# Frequent Detection of HIV-1 Variants With Mixed Coreceptor Usage Among People Who Inject Drugs Infected With CRF01_AE: Possible Association With Coreceptor Switch

**Authors:** Yosuke Maeda, Takayuki Chikata, Takeo Kuwata, Hiromi Terasawa, Giang Van Tran, Shuzo Matsushita, Tomohiro Sawa, Futoshi Hasebe, Masafumi Takiguchi

PMC · DOI: 10.1093/ofid/ofag080 · Open Forum Infectious Diseases · 2026-02-21

## TL;DR

This study found that people who inject drugs infected with a specific HIV subtype often have mixed HIV variants that use different cell receptors, which may be linked to changes in virus behavior and higher virus levels.

## Contribution

The study reveals a possible link between mixed HIV-1 coreceptor usage and coreceptor switch in CRF01_AE-infected PWID.

## Key findings

- Mixed HIV-1 infection with R5 and X4/dual variants was detected in 36.1% of people who inject drugs.
- Mixed infections were associated with higher plasma viral RNA load compared to infections with only R5 HIV-1.
- Phylogenetic analysis showed R5 variants were dominant, but X4/dual variants were present as minor populations in most cases.

## Abstract

Our previous study suggested that mixed infection with R5 and X4/dual human immunodeficiency virus type 1 (HIV-1) may contribute to coreceptor switch from R5 to X4 HIV-1. To confirm this hypothesis, we investigated mixed HIV-1 infections in people who inject drugs (PWID) infected with the CRF01_AE subtype.

Viral plasma RNA from PWID were extracted, the V3 region of the HIV-1 gp120 gene was amplified, and deep sequencing was performed. Coreceptor usage was determined using phenotypic assay by cloning each V3 region. Coreceptor usage of minor HIV-1 variants detected by deep sequencing was predicted based on the amino acid sequences of the V3 region.

Deep sequencing of plasma from 36 PWID revealed that mixed HIV-1 infection involving different coreceptor usage occurred in 13 cases (36.1%). Phylogenetic analysis revealed that R5 variants were dominant, whereas X4/dual variants were detected as minor populations in most cases. In 1 case, however, R5 variants emerged as a distinct minor population mixed with X4/dual variants as the major population. Notably, plasma viral RNA load (pVL) was higher in cases of mixed infection with R5 and X4/dual HIV-1 than in those infected solely with R5 HIV-1.

Our observations suggest a possible association between mixed HIV-1 coreceptor usage and coreceptor switch in CRF01_AE–infected PWID, and that mixed infection may be associated with pVL.

This study investigated coreceptor switch from R5 to X4 HIV-1 in CRF01_AE-infected people who inject drugs. We found a high frequency of mixed infection with R5 and X4 HIV-1 and an association between mixed infection with elevated plasma viral load.

## Linked entities

- **Genes:** ITIH4 (inter-alpha-trypsin inhibitor heavy chain 4) [NCBI Gene 3700]

## Full-text entities

- **Genes:** CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, Env [NCBI Gene 155971], CCR5 (C-C motif chemokine receptor 5) [NCBI Gene 1234] {aka CC-CKR-5, CCCKR5, CCR-5, CD195, CKR-5, CKR5}, ITIH4 (inter-alpha-trypsin inhibitor heavy chain 4) [NCBI Gene 3700] {aka GP120, H4P, IHRP, ITI-HC4, ITIHL1, PK-120}, TMED2 (transmembrane p24 trafficking protein 2) [NCBI Gene 10959] {aka P24A, RNP24, p24, p24b1, p24beta1}, NRP2 (neuropilin 2) [NCBI Gene 8828] {aka NP2, NPN2, PRO2714, VEGF165R2}
- **Diseases:** PWID (MESH:C000719191), Infectious Diseases (MESH:D003141), X4 HIV-1 (MESH:D015658), CRF01_AE HIV-1 infection (MESH:D015490), Tropical Diseases (MESH:D015493), CRF01_AE infection (MESH:D007239), PNGS (MESH:D009371), NC (MESH:D058747), glioma (MESH:D005910)
- **Chemicals:** penicillin (MESH:D010406), G418 (MESH:C010680), Dulbecco's modified Eagle medium (-), Lipofectamine 2000 (MESH:C086724), PS (MESH:D010758), zeocin (MESH:C105427), streptomycin (MESH:D013307)
- **Species:** Human immunodeficiency virus (species) [taxon 12721], Homo sapiens (human, species) [taxon 9606], HIV-1 group M (no rank) [taxon 388795], Human immunodeficiency virus 1 (no rank) [taxon 11676]
- **Cell lines:** NP-2 — Homo sapiens (Human), Glioblastoma, Cancer cell line (CVCL_1R15), HEK-293T — Homo sapiens (Human), Transformed cell line (CVCL_0063)

## Full text

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## Figures

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## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12951246/full.md

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Source: https://tomesphere.com/paper/PMC12951246