Mathuria Jitendra Prasad, Anupurba Shampa
Department of Microbiology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India; Department of Medical Lab Technology, Paramedical Vigyaan Mahavidhyalaya, Uttar Pradesh University of Medical Sciences, Saifai, Etawah, India.
Department of Microbiology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Int J Mycobacteriol. 2016 Dec;5 Suppl 1:S176-S177. doi: 10.1016/j.ijmyco.2016.10.041. Epub 2016 Nov 27.
OBJECTIVE/BACKGROUND: World Health Organization estimates that approximately one-third of the global community is infected with Mycobatcerium tuberculosis (MTB). Various molecular epidemiology methods were developed and found very promising for assessing the genetic diversity among MTB complex strain. The two major tools restriction fragment length polymorphism (RFLP) and spoligotyping were commonly used in various studies. Some Indian studies raise the question about the utility of IS6110-RFLP in India due to the presence of zero and low copy number of IS6110 element in MTB isolates. In this short study, we attempt to evaluate the usefulness of IS6110-RFLP in genotyping of MTB isolates in North India.
We conducted a short study involving 26 MTB isolates collected from Sawai Madhopur, Rajasthan, India. IS6110-RFLP analysis was performed as previously described method. In brief, the procedure involve MTB DNA digestion (PvuII restriction enzyme), electrophoresis on 1% agarose gel, transfer of DNA fragments on positively charged nylon membrane, hybridization with digoxigenin-labeled IS6110 probe, and detection by digoxigenin nucleic acid labeling and detection kit.
IS6110-RFLP analysis of 26 MTB isolates showed presence of IS6110 element in varying range from 0 to 17 copies. Out of the 26 MTB isolates, two (7.8%), three (11.5%), and 21 (80.8%) showed zero, low, and multiple copy numbers, respectively. The isolates, which had IS6110 element, showed 22 different RFLP patterns. Two clusters of two isolates each were found, and 20 isolates showed unique RFLP pattern. The two clusters of isolates had 11 and 13 copy numbers of IS6110.
In this study, we found that the majority of isolates were having multiple copy numbers of IS6110 element and showed a very diverse pattern. These results showed that the IS6110-RFLP analysis is still a promising genotyping method and has good discriminatory power to differentiate strains of MTB isolates in India.
目的/背景:世界卫生组织估计,全球约三分之一的人感染了结核分枝杆菌(MTB)。人们开发了各种分子流行病学方法,发现这些方法在评估MTB复合菌株的遗传多样性方面非常有前景。两种主要工具,即限制性片段长度多态性(RFLP)和间隔寡核苷酸分型(spoligotyping),在各种研究中普遍使用。一些印度的研究对IS6110-RFLP在印度的实用性提出了质疑,因为MTB分离株中IS6110元件的拷贝数为零或很低。在这项简短的研究中,我们试图评估IS6110-RFLP在印度北部MTB分离株基因分型中的实用性。
我们进行了一项简短的研究,涉及从印度拉贾斯坦邦萨瓦伊马德霍布尔收集的26株MTB分离株。按照先前描述的方法进行IS6110-RFLP分析。简而言之,该程序包括MTB DNA消化(PvuII限制性酶)、在1%琼脂糖凝胶上进行电泳、将DNA片段转移到带正电荷的尼龙膜上、与地高辛标记的IS6110探针杂交,以及用地高辛核酸标记和检测试剂盒进行检测。
对26株MTB分离株的IS6110-RFLP分析显示,IS6110元件的拷贝数在0至17个之间变化。在26株MTB分离株中,分别有2株(7.8%)、3株(11.5%)和21株(80.8%)显示拷贝数为零、低拷贝数和多拷贝数。具有IS6110元件的分离株显示出22种不同的RFLP模式。发现了两个每组有两株分离株的簇,20株分离株显示出独特的RFLP模式。这两个分离株簇的IS6110拷贝数分别为11和13。
在本研究中,我们发现大多数分离株具有多个IS6110元件拷贝数,并且显示出非常多样的模式。这些结果表明,IS6110-RFLP分析仍然是一种有前景的基因分型方法,并且在区分印度MTB分离株菌株方面具有良好的鉴别力。