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Detection and Molecular Characterization of Cryptosporidium spp. from Wild Rodents and Insectivores in South Korea
Juha Song, C-Yoon Kim, Seo-Na Chang, Tamer Said Abdelkader, Juhee Han, Tae-Hyun Kim, Hanseul Oh, Ji Min Lee, Dong-Su Kim, Jong-Taek Kim, Hong-Shik Oh, Moonsuk Hur, Jae-Hwa Suh, Jae-Hak Park
Korean J Parasitol 2015;53(6):737-743.
Published online December 31, 2015
DOI: https://doi.org/10.3347/kjp.2015.53.6.737
In order to examine the prevalence of Cryptosporidium infection in wild rodents and insectivores of South Korea and to assess their potential role as a source of human cryptosporidiosis, a total of 199 wild rodents and insectivore specimens were collected from 10 regions of South Korea and screened for Cryptosporidium infection over a period of 2 years (2012-2013). A nested-PCR amplification of Cryptosporidium oocyst wall protein (COWP) gene fragment revealed an overall prevalence of 34.2% (68/199). The sequence analysis of 18S rRNA gene locus of Cryptosporidium was performed from the fecal and cecum samples that tested positive by COWP amplification PCR. As a result, we identified 4 species/genotypes; chipmunk genotype I, cervine genotype I, C. muris, and a new genotype which is closely related to the bear genotype. The new genotype isolated from 12 Apodemus agrarius and 2 Apodemus chejuensis was not previously identified as known species or genotype, and therefore, it is supposed to be a novel genotype. In addition, the host spectrum of Cryptosporidium was extended to A. agrarius and Crosidura lasiura, which had not been reported before. In this study, we found that the Korean wild rodents and insectivores were infected with various Cryptosporidium spp. with large intra-genotypic variationa, indicating that they may function as potential reservoirs transmitting zoonotic Cryptosporidium to livestock and humans.

Citations

Citations to this article as recorded by  Crossref logo
  • Prevalence and novel genetic characteristics of Cryptosporidium spp. in wild rodents in the northern foothills of the Dabie Mountains, southeast Henan Province, China
    Mengyao Yang, Yin Fu, Pitambar Dhakal, Zi Yan, Jiashu Lang, Chaofeng Ma, Yuhong Jiang, Congzhou Wang, Longxian Zhang, Lihua Xiao,
    PLOS Neglected Tropical Diseases.2025; 19(5): e0013117.     CrossRef
  • Critters and contamination: Zoonotic protozoans in urban rodents and water quality
    Siobhon Egan, Amanda D. Barbosa, Yaoyu Feng, Lihua Xiao, Una Ryan
    Water Research.2024; 251: 121165.     CrossRef
  • Detection and Molecular Characterization of Giardia and Cryptosporidium spp. Circulating in Wild Small Mammals from Portugal
    Laura Lux, Rainer G. Ulrich, Sérgio Santos-Silva, João Queirós, Christian Imholt, Christian Klotz, Joana Paupério, Ricardo Pita, Hélia Vale-Gonçalves, Paulo Célio Alves, João R. Mesquita
    Animals.2023; 13(3): 515.     CrossRef
  • Outbreak of severe diarrhea due to zoonotic Cryptosporidium parvum and C. xiaoi in goat kids in Chungcheongbuk-do, Korea
    Ah-Young Kim, Badriah Alkathiri, Subin Lee, Kyung-Duk Min, Soochong Kim, Sang-Myeong Lee, Wan-Kyu Lee, Dongmi Kwak, Seung-Hun Lee
    Parasitology Research.2023; 122(9): 2045.     CrossRef
  • Cryptosporidium mortiferum n. sp. (Apicomplexa: Cryptosporidiidae), the species causing lethal cryptosporidiosis in Eurasian red squirrels (Sciurus vulgaris)
    Lenka Tůmová, Jana Ježková, Jitka Prediger, Nikola Holubová, Bohumil Sak, Roman Konečný, Dana Květoňová, Lenka Hlásková, Michael Rost, John McEvoy, Lihua Xiao, Monica Santín, Martin Kváč
    Parasites & Vectors.2023;[Epub]     CrossRef
  • Public health and ecological significance of rodents in Cryptosporidium infections
    Kaihui Zhang, Yin Fu, Junqiang Li, Longxian Zhang
    One Health.2022; 14: 100364.     CrossRef
  • Cryptosporidium rattin. sp. (Apicomplexa: Cryptosporidiidae) and genetic diversity ofCryptosporidiumspp. in brown rats (Rattus norvegicus) in the Czech Republic
    Jana Ježková, Jitka Prediger, Nikola Holubová, Bohumil Sak, Roman Konečný, Yaoyu Feng, Lihua Xiao, Michael Rost, John McEvoy, Martin Kváč
    Parasitology.2021; 148(1): 84.     CrossRef
  • The Role of Peridomestic Rodents as Reservoirs for Zoonotic Foodborne Pathogens
    Nusrat A. Jahan, Laramie L. Lindsey, Peter A. Larsen
    Vector-Borne and Zoonotic Diseases.2021; 21(3): 133.     CrossRef
  • Biodiversity of the Coccidia (Apicomplexa: Conoidasida) in vertebrates: what we know, what we do not know, and what needs to be done
    Donald W. Duszynski
    Folia Parasitologica.2021;[Epub]     CrossRef
  • Genetic characterizations of Cryptosporidium spp. from pet rodents indicate high zoonotic potential of pathogens from chinchillas
    Jia Chen, Weijian Wang, Yu Lin, Lianbei Sun, Na Li, Yaqiong Guo, Martin Kvac, Una Ryan, Yaoyu Feng, Lihua Xiao
    One Health.2021; 13: 100269.     CrossRef
  • Zoonotic Cryptosporidium spp. in Wild Rodents and Shrews
    Rauni Kivistö, Sofia Kämäräinen, Otso Huitu, Jukka Niemimaa, Heikki Henttonen
    Microorganisms.2021; 9(11): 2242.     CrossRef
  • Taxonomy and molecular epidemiology of Cryptosporidium and Giardia – a 50 year perspective (1971–2021)
    Una M. Ryan, Yaoyu Feng, Ronald Fayer, Lihua Xiao
    International Journal for Parasitology.2021; 51(13-14): 1099.     CrossRef
  • Molecular Detection of Cryptosporidium spp. and Enterocytozoon bieneusi Infection in Wild Rodents From Six Provinces in China
    Hong-Bo Ni, Yu-Zhe Sun, Si-Yuan Qin, Yan-Chun Wang, Quan Zhao, Zheng-Yao Sun, Miao Zhang, Ding Yang, Zhi-Hui Feng, Zheng-Hao Guan, Hong-Yu Qiu, Hao-Xian Wang, Nian-Yu Xue, He-Ting Sun
    Frontiers in Cellular and Infection Microbiology.2021;[Epub]     CrossRef
  • Serosurvey and molecular detection of the main zoonotic parasites carried by commensal Rattus norvegicus population in Tehran, Iran
    Taher Azimi, Mohammad Reza Pourmand, Fatemeh Fallah, Abdollah Karimi, Roxana Mansour-Ghanaie, Seyedeh Mahsan Hoseini-Alfatemi, Mehdi Shirdoust, Leila Azimi
    Tropical Medicine and Health.2020;[Epub]     CrossRef
  • Diversity of Cryptosporidium spp. in wild rodents from the Canary Islands, Spain
    Katherine García-Livia, Aarón Martín-Alonso, Pilar Foronda
    Parasites & Vectors.2020;[Epub]     CrossRef
  • Diversity of Cryptosporidium spp. in Apodemus spp. in Europe
    Šárka Čondlová, Michaela Horčičková, Nikola Havrdová, Bohumil Sak, Lenka Hlásková, Agnieszka Perec-Matysiak, Marta Kicia, John McEvoy, Martin Kváč
    European Journal of Protistology.2019; 69: 1.     CrossRef
  • Cryptosporidium apodemi sp. n. and Cryptosporidium ditrichi sp. n. (Apicomplexa: Cryptosporidiidae) in Apodemus spp.
    Šárka Čondlová, Michaela Horčičková, Bohumil Sak, Dana Květoňová, Lenka Hlásková, Roman Konečný, Michal Stanko, John McEvoy, Martin Kváč
    European Journal of Protistology.2018; 63: 1.     CrossRef
  • Molecular characterizations of Cryptosporidium spp. and Enterocytozoon bieneusi in brown rats (Rattus norvegicus) from Heilongjiang Province, China
    Wei Zhao, Jianguang Wang, Guangxu Ren, Ziyin Yang, Fengkun Yang, Weizhe Zhang, Yingchu Xu, Aiqin Liu, Hong Ling
    Parasites & Vectors.2018;[Epub]     CrossRef
  • Subtype analysis of zoonotic pathogen Cryptosporidium skunk genotype
    Wenchao Yan, Kerri Alderisio, Dawn M. Roellig, Kristin Elwin, Rachel M. Chalmers, Fengkun Yang, Yuanfei Wang, Yaoyu Feng, Lihua Xiao
    Infection, Genetics and Evolution.2017; 55: 20.     CrossRef
  • Native and introduced squirrels in Italy host different Cryptosporidium spp.
    Jitka Prediger, Michaela Horčičková, Lada Hofmannová, Bohumil Sak, Nicola Ferrari, Maria Vittoria Mazzamuto, Claudia Romeo, Lucas A. Wauters, John McEvoy, Martin Kváč
    European Journal of Protistology.2017; 61: 64.     CrossRef
  • Cryptosporidium homai n. sp. (Apicomplexa: Cryptosporidiiae) from the guinea pig (Cavia porcellus)
    Alireza Zahedi, Zoey Durmic, Alexander W. Gofton, Susan Kueh, Jill Austen, Malcolm Lawson, Lauren Callahan, John Jardine, Una Ryan
    Veterinary Parasitology.2017; 245: 92.     CrossRef
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Comparative Sensitivity of PCR Primer Sets for Detection of Cryptosporidium parvum
Jae-Ran Yu, Soo-Ung Lee, Woo-Yoon Park
Korean J Parasitol 2009;47(3):293-297.
Published online August 28, 2009
DOI: https://doi.org/10.3347/kjp.2009.47.3.293

Improved methods for detection of Cryptosporidium oocysts in environmental and clinical samples are urgently needed to improve detection of cryptosporidiosis. We compared the sensitivity of 7 PCR primer sets for detection of Cryptosporidium parvum. Each target gene was amplified by PCR or nested PCR with serially diluted DNA extracted from purified C. parvum oocysts. The target genes included Cryptosporidium oocyst wall protein (COWP), small subunit ribosomal RNA (SSU rRNA), and random amplified polymorphic DNA. The detection limit of the PCR method ranged from 103 to 104 oocysts, and the nested PCR method was able to detect 100 to 102 oocysts. A second-round amplification of target genes showed that the nested primer set specific for the COWP gene proved to be the most sensitive one compared to the other primer sets tested in this study and would therefore be useful for the detection of C. parvum.

Citations

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  • Occurrence and molecular characterization of Cryptosporidium oocysts in chickens from Egypt, and a meta-analysis for Cryptosporidium infections in chickens worldwide
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    Veterinary Parasitology: Regional Studies and Reports.2025; 57: 101169.     CrossRef
  • Evaluating the role of synanthropic filth flies in the transmission of zoonotic parasites: field and laboratory evidence from different animal rearing sites in upper Egypt with focus on Cryptosporidium spp.
    Omaima Ragab AbdAllah, Refaat M. Gabre, Sara Abdelaal Mohammed, Ahmed Mohamed Korayem, Hala E. Hussein, Alzahraa Abdelraouf Ahmad
    BMC Veterinary Research.2025;[Epub]     CrossRef
  • Chemical profiling of Verbena officinalis and assessment of its anti-cryptosporidial activity in experimentally infected immunocompromised mice
    Eman S. El-Wakil, Maha A.M. El-Shazly, Ayman M. El-Ashkar, Tarek Aboushousha, Mosad A. Ghareeb
    Arabian Journal of Chemistry.2022; 15(7): 103945.     CrossRef
  • Anti-cryptosporidial activity of Camellia sinensis (green tea extract) in experimentally infected immunocompromised mice
    Eman S. El-Wakil, Eman Ali Mohamed, Eman Ahmed El-Wakil, Tarek S. AbouShousha, Neimat Mousa Amer
    Acta Protozoologica.2022; 61: 23.     CrossRef
  • Detection and Molecular Identification of Cryptosporidium Species Among Children with Malignancies
    Heba Said Ibrahim, Amel Youssef Shehab, Amal Farahat Allam, Mostafa Aboelhoda Mohamed, Hoda Fahmy Farag, Mona Mohamed Tolba
    Acta Parasitologica.2021; 66(2): 377.     CrossRef
  • Competency Assessment: Diagnostic Methods for Detection of Cryptosporidium, Microsporidia, and Toxoplasma in Bronchoalveolar Lavage Samples
    Zahra Eslamirad, Abdolatif Moini, Mojtaba Didehdar, Reza Hajihossein, Ali Arash Anoushiravani
    Jundishapur Journal of Microbiology.2021;[Epub]     CrossRef
  • Molecular epidemiology of Cryptosporidium spp. in an agricultural area of northern Vietnam: A community survey
    Hanako Iwashita, Taichiro Takemura, Asako Tokizawa, Tetsuhiro Sugamoto, Vu Dinh Thiem, Tuan Hai Nguyen, Tho Duc Pham, Anh Hong Quynh Pham, Hang Thi Doan, Na Ly Tran, Tetsu Yamashiro
    Parasitology International.2021; 83: 102341.     CrossRef
  • Genotype and subtype analyses of Cryptosporidium isolate from humans by gp60 PCR-RLFP in Zabol, Southeast of Iran
    Mansour Dabirzadeh, Habibeh Mohammadian, Hakim Azizi, Mahdi Khoshsima Shahreki
    Modern Medical Laboratory Journal.2021; 4(1): 5.     CrossRef
  • In vitro and in vivo anti-Cryptosporidium and anti-inflammatory effects of Aloe vera gel in dexamethasone immunosuppressed mice
    Alyaa Farid, Aya Tawfik, Basil Elsioufy, Gehan Safwat
    International Journal for Parasitology: Drugs and Drug Resistance.2021; 17: 156.     CrossRef
  • Prevalence and molecular characterization of Cryptosporidium species in poultry in Bangladesh
    Mohammad Hazzaz Bin Kabir, Yongmei Han, Seung-Hun Lee, Arifin Budiman Nugraha, Frances Recuenco, Fumi Murakoshi, Xuenan Xuan, Kentaro Kato
    One Health.2020; 9: 100122.     CrossRef
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    International Journal of Environmental Research and Public Health.2020; 17(14): 5048.     CrossRef
  • The Detection Limit of PCR Amplification for Cryptosporidium spp. Oocysts in Fecal Samples
    Harith Saeed Al-Warid, Ihsan M. Al-Saqur, Souhaila H. Mahmood
    National Academy Science Letters.2019; 42(5): 423.     CrossRef
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    Veterinary Parasitology: Regional Studies and Reports.2019; 16: 100280.     CrossRef
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    Shiraz E-Medical Journal.2019;[Epub]     CrossRef
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    The Korean Journal of Parasitology.2019; 57(5): 531.     CrossRef
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  • 17,609 View
  • 170 Download
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Original Article

Toxocariasis and Ingestion of Raw Cow Liver in Patients with Eosinophilia
Dongil Choi, Jae Hoon Lim, Dong-Chull Choi, Seung Woon Paik, Sun-Hee Kim, Sun Huh
Korean J Parasitol 2008;46(3):139-143.
Published online September 20, 2008
DOI: https://doi.org/10.3347/kjp.2008.46.3.139

Ingestion of raw animal liver has been suggested as a possible mode of infection of human toxocariasis. We evaluated the relationship between toxocariasis and the ingestion of raw meat in patients with eosinophilia of unknown etiology. The study population consisted of 120 patients presenting with peripheral blood eosinophilia (> 500 cells/?l or > 10% of the white blood cell count). They were divided into 2 groups: 104 seropositive patients based on a Toxocara excretory-secretory IgG ELISA and 16 seronegative patients. While 25.0% of seronegative patients had a recent history of eating raw cow liver, 87.5% of seropositive patients had this history. Multivariate statistical analysis showed that a recent history of eating raw cow liver was related to an increased risk of toxocariasis. Collectively, it is proposed that raw cow liver is a significant infection source of toxocariasis in the patients with eosinophilia of unknown etiology.

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Brief Communication
Examination of gastrointestinal helminth in livestock grazing in grassland of Bangladesh
M. Motahar-Hussain Mondal, M-Khyrul Islam, Jin Hur, John-Hwa Lee, Byeong-Kirl Baek
Korean J Parasitol 2000;38(3):187-190.
Published online September 30, 2000
DOI: https://doi.org/10.3347/kjp.2000.38.3.187

To determine association of grassland with parasitic diseases of livestock in Bangladesh, the 'Tracer' animals (two cow calves and two goats) were released for a month in a grassland used for communal grazing of livestock near school premise in Kanthal, Trishal, Mymensingh, Bangladesh. After slaughtering of the tracer animals, their gastrointestinal tract examination revealed six species of nematode and one cestode. The nematode species were Haemonchus contortus, Trichostrongylus axei, Mecistocirrus digitatus, Oesophagostomum spp., Trichuris spp. and Bunostomum sp. The cestode was one of the genus Moniezia. With this preliminary study, grasslands are thought to be one of the main sources of gastrointestinal parasitic diseases of livestock in Bangladesh.

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