.     CrossRef
  • Current Status of Tick-Borne Diseases in South Korea
    Jae Hyoung Im, JiHyeon Baek, Areum Durey, Hea Yoon Kwon, Moon-Hyun Chung, Jin-Soo Lee
    Vector-Borne and Zoonotic Diseases.2019; 19(4): 225.     CrossRef
  • Detection and characterization of an emerging type of Babesia sp. similar to Babesia motasi for the first case of human babesiosis and ticks in Korea
    Sung-Hee Hong, Seong-Yoon Kim, Bong Goo Song, Jong Yul Roh, Chong Rae Cho, Chul-Nam Kim, Tae-Hyun Um, Yee Gyung Kwak, Shin-Hyeong Cho, Sang-Eun Lee
    Emerging Microbes & Infections.2019; 8(1): 869.     CrossRef
  • 11,013 View
  • 191 Download
  • 16 Web of Science
  • Crossref
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

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.

Citations

Citations to this article as recorded by  Crossref logo
  • Navigating the Landscape of Tick Diversity: Integrating Molecular Approaches for Enhanced Control Measures
    Donath Damian
    Vector-Borne and Zoonotic Diseases.2025; 25(1): 1.     CrossRef
  • Tick Control Strategies: Critical Insights into Chemical, Biological, Physical, and Integrated Approaches for Effective Hard Tick Management
    Tsireledzo Goodwill Makwarela, Nimmi Seoraj-Pillai, Tshifhiwa Constance Nangammbi
    Veterinary Sciences.2025; 12(2): 114.     CrossRef
  • Study on Frequency of Hard Tick Isolated from Goat (Capra hircus Linnaeus, 1758) in Iraq
    Z A Makawi, H M Jihad, S Y Jasim
    IOP Conference Series: Earth and Environmental Science.2025; 1449(1): 012036.     CrossRef
  • Cross-continental hitchhiking of exotic ticks on human travelers and ensuing public health challenges in the USA
    Noelle Khalil, Lorelei Sandland, Goudarz Molaei
    iScience.2025; 28(8): 113223.     CrossRef
  • Hard Tick Species Parasitism Levels in Domestic Ruminants with Their Distribution and Role as Vectors: A Detailed Global Meta-analysis and Systematic Review
    Hassan Nasirian
    Acta Parasitologica.2024; 69(1): 1.     CrossRef
  • Data release: targeted systematic literature search for tick and tick-borne pathogen distributions in six countries in sub-Saharan Africa from 1901 to 2020
    Abigail A. Lilak, David B. Pecor, Graham Matulis, Alexander M. Potter, Rachel N. Wofford, Mary F. Kearney, Stephanie Mitchell, Fatima Jaradat, Arisa Kano, Dawn M. Zimmerman, James M. Hassell, Bersissa Kumsa, Maureen Kamau, Yvonne-Marie Linton, Michael E.
    Parasites & Vectors.2024;[Epub]     CrossRef
  • Detailed new insights about tick infestations in domestic ruminant groups: a global systematic review and meta-analysis
    Hassan Nasirian
    Journal of Parasitic Diseases.2022; 46(2): 526.     CrossRef
  • Epidemiology of tick-borne pathogens of cattle and tick control practices among mixed farming and pastoral communities in Gairo and Monduli districts, Tanzania
    Isihaka Haji, Martin Simuunza, Isack Ibrahim Kerario, Ning Jiang, Qijun Chen
    Veterinary Parasitology: Regional Studies and Reports.2022; 32: 100738.     CrossRef
  • Molecular Diversity of Hard Tick Species from Selected Areas of a Wildlife-Livestock Interface Ecosystem at Mikumi National Park, Morogoro Region, Tanzania
    Donath Damian, Modester Damas, Jonas Johansson Wensman, Mikael Berg
    Veterinary Sciences.2021; 8(3): 36.     CrossRef
  • Seroprevalence and associated risk factors of selected zoonotic viral hemorrhagic fevers in Tanzania
    Sima Rugarabamu, Gaspary O. Mwanyika, Susan F. Rumisha, Calvin Sindato, Hee-Young Lim, Gerald Misinzo, Leonard E.G. Mboera
    International Journal of Infectious Diseases.2021; 109: 174.     CrossRef
  • Development of a practical framework for sustainable surveillance and control of ticks and tick-borne diseases in Africa
    Felix Nchu, Nkululeko Nyangiwe, Dennis Muhanguzi, Jahashi Nzalawahe, Yakob Petro Nagagi, George Msalya, Natala Audu Joseph, Esther Gwae Kimaro, Margaret Mollel, Violet Temba, Difo Voukang Harouna
    Veterinary World.2020; 13(9): 1910.     CrossRef
  • Sensitivity of Different Cattle Breeds to the Infestation of Cattle Ticks Amblyomma variegatum, Rhipicephalus microplus, and Hyalomma spp. on the Natural Pastures of Opkara Farm, Benin
    Roland Eric Yessinou, Camus Adoligbe, Yao Akpo, Justin Adinci, Issaka Youssao Abdou Karim, Souaïbou Farougou
    Journal of Parasitology Research.2018; 2018: 1.     CrossRef
  • 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
    The Korean Journal of Parasitology.2018; 56(3): 305.     CrossRef
  • Abundance and distribution of Ixodid tick species infesting cattle reared under traditional farming systems in Tanzania
    Ibrahim Kerario Isack, Muleya Walter, Chenyambuga Sebastian, Koski Marja, Hwang Seong-Gu, Simuunza Martin
    African Journal of Agricultural Research.2017; 12(4): 286.     CrossRef
  • 10,918 View
  • 132 Download
  • 12 Web of Science
  • Crossref
Original Article
Sarcocystosis among Wild Captive and Zoo Animals in Malaysia
Baha Latif, Subramaniam Vellayan, Effat Omar, Suliman Abdullah, Noryatimah Mat Desa
Korean J Parasitol 2010;48(3):213-217.
Published online September 16, 2010
DOI: https://doi.org/10.3347/kjp.2010.48.3.213

Sarcocystis sp. infection was investigated in 20 necropsied captive wild mammals and 20 birds in 2 petting zoos in Malaysia. The gross post-mortem lesions in mammals showed marbling of the liver with uniform congestion of the intestine, and for birds, there was atrophy of the sternal muscles with hemorrhage and edema of the lungs in 2 birds. Naked eye examination was used for detection of macroscopic sarcocysts, and muscle squash for microscopic type. Only microscopically visible cysts were detected in 8 animals and species identification was not possible. Histological examination of the sections of infected skeletal muscles showed more than 5 sarcocysts in each specimen. No leukocytic infiltration was seen in affected organs. The shape of the cysts was elongated or circular, and the mean size reached 254 × 24.5 ?m and the thickness of the wall up to 2.5 ?m. Two stages were recognized in the cysts, the peripheral metrocytes and large numbers of crescent shaped merozoites. Out of 40 animals examined, 3 mammals and 5 birds were positive (20%). The infection rate was 15% and 25% in mammals and birds, respectively. Regarding the organs, the infection rate was 50% in the skeletal muscles followed by tongue and heart (37.5%), diaphragm (25%), and esophagus (12.5%). Further ultrastructural studies are required to identify the species of Sarcocystis that infect captive wild animals and their possible role in zoonosis.

Citations

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  • Gastrointestinal parasites of zoonotic importance observed in the wild, urban, and captive populations of non‐human primates in Malaysia
    Madinah Adrus, Ramlah Zainudin, Mariana Ahamad, Mohd‐Azlan Jayasilan, Mohd Tajuddin Abdullah
    Journal of Medical Primatology.2019; 48(1): 22.     CrossRef
  • Prevalence of parasites in working pig‐tailed Macaques (Macaca nemestrina) in Kelantan, Malaysia
    Siew Shean Choong, Mohamad Mimi Armiladiana, Hayati Hamdan Ruhil, Tan Li Peng
    Journal of Medical Primatology.2019; 48(4): 207.     CrossRef
  • Human and animal sarcocystosis in Malaysia: A review
    Baha Latif, Azdayanti Muslim
    Asian Pacific Journal of Tropical Biomedicine.2016; 6(11): 982.     CrossRef
  • Neglected Tropical Diseases among Two Indigenous Subtribes in Peninsular Malaysia: Highlighting Differences and Co-Infection of Helminthiasis and Sarcocystosis
    Soo Ching Lee, Romano Ngui, Tiong Kai Tan, Roslan Muhammad Aidil, Yvonne Ai Lian Lim, David Joseph Diemert
    PLoS ONE.2014; 9(9): e107980.     CrossRef
  • Initial Patient Cluster and First Positive Biopsy Findings in an Outbreak of Acute Muscular Sarcocystis-Like Infection in Travelers Returning from Tioman Island, Peninsular Malaysia, in 2011
    Dennis Tappe, Karen Ernestus, Stephan Rauthe, Christoph Schoen, Matthias Frosch, Andreas Müller, August Stich
    Journal of Clinical Microbiology.2013; 51(2): 725.     CrossRef
  • Zoonoses: a potential obstacle to the growing wildlife industry of Namibia
    Kudakwashe Magwedere, Maria Y. Hemberger, Louw C. Hoffman, Francis Dziva
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