# Gut microbiota alterations and microbial translocation in HIV/SARS-CoV-2 co-infected patients

**Authors:** Xuan Yan, Xinyu Zhang, Lin Wang, Wei Song, Tangkai Qi, Zhenyan Wang, Yang Tang, Jianjun Sun, Shuibao Xu, Junyang Yang, Yueming Shao, Youming Chen, Jiangrong Wang, Jun Chen, Renfang Zhang, Li Liu, Yinzhong Shen

PMC · DOI: 10.3389/fcimb.2026.1688580 · Frontiers in Cellular and Infection Microbiology · 2026-02-12

## TL;DR

This study finds that HIV/SARS-CoV-2 co-infection causes gut microbiome changes and increased microbial translocation, with certain microbes linked to disease severity.

## Contribution

The study identifies specific microbial signatures and translocation markers in HIV/SARS-CoV-2 co-infected patients, linking Blautia depletion to severe COVID-19.

## Key findings

- Co-infected patients had higher LPS and sCD14 levels, indicating increased microbial translocation.
- Blautia abundance was reduced in severe-to-critical co-infected cases compared to mild cases and controls.
- Akkermansia showed the highest diagnostic potential for co-infection with an AUC of 0.811.

## Abstract

To characterize gut microbiome alterations and microbial translocation in human immunodeficiency virus (HIV)/severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) co-infected patients and identify microbial signatures associated with COVID-19 severity.

In this cohort study, blood and fecal samples from 38 HIV/AIDS patients (20 SARS-CoV-2 co-infected [PC group]; 18 SARS-CoV-2-negative [NC group]) were analyzed. The PC group was stratified by COVID-19 severity: mild-to-moderate (PC1, n=13), severe-to-critical (PC2, n=3), and mixed infections (PC3, n=4). Serum lipopolysaccharide (LPS), soluble CD14 (sCD14), and zonulin levels were measured to assess microbial translocation and gut barrier integrity. Fecal metagenomic profiling was performed via whole-genome shotgun sequencing (Illumina NovaSeq/HiSeq).

Co-infected patients exhibited significantly elevated plasma LPS (78.09 vs 48.72 pg/mL, p=0.032) and sCD14 (2667 vs 1927 ng/mL, p=0.0015) compared to controls. Although no differences in α-diversity or overall taxonomic abundance were observed between the PC and NC groups, 329 PC-unique and 216 NC-unique microbial species were identified. Nine genera demonstrated diagnostic potential for co-infection [Area Under the Curve (AUC), >0.7] with Akkermansia showing the highest predictive value (AUC = 0.811). Critically, Blautia abundance was significantly reduced in severe-to-critical cases (PC2) versus mild-moderate cases (PC1, p=0.043) and controls (NC, p=0.006). Besides, our function prediction for gut microbiota suggested that SARS-CoV-2 may exacerbate lipid metabolic dysregulation in HIV-infected individuals.

HIV/SARS-CoV-2 co-infection is characterized by heightened microbial translocation and species-specific microbiota alterations rather than global dysbiosis. Blautia depletion may correlate with COVID-19 severity.

## Linked entities

- **Proteins:** IRF6 (interferon regulatory factor 6), Scd1_1 (acyl-CoA Delta-9 desaturase), Hp (haptoglobin)
- **Diseases:** SARS-CoV-2 (MONDO:0100096), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** PCSK1 (proprotein convertase subtilisin/kexin type 1) [NCBI Gene 5122] {aka BMIQ12, NEC1, PC1, PC1/3, PC3, SPC3}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD14 (CD14 molecule) [NCBI Gene 929], IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, HP (haptoglobin) [NCBI Gene 3240] {aka HP2ALPHA2, HPA1S}, CBX8 (chromobox 8) [NCBI Gene 57332] {aka PC3, RC1}
- **Diseases:** ulcerative colitis (MESH:D003093), sepsis (MESH:D018805), infectious diseases (MESH:D003141), HIV (MESH:D015658), pathologies (MESH:D005598), cardiac complications (MESH:D006331), intestinal tuberculosis (MESH:D014376), constipation (MESH:D003248), bacterial (MESH:D001424), cytotoxicity (MESH:D064420), Crohn's disease (MESH:D003424), -infected (MESH:D007239), HIV/SARS-CoV-2 co-infected (MESH:D000086382), malnutrition (MESH:D044342), HIV co-infection (MESH:D060085), HIV/AIDS (MESH:D016263), hypoxemia (MESH:D000860), metabolic dysregulation (MESH:D021081), Akkermansia overgrowth (MESH:C537340), acute respiratory distress syndrome (MESH:D012128), diarrhea (MESH:D003967), respiratory pathogens (MESH:D012131), AIDS (MESH:D000163), autoimmune disorders (MESH:D001327), substance addiction (MESH:D019966), pulmonary disease (MESH:D008171), Dysbiosis (MESH:D064806), cancer (MESH:D009369), PC (MESH:D015324), Diseases (MESH:D004194), intracranial aneurysms (MESH:D002532), inflammation (MESH:D007249), metabolic syndrome (MESH:D024821), critically ill (MESH:D016638)
- **Chemicals:** short-chain fatty acid (MESH:D005232), LPS (MESH:D008070), Lipid (MESH:D008055), PC (MESH:C053518), Fatty_acid (MESH:D005227), carbohydrate (MESH:D002241), Blautia (-), bile acids (MESH:D001647), trimethylamine (MESH:C023336), Limonene (MESH:D000077222)
- **Species:** gut metagenome (species) [taxon 749906], Anaerobutyricum (genus) [taxon 2569097], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Human immunodeficiency virus (species) [taxon 12721], Akkermansia muciniphila (species) [taxon 239935], Romboutsia (genus) [taxon 1501226], Roseburia (genus) [taxon 841], Human immunodeficiency virus 1 (no rank) [taxon 11676], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Actinomyces (genus) [taxon 1654], Parvimonas (genus) [taxon 543311], Eubacterium (genus) [taxon 1730], Lachnoclostridium (genus) [taxon 1506553], Pneumocystis (genus) [taxon 4753]

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935960/full.md

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Source: https://tomesphere.com/paper/PMC12935960