# Metagenomic analysis of blood microbiota alterations: insights into HIV progression and immune restoration

**Authors:** Yingjie Chen, Rongqiu Zhang, Juan Wen, Jingyue Zhao, Jianmei Zhang

PMC · DOI: 10.3389/fcimb.2025.1619059 · Frontiers in Cellular and Infection Microbiology · 2025-10-20

## TL;DR

This study explores how the blood microbiome changes in HIV patients and how these changes could help track disease progression and treatment success.

## Contribution

The study identifies specific blood microbiota markers associated with HIV progression and immune restoration following ART.

## Key findings

- HIV infection significantly reduces blood microbiota diversity and increases opportunistic pathogens like Pseudomonas aeruginosa.
- ART partially restores microbial diversity but does not fully return a healthy microbiota profile.
- Certain microbes, such as Acinetobacter pittii, are strongly correlated with viral load and immune markers like CD4/CD8 ratio.

## Abstract

Emerging evidence suggests that the blood microbiome may influence the progression of HIV infection and immune restoration. This study aims to comprehensively characterize blood microbiota alterations associated with HIV infection and antiretroviral therapy (ART), and to evaluate their potential as microbial indicators for assessing infection status and immune restoration.

We recruited 91 participants, including 31 treatment-naïve HIV-infected individuals, 30 ART-treated individuals with undetectable viral loads, and 30 healthy controls. Blood samples were collected for metagenomic sequencing and immunological profiling.

HIV infection profoundly disrupted blood microbiota diversity and composition, with a marked reduction in α-diversity and enrichment of opportunistic pathogens such as Pseudomonas aeruginosa, Acinetobacter baumannii and Stenotrophomonas maltophilia, alongside depletion of beneficial taxa like Bifidobacterium longum. ART partially restored microbial diversity but did not fully reestablish a healthy microbiota. Correlation analysis revealed that Acinetobacter pittii, Xanthomonas campestris and Diaphorobacter nitroreducens were significantly associated with viral load, suggesting their potential role in HIV progression. Additionally, after ART, Acinetobacter junii and Pseudomonas putida were significantly correlated with the CD4/CD8 ratio, indicating their potential role in immune restoration.

These findings provide new insights into the interactions between blood microbiota and HIV progression. The identified blood microbiota may serve as potential indicators for evaluating HIV infection status and treatment efficacy, offering a basis for microbial-based diagnostic and therapeutic strategies.

## Linked entities

- **Species:** Pseudomonas aeruginosa (taxon 287), Acinetobacter baumannii (taxon 470), Stenotrophomonas maltophilia (taxon 40324), Bifidobacterium longum (taxon 216816), Acinetobacter pittii (taxon 48296), Xanthomonas campestris (taxon 339), Diaphorobacter nitroreducens (taxon 164759), Acinetobacter junii (taxon 40215), Pseudomonas putida (taxon 303)

## Full-text entities

- **Genes:** 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}
- **Diseases:** infection (MESH:D007239), HIV infection (MESH:D015658)
- **Species:** Stenotrophomonas maltophilia (species) [taxon 40324], Pseudomonas aeruginosa (species) [taxon 287], Human immunodeficiency virus 1 (no rank) [taxon 11676], Acinetobacter pittii (species) [taxon 48296], Bifidobacterium longum (species) [taxon 216816], Xanthomonas campestris (species) [taxon 339], Diaphorobacter nitroreducens (species) [taxon 164759], Acinetobacter baumannii (species) [taxon 470], Acinetobacter junii (species) [taxon 40215], Pseudomonas putida (species) [taxon 303]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12580212/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12580212/full.md

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Source: https://tomesphere.com/paper/PMC12580212