Background: HIV-1 subtype B, introduced to mainland China at an early stage, rapidly spread among commercial plasma donors and heterosexuals (HETs) during the 1990s. It was first identified in Hainan, which has a population of 10 million, in 2007. Nevertheless, there is a paucity of data about the molecular-epidemiological characteristics, spatial origins, and transmission patterns of this strain on the island of China.
Methods: Pol sequences for HIV-1 subtype B from Hainan Island (2007-2024) were obtained from our research and global databases. An analysis of phylogenetic data, molecular clock models, and a Bayesian coalescent-based approach was performed to investigate how HIV-1 subtype B was introduced and disseminated on this island.
Results: A total of 76 sequences were obtained from Hainan Island, of which 52.63% were collected from men who have sex with men (MSM). Phylogenetic analysis demonstrated that HIV-1 subtype B circulating on the island was closely related to HIV-1 sequence lineages in Guangdong (22.84%, 127/556), Hubei (12.59%, 70/556), and Beijing (14.03%, 78/556), indicating multiple introductions from various cities in China. Bayesian time-scaled phylogenetic reconstructions revealed that 27 Hainan sequences were together in clusters [posterior probability (PP) > 0.90], and 18 Hainan sequences were intermixed in larger clades containing sequences from other provinces (PP > 0.90). Bayes factors (BF) demonstrated that subtype B on the Island originated from Guangdong Province (BF > 100) in 1999.9 (95% HPD:1996.7, 2002.7) and Hubei Province (BF > 100) in 2007.9 (95% HPD:2004.4, 2011.2). Subsequently, HIV-1 subtype B was introduced to Beijing from the island (BF > 100). The analysis of viral migration patterns among risk subgroups revealed that subtype B was introduced to the island by MSMs (BF > 100). Within the island, this strain was from MSM to HETs (BF > 100).
Conclusion: Using Hainan Island as a case study, our findings shed light on the intricate evolution and transmission dynamics of HIV-1 subtype B on the island, revealing crucial insights for HIV prevention efforts in the future.
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http://dx.doi.org/10.1186/s12879-025-10703-1 | DOI Listing |
Front Immunol
March 2025
Department of Neurology, Yale University School of Medicine, New Haven, CT, United States.
Background: Trafficking of immune cells to the central nervous system is hypothesized to facilitate HIV entry and immune-induced neuronal injury and is mediated by surface proteins such as chemokine receptors and α4 integrin. We longitudinally assessed immune cell activation and surface marker expression in cerebrospinal fluid (CSF) and blood and their relationship with CSF HIV RNA beginning during primary HIV infection (PHI) before and after antiretroviral therapy (ART).
Methods: Longitudinal paired blood and CSF were obtained in ART-naïve PHI (<12 month since infection) participants; some independently initiated ART during follow up.
BMC Infect Dis
March 2025
School of Public Health, Heinz Mehlhorn Academician Workstation, Key Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, Hainan, 571199, China.
Background: HIV-1 subtype B, introduced to mainland China at an early stage, rapidly spread among commercial plasma donors and heterosexuals (HETs) during the 1990s. It was first identified in Hainan, which has a population of 10 million, in 2007. Nevertheless, there is a paucity of data about the molecular-epidemiological characteristics, spatial origins, and transmission patterns of this strain on the island of China.
View Article and Find Full Text PDFBiochem Biophys Rep
March 2025
HIV/AIDS Research Center, Institute of Health, Shiraz University of Medical Sciences, Shiraz, Iran.
HIV-1 has various subtypes and CRFs, each with unique genetic attributes that impact the virus's spread, disease development, and response to treatment in different populations. Determining V3 tropism is crucial for utilizing CCR5 antagonists and understanding why certain HIV-1 subtypes are more pathogenic than others are. Genotypic coreceptor usage of 603 major subtypes of A, B, C, AE, and CRF35-AD is investigated via five bioinformatics tools (PhenoSeq, WebPSSM, Geno2Pheno, Net charge, and the 11/25 rule).
View Article and Find Full Text PDFProteins
March 2025
Department of Biotechnology, Bhupat and Jyoti Mehta School of Biosciences, Indian Institute of Technology Madras, Chennai, India.
In recent years, Human Immunodeficiency Virus (HIV) remains a significant global health challenge, with millions affected worldwide, particularly in Africa and sub-Saharan regions. Despite advances in antiretroviral therapies, the genetic variability of HIV, including different subtypes and drug-resistant strains, poses persistent obstacles in the development of universally effective treatments. This study focuses on the dynamics of HIV protease, a key enzyme in viral replication and maturation, particularly targeting subtype C and its double insertion (HL) variant L38HL, in the context of interaction with Darunavir (DRV), a second-generation nonpeptidic protease inhibitor approved by the FDA in 2006.
View Article and Find Full Text PDFSex Transm Infect
February 2025
Infectious, Tropical Diseases and Acquired Immunodeficiency, Pomeranian Medical University in Szczecin, Szczecin, Poland.
Objectives: The efficacy of pre-exposure prophylaxis (PrEP) relies on adherence to effective regimens. As data on real-life PrEP roll-out and efficacy from Central and Eastern Europe are scarce, we explored the HIV incident infections among PrEP users in an observational cohort in Poland.
Methods: A cohort of 887 men having sex with men (MSM) on generic emtricitabine/tenofovir disoproxil (FTC/TDF) were followed for a cumulative 2587 person years (PY).
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