Return to search

Investigation of the distribution and risk factors associated with Mycobacterium avium subspecies paratuberculosis in cow-calf herds in Canada

This thesis summarizes an investigation of Mycobacterium avium subspecies paratuberculosis (Map) as a pathogen within the cow-calf industry in Canada. The specific objectives of this project were to describe the distribution of this pathogen in this industry provincially, as well as at the individual farm level in wildlife species, and in the environment. Secondary objectives of this project were to identify on-farm management risk factors that are associated with this disease and to examine potential options for herd level diagnostic capabilities. Nationally, 0.8% (95%CI = 0.4-1.1%) of the cows in the cow-calf industry were seropositive for Map with 11.7% (95%CI=7.0-16.5%) of the herds sampled having a minimum of one positive test result or 4.5% (95%CI=1.4-7.5%) of the herds having a minimum of two positive test results. The true cow prevalence was estimated as 1.8% (95%CI= 0.4 3.1). No Map was detected in any of the non-ruminant wildlife species sampled on cow-calf operations suggesting that these species were not of primary concern when dealing with the management of this disease. In a study not focussed on a cow-calf operation, Map was detected in one cluster of trapped coyote samples in a region with cow-calf production. The prevalence of Map infection in this cluster of coyotes was calculated to be 9.1% (CI: 5.7-12.5). The prevalence of infection in coyotes including all sites, ignoring the effect of clustering, was calculated to be 3.7% (CI: 2.3-5.1). The use of a commercial colostrum replacement on farm (Odds Ratio =3.96; 95% CI = 1.1014.23, p=0.035) and the presence of wild deer interacting with the cattle (Odds Ratio = 14.32; 95% CI = 1.13181.90, p=0.040) were positively associated with being a herd infected with paratuberculosis. The use of rotational grazing practices was protective (Odds Ratio = 0.20; 95% CI = 0.040.93, p=0.039). It was possible to detect environmental contamination with Map on cow-calf farms using bacterial culture and PCR for confirmation. No water samples were positive to Map; however, 6.2% of the non-water environmental samples were positive. The use of an environmental sampling protocol had a herd sensitivity of 29.6%. This finding led to a simulation modelling study to evaluate how various testing methods would compare in the broader population of cow-calf herds. The final mean risk of selecting a herd infected with Map that was not identified as positive via the herd screen test strategy was 12.9%, 9.8%, 9.6%, and 6.1% for no herd screen test, environmental sampling, ELISA serology, and pooled fecal culture strategies, respectively.

Identiferoai:union.ndltd.org:USASK/oai:usask.ca:etd-03312011-114913
Date14 April 2011
CreatorsDouma, Dale Peter
ContributorsStookey, Joseph, VanLeeuwen, John, Hendrick, Steve, Waldner, Cheryl, Campbell, John, Wobeser, Gary
PublisherUniversity of Saskatchewan
Source SetsUniversity of Saskatchewan Library
LanguageEnglish
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://library.usask.ca/theses/available/etd-03312011-114913/
Rightsunrestricted, I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to University of Saskatchewan or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.

Page generated in 0.0019 seconds