Sekar Balaraman, Arunagiri Kamalanathan, Selvakumar Nagamiah, Preethi Kaluvuri Serena, Menaka Kandhaswami
Division of Laboratories, Central Leprosy Teaching and Research Institute, Chengalpattu, Tamil Nadu, India.
BMC Infect Dis. 2009 Jul 25;9:114. doi: 10.1186/1471-2334-9-114.
Comparative genomic analysis of M. tuberculosis H37Rv and M. bovis BCG have shown that 16 RDs (Regions of Differences) are deleted in BCG and have shown six deletion regions in M. tuberculosis H37Rv. RD1, is present in M. tuberculosis but is absent in all M. bovis BCG sub-strains. A study from Kerala, a south-western coastal state of India aimed to find out differences in RD1 region showed for the first time the presence of moaA3 gene in majority of their clinical isolates, that was absent in type strain H37Rv. We attempted to find out such polymorphism between type strains and the clinical isolates within RD1, targeting moaA3 gene among the clinical isolates of Tamil Nadu & Pondicherry, south-eastern coastal states of India
One hundred and sixteen clinical isolates of M. tuberculosis were included in the study. PCR using RD1DLa and RD1DRa primers was carried out to amplify a 652 bp fragment, encoding for cfp10 and esat 6 proteins of RD1. A second PCR using primers designed from the surrounding regions of moaA3 gene was done to confirm the presence of the full Open Reading Frame (ORF) in clinical isolates.
In M. tuberculosis H37Rv the expected 652 bp band was present. In BCG it was absent as expected, but a 386 bp fragment was amplified. Around 12/116 (10.3%) of our clinical isolates showed both 652 and 386 bp fragments. The additional 386 bp amplicon is a part of the moaA3 gene which codes for molybdopterin cofactor protein A in M. bovis. The second PCR amplified the flanking sequence of moaA3 and yielded the expected amplicon of 1254 bp in all those 10.3% of clinical isolates which had the 386 bp fragment. However the earlier study carried out in Kerala, reported the presence of moaA3 gene in majority (97%) of their clinical isolates.
This finding showed that there was regional variation presenting polymorphism in moA3 gene, among the strains of M. tuberculosis and further strengthens the speculation of genetic differences among the strains of Kerala and Tamil Nadu & Pondicherry, the South Indian states.
结核分枝杆菌H37Rv和牛分枝杆菌卡介苗的比较基因组分析表明,卡介苗中有16个差异区域(RDs)缺失,而结核分枝杆菌H37Rv中有6个缺失区域。RD1存在于结核分枝杆菌中,但在所有牛分枝杆菌卡介苗亚菌株中均不存在。印度西南部沿海邦喀拉拉邦的一项研究旨在找出RD1区域的差异,该研究首次发现其大多数临床分离株中存在moaA3基因,而在标准菌株H37Rv中不存在。我们试图找出标准菌株与RD1内临床分离株之间的这种多态性,以印度东南部沿海邦泰米尔纳德邦和本地治里的临床分离株中的moaA3基因为靶点。
本研究纳入了116株结核分枝杆菌临床分离株。使用RD1DLa和RD1DRa引物进行PCR,以扩增一个652 bp的片段,该片段编码RD1的cfp10和esat 6蛋白。使用从moaA3基因周围区域设计的引物进行第二次PCR,以确认临床分离株中完整开放阅读框(ORF)的存在。
在结核分枝杆菌H37Rv中出现了预期的652 bp条带。在卡介苗中,如预期的那样没有该条带,但扩增出了一个386 bp的片段。在我们的临床分离株中,约12/116(10.3%)同时显示出652 bp和386 bp的片段。额外的386 bp扩增子是moaA3基因的一部分,该基因在牛分枝杆菌中编码钼蝶呤辅因子蛋白A。第二次PCR扩增了moaA3的侧翼序列,并在所有具有386 bp片段的10.3%临床分离株中产生了预期大小为1254 bp的扩增子。然而,喀拉拉邦 earlier进行的研究报告称,其大多数(97%)临床分离株中存在moaA3基因。
这一发现表明,结核分枝杆菌菌株之间存在区域差异,moA基因呈现多态性,进一步强化了对印度南部喀拉拉邦与泰米尔纳德邦和本地治里邦菌株之间基因差异的推测。