Literature DB >> 11849717

Sensitivity and specificity of pooled faecal culture and serology as flock-screening tests for detection of ovine paratuberculosis in Australia.

E S G Sergeant1, R J Whittington, S J More.   

Abstract

The flock-level sensitivity of pooled faecal culture and serological testing using AGID for the detection of ovine Johne's disease-infected flocks were estimated using non-gold-standard methods. The two tests were compared in an extensive field trial in 296 flocks in New South Wales during 1998. In each flock, a sample of sheep was selected and tested for ovine Johne's disease using both the AGID and pooled faecal culture. The flock-specificity of pooled faecal culture also was estimated from results of surveillance and market-assurance testing in New South Wales. The overall flock-sensitivity of pooled faecal culture was 92% (95% CI: 82.4 and 97.4%) compared to 61% (50.5 and 70.9%) for serology (assuming that both tests were 100% specific). In low-prevalence flocks (estimated prevalence <2%), the flock-sensitivities of pooled faecal culture and serology were 82% (57 and 96%) and 33% (19 and 49%), respectively, compared to 96% (85 and 99.5%) and 85% (72 and 93%), respectively, in higher-prevalence flocks (estimated prevalence > or =2%). A Bayesian approach incorporating prior knowledge on flock-specificity of pooled culture produced similar estimates and probability intervals. These estimates assume conditional independence of the two tests, and therefore might have over-estimated the true flock-sensitivities of the tests if the flock-sensitivities of pooled faecal culture and serology were correlated. The estimated minimum flock-specificity of pooled culture when used for surveillance and assurance testing was 99.1% (96.9 and 99.9%). Surveillance and assurance programs in Australia are designed to provide a flock-sensitivity of 95% for an assumed prevalence of 2%. Pooled faecal culture is performing at close to this level--whereas the flock-sensitivity of serology appears to be lower than expected, particularly in lower prevalence flocks.

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Year:  2002        PMID: 11849717     DOI: 10.1016/s0167-5877(01)00261-6

Source DB:  PubMed          Journal:  Prev Vet Med        ISSN: 0167-5877            Impact factor:   2.670


  5 in total

1.  Survival of Mycobacterium avium subsp. paratuberculosis in dam water and sediment.

Authors:  Richard J Whittington; Ian B Marsh; Leslie A Reddacliff
Journal:  Appl Environ Microbiol       Date:  2005-09       Impact factor: 4.792

2.  Estimated within-herd prevalence (WHP) of Mycobacterium avium subsp. paratuberculosis in a sample of Minnesota dairy herds using bacterial culture of pooled fecal samples.

Authors:  Eran A Raizman; Scott J Wells; Claudia A Muñoz-Zanzi; Saraya Tavornpanich
Journal:  Can J Vet Res       Date:  2011-04       Impact factor: 1.310

3.  Factors affecting isolation and identification of Mycobacterium avium subsp. paratuberculosis from fecal and tissue samples in a liquid culture system.

Authors:  Richard J Whittington
Journal:  J Clin Microbiol       Date:  2009-01-14       Impact factor: 5.948

4.  Detection of Mycobacterium avium subsp. paratuberculosis by a sonicate immunoassay based on surface-enhanced Raman scattering.

Authors:  Betsy Jean Yakes; Robert J Lipert; John P Bannantine; Marc D Porter
Journal:  Clin Vaccine Immunol       Date:  2007-12-12

5.  Impact of protein shedding on detection of Mycobacterium avium subsp. paratuberculosis by a whole-cell immunoassay incorporating surface-enhanced Raman scattering.

Authors:  Betsy Jean Yakes; Robert J Lipert; John P Bannantine; Marc D Porter
Journal:  Clin Vaccine Immunol       Date:  2007-12-12
  5 in total

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