Emerging Trends in HIV-1 Sub-Subtype A6 in Belgium: Transmission Dynamics, Drug Resistance, and Subtyping Tool Evaluation
Authors:
- Virginie MortierVirginie Mortier
- Laurent DebaisieuxLaurent Debaisieux
- Deborah De GeyterDeborah De Geyter
- Marie-Luce DelforgeMarie-Luce Delforge
- Melissa DepypereMelissa Depypere
- Géraldine DessillyGéraldine Dessilly
- Benoît Kabamba-MukadiBenoît Kabamba-Mukadi
- Khalid El MoussaouiKhalid El Moussaoui
- Samy MzouguiSamy Mzougui
- Ben SerrienBen Serrien
- Karolien StoffelsKarolien Stoffels
- Dominique Van BeckhovenDominique Van Beckhoven
Open Access
Abstract
The international spread of HIV-1 sub-subtype A6 raises concerns due to its association with contraindications for long-acting injectable formulations of cabotegravir (LA-CAB) and rilpivirine (LA-RPV). This study investigated its increasing proportion in Belgium, assessing transmission dynamics and potential migration links. Additionally, genotypic drug resistance in the Belgian HIV-1 sub-subtype A6 population were analyzed and four automatic subtyping tools were compared. A dataset of 4764 HIV-1 protease and reverse transcriptase (RT) sequences from newly diagnosed, treatment-naïve individuals in Belgium (2013–2022) was analyzed. A combination of phylogenetic analysis and online subtyping tools identified 136 sub-subtype A6 sequences. The increase in the proportion of HIV-1 sub-subtype A6 observed in Belgium since 2020 reflects changing transmission patterns, especially among Belgium-born men having sex with men, and cannot be solely linked to the recent influx of Ukrainian migrants. Of these sub-subtype A6 sequences, less than 10% showed LA-CAB + LA-RPV resistance, mainly due to E138A within RT. HIVdb and ANRS reliably assessed resistance in this therapy-naïve cohort, and HIVdb, COMET, and SmartGene® produced concordant subtyping results. While algorithm choice has little impact at low resistance prevalence, further research is necessary and HIVdb and ANRS remain more suitable for ongoing clinical and research use.Keywords
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