2014
DOI: 10.1371/journal.pone.0095698
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Safety and Immunogenicity of a Mycoplasma ovipneumoniae Bacterin for Domestic Sheep (Ovis aries)

Abstract: BackgroundMortality from epizootic pneumonia is hindering re-establishment of bighorn sheep populations in western North America. Mycoplasma ovipneumoniae, a primary agent of this disease, is frequently carried asymptomatically by the domestic sheep and goats that constitute the reservoir of this agent for transmission to bighorn sheep. Our long-term objective is to reduce the risk of M. ovipneumoniae infection of bighorn sheep; one approach to this objective is to control the pathogen in its reservoir hosts.M… Show more

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Cited by 41 publications
(53 citation statements)
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References 26 publications
(46 reference statements)
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“…() and Ziegler et al . (), respectively. Both tests were used to ascribe infection status to a sample, and RT‐PCR was also used to estimate relative pathogen load.…”
Section: Methodsmentioning
confidence: 95%
See 1 more Smart Citation
“…() and Ziegler et al . (), respectively. Both tests were used to ascribe infection status to a sample, and RT‐PCR was also used to estimate relative pathogen load.…”
Section: Methodsmentioning
confidence: 95%
“…We collected nasal samples with dacron swabs and placed these samples into mycoplasma broth (Hardy Diagnostics, Santa Maria, CA) for culture enrichment or into sterile tubes (dry swabs). We conducted PCR and RT-PCR (realtime PCR) detection of M. ovipneumoniae with the methods described in McAuliffe et al (2003) and Ziegler et al (2014), respectively. Both tests were used to ascribe infection status to a sample, and RT-PCR was also used to estimate relative pathogen load.…”
Section: Sampling Methods and Diagnostic Testingmentioning
confidence: 99%
“…We extracted DNA from a subset of these sources to detect and strain type M. ovipneumoniae within the study population and the metapopulation through time. Detection was based on conventional (McAuliffe et al ) and realtime (Ziegler et al ) PCR.…”
Section: Methodsmentioning
confidence: 99%
“…We extracted DNA from a subset of these sources to detect and strain type M. ovipneumoniae within the study population and the metapopulation through time. Detection was based on conventional (McAuliffe et al 2003) and realtime (Ziegler et al 2014) PCR. We used multi-locus sequence typing (MLST) to characterize strains using partial DNA sequences of the 16S-23S intergenic spacer region (IGS), the small ribosomal subunit (16S), and the genes encoding RNA polymerase B (rpoB) and gyrase B (gyrB).…”
Section: Strain Typingmentioning
confidence: 99%
“…Nasal swabs were obtained from most (82 of 129, accounting for 74% of all observations) of the marked animals in the winter preceding summer observations. Samples were analysed at the Washington Disease Diagnostic Laboratory, who measured per cent inhibition by an anti-M. ovi antibody using a competitive ELISA, and identified active current infections on a categorical basis (an animal was infected or not) using real-time M. ovi-specific PCR (Ziegler et al 2014). We assume PCR status during the preceding winter was a reasonable proxy for an active infection throughout this manuscript.…”
Section: Materials and Methods Study Populations And Field Data Collementioning
confidence: 99%