O'Toole Ronan F, Gautam Sanjay S
School of Medicine, Faculty of Health, University of Tasmania, Hobart TAS 7000, Australia; Department of Clinical Microbiology, Sir Patrick Dun Laboratory, School of Medicine, Trinity College Dublin, Dublin 8, Ireland.
School of Medicine, Faculty of Health, University of Tasmania, Hobart TAS 7000, Australia.
Genomics. 2017 Oct;109(5-6):471-474. doi: 10.1016/j.ygeno.2017.07.004. Epub 2017 Jul 22.
The genome sequence of Mycobacterium tuberculosis strain H37Rv is an important and valuable reference point in the study of M. tuberculosis phylogeny, molecular epidemiology, and drug-resistance mutations. However, it is becoming apparent that use of H37Rv as a sole reference genome in analysing clinical isolates presents some limitations to fully investigating M. tuberculosis virulence. Here, we examine the presence of single locus variants and the absence of entire genes in H37Rv with respect to strains that are responsible for cases and outbreaks of tuberculosis. We discuss how these polymorphisms may affect phenotypic properties of H37Rv including pathogenicity. Based on our observations and those of other researchers, we propose that use of a single reference genome, H37Rv, is not sufficient for the detection and characterisation of M. tuberculosis virulence-related loci. We recommend incorporation of genome sequences of other reference strains, in particular, direct clinical isolates, in such analyses in addition to H37Rv.
结核分枝杆菌H37Rv菌株的基因组序列是研究结核分枝杆菌系统发育、分子流行病学和耐药性突变的重要且有价值的参考点。然而,越来越明显的是,在分析临床分离株时仅使用H37Rv作为参考基因组,在全面研究结核分枝杆菌毒力方面存在一些局限性。在此,我们针对导致结核病病例和暴发的菌株,研究了H37Rv中单个位点变异的存在情况以及完整基因的缺失情况。我们讨论了这些多态性如何可能影响H37Rv的表型特性,包括致病性。基于我们的观察以及其他研究人员的观察,我们提出仅使用单个参考基因组H37Rv不足以检测和鉴定结核分枝杆菌毒力相关位点。我们建议在这类分析中,除了H37Rv之外,还应纳入其他参考菌株的基因组序列,特别是直接从临床分离得到的菌株。