Beste Dany J V, Espasa Mateus, Bonde Bhushan, Kierzek Andrzej M, Stewart Graham R, McFadden Johnjoe
FHMS, University of Surrey, Guildford, United Kingdom.
PLoS One. 2009 Apr 28;4(4):e5349. doi: 10.1371/journal.pone.0005349.
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.
结核分枝杆菌感染了世界三分之一的人口。原发性肺结核涉及活跃的快速细菌复制,之后通常会出现无症状的潜伏性肺结核,其特征是细菌生长缓慢或不复制。潜伏感染的重新激活,即转变回活跃的细菌复制,可导致继发性可传播肺结核。参与缓慢生长或改变生长速率的分枝杆菌机制为开发针对持续性分枝杆菌感染的新药提供了合理的靶点。利用恒化器培养来控制生长速率,我们通过转座子位点杂交(TraSH)筛选了一个转座子突变体文库,以确定牛分枝杆菌(卡介苗)缓慢和快速生长的遗传需求以及生长速率转变的需求。我们鉴定出84个仅在缓慢生长(倍增时间为69小时)时所需的基因,以及256个从缓慢生长转变为快速生长所需的基因。为了验证这些发现,我们使用单个结核分枝杆菌和牛分枝杆菌卡介苗基因敲除突变体进行了实验。我们已经证明,生长速率控制是一个精心编排的过程,需要一组独特的基因,这些基因编码几种毒力决定因素、基因调节因子和代谢酶。mce1位点似乎是转变为缓慢生长速率的一个组成部分,这与结核分枝杆菌在毒力方面的假定作用一致。这些结果为揭示急性和持续性结核感染之间转变所涉及的机制提供了新的视角,并提供了一种在体外研究这一重要现象的方法。