Huard Richard C, Fabre Michel, de Haas Petra, Lazzarini Luiz Claudio Oliveira, van Soolingen Dick, Cousins Debby, Ho John L
Division of International Medicine and Infectious Diseases, Department of Medicine, Joan and Sanford I. Weill Medical College, Cornell University, Room A-421, 525 East 68th St., New York, NY 10021, USA.
J Bacteriol. 2006 Jun;188(12):4271-87. doi: 10.1128/JB.01783-05.
In a previous report, we described a PCR protocol for the differentiation of the various species of the Mycobacterium tuberculosis complex (MTC) on the basis of genomic deletions (R. C. Huard, L. C. de Oliveira Lazzarini, W. R. Butler, D. van Soolingen, and J. L. Ho, J. Clin. Microbiol. 41:1637-1650, 2003). That report also provided a broad cross-comparison of several previously identified, phylogenetically relevant, long-sequence and single-nucleotide polymorphisms (LSPs and SNPs, respectively). In the present companion report, we expand upon the previous work (i) by continuing the evaluation of known MTC phylogenetic markers in a larger collection of tubercle bacilli (n = 125), (ii) by evaluating additional recently reported MTC species-specific and interspecific polymorphisms, and (iii) by describing the identification and distribution of a number of novel LSPs and SNPs. Notably, new genomic deletions were found in various Mycobacterium tuberculosis strains, new species-specific SNPs were identified for "Mycobacterium canettii," Mycobacterium microti, and Mycobacterium pinnipedii, and, for the first time, intraspecific single-nucleotide DNA differences were discovered for the dassie bacillus, the oryx bacillus, and the two Mycobacterium africanum subtype I variants. Surprisingly, coincident polymorphisms linked one M. africanum subtype I genotype with the dassie bacillus and M. microti with M. pinnipedii, thereby suggesting closer evolutionary ties within each pair of species than had been previously thought. Overall, the presented data add to the genetic definitions of several MTC organisms as well as fine-tune current models for the evolutionary history of the MTC.
在之前的一份报告中,我们描述了一种基于基因组缺失来区分结核分枝杆菌复合群(MTC)各菌种的PCR方案(R. C. Huard、L. C. de Oliveira Lazzarini、W. R. Butler、D. van Soolingen和J. L. Ho,《临床微生物学杂志》41:1637 - 1650,2003年)。该报告还对几个先前鉴定的、系统发育相关的长序列和单核苷酸多态性(分别为LSPs和SNPs)进行了广泛的交叉比较。在本配套报告中,我们扩展了先前的工作:(i)通过在更大的结核杆菌集合(n = 125)中继续评估已知的MTC系统发育标记;(ii)通过评估其他最近报道的MTC菌种特异性和种间多态性;(iii)通过描述一些新的LSPs和SNPs的鉴定及分布。值得注意的是,在各种结核分枝杆菌菌株中发现了新的基因组缺失,为“卡内蒂分枝杆菌”、田鼠分枝杆菌和海豹分枝杆菌鉴定了新的菌种特异性SNPs,并且首次发现了南非山兔分枝杆菌、羚羊分枝杆菌以及两种非洲分枝杆菌I型变种的种内单核苷酸DNA差异。令人惊讶的是,重合的多态性将一种非洲分枝杆菌I型基因型与南非山兔分枝杆菌联系起来,将田鼠分枝杆菌与海豹分枝杆菌联系起来,从而表明每对物种之间的进化关系比之前认为的更为密切。总体而言,所呈现的数据增加了几种MTC生物体的遗传定义,并对当前MTC进化历史模型进行了微调。