Literature DB >> 21775002

Environmental contamination with Mycobacterium avium subsp. paratuberculosis in endemically infected dairy herds.

R L Smith1, Y H Schukken, A K Pradhan, J M Smith, R H Whitlock, J S Van Kessel, D R Wolfgang, Y T Grohn.   

Abstract

Environmental contamination with Mycobacterium avium subsp. paratuberculosis (MAP) is thought to be one of the primary sources of infection for dairy cattle. The exact link between fecal shedding of MAP by individual cows and environmental contamination levels at the herd level was explored with a cross-sectional analysis of longitudinally collected samples on 3 dairy farms. Composite samples from multiple environmental sites in 3 commercial dairy herds in the Northeast US were cultured quarterly for MAP, providing 1131 samples (133 (11.8%) were culture-positive), and all adult animals in the herds were tested biannually by fecal culture (FC), for 6 years. Of the environmental sites sampled, manure storage areas and shared alleyways were most likely to be culture-positive. Environmental sample results were compared to FC results from either the concurrent or previous sampling date at both the herd and the pen level. At the herd level, a 1 log unit increase in average fecal shedding increased the odds of a positive non-pen environmental sample by a factor of 6 and increased the average amount of MAP in non-pen samples by 2.9 cfu/g. At the pen level, a 1 log unit increase in average fecal shedding in the pen increased the odds of a positive environment by a factor of 2.4 and the average amount of MAP was increased by 3.5 cfu/g. We were not able to model the relationship between non-pen environmental sample status and the distance between shedding animals and the sample's location, and neighboring pens did not significantly affect the results of the pen-level analysis. The amount of MAP in pen-level samples and the probability of a pen testing positive for MAP were both positively but non-significantly correlated with the number of animals in the pen shedding >30 cfu/g of MAP. At least 6 environmental samples met the criteria for the U.S. Voluntary Bovine Johne's Disease Control Program on 47 of the 72 sampling dates; of these, 19 of the 47 FC-positive sampling dates were positive by the 6-sample environmental testing method, resulting in a herd sensitivity of 0.40 (95% CI: 0.26-0.54). None of the 3 FC-negative sampling dates produced positive environmental samples. Although environmental sampling can be used as a tool in understanding the level of MAP infection in a herd or pen, it did not appear to be a sensitive diagnostic method for herd positivity in these low prevalence herds, and its use may require caution.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21775002     DOI: 10.1016/j.prevetmed.2011.06.009

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


  14 in total

1.  Culture- and quantitative IS900 real-time PCR-based analysis of the persistence of Mycobacterium avium subsp. paratuberculosis in a controlled dairy cow farm environment.

Authors:  M Moravkova; V Babak; A Kralova; I Pavlik; I Slana
Journal:  Appl Environ Microbiol       Date:  2012-07-06       Impact factor: 4.792

2.  Evaluation of environmental fecal culture for Mycobacterium avium subspecies paratuberculosis detection in dairy herds and association with apparent within-herd prevalence.

Authors:  Carrie J Lavers; Shawn L B McKenna; Ian R Dohoo; Herman W Barkema; Greg P Keefe
Journal:  Can Vet J       Date:  2013-11       Impact factor: 1.008

3.  Detection of Mycobacterium avium subspecies paratuberculosis in tie-stall dairy herds using a standardized environmental sampling technique and targeted pooled samples.

Authors:  Juan C Arango-Sabogal; Geneviève Côté; Julie Paré; Olivia Labrecque; Jean-Philippe Roy; Sébastien Buczinski; Elizabeth Doré; Julie H Fairbrother; Nathalie Bissonnette; Vincent Wellemans; Gilles Fecteau
Journal:  Can J Vet Res       Date:  2016-07       Impact factor: 1.310

4.  Relationship between presence of cows with milk positive for Mycobacterium avium subsp. paratuberculosis-specific antibody by enzyme-linked immunosorbent assay and viable M. avium subsp. paratuberculosis in dust in cattle barns.

Authors:  Susanne W F Eisenberg; Ruj Chuchaisangrat; Mirjam Nielen; Ad P Koets
Journal:  Appl Environ Microbiol       Date:  2013-06-21       Impact factor: 4.792

5.  Sensitivities of a bulk-tank milk ELISA and composite fecal qPCR to detect various seroprevalence levels of paratuberculosis in cattle herds in Normandy, France.

Authors:  Arnaud Delafosse; Eric Meens; Thomas Rambaud; François Hanoy; Hamid Achour
Journal:  Can Vet J       Date:  2019-03       Impact factor: 1.008

6.  A new compartmental model of Mycobacterium avium subsp. paratuberculosis infection dynamics in cattle.

Authors:  Rebecca L Smith; Ynte H Schukken; Yrjö T Gröhn
Journal:  Prev Vet Med       Date:  2015-10-21       Impact factor: 2.670

Review 7.  Phage Amplification Assay for Detection of Mycobacterial Infection: A Review.

Authors:  Monika Beinhauerova; Iva Slana
Journal:  Microorganisms       Date:  2021-01-23

8.  Detection of Mycobacterium avium subspecies paratuberculosis in environmental samples by faecal culture and real-time PCR in relation to apparent within-herd prevalence as determined by individual faecal culture.

Authors:  K Donat; J Kube; J Dressel; E Einax; M Pfeffer; K Failing
Journal:  Epidemiol Infect       Date:  2014-10-02       Impact factor: 4.434

9.  Longitudinal data collection of Mycobacterium avium subspecies Paratuberculosis infections in dairy herds: the value of precise field data.

Authors:  Ynte H Schukken; Robert H Whitlock; Dave Wolfgang; Yrjo Grohn; Annabelle Beaver; JoAnn VanKessel; Mike Zurakowski; Rebecca Mitchell
Journal:  Vet Res       Date:  2015-06-19       Impact factor: 3.683

10.  Johne's disease: reliability of environmental sampling to characterize Mycobacterium avium subspecies paratuberculosis (MAP) infection in beef cow-calf herds.

Authors:  W Klawonn; E Einax; R Pützschel; M Schmidt; K Donat
Journal:  Epidemiol Infect       Date:  2016-04-20       Impact factor: 4.434

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