Comparative genomics shows differences in the electron transport and carbon metabolic pathways of Mycobacterium africanum relative to Mycobacterium tuberculosis and suggests an adaptation to low oxygen tension

被引:11
作者
Ofori-Anyinam, Boatema [1 ,2 ,3 ]
Riley, Abi Janet [2 ]
Jobarteh, Tijan [2 ]
Gitteh, Ensa [2 ]
Sarr, Binta [2 ]
Faal-Jawara, Tutty Isatou [2 ]
Rigouts, Leen [1 ,4 ]
Senghore, Madikay [2 ]
Kehinde, Aderemi [5 ,6 ]
Onyejepu, Nneka [7 ]
Antonio, Martin [2 ,8 ,9 ]
de Jong, Bouke C. [1 ]
Gehre, Florian [1 ,2 ,10 ]
Meehan, Conor J. [1 ,11 ]
机构
[1] Inst Trop Med, Mycobacteriol Unit, Antwerp, Belgium
[2] MRC Unit, Vaccines & Immun Theme, Banjul, Gambia
[3] Ctr Global Hlth Secur & Diplomacy, Ottawa, ON, Canada
[4] Antwerp Univ, Dept Biomed Sci, Antwerp, Belgium
[5] Univ Coll Hosp, Dept Med Microbiol & Parasitol, Ibadan, Nigeria
[6] Univ Ibadan, Coll Med, Dept Med Microbiol & Parasitol, Ibadan, Nigeria
[7] Nigeria Inst Med Res, Ctr TB Res, Lagos, Nigeria
[8] London Sch Hyg & Trop Med, Div Infect & Trop Dis, London, England
[9] Univ Warwick, Med Sch, Coventry, W Midlands, England
[10] Bernhard Nocht Inst Trop Med, Hamburg, Germany
[11] Univ Bradford, Sch Chem & Biosci, Bradford, W Yorkshire, England
基金
英国医学研究理事会; 欧洲研究理事会;
关键词
Tuberculosis; Mycobacterium africanum; Mycobacterium tuberculosis; Genome; Electron transport; Carbon metabolism; MESSENGER-RNA STABILITY; PULMONARY TUBERCULOSIS; DOSR REGULON; LINEAGE; COMPLEX; TOOL; DIVERSITY; STRAINS; MUTATIONS; VIRULENCE;
D O I
10.1016/j.tube.2020.101899
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The geographically restricted Mycobacterium africanum lineages (MAF) are primarily found in West Africa, where they account for a significant proportion of tuberculosis. Despite this phenomenon, little is known about the coevolution of these ancient lineages with West Africans. MAF and M. tuberculosis sensu stricto lineages (MTB) differ in their clinical, in vitro and in vivo characteristics for reasons not fully understood. Therefore, we compared genomes of 289 MAF and 205 MTB clinical isolates from the 6 main human-adapted M. tuberculosis complex lineages, for mutations in their Electron Transport Chain and Central Carbon Metabolic pathway in order to explain these metabolic differences. Furthermore, we determined, in silico, whether each mutation could affect the function of genes encoding enzymes in these pathways. We found more mutations with the potential to affect enzymes in these pathways in MAF lineages compared to MTB lineages. We also found that similar mutations occurred in these pathways between MAF and some MTB lineages. Generally, our findings show further differences between MAF and MTB lineages that may have contributed to the MAF clinical and growth phenotype and indicate potential adaptation of MAF lineages to a distinct ecological niche, which we suggest includes areas characterized by low oxygen tension.
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页数:12
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