Molecular characterization of Cryptosporidium isolates from humans in Ontario, Canada

被引:33
作者
Guy, Rebecca A. [1 ]
Yanta, Christine A. [1 ]
Muchaal, Pia K. [2 ]
Rankin, Marisa A. [1 ]
Thivierge, Karine [3 ]
Lau, Rachel [4 ]
Boggild, Andrea K. [4 ,5 ,6 ]
机构
[1] Publ Hlth Agcy Canada, Parasite Biol Unit, Natl Microbiol Lab, Div Enter Dis, 110 Stone Rd West, Guelph, ON N1G 3W4, Canada
[2] Publ Hlth Agcy Canada, Ctr Food Borne Environm & Zoonot Infect Dis, 370 Woodlawn Rd West, Guelph, ON N1H 7M7, Canada
[3] Inst Natl Sante Publ Quebec, Lab Sante Publ Quebec, 20045 Chemin St Marie, Ste Anne De Bellevue, PQ H9X 3R5, Canada
[4] Publ Hlth Ontario, Publ Hlth Ontario Lab, Toronto, ON M5G 1M1, Canada
[5] Toronto Gen Hosp, Trop Dis Unit, Toronto, ON M5G 2C4, Canada
[6] Univ Toronto, Fac Med, Toronto, ON M5S 1A8, Canada
关键词
Coccidiosis; Cryptosporidium parvum; Cryptosporidium hominis; Gp60; Sanger sequencing; Zoonosis; SUBTYPING CRYPTOSPORIDIUM; ZOONOTIC TRANSMISSION; WIDESPREAD OCCURRENCE; HOMINIS SUBTYPE; EPIDEMIOLOGY; INFECTIONS; SPP; CONSEQUENCES; MELEAGRIDIS; DIVERSITY;
D O I
10.1186/s13071-020-04546-9
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
BackgroundCryptosporidiosis is a gastrointestinal disease with global distribution. It has been a reportable disease in Canada since 2000; however, routine molecular surveillance is not conducted. Therefore, sources of contamination are unknown. The aim of this project was to identify species and subtypes of Cryptosporidium in clinical cases from Ontario, the largest province in Canada, representing one third of the Canadian population, in order to understand transmission patterns.MethodsA total of 169 frozen, banked, unpreserved stool specimens that were microscopy positive for Cryptosporidium over the period 2008-2017 were characterized using molecular tools. A subset of the 169 specimens were replicate samples from individual cases. DNA was extracted directly from the stool and nested PCR followed by Sanger sequencing was conducted targeting the small subunit ribosomal RNA (SSU) and glycoprotein 60 (gp60) genes.ResultsMolecular typing data and limited demographic data were obtained for 129 cases of cryptosporidiosis. Of these cases, 91 (70.5 %) were due to Cryptosporidium parvum and 24 (18.6%) were due to Cryptosporidium hominis. Mixed infections of C. parvum and C. hominis occurred in four (3.1%) cases. Five other species observed were Cryptosporidium ubiquitum (n = 5), Cryptosporidium felis (n = 2), Cryptosporidium meleagridis (n = 1), Cryptosporidium cuniculus (n = 1) and Cryptosporidium muris (n = 1). Subtyping the gp60 gene revealed 5 allelic families and 17 subtypes of C. hominis and 3 allelic families and 17 subtypes of C. parvum. The most frequent subtype of C. hominis was IbA10G2 (22.3%) and of C. parvum was IIaA15G2R1 (62.4%).ConclusionsThe majority of isolates in this study were C. parvum, supporting the notion that zoonotic transmission is the main route of cryptosporidiosis transmission in Ontario. Nonetheless, the observation of C. hominis in about a quarter of cases suggests that anthroponotic transmission is also an important contributor to cryptosporidiosis pathogenesis in Ontario.
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