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Scientific Articles

Prevalence of endemic enteropathogens of calves in New Zealand dairy farms

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Pages 147-152 | Received 23 Feb 2014, Accepted 08 Sep 2014, Published online: 17 Mar 2015
 

Abstract

AIM: To conduct a country-wide prevalence study of bovine group A rotavirus, coronavirus, Cryptosporidium parvum, Salmonella spp. and enterotoxigenic K99+ Escherichia coli (K99) in calves on New Zealand dairy farms.

METHODS: Faecal samples (n=1,283) were collected during the 2011 calving season from calves that were 1–5 and 9–21 days-old on 97 dairy farms, and were analysed for the presence of bovine group A rotavirus, coronavirus, Cryptosporidium and Salmonella spp., and K99. Farm-level prevalences were calculated and relationships between demographic variables and the presence of enteropathogens were examined using logistic regression models.

RESULTS: Of the 97 farms, 93 (96%) had at least one sample infected with enteropathogens. The standardised farm prevalences of bovine group A rotavirus, bovine coronavirus and C. parvum were 46, 14 and 18%, respectively, in calves that were 1–5 days-old, and 57, 31 and 52%, respectively, in calves that were 9–21 days-old. The farm-level prevalence of K99 was 11% in calves that were 1–5 days-old. Salmonella spp. were found in three and four samples, from calves that were 1–5 and 9–21 days-old, respectively. No associations between explanatory variables and the presence of the enteropathogens were identified at the farm level. At the calf level, the odds of C. parvum shedding and of co-infection with any combination of pathogens were greater in calves that were 9–21 than 1–5 days-old.

CONCLUSIONS AND CLINICAL RELEVANCE: This study provides epidemiological estimates of the prevalence of calves’ enteropathogens in New Zealand, which could be used for infection risk assessment or estimation of the environmental loads of pathogens shed in cattle faeces.

Acknowledgments

This project was funded by MSD Animal Health and Massey University. We thank the farmers and the sampling staff, and Liz Burrows and Laryssa Howe (Massey University) for technical assistance with the reverse transcriptase PCR.

Notes

*Non-peer-reviewed

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