Second line molecular diagnosis for bovine tuberculosis to improve diagnostic schemes
Surveillance of bovine tuberculosis (bTB) is partly based on the sanitary inspection of carcasses at the abattoir to detect bTB-like lesions which, in compliance with EU recommendations, are analysed by bacteriology and histopathology to disclose Mycobacterium bovis (or M. caprae) infection. Moreove...
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description | Surveillance of bovine tuberculosis (bTB) is partly based on the sanitary inspection of carcasses at the abattoir to detect bTB-like lesions which, in compliance with EU recommendations, are analysed by bacteriology and histopathology to disclose Mycobacterium bovis (or M. caprae) infection. Moreover, since 2012, a PCR method with similar sensitivity and specificity values of histopathology and bacteriology respectively is additionally employed in France, partially compensating for the weaknesses of classical diagnostic methods. We analysed a collection of bTB-like lesions from cattle presenting positive histological results albeit with negative PCR results. We present here the results of these samples, recovered from 292 animals culled between 2013 and 2016, analysed with a second line molecular diagnosis approach that consists in a combination of PCRs targeting the M. tuberculosis-M. avium complexes as well as the Mycobacterium genus and sequencing of hsp65 gene. These molecular analyses disclosed to identify the presence of non-tuberculous bacteria which could be responsible for most of these non-specific TB lesions: non tuberculous mycobacteria (24%) or Actinomycetales (56%) such as Rhodococcus equi (53%); 24% of the samples were negative. M. bovis -or any other MTBC members- was neither detected by molecular methods nor isolated in any of them at the end of the 3 months of culture. In conclusion, these results highlight the lack of specificity of histopathology and the usefulness of a first line PCR with a second line molecular diagnostic test to circumvent it. This diagnostic strategy makes it possible to reduce the number of suspect bTB cases raised at the abattoir or shortening their lock-up periods. By simplifying diagnostic schemes, the use of this tool could improve bTB surveillance and make eradication programs more efficient in the future. |
doi_str_mv | 10.1371/journal.pone.0207614 |
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Moreover, since 2012, a PCR method with similar sensitivity and specificity values of histopathology and bacteriology respectively is additionally employed in France, partially compensating for the weaknesses of classical diagnostic methods. We analysed a collection of bTB-like lesions from cattle presenting positive histological results albeit with negative PCR results. We present here the results of these samples, recovered from 292 animals culled between 2013 and 2016, analysed with a second line molecular diagnosis approach that consists in a combination of PCRs targeting the M. tuberculosis-M. avium complexes as well as the Mycobacterium genus and sequencing of hsp65 gene. These molecular analyses disclosed to identify the presence of non-tuberculous bacteria which could be responsible for most of these non-specific TB lesions: non tuberculous mycobacteria (24%) or Actinomycetales (56%) such as Rhodococcus equi (53%); 24% of the samples were negative. M. bovis -or any other MTBC members- was neither detected by molecular methods nor isolated in any of them at the end of the 3 months of culture. In conclusion, these results highlight the lack of specificity of histopathology and the usefulness of a first line PCR with a second line molecular diagnostic test to circumvent it. This diagnostic strategy makes it possible to reduce the number of suspect bTB cases raised at the abattoir or shortening their lock-up periods. By simplifying diagnostic schemes, the use of this tool could improve bTB surveillance and make eradication programs more efficient in the future.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0207614</identifier><identifier>PMID: 30475835</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Abattoirs ; Actinomycetales - genetics ; Actinomycetales - isolation & purification ; Animal biology ; Animals ; Bacteria ; Bacterial Proteins - genetics ; Bacteriology ; Beef cattle ; Biology and Life Sciences ; Bovine tuberculosis ; Carcasses ; Cattle ; Chaperonin 60 - genetics ; Deoxyribonucleic acid ; Diagnosis ; Diagnostic software ; Diagnostic systems ; DNA ; DNA, Bacterial - metabolism ; DNA-Directed RNA Polymerases - genetics ; Food ; Gene sequencing ; Genes ; Heat shock proteins ; Histochemistry ; Histopathology ; Hsp65 gene ; Hsp65 protein ; Inspection ; Intelligence gathering ; Laboratories ; Lesions ; Life Sciences ; Lymphatic system ; Medical diagnosis ; Medicine and Health Sciences ; Methods ; Microbiology and Parasitology ; Molecular modeling ; Mycobacterium - genetics ; Mycobacterium - isolation & purification ; Nontuberculous Mycobacteria - genetics ; Nontuberculous Mycobacteria - isolation & purification ; Occupational health ; Polymerase Chain Reaction ; Research and Analysis Methods ; Retrospective Studies ; Rhodococcus ; Rhodococcus equi ; Risk factors ; Surveillance ; Tuberculosis ; Tuberculosis, Bovine - diagnosis ; Tuberculosis, Bovine - microbiology ; Tuberculosis, Bovine - pathology ; Veterinary medicine and animal Health</subject><ispartof>PloS one, 2018-11, Vol.13 (11), p.e0207614-e0207614</ispartof><rights>COPYRIGHT 2018 Public Library of Science</rights><rights>2018 Michelet et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2018 Michelet et al 2018 Michelet et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c728t-5821536a381dac482afe71a95a7979f9a9db5a57d3f23152abb182970eee924a3</citedby><cites>FETCH-LOGICAL-c728t-5821536a381dac482afe71a95a7979f9a9db5a57d3f23152abb182970eee924a3</cites><orcidid>0000-0002-6705-1684 ; 0000-0003-2991-1660</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261039/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261039/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30475835$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://anses.hal.science/anses-03910916$$DView record in HAL$$Hfree_for_read</backlink></links><search><contributor>Chatterjee, Delphi</contributor><creatorcontrib>Michelet, Lorraine</creatorcontrib><creatorcontrib>de Cruz, Krystel</creatorcontrib><creatorcontrib>Karoui, Claudine</creatorcontrib><creatorcontrib>Tambosco, Jennifer</creatorcontrib><creatorcontrib>Moyen, Jean-Louis</creatorcontrib><creatorcontrib>Hénault, Sylvie</creatorcontrib><creatorcontrib>Boschiroli, María Laura</creatorcontrib><title>Second line molecular diagnosis for bovine tuberculosis to improve diagnostic schemes</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Surveillance of bovine tuberculosis (bTB) is partly based on the sanitary inspection of carcasses at the abattoir to detect bTB-like lesions which, in compliance with EU recommendations, are analysed by bacteriology and histopathology to disclose Mycobacterium bovis (or M. caprae) infection. Moreover, since 2012, a PCR method with similar sensitivity and specificity values of histopathology and bacteriology respectively is additionally employed in France, partially compensating for the weaknesses of classical diagnostic methods. We analysed a collection of bTB-like lesions from cattle presenting positive histological results albeit with negative PCR results. We present here the results of these samples, recovered from 292 animals culled between 2013 and 2016, analysed with a second line molecular diagnosis approach that consists in a combination of PCRs targeting the M. tuberculosis-M. avium complexes as well as the Mycobacterium genus and sequencing of hsp65 gene. These molecular analyses disclosed to identify the presence of non-tuberculous bacteria which could be responsible for most of these non-specific TB lesions: non tuberculous mycobacteria (24%) or Actinomycetales (56%) such as Rhodococcus equi (53%); 24% of the samples were negative. M. bovis -or any other MTBC members- was neither detected by molecular methods nor isolated in any of them at the end of the 3 months of culture. In conclusion, these results highlight the lack of specificity of histopathology and the usefulness of a first line PCR with a second line molecular diagnostic test to circumvent it. This diagnostic strategy makes it possible to reduce the number of suspect bTB cases raised at the abattoir or shortening their lock-up periods. By simplifying diagnostic schemes, the use of this tool could improve bTB surveillance and make eradication programs more efficient in the future.</description><subject>Abattoirs</subject><subject>Actinomycetales - genetics</subject><subject>Actinomycetales - isolation & purification</subject><subject>Animal biology</subject><subject>Animals</subject><subject>Bacteria</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacteriology</subject><subject>Beef cattle</subject><subject>Biology and Life Sciences</subject><subject>Bovine tuberculosis</subject><subject>Carcasses</subject><subject>Cattle</subject><subject>Chaperonin 60 - genetics</subject><subject>Deoxyribonucleic acid</subject><subject>Diagnosis</subject><subject>Diagnostic software</subject><subject>Diagnostic systems</subject><subject>DNA</subject><subject>DNA, Bacterial - metabolism</subject><subject>DNA-Directed RNA Polymerases - genetics</subject><subject>Food</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>Heat shock proteins</subject><subject>Histochemistry</subject><subject>Histopathology</subject><subject>Hsp65 gene</subject><subject>Hsp65 protein</subject><subject>Inspection</subject><subject>Intelligence gathering</subject><subject>Laboratories</subject><subject>Lesions</subject><subject>Life Sciences</subject><subject>Lymphatic system</subject><subject>Medical diagnosis</subject><subject>Medicine and Health Sciences</subject><subject>Methods</subject><subject>Microbiology and Parasitology</subject><subject>Molecular modeling</subject><subject>Mycobacterium - genetics</subject><subject>Mycobacterium - isolation & purification</subject><subject>Nontuberculous Mycobacteria - genetics</subject><subject>Nontuberculous Mycobacteria - isolation & purification</subject><subject>Occupational health</subject><subject>Polymerase Chain Reaction</subject><subject>Research and Analysis Methods</subject><subject>Retrospective Studies</subject><subject>Rhodococcus</subject><subject>Rhodococcus equi</subject><subject>Risk factors</subject><subject>Surveillance</subject><subject>Tuberculosis</subject><subject>Tuberculosis, Bovine - diagnosis</subject><subject>Tuberculosis, Bovine - microbiology</subject><subject>Tuberculosis, Bovine - pathology</subject><subject>Veterinary medicine and animal Health</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNk2-L00AQxoMo3nn6DUQDgijSun-STfaNUA71CoUDz_PtMslO2i1Jtu4mRb-9m2t6NMe9kLzYMPN7np2ZZKLoNSVzyjP6eWt710I939kW54SRTNDkSXROJWczwQh_evJ-Fr3wfktIynMhnkdnnCRZmvP0PLq9wdK2Oq5Ni3Fjayz7GlysDaxb642PK-viwu6HdNcX6EL-Lt7Z2DQ7Z_d4hDtTxr7cYIP-ZfSsgtrjq_G8iG6_ff15eTVbXX9fXi5WszJjeTdLc0ZTLoDnVEOZ5AwqzCjIFDKZyUqC1EUKaaZ5xThNGRQFzZnMCCJKlgC_iN4efHehKDVOxCtGeU5E6DAPxPJAaAtbtXOmAfdXWTDqLmDdWoELldeoKiFlkmMqWThLLaGqNAqtgTJaiEIGry_jbX3RoC6x7RzUE9NppjUbtbZ7JZighA8Gnw4Gmweyq8VKQevRq4BRIqnY00B_GK9z9nePvlON8SXWNbRo-0OXgotEkoC-e4A-PouRWkNo17SVDVWWg6lapIInjMqEBWr-CBUejY0J_wpWJsQngo8TQWA6_NOtofdeLW9-_D97_WvKvj9hNwh1t_G27jtjWz8FkwNYOuu9w-p-tpSoYVeO01DDrqhxV4LszennvBcdl4P_A1HuDng</recordid><startdate>20181126</startdate><enddate>20181126</enddate><creator>Michelet, Lorraine</creator><creator>de Cruz, Krystel</creator><creator>Karoui, Claudine</creator><creator>Tambosco, Jennifer</creator><creator>Moyen, Jean-Louis</creator><creator>Hénault, Sylvie</creator><creator>Boschiroli, María Laura</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-6705-1684</orcidid><orcidid>https://orcid.org/0000-0003-2991-1660</orcidid></search><sort><creationdate>20181126</creationdate><title>Second line molecular diagnosis for bovine tuberculosis to improve diagnostic schemes</title><author>Michelet, Lorraine ; de Cruz, Krystel ; Karoui, Claudine ; Tambosco, Jennifer ; Moyen, Jean-Louis ; Hénault, Sylvie ; Boschiroli, María Laura</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c728t-5821536a381dac482afe71a95a7979f9a9db5a57d3f23152abb182970eee924a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Abattoirs</topic><topic>Actinomycetales - 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Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Michelet, Lorraine</au><au>de Cruz, Krystel</au><au>Karoui, Claudine</au><au>Tambosco, Jennifer</au><au>Moyen, Jean-Louis</au><au>Hénault, Sylvie</au><au>Boschiroli, María Laura</au><au>Chatterjee, Delphi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Second line molecular diagnosis for bovine tuberculosis to improve diagnostic schemes</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2018-11-26</date><risdate>2018</risdate><volume>13</volume><issue>11</issue><spage>e0207614</spage><epage>e0207614</epage><pages>e0207614-e0207614</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Surveillance of bovine tuberculosis (bTB) is partly based on the sanitary inspection of carcasses at the abattoir to detect bTB-like lesions which, in compliance with EU recommendations, are analysed by bacteriology and histopathology to disclose Mycobacterium bovis (or M. caprae) infection. Moreover, since 2012, a PCR method with similar sensitivity and specificity values of histopathology and bacteriology respectively is additionally employed in France, partially compensating for the weaknesses of classical diagnostic methods. We analysed a collection of bTB-like lesions from cattle presenting positive histological results albeit with negative PCR results. We present here the results of these samples, recovered from 292 animals culled between 2013 and 2016, analysed with a second line molecular diagnosis approach that consists in a combination of PCRs targeting the M. tuberculosis-M. avium complexes as well as the Mycobacterium genus and sequencing of hsp65 gene. These molecular analyses disclosed to identify the presence of non-tuberculous bacteria which could be responsible for most of these non-specific TB lesions: non tuberculous mycobacteria (24%) or Actinomycetales (56%) such as Rhodococcus equi (53%); 24% of the samples were negative. M. bovis -or any other MTBC members- was neither detected by molecular methods nor isolated in any of them at the end of the 3 months of culture. In conclusion, these results highlight the lack of specificity of histopathology and the usefulness of a first line PCR with a second line molecular diagnostic test to circumvent it. This diagnostic strategy makes it possible to reduce the number of suspect bTB cases raised at the abattoir or shortening their lock-up periods. By simplifying diagnostic schemes, the use of this tool could improve bTB surveillance and make eradication programs more efficient in the future.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>30475835</pmid><doi>10.1371/journal.pone.0207614</doi><tpages>e0207614</tpages><orcidid>https://orcid.org/0000-0002-6705-1684</orcidid><orcidid>https://orcid.org/0000-0003-2991-1660</orcidid><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2018-11, Vol.13 (11), p.e0207614-e0207614 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2138067588 |
source | MEDLINE; PubMed Central(OpenAccess); DOAJ Directory of Open Access Journals; Public Library of Science (PLoS) Journals Open Access; Free Full-Text Journals in Chemistry; EZB Electronic Journals Library |
subjects | Abattoirs Actinomycetales - genetics Actinomycetales - isolation & purification Animal biology Animals Bacteria Bacterial Proteins - genetics Bacteriology Beef cattle Biology and Life Sciences Bovine tuberculosis Carcasses Cattle Chaperonin 60 - genetics Deoxyribonucleic acid Diagnosis Diagnostic software Diagnostic systems DNA DNA, Bacterial - metabolism DNA-Directed RNA Polymerases - genetics Food Gene sequencing Genes Heat shock proteins Histochemistry Histopathology Hsp65 gene Hsp65 protein Inspection Intelligence gathering Laboratories Lesions Life Sciences Lymphatic system Medical diagnosis Medicine and Health Sciences Methods Microbiology and Parasitology Molecular modeling Mycobacterium - genetics Mycobacterium - isolation & purification Nontuberculous Mycobacteria - genetics Nontuberculous Mycobacteria - isolation & purification Occupational health Polymerase Chain Reaction Research and Analysis Methods Retrospective Studies Rhodococcus Rhodococcus equi Risk factors Surveillance Tuberculosis Tuberculosis, Bovine - diagnosis Tuberculosis, Bovine - microbiology Tuberculosis, Bovine - pathology Veterinary medicine and animal Health |
title | Second line molecular diagnosis for bovine tuberculosis to improve diagnostic schemes |
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