Evaluation of the limitations and methods to improve rapid phage-based detection of viable Mycobacterium avium subsp. paratuberculosis in the blood of experimentally infected cattle

Background Disseminated infection and bacteraemia is an underreported and under-researched aspect of Johne’s disease. This is mainly due to the time it takes for Mycobacterium avium subsp. paratuberculosis (MAP) to grow and lack of sensitivity of culture. Viable MAP cells can be detected in the b...

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Main Authors: Swift, Benjamin M.C., Huxley, J.N., Plain, Karen M., Begg, Douglas J., de Silva, Kumidika, Purdie, Auriol C., Whittington, Richard J., Rees, Catherine
Format: Article
Published: BioMed Central 2016
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Online Access:https://eprints.nottingham.ac.uk/37976/
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author Swift, Benjamin M.C.
Huxley, J.N.
Plain, Karen M.
Begg, Douglas J.
de Silva, Kumidika
Purdie, Auriol C.
Whittington, Richard J.
Rees, Catherine
author_facet Swift, Benjamin M.C.
Huxley, J.N.
Plain, Karen M.
Begg, Douglas J.
de Silva, Kumidika
Purdie, Auriol C.
Whittington, Richard J.
Rees, Catherine
author_sort Swift, Benjamin M.C.
building Nottingham Research Data Repository
collection Online Access
description Background Disseminated infection and bacteraemia is an underreported and under-researched aspect of Johne’s disease. This is mainly due to the time it takes for Mycobacterium avium subsp. paratuberculosis (MAP) to grow and lack of sensitivity of culture. Viable MAP cells can be detected in the blood of cattle suffering from Johne’s disease within 48 h using peptide-mediated magnetic separation (PMMS) followed by bacteriophage amplification. The aim of this study was to demonstrate the first detection of MAP in the blood of experimentally exposed cattle using the PMMS-bacteriophage assay and to compare these results with the immune response of the animal based on serum ELISA and shedding of MAP by faecal culture. Results Using the PMMS-phage assay, seven out of the 19 (37 %) MAP-exposed animals that were tested were positive for viable MAP cells although very low numbers of MAP were detected. Two of these animals were positive by faecal culture and one was positive by serum ELISA. There was no correlation between PMMS-phage assay results and the faecal and serum ELISA results. None of the control animals (10) were positive for MAP using any of the four detection methods. Investigations carried out into the efficiency of the assay; found that the PMMS step was the limiting factor reducing the sensitivity of the phage assay. A modified method using the phage assay directly on isolated peripheral blood mononuclear cells (without PMMS) was found to be superior to the PMMS isolation step. Conclusions This proof of concept study has shown that viable MAP cells are present in the blood of MAP-exposed cattle prior to the onset of clinical signs. Although only one time point was tested, the ability to detect viable MAP in the blood of subclinically infected animals by the rapid phage-based method has the potential to increase the understanding of the pathogenesis of Johne’s disease progression by warranting further research on the presence of MAP in blood.
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spelling nottingham-379762020-05-04T17:56:22Z https://eprints.nottingham.ac.uk/37976/ Evaluation of the limitations and methods to improve rapid phage-based detection of viable Mycobacterium avium subsp. paratuberculosis in the blood of experimentally infected cattle Swift, Benjamin M.C. Huxley, J.N. Plain, Karen M. Begg, Douglas J. de Silva, Kumidika Purdie, Auriol C. Whittington, Richard J. Rees, Catherine Background Disseminated infection and bacteraemia is an underreported and under-researched aspect of Johne’s disease. This is mainly due to the time it takes for Mycobacterium avium subsp. paratuberculosis (MAP) to grow and lack of sensitivity of culture. Viable MAP cells can be detected in the blood of cattle suffering from Johne’s disease within 48 h using peptide-mediated magnetic separation (PMMS) followed by bacteriophage amplification. The aim of this study was to demonstrate the first detection of MAP in the blood of experimentally exposed cattle using the PMMS-bacteriophage assay and to compare these results with the immune response of the animal based on serum ELISA and shedding of MAP by faecal culture. Results Using the PMMS-phage assay, seven out of the 19 (37 %) MAP-exposed animals that were tested were positive for viable MAP cells although very low numbers of MAP were detected. Two of these animals were positive by faecal culture and one was positive by serum ELISA. There was no correlation between PMMS-phage assay results and the faecal and serum ELISA results. None of the control animals (10) were positive for MAP using any of the four detection methods. Investigations carried out into the efficiency of the assay; found that the PMMS step was the limiting factor reducing the sensitivity of the phage assay. A modified method using the phage assay directly on isolated peripheral blood mononuclear cells (without PMMS) was found to be superior to the PMMS isolation step. Conclusions This proof of concept study has shown that viable MAP cells are present in the blood of MAP-exposed cattle prior to the onset of clinical signs. Although only one time point was tested, the ability to detect viable MAP in the blood of subclinically infected animals by the rapid phage-based method has the potential to increase the understanding of the pathogenesis of Johne’s disease progression by warranting further research on the presence of MAP in blood. BioMed Central 2016-06-16 Article PeerReviewed Swift, Benjamin M.C., Huxley, J.N., Plain, Karen M., Begg, Douglas J., de Silva, Kumidika, Purdie, Auriol C., Whittington, Richard J. and Rees, Catherine (2016) Evaluation of the limitations and methods to improve rapid phage-based detection of viable Mycobacterium avium subsp. paratuberculosis in the blood of experimentally infected cattle. BMC Veterinary Research, 12 . 115/1-115/8. ISSN 1746-6148 Johne’s disease Paratuberculosis Mycobacteria Bacteriophage Bacteraemia Blood test Detection method http://bmcvetres.biomedcentral.com/articles/10.1186/s12917-016-0728-2 doi:10.1186/s12917-016-0728-2 doi:10.1186/s12917-016-0728-2
spellingShingle Johne’s disease
Paratuberculosis
Mycobacteria
Bacteriophage
Bacteraemia
Blood test
Detection method
Swift, Benjamin M.C.
Huxley, J.N.
Plain, Karen M.
Begg, Douglas J.
de Silva, Kumidika
Purdie, Auriol C.
Whittington, Richard J.
Rees, Catherine
Evaluation of the limitations and methods to improve rapid phage-based detection of viable Mycobacterium avium subsp. paratuberculosis in the blood of experimentally infected cattle
title Evaluation of the limitations and methods to improve rapid phage-based detection of viable Mycobacterium avium subsp. paratuberculosis in the blood of experimentally infected cattle
title_full Evaluation of the limitations and methods to improve rapid phage-based detection of viable Mycobacterium avium subsp. paratuberculosis in the blood of experimentally infected cattle
title_fullStr Evaluation of the limitations and methods to improve rapid phage-based detection of viable Mycobacterium avium subsp. paratuberculosis in the blood of experimentally infected cattle
title_full_unstemmed Evaluation of the limitations and methods to improve rapid phage-based detection of viable Mycobacterium avium subsp. paratuberculosis in the blood of experimentally infected cattle
title_short Evaluation of the limitations and methods to improve rapid phage-based detection of viable Mycobacterium avium subsp. paratuberculosis in the blood of experimentally infected cattle
title_sort evaluation of the limitations and methods to improve rapid phage-based detection of viable mycobacterium avium subsp. paratuberculosis in the blood of experimentally infected cattle
topic Johne’s disease
Paratuberculosis
Mycobacteria
Bacteriophage
Bacteraemia
Blood test
Detection method
url https://eprints.nottingham.ac.uk/37976/
https://eprints.nottingham.ac.uk/37976/
https://eprints.nottingham.ac.uk/37976/