...
首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Effect of diversity in gp41 membrane proximal external region of primary HIV-1 Indian subtype C sequences on interaction with broadly neutralizing antibodies 4E10 and 10E8
【24h】

Effect of diversity in gp41 membrane proximal external region of primary HIV-1 Indian subtype C sequences on interaction with broadly neutralizing antibodies 4E10 and 10E8

机译:初级HIV-1印度亚型C序列近端外部区域对近中和抗体4E10和10E8的相互作用近外区域的影响

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Human Immunodeficiency Virus-1 Clade C (HIV-1C) dominates the AIDS epidemic in India, afflicting 2.1 million individuals within the country and more than 15 million people worldwide. Membrane proximal external region (MPER) is an attractive target for broadly neutralizing antibody (bNAb) based therapies. However, information on MPER sequence diversity from India is meagre due to limited sampling of primary viral sequences. In the present study, we examined the variation in MPER of HIV-1C from 24 individuals in Mumbai, India by high throughput sequencing of uncultured viral sequences. Deep sequencing of MPER (662-683; HXB2 envelope amino acid numbering) allowed quantification of intra-individual variation up to 65% at positions 662, 665, 668, 674 and 677 within this region. These variable positions included contact sites targeted by bNAbs 2F5, Z13e1, 4E10 as well as 10E8. Both major and minor epitope variants i.e. 'haplotypes' were generated for each sample dataset. A total of 23, 34 and 25 unique epitope haplotypes could be identified for bNAbs 2F5, Z13e1 and 4E10/10E8 respectively. Further analysis of 4E10 and 10E8 epitopes from our dataset and meta-analysis of previously reported HIV-1 sequences from India revealed 26 epitopes (7 India-specific), heretofore untested for neutralization sensitivity. Peptide-Ab docking predicted 13 of these to be non-binding to 10E8. ELISA, Surface Plasmon Resonance and peptide inhibition of HIV-1 neutralization assays were then performed which validated predicted weak/non-binding interactions for peptides corresponding to six of these epitopes. These results highlight the under-representation of 10E8 non-binding HIV-1C MPER sequences from India. Our study thus underscores the need for increased surveillance of primary circulating envelope sequences for development of efficacious bNAb-based interventions in India.
机译:人类免疫缺陷病毒-1 CLADE C(HIV-1C)在印度占据艾滋病流行病,折磨了该国内的210万人,全世界超过1500万人。膜近端外部区域(MPER)是一种有吸引力的基于抗体(BNAB)的疗法的吸引力。然而,由于原发性病毒序列的采样有限,有关印度的MPER序列多样性的信息。在本研究中,通过未培养的病毒序列的高通量测序检查了来自印度的24个个体的HIV-1C的MPER的变异。 MPER的深度测序(662-683; HXB2包络氨基酸编号)允许在该区域内的位置662,665,668,674和677处定量高达65%的内变化。这些可变位置包括由BNABS 2F5,Z13E1,4E10以及10E8靶向的接触位点。主要和次要表位变体都是对每个样本数据集产生的'单倍型'。可以分别为BNABS 2F5,Z13E1和4E10 / 10E8识别总共23,34和25个独特的表位单倍型。从我们的数据集和荟萃分析的进一步分析来自我们先前报道的印度的HIV-1序列的荟萃分析显示出26个表位(特异性7个特异性),迄今为止不受中和敏感性。肽-B肽对接预测的13与10E8无结合。然后进行ELISA,表面等离子体共振和肽的HIV-1中和测定的抑制,其验证了对应于这些表位的六个表位的肽的预测弱/不结合相互作用。这些结果突出了来自印度的10E8非结合HIV-1C MPER序列的表示。因此,我们的研究强调了对印度有效的BNAB干预措施的初级循环包络序列的序列增加了需求。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号