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Drug resistance-conferring mutations in Mycobacterium tuberculosis from Madang, Papua New Guinea
BACKGROUND: Monitoring drug resistance in Mycobacterium tuberculosis is essential to curb the spread of tuberculosis (TB). Unfortunately, drug susceptibility testing is currently not available in Papua New Guinea (PNG) and that impairs TB control in this country. We report for the first time M. tube...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3478209/ https://www.ncbi.nlm.nih.gov/pubmed/22943573 http://dx.doi.org/10.1186/1471-2180-12-191 |
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author | Ballif, Marie Harino, Paul Ley, Serej Coscolla, Mireia Niemann, Stefan Carter, Robyn Coulter, Christopher Borrell, Sonia Siba, Peter Phuanukoonnon, Suparat Gagneux, Sebastien Beck, Hans-Peter |
author_facet | Ballif, Marie Harino, Paul Ley, Serej Coscolla, Mireia Niemann, Stefan Carter, Robyn Coulter, Christopher Borrell, Sonia Siba, Peter Phuanukoonnon, Suparat Gagneux, Sebastien Beck, Hans-Peter |
author_sort | Ballif, Marie |
collection | PubMed |
description | BACKGROUND: Monitoring drug resistance in Mycobacterium tuberculosis is essential to curb the spread of tuberculosis (TB). Unfortunately, drug susceptibility testing is currently not available in Papua New Guinea (PNG) and that impairs TB control in this country. We report for the first time M. tuberculosis mutations associated with resistance to first and second-line anti-TB drugs in Madang, PNG. A molecular cluster analysis was performed to identify M. tuberculosis transmission in that region. RESULTS: Phenotypic drug susceptibility tests showed 15.7% resistance to at least one drug and 5.2% multidrug resistant (MDR) TB. Rifampicin resistant strains had the rpoB mutations D516F, D516Y or S531L; Isoniazid resistant strains had the mutations katG S315T or inhA promoter C15T; Streptomycin resistant strains had the mutations rpsL K43R, K88Q, K88R), rrs A514C or gidB V77G. The molecular cluster analysis indicated evidence for transmission of resistant strain. CONCLUSIONS: We observed a substantial rate of MDR-TB in the Madang area of PNG associated with mutations in specific genes. A close monitoring of drug resistance is therefore urgently required, particularly in the presence of drug-resistant M. tuberculosis transmission. In the absence of phenotypic drug susceptibility testing in PNG, molecular assays for drug resistance monitoring would be of advantage. |
format | Online Article Text |
id | pubmed-3478209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34782092012-10-23 Drug resistance-conferring mutations in Mycobacterium tuberculosis from Madang, Papua New Guinea Ballif, Marie Harino, Paul Ley, Serej Coscolla, Mireia Niemann, Stefan Carter, Robyn Coulter, Christopher Borrell, Sonia Siba, Peter Phuanukoonnon, Suparat Gagneux, Sebastien Beck, Hans-Peter BMC Microbiol Research Article BACKGROUND: Monitoring drug resistance in Mycobacterium tuberculosis is essential to curb the spread of tuberculosis (TB). Unfortunately, drug susceptibility testing is currently not available in Papua New Guinea (PNG) and that impairs TB control in this country. We report for the first time M. tuberculosis mutations associated with resistance to first and second-line anti-TB drugs in Madang, PNG. A molecular cluster analysis was performed to identify M. tuberculosis transmission in that region. RESULTS: Phenotypic drug susceptibility tests showed 15.7% resistance to at least one drug and 5.2% multidrug resistant (MDR) TB. Rifampicin resistant strains had the rpoB mutations D516F, D516Y or S531L; Isoniazid resistant strains had the mutations katG S315T or inhA promoter C15T; Streptomycin resistant strains had the mutations rpsL K43R, K88Q, K88R), rrs A514C or gidB V77G. The molecular cluster analysis indicated evidence for transmission of resistant strain. CONCLUSIONS: We observed a substantial rate of MDR-TB in the Madang area of PNG associated with mutations in specific genes. A close monitoring of drug resistance is therefore urgently required, particularly in the presence of drug-resistant M. tuberculosis transmission. In the absence of phenotypic drug susceptibility testing in PNG, molecular assays for drug resistance monitoring would be of advantage. BioMed Central 2012-09-04 /pmc/articles/PMC3478209/ /pubmed/22943573 http://dx.doi.org/10.1186/1471-2180-12-191 Text en Copyright ©2012 Ballif et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Ballif, Marie Harino, Paul Ley, Serej Coscolla, Mireia Niemann, Stefan Carter, Robyn Coulter, Christopher Borrell, Sonia Siba, Peter Phuanukoonnon, Suparat Gagneux, Sebastien Beck, Hans-Peter Drug resistance-conferring mutations in Mycobacterium tuberculosis from Madang, Papua New Guinea |
title | Drug resistance-conferring mutations in Mycobacterium tuberculosis from Madang, Papua New Guinea |
title_full | Drug resistance-conferring mutations in Mycobacterium tuberculosis from Madang, Papua New Guinea |
title_fullStr | Drug resistance-conferring mutations in Mycobacterium tuberculosis from Madang, Papua New Guinea |
title_full_unstemmed | Drug resistance-conferring mutations in Mycobacterium tuberculosis from Madang, Papua New Guinea |
title_short | Drug resistance-conferring mutations in Mycobacterium tuberculosis from Madang, Papua New Guinea |
title_sort | drug resistance-conferring mutations in mycobacterium tuberculosis from madang, papua new guinea |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3478209/ https://www.ncbi.nlm.nih.gov/pubmed/22943573 http://dx.doi.org/10.1186/1471-2180-12-191 |
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