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在无血浆病毒载量情况下,解剖组织中HIV-1 gp120可变区的新出现模式

Emerging Patterns in HIV-1 gp120 Variable Domains in Anatomical Tissues in the Absence of a Plasma Viral Load.

作者信息

Lamers Susanna L, Fogel Gary B, Nolan David J, Barbier Andrew E, Rose Rebecca, Singer Elyse J, Gonzalez-Perez Maria Paz, McGrath Michael S

机构信息

1 BioInfoExperts LLC, Thibodaux, Louisiana.

2 Natural Selection, Inc., San Diego, California.

出版信息

AIDS Res Hum Retroviruses. 2019 Jun;35(6):588-596. doi: 10.1089/AID.2018.0267. Epub 2019 Apr 10.

DOI:10.1089/AID.2018.0267
PMID:30793919
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6588100/
Abstract

The HIV envelope protein contains five hypervariable domains (V1-V5) that are fundamental for cell entry. We contrasted modifications in the variable domains derived from a panel of 24 tissues from 7 subjects with no measurable plasma viral load (NPVL) to variable domains from 76 tissues from 15 subjects who had a detectable plasma viral load (PVL) at death. NPVL subject's V1 and V2 domains were usually highly length variable, whereas length variation in PVL sequences was more conserved. Longer V1s contained more charged residues, whereas longer V2s were more glycosylated. Structural analysis demonstrated V1/V2 charge, and N-site additions/subtractions were localized to the CD4 binding pocket. Diversified envelopes in tissues during therapy may represent a mechanism for HIV persistence in tissues, as binding pocket complexity is associated with HIV that may escape neutralization, whereas shorter envelopes are associated with increased infectivity. Further analysis of tissue-derived envelope sequences may enable better understanding of potential immunological approaches targeting the persistent HIV reservoir.

摘要

HIV包膜蛋白包含五个高变区(V1-V5),这些区域对细胞进入至关重要。我们将来自7名无可测血浆病毒载量(NPVL)受试者的24个组织的可变区修饰与来自15名死亡时具有可检测血浆病毒载量(PVL)受试者的76个组织的可变区进行了对比。NPVL受试者的V1和V2结构域通常长度高度可变,而PVL序列中的长度变异则更为保守。较长的V1含有更多带电荷的残基,而较长的V2则糖基化程度更高。结构分析表明,V1/V2电荷以及N位点的添加/缺失定位于CD4结合口袋。治疗期间组织中多样化的包膜可能代表了HIV在组织中持续存在的一种机制,因为结合口袋的复杂性与可能逃避中和的HIV相关,而较短的包膜则与感染性增加相关。对组织来源的包膜序列进行进一步分析可能有助于更好地理解针对持续性HIV储存库的潜在免疫方法。