First identification of Cryptosporidium parvum virus 1 (CSpV1) in various subtypes of Cryptosporidium parvum from diarrheic calves, lambs and goat kids from France

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作者
Karim Tarik Adjou
Aurélie Chevillot
Pierrick Lucas
Yannick Blanchard
Houria Louifi
Razika Arab
Mohamed Mammeri
Myriam Thomas
Bruno Polack
Grégory Karadjian
Nolwenn M. Dheilly
机构
[1] Ecole Nationale Vétérinaire d’Alfort,Laboratoire de Santé Animale
[2] Anses,Anses Animal Health Laboratory
[3] INRAE,Laboratoire de Ploufragan
[4] UMR BIPAR,Plouzané
[5] UMR1161 Virology,Niort, Unité Génétique virale et biosécurité
[6] INRAE,undefined
[7] Anses,undefined
[8] ENVA,undefined
[9] ANSES,undefined
[10] Agence Nationale de Sécurité Sanitaire de l’Alimentation,undefined
[11] de l’Environnement et du Travail,undefined
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关键词
cryspovirus; calves; lambs; kids; France;
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摘要
Cryptosporidium spp. remain a major cause of waterborne diarrhea and illness in developing countries and represent a significant burden to farmers worldwide. Cryptosporidium parvum virus 1 (CSpV1), of the genus Cryspovirus, was first reported to be present in the cytoplasm of C. parvum in 1997. Full-length genome sequences have been obtained from C. parvum from Iowa (Iowa), Kansas (KSU) and China. We aimed at characterizing the genome of CSpV1 from France and used sequence analysis from Cryptosporidium isolates to explore whether CSpV1 genome diversity varies over time, with geographical sampling location, C. parvum genetic diversity, or ruminant host species. A total of 123 fecal samples of cattle, sheep and goats were collected from 17 different French departments (57 diseased animal fecal samples and 66 healthy animal fecal samples). Subtyping analysis of the C. parvum isolates revealed the presence of two zoonotic subtype families IIa and IId. Sequence analysis of CSpV1 revealed that all CSpV1 from France, regardless of the subtype of C. parvum (IIaA15G2R1, IIaA17G2R1 and IIdA18G1R1) are more closely related to CSpV1 from Turkey, and cluster on a distinct branch from CSpV1 collected from C. parvum subtype IIaA15G2R1 from Asia and North America. We also found that samples collected on a given year or successive years in a given location are more likely to host the same subtype of C. parvum and the same CSpV1 strain. Yet, there is no distinct clustering of CSpV1 per French department or ruminants, probably due to trade, and transmission of C. parvum among host species. Our results point towards (i) a close association between CSpV1 movement and C. parvum movement, (ii) recent migrations of C. parvum among distantly located departments and (iii) incidental transmission of C. parvum between ruminants. All together, these results provide insightful information regarding CSpV1 evolution and suggest the virus might be used as an epidemiological tracer for C. parvum. Future studies need to investigate CSpV1’s role in C. parvum virulence and on subtype ability to infect different species.
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