Near-Full-Length Genomic Characterization of Two Novel Unique Recombinants (CRF01_AE/CRF07_BC) in Shenzhen, Guangdong Province, China.

IF 1 4区 医学 Q4 IMMUNOLOGY
AIDS research and human retroviruses Pub Date : 2026-05-01 Epub Date: 2026-04-09 DOI:10.1177/08892229261439998
Chang Liu, Bo Zhu, Dandan Lin, Pinghui Wu, Wenbo Rong, Binglou He, Hanping Li, Yongjian Liu, Lei Jia, Xiaolin Wang, Jingyun Li, Bohan Zhang, Jingwan Han, Hongling Wen, Lin Li
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引用次数: 0

Abstract

Extensive cocirculation of CRF01_AE and CRF07_BC in China has created favorable conditions for ongoing intersubtype recombination, contributing to increasing genetic complexity within the local HIV-1 epidemic. In this study, two novel unique recombinant forms composed of CRF01_AE and CRF07_BC were identified in Shenzhen, Guangdong Province. Near-full-length genome sequences were obtained for isolates LS11654 and LS16824. Phylogenetic analysis indicated that both sequences clustered within a CRF01_AE-/CRF07_BC-related lineage but were distinct from previously reported strains. Recombination analysis revealed markedly different mosaic structures: LS11654 contained two recombination breakpoints, whereas LS16824 exhibited a more complex genome with eight breakpoints and multiple inserted fragments. Subregion phylogenetic analysis further confirmed the parental origins of the recombinant segments. These findings reflect ongoing recombination driven by sustained cocirculation of CRF01_AE and CRF07_BC in Shenzhen and highlight the importance of continued molecular surveillance.

中国广东深圳两个新的独特重组基因CRF01_AE/CRF07_BC的近全长基因组特征
CRF01_AE和CRF07_BC在中国的广泛共循环为正在进行的亚型间重组创造了有利条件,从而增加了当地HIV-1流行的遗传复杂性。本研究在广东深圳鉴定了两种由CRF01_AE和CRF07_BC组成的新型独特重组形式。分离株LS11654和LS16824获得了接近全长的基因组序列。系统发育分析表明,这两个序列都聚集在CRF01_AE-/ crf07_bc相关谱系中,但与先前报道的菌株不同。重组分析显示,LS11654包含两个重组断点,而LS16824具有更复杂的基因组,有8个断点和多个插入片段。亚区系统发育分析进一步证实了重组片段的亲本来源。这些发现反映了深圳CRF01_AE和CRF07_BC持续共循环驱动的持续重组,并强调了持续分子监测的重要性。
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来源期刊
CiteScore
3.10
自引率
6.70%
发文量
201
审稿时长
3-6 weeks
期刊介绍: AIDS Research and Human Retroviruses was the very first AIDS publication in the field over 30 years ago, and today it is still the critical resource advancing research in retroviruses, including AIDS. The Journal provides the broadest coverage from molecular biology to clinical studies and outcomes research, focusing on developments in prevention science, novel therapeutics, and immune-restorative approaches. Cutting-edge papers on the latest progress and research advances through clinical trials and examination of targeted antiretroviral agents lead to improvements in translational medicine for optimal treatment outcomes. AIDS Research and Human Retroviruses coverage includes: HIV cure research HIV prevention science - Vaccine research - Systemic and Topical PreP Molecular and cell biology of HIV and SIV Developments in HIV pathogenesis and comorbidities Molecular biology, immunology, and epidemiology of HTLV Pharmacology of HIV therapy Social and behavioral science Rapid publication of emerging sequence information.
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