首页> 美国卫生研究院文献>Journal of Virology >Full-Length Human Immunodeficiency Virus Type 1 Genomes from Subtype C-Infected Seroconverters in India with Evidence of Intersubtype Recombination
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Full-Length Human Immunodeficiency Virus Type 1 Genomes from Subtype C-Infected Seroconverters in India with Evidence of Intersubtype Recombination

机译:来自印度亚型C感染的血清转化者的全长人类免疫缺陷病毒1型基因组具有亚型重组的证据。

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摘要

The development of an effective human immunodeficiency virus type 1 (HIV-1) vaccine is likely to depend on knowledge of circulating variants of genes other than the commonly sequenced gag and env genes. In addition, full-genome data are particularly limited for HIV-1 subtype C, currently the most commonly transmitted subtype in India and worldwide. Likewise, little is known about sequence variation of HIV-1 in India, the country facing the largest burden of HIV worldwide. Therefore, the objective of this study was to clone and characterize the complete genome of HIV-1 from seroconverters infected with subtype C variants in India. Cocultured HIV-1 isolates were obtained from six seroincident individuals from Pune, India, and virtually full-length HIV-1 genomes were amplified, cloned, and sequenced from each. Sequence analysis revealed that five of the six genomes were of subtype C, while one was a mosaic of subtypes A and C, with multiple breakpoints in env, nef, and the 3′ long terminal repeat as determined by both maximal χ2 analysis and phylogenetic bootstrapping. Sequences were compared for preservation of known cytotoxic T lymphocyte (CTL) epitopes. Compared with those of the HIV-1LAI sequence, 38% of well-defined CTL epitopes were identical. The proportion of nonconservative substitutions for Env, at 61%, was higher (P < 0.001) than those for Gag (24%), Pol (18%), and Nef (32%). Therefore, characterized CTL epitopes demonstrated substantial differences from subtype B laboratory strains, which were most pronounced in Env. Because these clones were obtained from Indian seroconverters, they are likely to facilitate vaccine-related efforts in India by providing potential antigens for vaccine candidates as well as for assays of vaccine responsiveness.
机译:有效的1型人类免疫缺陷病毒(HIV-1)疫苗的研发可能取决于对基因的循环变异体(通常测序的gag和env基因除外)的了解。此外,HIV-1 C亚型的全基因组数据特别有限,HIV-1 C亚型目前是印度和世界范围内最常见的传播亚型。同样,对印度的HIV-1序列变异知之甚少,印度是全世界HIV负担最大的国家。因此,这项研究的目的是从印度感染C型亚型的血清转化者中克隆和鉴定HIV-1的完整基因组。共培养的HIV-1分离株是从印度浦那的六名血清事件个体获得的,实际上,从每个个体扩增,克隆和测序了全长的HIV-1基因组。序列分析显示,六个基因组中的五个基因组属于C型,而一个基因组是A型和C型亚型的镶嵌体,在env,nef和多个3'长末端重复序列上均由最大χ 2确定, 分析和系统发育自举。比较序列以保存已知的细胞毒性T淋巴细胞(CTL)表位。与HIV-1LAI序列相比,38%的明确CTL表位相同。 Env的非保守取代比例为61%,高于Gag(24%),Pol(18%)和Nef(32%)(P <0.001)。因此,特征化的CTL表位与B亚型实验室菌株显示出实质性差异,这在Env中最为明显。因为这些克隆是从印度的血清转化者获得的,所以它们有可能通过为候选疫苗提供潜在的抗原以及进行疫苗反应性的测定,从而促进印度与疫苗相关的工作。

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