Application of molecular epidemiology in revealing HIV‐1 transmission network and recombination patterns in Tianjin, China

Author:

Hehe Zhao1ORCID,Minna Zheng23,Qin Fan4,Tielin Ning23,Yi Feng15,Liping Fei1,Fangfang Chen1,Houlin Tang1,Shi Wang1,Maohe Yu23,Fan Lyu16

Affiliation:

1. National Center for AIDS/STD Control and Prevention Chinese Center for Disease Control and Prevention Beijing China

2. Department of HIV/AIDS and STDs Control and Prevention Tianjin Provincial Center for Disease Control and Prevention Tianjin China

3. Tianjin Key Laboratory of Pathogenic Microbiology of Infectious Disease Tianjin China

4. Department of HIV/AIDS and STDs Control and Prevention Zhejiang Provincial Center for Disease Control and Prevention Hangzhou China

5. State Key Laboratory for Infectious Disease Prevention and Control Beijing China

6. National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases Beijing China

Abstract

AbstractUsing a comprehensive molecular epidemiological approach, we characterized the transmission dynamics of HIV‐1 among the MSM population in Tianjin, China. Our findings revealed that 38.56% (386/1001) of individuals clustered across 109 molecular transmission clusters (TCs), with MSM aged 50 and below being the group most commonly transmitting HIV‐1. Among the identified TCs, CRF01_AE predominated, followed by CRF07_BC. Notably, CRF07_BC demonstrated a higher propensity for forming large clusters compared to CRF01_AE. Birth‐death skyline analyses of the two largest clusters indicated that the HIV/AIDS transmission may be at a critical point, nearly all had Re approximately 1 by now. A retrospective analysis revealed that the rapid expansion of these large clusters was primarily driven by the introduction of viruses in 2021, highlighting the crucial importance of continuous molecular surveillance in identifying newly emerging high‐risk transmission chains and adapting measures to address evolving epidemic dynamics. Furthermore, we detected the transmission of drug‐resistant mutations (DRMs) within the TCs, particularly in the CRF07_BC clusters (K103N, Y181C, and K101E) and CRF01_AE clusters (P225H and K219R), emphasizing the importance of monitoring to support the continued efficacy of first‐line therapies and pre‐exposure prophylaxis (PrEP). Recombination analyses indicated that complex recombinant patterns, associated with increased amino acid variability, could confer adaptive traits to the viruses, potentially providing a competitive advantage in certain host populations or regions. Our study highlights the potential of integrating molecular epidemiological and phylodynamic approaches to inform targeted interventions.

Publisher

Wiley

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