Gupta Debanjali, Saha Kallol, Biswas Aritra, Firdaus Rushna, Ghosh Monika, Sadhukhan Provash Chandra
ICMR Virus Unit, 57, Dr. Suresh Chandra Banerjee Road, Beliaghata, Kolkata 700010, West Bengal, India.
ICMR Virus Unit, 57, Dr. Suresh Chandra Banerjee Road, Beliaghata, Kolkata 700010, West Bengal, India.
Infect Genet Evol. 2017 Mar;48:156-163. doi: 10.1016/j.meegid.2016.12.001. Epub 2016 Dec 5.
Recombination in RNA virus is a rare event in the survival and evolution to evade host immune system. This is increasing within high risk group population (HRG) due to super infection that occurs by continuous sharing of common drug equipment by HCV infected or HIV-HCV co-infected recurrent drug users. Recombination causes impediment to vaccine development and therapeutic intervention as standard HCV treatment is still genotype specific. Blood samples of 194 people who inject drugs (PWID) were collected from an Opioid Substitution Therapy Centre in Kolkata, India. HCV sero-reactivity was checked by ELISA. Detection of HCV RNA by nested RT-PCR and genotyping by DNA sequencing were done. Phylogenetic analysis, Simplot, Bootscan plot, Recombination Detection Program were used for recombinant strain identification. Out of 80 HCV sero-reactive samples, 77 were RNA positive (96.25%). Out of 74 HIV mono-infected individuals, 12 HCV sero-nonreactive samples were HCV RNA positive. Out of total 89 RNA positive samples, 64 paired partial core and NS5B region (71.9%) were sequenced by Sanger's method. Two major genotypes (1 and 3), four subtypes and an inter-genotype recombinant strain (3a/1a) with a novel breakpoint in the NS4B coding region were found.
在RNA病毒的生存和进化以逃避宿主免疫系统的过程中,重组是一个罕见事件。由于丙型肝炎病毒(HCV)感染者或HIV-HCV合并感染者反复使用毒品者持续共用普通吸毒器具而发生的重复感染,在高危人群(HRG)中这种情况正在增加。重组对疫苗开发和治疗干预造成阻碍,因为标准的HCV治疗仍然是基因型特异性的。从印度加尔各答的一个阿片类药物替代治疗中心收集了194名注射毒品者(PWID)的血样。通过酶联免疫吸附测定(ELISA)检查HCV血清反应性。通过巢式逆转录聚合酶链反应(RT-PCR)检测HCV RNA并通过DNA测序进行基因分型。使用系统发育分析、Simplot分析、Bootscan分析图、重组检测程序来鉴定重组毒株。在80份HCV血清反应性样本中,77份RNA呈阳性(96.25%)。在74名单纯感染HIV的个体中,12份HCV血清反应阴性样本HCV RNA呈阳性。在总共89份RNA阳性样本中,64份配对的部分核心区和NS5B区(71.9%)通过桑格法进行了测序。发现了两种主要基因型(1型和3型)、四种亚型以及一种在NS4B编码区有一个新断点的基因型间重组毒株(3a/1a)。