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dc.contributor.authorButler, Carson J.
dc.contributor.authorEdwards, William H.
dc.contributor.authorJennings-Gaines, Jessica E.
dc.contributor.authorKillion, Halcyon J.
dc.contributor.authorWood, Mary E.
dc.contributor.authorMcWhirter, Douglas E.
dc.contributor.authorPaterson, J. Terrill
dc.contributor.authorProffitt, Kelly M.
dc.contributor.authorAlmberg, Emily S.
dc.contributor.authorWhite, Patrick J.
dc.contributor.authorRotella, Jay J.
dc.contributor.authorGarrott, Robert A.
dc.date.accessioned2017-09-20T15:44:54Z
dc.date.available2017-09-20T15:44:54Z
dc.date.issued2017-07
dc.identifier.citationButler, Carson J. , William H. Edwards, Jessica E. Jennings-Gaines, Halcyon J. Killion, Mary E. Woode, Douglas E. McWhirter, John Terrill Paterson, Kelly M. Proffitt, Emily S. Almberg, P. J. White, Jay J. Rotella, and Robert A. Garrott. "Assessing respiratory pathogen communities in bighorn sheep populations: Sampling realities, challenges, and improvements." PLoS One 12, no. 7 (July 2017): e0180689. DOI: 10.1371/journal.pone.0180689.en_US
dc.identifier.issn1932-6203
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/13716
dc.description.abstractRespiratory disease has been a persistent problem for the recovery of bighorn sheep (Ovis canadensis), but has uncertain etiology. The disease has been attributed to several bacterial pathogens including Mycoplasma ovipneumoniae and Pasteurellaceae pathogens belonging to the Mannheimia, Bibersteinia, and Pasteurella genera. We estimated detection probability for these pathogens using protocols with diagnostic tests offered by a fee-for-service laboratory and not offered by a fee-for-service laboratory. We conducted 2861 diagnostic tests on swab samples collected from 476 bighorn sheep captured across Montana and Wyoming to gain inferences regarding detection probability, pathogen prevalence, and the power of different sampling methodologies to detect pathogens in bighorn sheep populations. Estimated detection probability using fee-for-service protocols was less than 0.50 for all Pasteurellaceae and 0.73 for Mycoplasma ovipneumoniae. Non-fee-for-service Pasteurellaceae protocols had higher detection probabilities, but no single protocol increased detection probability of all Pasteurellaceae pathogens to greater than 0.50. At least one protocol resulted in an estimated detection probability of 0.80 for each pathogen except Mannheimia haemolytica, for which the highest detection probability was 0.45. In general, the power to detect Pasteurellaceae pathogens at low prevalence in populations was low unless many animals were sampled or replicate samples were collected per animal. Imperfect detection also resulted in low precision when estimating prevalence for any pathogen. Low and variable detection probabilities for respiratory pathogens using live-sampling protocols may lead to inaccurate conclusions regarding pathogen community dynamics and causes of bighorn sheep respiratory disease epizootics. We recommend that agencies collect multiples samples per animal for Pasteurellaceae detection, and one sample for Mycoplasma ovipneumoniae detection from at least 30 individuals to reliably detect both Pasteurellaceae and Mycoplasma ovipneumoniae at the population-level. Availability of PCR diagnostic tests to wildlife management agencies would improve the ability to reliably detect Pasteurellaceae in bighorn sheep populations.en_US
dc.titleAssessing respiratory pathogen communities in bighorn sheep populations: Sampling realities, challenges, and improvementsen_US
mus.citation.extentfirstpagee0180689en_US
mus.citation.extentlastpagee0180689en_US
mus.citation.issue7en_US
mus.citation.journaltitlePLoS Oneen_US
mus.citation.volume12en_US
mus.identifier.categoryLife Sciences & Earth Sciencesen_US
mus.identifier.doi10.1371/journal.pone.0180689en_US
mus.relation.collegeCollege of Letters & Scienceen_US
mus.relation.departmentEcology.en_US
mus.relation.universityMontana State University - Bozemanen_US
mus.data.thumbpage11en_US


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