The complete genome sequence of Mycobacterium bovis

被引:709
|
作者
Garnier, T
Eiglmeier, K
Camus, JC
Medina, N
Mansoor, H
Pryor, M
Duthoy, S
Grondin, S
Lacroix, C
Monsempe, C
Simon, S
Harris, B
Atkin, R
Doggett, J
Mayes, R
Keating, L
Wheeler, PR
Parkhill, J
Barrell, BG
Cole, ST
Gordon, SV
Hewinson, RG
机构
[1] Inst Pasteur, Unite Genet Mol Bacterienne, F-75724 Paris 15, France
[2] Vet Labs Agcy Weybridge, TB Res Grp, Surrey KT15 3NB, England
[3] Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England
关键词
D O I
10.1073/pnas.1130426100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mycobacterium bovis is the causative agent of tuberculosis in a range of animal species and man, with worldwide annual losses to agriculture of $3 billion. The human burden of tuberculosis caused by the bovine tubercle bacillus is still largely unknown. M. bovis was also the progenitor for the M. bovis bacillus Calmette-Guerin vaccine strain, the most widely used human vaccine. Here we describe the 4,345,492-bp genome sequence of M. bovis AF2122/97 and its comparison with the genomes of Mycobacterium tuberculosis and Mycobacterium leprae. Strikingly, the genome sequence of M. bovis is >99.95% identical to that of M. tuberculosis, but deletion of genetic information has led to a reduced genome size. Comparison with M. leprae reveals a number of common gene losses, suggesting the removal of functional redundancy. Cell wall components and secreted proteins show the greatest variation, indicating their potential role in host-bacillus interactions or immune evasion. Furthermore, there are no genes unique to M. bovis, implying that differential gene expression may be the key to the host tropisms of human and bovine bacilli. The genome sequence therefore offers major insight on the evolution, host preference, and pathobiology of M. bovis.
引用
收藏
页码:7877 / 7882
页数:6
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