Evidence map›Paper›PMID 40660300›Full record

ArticleVirology journal2025

Genetic diversity of HIV in Yunnan, China: the role of second-generation recombination involving circulating and unique recombinant forms.

Ying-Na Xie, Zheng-Xu Li, Ya-Ting Chen, Yong-Juan Li, Zhu-Qian Yang, Yuan Ren, Zi-Xuan Yang, Xin Chen

Abstract read
In one paragraph

Article in Virology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ying-Na Xie *Department of Pathogenic Biology, School of Basic Medical Sciences, Gannan Medical University, Ganzhou, 341000, China.
Zheng-Xu Li *Department of HIV/AIDS and STD Prevention and Control, Baoshan Center for Disease Control and Prevention, Baoshan, 678000, China.
Ya-Ting ChenDepartment of Pathogenic Biology, School of Basic Medical Sciences, Gannan Medical University, Ganzhou, 341000, China.
Yong-Juan LiBaoshan People's Hospital, Baoshan, 678000, China.
Zhu-Qian YangBaoshan People's Hospital, Baoshan, 678000, China.
Yuan RenSchool of Basic Medical Sciences, Baoshan College of Traditional Chinese Medicine, Baoshan, 678000, China.
Zi-Xuan YangBaoshan People's Hospital, Baoshan, 678000, China.
Xin ChenDepartment of Pathogenic Biology, School of Basic Medical Sciences, Gannan Medical University, Ganzhou, 341000, China. baiyjqqq@126.com.

Funding

National Natural Science Foundation of China 32460043, 81902106Natural Science Foundation of Jiangxi Province 20242BAB25538
6 · The paper itself

Abstract

backgroundThe genetic diversity of HIV is significantly influenced by second-generation recombination events involving circulating recombinant forms (CRFs) and unique recombinant forms (URFs), which are crucial for the virus's evolution and dissemination. The China-Myanmar border region is recognized as a focal point for inter-subtype recombination of HIV, with recombinant strains predominating in this area.

methodsNear full-length HIV genomes were amplified from plasma samples of eight Burmese individuals newly diagnosed with HIV in Baoshan, China, from 2006 to 2020. Phylogenetic trees were constructed using maximum likelihood methods, and Bootscan analysis was conducted to identify recombination structures.

resultsAmong the eight sequences, one (YN33F28) clustered with subtype C, and one (YN9M24) with CRF08_BC. The remaining six sequences did not cluster with any known HIV subtypes, indicating they might represent novel recombinant strains. Bootscan analysis revealed that three sequences (YN36F38, YN35F22, and YN32M22) were likely formed through second-generation recombination involving known CRFs (CRF82_cpx and CRF86_BC) and a URF (KY406739). Additionally, three sequences (YN34F21, YN7F27, and YN8F28) were identified as newly formed URFs, resulting from complex recombination events between HIV subtypes B, C, and CRF01_AE.

conclusionThese results underscore the continuous evolution of HIV via recombination in the China-Myanmar border region. The identification of second-generation recombinants and newly formed URFs highlights the importance of continuous molecular surveillance to better understand HIV diversity and to inform strategies for prevention, treatment, and vaccine development.

Indexed as

Genetic VariationHIV-1HIV InfectionsRecombination, GeneticAdultChinaEvolution, MolecularFemaleGenome, ViralGenotypeHumansMaleMiddle AgedPhylogenyGenetic diversityHIVMolecular epidemiologyRecombinationRevolution

Identifiers

PMID40660300
PMCPMC12257697

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