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Mycobacterium africanum (Lineage 6) shows slower sputum smear conversion on tuberculosis treatment than Mycobacterium tuberculosis (Lineage 4) in Bamako, Mali
OBJECTIVE: Ancestral M. tuberculosis complex lineages such as M. africanum are underrepresented among retreatment patients and those with drug resistance. To test the hypothesis that they respond faster to TB treatment, we determined the rate of smear conversion of new pulmonary tuberculosis patient...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291124/ https://www.ncbi.nlm.nih.gov/pubmed/30540823 http://dx.doi.org/10.1371/journal.pone.0208603 |
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author | Diarra, Bassirou Kone, Mahamadou Togo, Antieme Combo Georges Sarro, Yeya dit Sadio Cisse, Aissata Boubakar Somboro, Amadou Degoga, Boureima Tolofoudie, Mohamed Kone, Bourahima Sanogo, Moumine Baya, Bocar Kodio, Ousmane Maiga, Mamoudou Belson, Michael Orsega, Susan Krit, Meryam Dao, Sounkalo Maiga, Ibrahim Izétiegouma Murphy, Robert L. Rigouts, Leen Doumbia, Seydou Diallo, Souleymane de Jong, Bouke Catherine |
author_facet | Diarra, Bassirou Kone, Mahamadou Togo, Antieme Combo Georges Sarro, Yeya dit Sadio Cisse, Aissata Boubakar Somboro, Amadou Degoga, Boureima Tolofoudie, Mohamed Kone, Bourahima Sanogo, Moumine Baya, Bocar Kodio, Ousmane Maiga, Mamoudou Belson, Michael Orsega, Susan Krit, Meryam Dao, Sounkalo Maiga, Ibrahim Izétiegouma Murphy, Robert L. Rigouts, Leen Doumbia, Seydou Diallo, Souleymane de Jong, Bouke Catherine |
author_sort | Diarra, Bassirou |
collection | PubMed |
description | OBJECTIVE: Ancestral M. tuberculosis complex lineages such as M. africanum are underrepresented among retreatment patients and those with drug resistance. To test the hypothesis that they respond faster to TB treatment, we determined the rate of smear conversion of new pulmonary tuberculosis patients in Bamako, Mali by the main MTBc lineages. METHODS: Between 2015 and 2017, we conducted a prospective cohort study of new smear positive pulmonary tuberculosis patients in Bamako. Confirmed MTBc isolates underwent genotyping by spoligotyping for lineage classification. Patients were followed at 1 month (M), 2M and 5M to measure smear conversion in auramine (AR) and Fluorescein DiAcetate (FDA) vital stain microscopy. RESULT: All the first six human MTBc lineages were represented in the population, plus M. bovis in 0.8% of the patients. The most widely represented lineage was the modern Euro-American lineage (L) 4, 57%, predominantly the T family, followed by L6 (M. africanum type 2) in 22.9%. Ancestral lineages 1, 5, 6 and M. bovis combined amounted to 28.8%. Excluding 25 patients with rifampicin resistance, smear conversion, both by AR and FDA, occurred later in L6 compared to L4 (HR 0.80 (95% CI 0.66–0.97) for AR, and HR 0.81 (95%CI 0.68–0.97) for FDA). In addition we found that HIV negative status, higher BMI at day 0, and patients with smear grade at baseline ≤ 1+ were associated with earlier smear conversion. CONCLUSION: The six major human lineages of the MTBc all circulate in Bamako. Counter to our hypothesis, we found that patients diseased with modern M. tuberculosis complex L4 respond faster to TB treatment than those with M. africanum L6. |
format | Online Article Text |
id | pubmed-6291124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62911242018-12-28 Mycobacterium africanum (Lineage 6) shows slower sputum smear conversion on tuberculosis treatment than Mycobacterium tuberculosis (Lineage 4) in Bamako, Mali Diarra, Bassirou Kone, Mahamadou Togo, Antieme Combo Georges Sarro, Yeya dit Sadio Cisse, Aissata Boubakar Somboro, Amadou Degoga, Boureima Tolofoudie, Mohamed Kone, Bourahima Sanogo, Moumine Baya, Bocar Kodio, Ousmane Maiga, Mamoudou Belson, Michael Orsega, Susan Krit, Meryam Dao, Sounkalo Maiga, Ibrahim Izétiegouma Murphy, Robert L. Rigouts, Leen Doumbia, Seydou Diallo, Souleymane de Jong, Bouke Catherine PLoS One Research Article OBJECTIVE: Ancestral M. tuberculosis complex lineages such as M. africanum are underrepresented among retreatment patients and those with drug resistance. To test the hypothesis that they respond faster to TB treatment, we determined the rate of smear conversion of new pulmonary tuberculosis patients in Bamako, Mali by the main MTBc lineages. METHODS: Between 2015 and 2017, we conducted a prospective cohort study of new smear positive pulmonary tuberculosis patients in Bamako. Confirmed MTBc isolates underwent genotyping by spoligotyping for lineage classification. Patients were followed at 1 month (M), 2M and 5M to measure smear conversion in auramine (AR) and Fluorescein DiAcetate (FDA) vital stain microscopy. RESULT: All the first six human MTBc lineages were represented in the population, plus M. bovis in 0.8% of the patients. The most widely represented lineage was the modern Euro-American lineage (L) 4, 57%, predominantly the T family, followed by L6 (M. africanum type 2) in 22.9%. Ancestral lineages 1, 5, 6 and M. bovis combined amounted to 28.8%. Excluding 25 patients with rifampicin resistance, smear conversion, both by AR and FDA, occurred later in L6 compared to L4 (HR 0.80 (95% CI 0.66–0.97) for AR, and HR 0.81 (95%CI 0.68–0.97) for FDA). In addition we found that HIV negative status, higher BMI at day 0, and patients with smear grade at baseline ≤ 1+ were associated with earlier smear conversion. CONCLUSION: The six major human lineages of the MTBc all circulate in Bamako. Counter to our hypothesis, we found that patients diseased with modern M. tuberculosis complex L4 respond faster to TB treatment than those with M. africanum L6. Public Library of Science 2018-12-12 /pmc/articles/PMC6291124/ /pubmed/30540823 http://dx.doi.org/10.1371/journal.pone.0208603 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Diarra, Bassirou Kone, Mahamadou Togo, Antieme Combo Georges Sarro, Yeya dit Sadio Cisse, Aissata Boubakar Somboro, Amadou Degoga, Boureima Tolofoudie, Mohamed Kone, Bourahima Sanogo, Moumine Baya, Bocar Kodio, Ousmane Maiga, Mamoudou Belson, Michael Orsega, Susan Krit, Meryam Dao, Sounkalo Maiga, Ibrahim Izétiegouma Murphy, Robert L. Rigouts, Leen Doumbia, Seydou Diallo, Souleymane de Jong, Bouke Catherine Mycobacterium africanum (Lineage 6) shows slower sputum smear conversion on tuberculosis treatment than Mycobacterium tuberculosis (Lineage 4) in Bamako, Mali |
title | Mycobacterium africanum (Lineage 6) shows slower sputum smear conversion on tuberculosis treatment than Mycobacterium tuberculosis (Lineage 4) in Bamako, Mali |
title_full | Mycobacterium africanum (Lineage 6) shows slower sputum smear conversion on tuberculosis treatment than Mycobacterium tuberculosis (Lineage 4) in Bamako, Mali |
title_fullStr | Mycobacterium africanum (Lineage 6) shows slower sputum smear conversion on tuberculosis treatment than Mycobacterium tuberculosis (Lineage 4) in Bamako, Mali |
title_full_unstemmed | Mycobacterium africanum (Lineage 6) shows slower sputum smear conversion on tuberculosis treatment than Mycobacterium tuberculosis (Lineage 4) in Bamako, Mali |
title_short | Mycobacterium africanum (Lineage 6) shows slower sputum smear conversion on tuberculosis treatment than Mycobacterium tuberculosis (Lineage 4) in Bamako, Mali |
title_sort | mycobacterium africanum (lineage 6) shows slower sputum smear conversion on tuberculosis treatment than mycobacterium tuberculosis (lineage 4) in bamako, mali |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291124/ https://www.ncbi.nlm.nih.gov/pubmed/30540823 http://dx.doi.org/10.1371/journal.pone.0208603 |
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