» Articles » PMID: 38724547

Characteristics of Drug Resistance Mutations in ART-experienced HIV-1 Patients with Low-level Viremia in Zhengzhou City, China

Overview
Journal Sci Rep
Specialty Science
Date 2024 May 9
PMID 38724547
Authors
Affiliations
Soon will be listed here.
Abstract

Although most people living with HIV (PLWH) receiving antiretroviral therapy (ART) achieve continuous viral suppression, some show detectable HIV RNA as low-level viremia (LLV) (50-999 copies/mL). Drug resistance mutations (DRMs) in PLWH with LLV is of particular concern as which may lead to treatment failure. In this study, we investigated the prevalence of LLV and LLV-associated DRMs in PLWH in Zhengzhou City, China. Of 3616 ART-experienced PLWH in a long-term follow-up cohort from Jan 2022 to Aug 2023, 120 were identified as having LLV. Of these PLWH with LLV, we obtained partial pol and integrase sequences from 104 (70 from HIV-1 RNA and 34 from proviral DNA) individuals. DRMs were identified in 44 individuals. Subtyping analysis indicated that the top three subtypes were B (48.08%, 50/104), CRF07_BC (31.73%, 33/104), and CRF01_AE (15.38%, 16/104). The proportions of nucleoside reverse transcriptase inhibitors (NRTIs), non-nucleoside reverse transcriptase inhibitors (NNRTIs), protease inhibitors (PIs), and integrase strand transfer inhibitors (INSTIs) associated DRMs were 23.83% (24/104), 35.58% (37/104), 5.77% (6/104), and 3.85% (4/104), respectively, which contributed to an overall prevalence of 42.31% (44/104). When analyzed by individual DRMs, the most common mutation(s) were V184 (18.27%, 19/104), followed by V179 (11.54%, 12/104), K103 (9.62%, 10/104), Y181 (9.62%, 10/104), M41 (7.69%, 8/104), and K65R (7.69%, 8/104). The prevalence of DRMs in ART-experienced PLWH with LLV is high in Zhengzhou City and continuous surveillance can facilitate early intervention and provision of effective treatment.

Citing Articles

High prevalence of reverse transcriptase inhibitors associated resistance mutations among people living with HIV on dolutegravir-based antiretroviral therapy in Francistown, Botswana.

Choga O, Lemogang G, Choga W, Muzanywa G, Shadreck T, Ralegoreng C J Antimicrob Chemother. 2025; 80(3):767-776.

PMID: 39764689 PMC: 11879200. DOI: 10.1093/jac/dkae472.


The prevalence of low-level viraemia and its association with virological failure in people living with HIV: a systematic review and meta-analysis.

Zhao S, Wang W, Li S, He J, Duan W, Fang Z Emerg Microbes Infect. 2024; 14(1):2447613.

PMID: 39727007 PMC: 11722027. DOI: 10.1080/22221751.2024.2447613.


Archived HIV-1 Drug Resistance Mutations: Role of Proviral HIV-1 DNA Genotype for the Management of Virological Responder People Living with HIV.

Campagna R, Nonne C, Antonelli G, Turriziani O Viruses. 2024; 16(11).

PMID: 39599811 PMC: 11599110. DOI: 10.3390/v16111697.


Risk factors and clinical prediction models for low-level viremia in people living with HIV receiving antiretroviral therapy: an 11-year retrospective study.

Zhang W, Shi J, Wang Y, Li E, Yan D, Zhang Z Front Microbiol. 2024; 15:1451201.

PMID: 39552647 PMC: 11563986. DOI: 10.3389/fmicb.2024.1451201.

References
1.
Elvstam O, Marrone G, Medstrand P, Treutiger C, Sonnerborg A, Gisslen M . All-Cause Mortality and Serious Non-AIDS Events in Adults With Low-level Human Immunodeficiency Virus Viremia During Combination Antiretroviral Therapy: Results From a Swedish Nationwide Observational Study. Clin Infect Dis. 2020; 72(12):2079-2086. PMC: 8204776. DOI: 10.1093/cid/ciaa413. View

2.
Melikian G, Rhee S, Varghese V, Porter D, White K, Taylor J . Non-nucleoside reverse transcriptase inhibitor (NNRTI) cross-resistance: implications for preclinical evaluation of novel NNRTIs and clinical genotypic resistance testing. J Antimicrob Chemother. 2013; 69(1):12-20. PMC: 3861329. DOI: 10.1093/jac/dkt316. View

3.
Taramasso L, Magnasco L, Bruzzone B, Caligiuri P, Bozzi G, Mora S . How relevant is the HIV low level viremia and how is its management changing in the era of modern ART? A large cohort analysis. J Clin Virol. 2020; 123:104255. DOI: 10.1016/j.jcv.2019.104255. View

4.
Simonetti F, Sobolewski M, Fyne E, Shao W, Spindler J, Hattori J . Clonally expanded CD4+ T cells can produce infectious HIV-1 in vivo. Proc Natl Acad Sci U S A. 2016; 113(7):1883-8. PMC: 4763755. DOI: 10.1073/pnas.1522675113. View

5.
Bareng O, Choga W, Maphorisa S, Seselamarumo S, Seatla K, Mokgethi P . HIV-1C in-House RNA-Based Genotyping Assay for Detection of Drug Resistance Mutations in Samples with Low-Level Viral Loads. Infect Drug Resist. 2022; 15:7565-7576. PMC: 9792565. DOI: 10.2147/IDR.S388816. View