Bukka Archana, Price Christopher T D, Kernodle Douglas S, Graham James E
Department of Microbiology and Immunology, University of Louisville School of Medicine Louisville, KY, USA.
Front Microbiol. 2012 Jan 10;2:266. doi: 10.3389/fmicb.2011.00266. eCollection 2011.
To identify factors contributing to the ability of tubercle bacilli to grow in the lung during active infection, we analyzed RNA expression patterns in bacteria present in patient sputum. Prominent among bacterial transcripts identified were those encoding secreted peptides of the Esat-6 subfamily that includes EsxK and EsxL (Rv1197 and Rv1198). H37Rv esxKL and esxJI transcripts were differentially expressed under different growth conditions, and disruption of these genes altered growth phase kinetics in typical laboratory batch broth cultures. These growth defects, including the reduced intracellular growth of an ΔesxKL mutant in primary human macrophages, were reversed by either low multiplicity co-infection or co-culture with wild-type bacteria, demonstrating the ability of the secreted factors to rescue isogenic mutants. Complementing either only esxL or esxI alone (Rv1198 or Rv1037c) also reduced observed growth defects, indicating these genes encode factors capable of contributing to growth. Our studies indicate that the Mycobacterium tuberculosis Mtb9.9 family secreted factors EsxL and EsxI can act in trans to modulate growth of intracellular bacteria, and are highly expressed during active human lung infection.
为了确定在活动性感染期间促成结核杆菌在肺部生长能力的因素,我们分析了患者痰液中细菌的RNA表达模式。在鉴定出的细菌转录本中,突出的是那些编码Esat-6亚家族分泌肽的转录本,该亚家族包括EsxK和EsxL(Rv1197和Rv1198)。H37Rv esxKL和esxJI转录本在不同生长条件下差异表达,这些基因的破坏改变了典型实验室分批肉汤培养中的生长阶段动力学。这些生长缺陷,包括ΔesxKL突变体在原代人巨噬细胞中细胞内生长的减少,通过低 multiplicity 共感染或与野生型细菌共培养得以逆转,证明了分泌因子拯救同基因突变体的能力。单独补充esxL或esxI(Rv1198或Rv1037c)也减少了观察到的生长缺陷,表明这些基因编码有助于生长的因子。我们的研究表明,结核分枝杆菌Mtb9.9家族分泌因子EsxL和EsxI可以反式作用来调节细胞内细菌的生长,并且在人类肺部活动性感染期间高度表达。