Department of Medicine, University of Cambridge, Cambridge, UK.
Antimicrob Agents Chemother. 2012 Dec;56(12):6080-7. doi: 10.1128/AAC.01641-12. Epub 2012 Sep 24.
Despite being genetically monomorphic, the limited genetic diversity within the Mycobacterium tuberculosis complex (MTBC) has practical consequences for molecular methods for drug susceptibility testing and for the use of current antibiotics and those in clinical trials. It renders some representatives of MTBC intrinsically resistant against one or multiple antibiotics and affects the spectrum and consequences of resistance mutations selected for during treatment. Moreover, neutral or silent changes within genes responsible for drug resistance can cause false-positive results with hybridization-based assays, which have been recently introduced to replace slower phenotypic methods. We discuss the consequences of these findings and propose concrete steps to rigorously assess the genetic diversity of MTBC to support ongoing clinical trials.
尽管结核分枝杆菌复合群(MTBC)在基因上是单态的,但它的遗传多样性有限,这对药物敏感性检测的分子方法以及当前抗生素和临床试验中的抗生素的使用都有实际影响。这使得 MTBC 的一些代表对一种或多种抗生素具有内在抗性,并影响了治疗过程中选择的耐药突变的范围和后果。此外,负责耐药性的基因中的中性或沉默变化会导致基于杂交的检测出现假阳性结果,这些检测最近已被引入以替代较慢的表型方法。我们讨论了这些发现的后果,并提出了具体步骤来严格评估 MTBC 的遗传多样性,以支持正在进行的临床试验。