Sankar Sathish, Kuppanan Suresh, Balakrishnan Babu, Nandagopal Balaji
Division of Biomedical Research, Sri Narayani Hospital and Research Centre, Thirumalaikodi, Sripuram, Vellore - 632 055, Tamil Nadu, India.
Bioinformation. 2011;6(7):283-5. doi: 10.6026/97320630006283. Epub 2011 Jun 23.
The IS6110 belongs to the family of insertion sequences (IS) of the IS3 category. This insertion sequence was reported to be specific for Mycobacterium tuberculosis complex and hence is extensively exploited for laboratory detection of the agent of tuberculosis and for epidemiological investigations based on polymerase chain reaction. IS6110 is 1361-bp long and within this sequence different regions have been utilized as targets in the identification of M. tuberculosis by PCR. However, the results are not always consistent, specific and sensitive. In recent years, a few clinical investigations raised concerns over IS6110 specificity and sensitivity in the diagnosis of tuberculosis due to false-positive (homology with other target DNA besides M. tuberculosis) or false negative (due to absence of copies of IS6110) results with IS6110 specific primers. To unravel the variations in IS6110 sequences, an insilico analysis of IS6110 sequence of different strains of M. tuberculosis was carried out. Our results of comparative analysis of IS6110 insertion sequences of M. tuberculosis complex suggests that, IS6110 insertion sequences harbored variations in its sequence, which is evident from the phylogenetic analysis. Importantly, IS6110 sequence has divergence within the copies of same strain and formed different clusters. A list of IS6110 specific primers used in various clinical investigation of tuberculosis was obtained from the literature and their performance scrutinized. Our study emphasizes the need to develop PCR assays (multiplex format) targeting more than one region of the genome of M. tuberculosis.
IS6110属于IS3类插入序列(IS)家族。据报道,这种插入序列是结核分枝杆菌复合群特有的,因此被广泛用于结核病病原体的实验室检测以及基于聚合酶链反应的流行病学调查。IS6110长1361个碱基对,在这个序列中,不同区域已被用作通过PCR鉴定结核分枝杆菌的靶标。然而,结果并不总是一致、特异和灵敏的。近年来,一些临床研究对IS6110在结核病诊断中的特异性和敏感性提出了担忧,因为使用IS6110特异性引物会出现假阳性(与除结核分枝杆菌外的其他靶标DNA同源)或假阴性(由于缺乏IS6110拷贝)结果。为了揭示IS6110序列的变异情况,对不同结核分枝杆菌菌株的IS6110序列进行了电子分析。我们对结核分枝杆菌复合群IS6110插入序列的比较分析结果表明,IS6110插入序列在其序列中存在变异,这从系统发育分析中可以明显看出。重要的是,IS6110序列在同一菌株的拷贝内存在差异,并形成了不同的簇。从文献中获得了在各种结核病临床研究中使用的IS6110特异性引物列表,并对其性能进行了审查。我们的研究强调了开发针对结核分枝杆菌基因组多个区域的PCR检测方法(多重形式)的必要性。