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Mapping HIV-1 Subtype C gp120 Epitopes Using a Bioinformatic Approach

机译:使用生物信息方法映射HIV-1亚型C GP120表位

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Human Immunodeficiency Type-1 subtype C (HIV-IC) is rapidly diverging among populations causing more than 48% of infections worldwide. HIV-IC gp120's 128 sequences available at Genbank were aligned and submitted to phylogenetic analysis. Three major clusters were identified: 72 sequences aligned with a Brazilian 0072eference sequence; 44 sequences aligned with an Ethiopian sequence and 12 could be group along with Indian isolates. A search was made for conserved HIV-IC cytotoxic T lymphocyte (CTL) epitopes to A*0201, A*0301, A*1101 e B*07 human leukocyte antigen (HLA) alleles (using Epijen software). Five most conserved epitopes were recognized: QMHEDIISL, CTHGIKPVV, NLTNNVKTI, AITQACPKV, CTRPNNNTR. Our results showed a recognized evolutionary force of HIV-1 to escape from CTL responses mutating sites that can be negatively select by host's immune system. The present study brings up a new approach to in silico epitope analysis taking into account geographical informations on virus diversity and host genetic background.
机译:人类免疫缺陷型-1亚型C(HIV-IC)在全世界群体的群体中迅速发散,导致超过48%的感染。 Genbank可获得的HIV-IC GP120的128序列被对齐并提交给系统发育分析。确定了三个主要簇:72个与巴西00722eference序列对齐的序列; 44与埃塞俄比亚序列和12对齐的序列可以是群体以及印度分离株。将保守的HIV-IC细胞毒性T淋巴细胞(CTL)表位为A * 0201,A * 0301,A * 0301,A * 1101e B * 07人白细胞抗原(HLA)等位基因(使用EPIJEN软件)进行搜索。识别出五种最保守的表位:QMHEDIISL,CTHGIKPVV,NLTNVKTI,AITQACPKV,CTRPNNTR。我们的结果表明,HIV-1的公认进化力,以逃离CTL响应突变位点,这些位点通过宿主的免疫系统提供负面选择。本研究为考虑到病毒多样性和宿主遗传背景的地理信息,提出了一种新的硅表位分析方法。

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