TY - JOUR
T1 - Mycobacterium africanum (Lineage 6) shows slower sputum smear conversion on tuberculosis treatment than Mycobacterium tuberculosis (Lineage 4) in Bamako, Mali
AU - Diarra, Bassirou
AU - Kone, Mahamadou
AU - Togo, Antieme Combo Georges
AU - Sarro, Yeya dit Sadio
AU - Cisse, Aissata Boubakar
AU - Somboro, Amadou
AU - Degoga, Boureima
AU - Tolofoudie, Mohamed
AU - Kone, Bourahima
AU - Sanogo, Moumine
AU - Baya, Bocar
AU - Kodio, Ousmane
AU - Maiga, Mamoudou
AU - Belson, Michael
AU - Orsega, Susan
AU - Krit, Meryam
AU - Dao, Sounkalo
AU - Maiga, Ibrahim Izétiegouma
AU - Murphy, Robert L.
AU - Rigouts, Leen
AU - Doumbia, Seydou
AU - Diallo, Souleymane
AU - de Jong, Bouke Catherine
N1 - Funding Information:
Funding:ThisstudywaspartiallyfundedbyaTDR fellowship,TIMSIDB40072toBD,thespecial programmeforresearchandtrainingintropical diseases,co-sponsoredbyUNICEF,UNDP,World BankandWHO;theNorthwesternUniversity (Chicago,IL,USA)throughNIH/FICD43TW10350 toRLM,andtheUniversityofSciences,
Funding Information:
This study was partially funded by a TDR fellowship, TIMS ID B40072 to BD, the special programme for research and training in tropical diseases, co-sponsored by UNICEF, UNDP, World Bank and WHO; the Northwestern University (Chicago, IL, USA) through NIH/FIC D43 TW10350 to RLM, and the University of Sciences, Techniques and Technologies of Bamako (USTTB) through NIH/ R01 grant R01AI110386 to SD. Bouke de Jong was supported by ERC starting grant INTERRUPTB (311725), and Bassirou Diarra was partially supported by NIH/FIC D71 TW010428-01A1. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We express our special thanks to all the health centers in Bamako district for their assistance in the recruitment of patients, and also thank all the study volunteers for participating in this study. We expressed our special thanks to Gagni Coulibaly, Fatimata Diallo, Bintou Fane, N’guiakam Natacha and Mandou-Han Christiane Marie Laure Keita for their assistance in collecting/testing the samples. We thank Armand Van Deun, Pim De Rijk, Wim Mulders, Viviane Hanquart, Cécile Uwizeye, and Jelle Keysers all at the department of Mycobacteriology at ITM, Antwerp, for their assistance. We are very grateful of Guislaine Refregier for her assistance in interpreting some of our spoligotype results for classification into lineages.
Publisher Copyright:
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 public domain dedication.
PY - 2018/12
Y1 - 2018/12
N2 - 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 genotyp-ing 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.
AB - 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 genotyp-ing 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.
UR - http://www.scopus.com/inward/record.url?scp=85058443686&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85058443686&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0208603
DO - 10.1371/journal.pone.0208603
M3 - Article
C2 - 30540823
AN - SCOPUS:85058443686
SN - 1932-6203
VL - 13
JO - PloS one
JF - PloS one
IS - 12
M1 - e0208603
ER -