Microbiome profiling reveals gut bacterial species associated with rapid lung function decline in people with HIV

TL;DR

This study finds that certain gut bacteria are linked to faster lung function decline in people with HIV, suggesting a possible role in lung disease.

Contribution

Identifies specific gut bacterial species associated with rapid lung function decline in people with HIV.

Findings

Bacteroides coprophilus, Klebsiella michiganensis, and Clostridium perfringens were enriched in PWH with rapid lung function decline.

A gut dysbiosis index was associated with rapid lung function decline and airflow limitation in adjusted analyses.

Abstract

People with HIV (PWH) have an increased risk of pulmonary comorbidities compared to people without HIV. The gut microbiome regulates host immunity and is altered in PWH. This study aims to determine potential associations between gut microbiome, lung function decline, and airflow limitation in PWH.

PWH from the Copenhagen Comorbidity in HIV Infection (COCOMO) Study with available lung function testing and microbiome data were included (n=385). The gut microbiome was characterized using shotgun metagenomic sequencing. Associations between gut microbiome, rapid lung function decline, and airflow limitation were analysed in multivariable logistic regressions adjusted for traditional and HIV-associated risk factors for lung disease.

Several bacterial species were significantly enriched in PWH with rapid lung function decline, including opportunistic pathogenic bacterial species Bacteroides coprophilus, Klebsiella michiganensis, and Clostridium perfringens. A gut microbial dysbiosis index based on compositional changes was associated with rapid lung function decline (adjusted odds ratio (aOR) 1.18, 95% confidence interval (CI) [1.11-1.27], p<0.001), and airflow limitation (aOR 1.16, 95% CI [1.04-1.29], p=0.007) in adjusted multivariable logistic regression analyses.

Associations between the gut dysbiosis index and rapid lung function decline and airflow limitation suggest a potential role of certain gut bacterial species in the pathogenesis of pulmonary comorbidities in PWH.

Figures