Kim Byoung-Jun, Kim Bo-Ram, Lee So-Young, Kook Yoon-Hoh, Kim Bum-Joon
Department of Microbiology and Immunology, Biomedical Sciences, Liver Research Institute, Cancer Research Institute and Seoul National University Medical Research Center (SNUMRC), Seoul National University College of Medicine, Seoul 110-799, Republic of Korea.
BMC Genomics. 2013 Dec 17;14:890. doi: 10.1186/1471-2164-14-890.
Recently, we introduced the complete genome sequence of Mycobacterium massiliense clinical isolates, Asan 50594 belonging to Type II genotype with rough colony morphology. Here, to address the issue of whether the rough colony morphotype of M. massiliense Type II genotype is genetically determined or not, we compared polymorphisms of the glycopeptidolipid (GPL) gene locus between M. massiliense Type II Asan 50594 and other rapidly growing mycobacteria (RGM) strains via analysis of genome databases.
We found deletions of 10 genes (24.8 kb), in the GPL biosynthesis related gene cluster of Asan 50594 genome, but no deletions in those of other smooth RGMs. To check the presence of deletions of GPL biosynthesis related genes in Mycobacterium abscessus--complex strains, PCRs targeting 12 different GPL genes (10 genes deleted in Asan 50594 genome as well as 2 conserved genes) were applied into 76 clinical strains of the M. abscessus complex strains [54 strains (Type I: 33, and Type II: 21) of M. massiliense and 22 strains (rough morphoype: 11 and smooth morphotype: 11) of M. abscessus]. No strains of the Type II genotype produced PCR amplicons in a total of 10 deleted GPL genes, suggesting loss of GPL biosynthesis genes in the genome of M. massiliense type II genotype strains.
Our data suggested that the rough colony morphotype of the M. massiliense Type II genotype may be acquired via deletion events at the GPL gene locus for evolutionary adaptation between the host and pathogen.
最近,我们公布了马赛分枝杆菌临床分离株阿山50594的全基因组序列,该菌株属于II型基因型,菌落形态粗糙。在此,为了解决马赛分枝杆菌II型基因型的粗糙菌落形态是否由基因决定这一问题,我们通过分析基因组数据库,比较了马赛分枝杆菌II型阿山50594与其他快速生长分枝杆菌(RGM)菌株之间糖肽脂(GPL)基因座的多态性。
我们发现阿山50594基因组中GPL生物合成相关基因簇有10个基因(24.8 kb)缺失,但其他光滑型RGM菌株中没有缺失。为检测脓肿分枝杆菌复合群菌株中GPL生物合成相关基因的缺失情况,针对12个不同的GPL基因(阿山50594基因组中缺失的10个基因以及2个保守基因)进行PCR,应用于76株脓肿分枝杆菌复合群临床菌株[54株马赛分枝杆菌(I型:33株,II型:21株)和22株脓肿分枝杆菌(粗糙形态型:11株,光滑形态型:11株)]。II型基因型菌株在总共10个缺失的GPL基因中均未产生PCR扩增产物,表明马赛分枝杆菌II型基因型菌株基因组中GPL生物合成基因缺失。
我们的数据表明,马赛分枝杆菌II型基因型的粗糙菌落形态可能是通过GPL基因座的缺失事件获得的,以实现宿主与病原体之间的进化适应。