The Genetic Requirements for Fast and Slow Growth in Mycobacteria
被引:97
作者:
Beste, Dany J. V.
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机构:FHMS, University of Surrey, Guildford
Beste, Dany J. V.
Espasa, Mateus
论文数: 0引用数: 0
h-index: 0
机构:FHMS, University of Surrey, Guildford
Espasa, Mateus
Bonde, Bhushan
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h-index: 0
机构:FHMS, University of Surrey, Guildford
Bonde, Bhushan
Kierzek, Andrzej M.
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h-index: 0
机构:FHMS, University of Surrey, Guildford
Kierzek, Andrzej M.
Stewart, Graham R.
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h-index: 0
机构:FHMS, University of Surrey, Guildford
Stewart, Graham R.
论文数: 引用数:
h-index:
机构:
McFadden, Johnjoe
机构:
[1] FHMS, University of Surrey, Guildford
来源:
PLOS ONE
|
2009年
/
4卷
/
04期
基金:
英国生物技术与生命科学研究理事会;
英国惠康基金;
关键词:
D O I:
10.1371/journal.pone.0005349
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 tuberculosis infects a third of the world's population. Primary tuberculosis involving active fast bacterial replication is often followed by asymptomatic latent tuberculosis, which is characterised by slow or non-replicating bacteria. Reactivation of the latent infection involving a switch back to active bacterial replication can lead to post-primary transmissible tuberculosis. Mycobacterial mechanisms involved in slow growth or switching growth rate provide rational targets for the development of new drugs against persistent mycobacterial infection. Using chemostat culture to control growth rate, we screened a transposon mutant library by Transposon site hybridization (TraSH) selection to define the genetic requirements for slow and fast growth of Mycobacterium bovis (BCG) and for the requirements of switching growth rate. We identified 84 genes that are exclusively required for slow growth (69 hours doubling time) and 256 genes required for switching from slow to fast growth. To validate these findings we performed experiments using individual M. tuberculosis and M. bovis BCG knock out mutants. We have demonstrated that growth rate control is a carefully orchestrated process which requires a distinct set of genes encoding several virulence determinants, gene regulators, and metabolic enzymes. The mce1 locus appears to be a component of the switch to slow growth rate, which is consistent with the proposed role in virulence of M. tuberculosis. These results suggest novel perspectives for unravelling the mechanisms involved in the switch between acute and persistent TB infections and provide a means to study aspects of this important phenomenon in vitro.
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