Unique genetic signatures in HIV-1 subtype A1 and A1D recombinant envelope glycoprotein distinguish contemporary transmitted/founder viruses from historical strains in East Africa.

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-08-04 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1632581
Frank Kato, Anne Kapaata, Ronald Galiwango, Angella Nakyanzi, Christian Ndekezi, Fortunate Natwijuka, Denis Omara, Andrew Ekii Obuku, Brian Foley, Pontiano Kaleebu, Eunice Nduati, Sheila Nina Balinda
{"title":"Unique genetic signatures in HIV-1 subtype A1 and A1D recombinant envelope glycoprotein distinguish contemporary transmitted/founder viruses from historical strains in East Africa.","authors":"Frank Kato, Anne Kapaata, Ronald Galiwango, Angella Nakyanzi, Christian Ndekezi, Fortunate Natwijuka, Denis Omara, Andrew Ekii Obuku, Brian Foley, Pontiano Kaleebu, Eunice Nduati, Sheila Nina Balinda","doi":"10.3389/fmicb.2025.1632581","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>The envelope glycoprotein (Env) of HIV-1 Transmitted/Founder (T/F) viruses in subtypes B and C carries distinct genetic signatures that enhance transmission fitness, augment infectivity and immune evasion. However, there is limited data on such signatures in T/F subtypes A1, D and A1D recombinants that predominate East Africa's HIV epidemic.</p><p><strong>Methods: </strong>We used phylogenetically corrected approaches to detect distinct genetic signatures by comparing 44 contemporary HIV-1 T/F Envs with 229 historical Envs of the same subtype in East Africa.</p><p><strong>Results and discussion: </strong>Subtype analysis based on the full-length Env gene of contemporary T/F viruses revealed a high proportion of subtype A1, followed by A1D recombinants, and fewer subtype D. Signature analysis revealed that the contemporary subtype A1 T/Fs were more likely to select distinct amino acids, including M22 in the signal peptide, R82 in gp120, A172 in the V2 loop, E230 in the glycosite 230, K275 in the D loop, Y317 in the V3 loop, K476 and N477 in the CD4 contact site, when compared with the historical Envs (q-value < 0.2). Conversely, the contemporary subtype A1 T/F Envs were less likely to carry the amino acids Q432 in the CD4 contact site, and the L784 signature within the LLP-2 (q-value < 0.2). The A1D recombinant T/Fs were more likely to select the D620 in the C-helix, but under selected the L34 in gp120, P299 in the V3 loop and Y643 in the Heptad repeat-2, compared to the historical Envs (q-value < 0.2). The distinct signature sites reported in this study may contribute to the successful establishment of acute infection as well as the persistence of long-term infection. Therefore, effective therapeutics and vaccines may target these distinct amino acid signatures especially for the East African region as it may be necessary to employ subtype-specific vaccines according to the subtype distribution.</p>","PeriodicalId":12466,"journal":{"name":"Frontiers in Microbiology","volume":"16 ","pages":"1632581"},"PeriodicalIF":4.0000,"publicationDate":"2025-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12358483/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fmicb.2025.1632581","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: The envelope glycoprotein (Env) of HIV-1 Transmitted/Founder (T/F) viruses in subtypes B and C carries distinct genetic signatures that enhance transmission fitness, augment infectivity and immune evasion. However, there is limited data on such signatures in T/F subtypes A1, D and A1D recombinants that predominate East Africa's HIV epidemic.

Methods: We used phylogenetically corrected approaches to detect distinct genetic signatures by comparing 44 contemporary HIV-1 T/F Envs with 229 historical Envs of the same subtype in East Africa.

Results and discussion: Subtype analysis based on the full-length Env gene of contemporary T/F viruses revealed a high proportion of subtype A1, followed by A1D recombinants, and fewer subtype D. Signature analysis revealed that the contemporary subtype A1 T/Fs were more likely to select distinct amino acids, including M22 in the signal peptide, R82 in gp120, A172 in the V2 loop, E230 in the glycosite 230, K275 in the D loop, Y317 in the V3 loop, K476 and N477 in the CD4 contact site, when compared with the historical Envs (q-value < 0.2). Conversely, the contemporary subtype A1 T/F Envs were less likely to carry the amino acids Q432 in the CD4 contact site, and the L784 signature within the LLP-2 (q-value < 0.2). The A1D recombinant T/Fs were more likely to select the D620 in the C-helix, but under selected the L34 in gp120, P299 in the V3 loop and Y643 in the Heptad repeat-2, compared to the historical Envs (q-value < 0.2). The distinct signature sites reported in this study may contribute to the successful establishment of acute infection as well as the persistence of long-term infection. Therefore, effective therapeutics and vaccines may target these distinct amino acid signatures especially for the East African region as it may be necessary to employ subtype-specific vaccines according to the subtype distribution.

Abstract Image

Abstract Image

Abstract Image

HIV-1亚型A1和A1D重组包膜糖蛋白的独特遗传特征将东非当代传播/创始人病毒与历史毒株区分开来。
HIV-1传播/方正(T/F)病毒B和C亚型的包膜糖蛋白(Env)携带不同的遗传特征,增强传播适应性,增强传染性和免疫逃避。然而,在主导东非艾滋病毒流行的T/F A1、D和A1D亚型重组中,关于这种特征的数据有限。方法:我们使用系统发育校正方法,通过比较44名当代HIV-1 T/F Envs与229名东非相同亚型的历史Envs,来检测不同的遗传特征。结果与讨论:亚型分析基于当代T / F的长篇Env基因病毒显示高比例的亚型A1,其次是A1D重组,和更少的亚型D特征分析表明当代亚型A1 T / Fs更有可能选择不同的氨基酸,包括锰在信号肽,在gp120 R82 A172 V2的循环,E230 230年glycosite K275 D环,Y317 V3中循环,K476和N477 CD4联系网站,与历史Envs相比(q值< 0.2)。相反,当代A1 T/F亚型Envs在CD4接触位点携带氨基酸Q432的可能性较小,在LLP-2中携带L784的可能性较小(q值< 0.2)。与历史Envs相比,A1D重组T/ f更倾向于选择C-helix中的D620,而较少选择gp120中的L34、V3环中的P299和Heptad repeat2中的Y643 (q值< 0.2)。本研究中报道的独特的特征位点可能有助于成功建立急性感染以及长期感染的持久性。因此,有效的治疗方法和疫苗可能针对这些不同的氨基酸特征,特别是对于东非地区,因为可能有必要根据亚型分布使用亚型特异性疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信