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Updated: Oct 6, 2025

Microbiota Analysis Using Two-step PCR and Next-generation 16S rRNA Gene Sequencing
Published on: October 15, 2019
Respiratory tract infections and gut microbiome modifications: A systematic review
Claire A Woodall1, Luke J McGeoch2, Alastair D Hay1
1Centre for Academic Primary Care, Bristol Medical School, Population Health Sciences, University of Bristol, Bristol, United Kingdom.
Abstract:
Respiratory tract infections (RTIs) are extremely common and can cause gastrointestinal tract symptoms and changes to the gut microbiota, yet these effects are poorly understood. We conducted a systematic review to evaluate the reported evidence of gut microbiome alterations in patients with a RTI compared to healthy controls (PROSPERO: CRD42019138853). We systematically searched Medline, Embase, Web of Science, Cochrane and the Clinical Trial Database for studies published between January 2015 and June 2021. Studies were eligible for inclusion if they were human cohorts describing the gut microbiome in patients with an RTI compared to healthy controls and the infection was caused by a viral or bacterial pathogen. Dual data screening and extraction with narrative synthesis was performed. We identified 1,593 articles and assessed 11 full texts for inclusion. Included studies (some nested) reported gut microbiome changes in the context of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) (n = 5), influenza (H1N1 and H7N9) (n = 2), Tuberculosis (TB) (n = 4), Community-Acquired Pneumonia CAP (n = 2) and recurrent RTIs (rRTI) (n = 1) infections. We found studies of patients with an RTI compared to controls reported a decrease in gut microbiome diversity (Shannon) of 1.45 units (95% CI, 0.15-2.50 [p, <0.0001]) and a lower abundance of taxa (p, 0.0086). Meta-analysis of the Shannon value showed considerable heterogeneity between studies (I2, 94.42). Unbiased analysis displayed as a funnel plot revealed a depletion of Lachnospiraceae, Ruminococcaceae and Ruminococcus and enrichment of Enterococcus. There was an important absence in the lack of cohort studies reporting gut microbiome changes and high heterogeneity between studies may be explained by variations in microbiome methods and confounder effects. Further human cohort studies are needed to understand RTI-induced gut microbiome changes to better understand interplay between microbes and respiratory health.
Insights
Respiratory tract infections (RTIs) significantly reduce gut microbiome diversity and abundance. This systematic review highlights a depletion of beneficial bacteria and an enrichment of others, underscoring the need for further research.
Area of Science:
- Microbiology
- Gastroenterology
- Infectious Diseases
Background:
- Respiratory tract infections (RTIs) are common and can impact the gut microbiome, but this relationship is not well understood.
- Changes in gut microbiota may contribute to gastrointestinal symptoms associated with RTIs.
Purpose of the Study:
- To systematically review and evaluate evidence on gut microbiome alterations in patients with RTIs compared to healthy controls.
- To synthesize findings from human cohort studies investigating the impact of viral and bacterial respiratory infections on gut microbial composition.
Main Methods:
- Systematic literature search of Medline, Embase, Web of Science, Cochrane, and Clinical Trial Database (Jan 2015-June 2021).
- Inclusion of human cohort studies comparing gut microbiome in RTI patients versus controls.
- Narrative synthesis of data from eligible studies, including meta-analysis of Shannon diversity.
Main Results:
- Eleven studies were included, focusing on SARS-CoV-2, influenza, Tuberculosis, Community-Acquired Pneumonia, and recurrent RTIs.
- A significant decrease in gut microbiome diversity (Shannon index: -1.45 units, p < 0.0001) and overall taxa abundance (p = 0.0086) was observed in RTI patients.
- Meta-analysis revealed depletion of Lachnospiraceae, Ruminococcaceae, and Ruminococcus, with enrichment of Enterococcus.
Conclusions:
- RTIs are associated with significant gut microbiome dysbiosis, characterized by reduced diversity and altered bacterial populations.
- High heterogeneity among studies suggests variations in methodology and confounding factors.
- Further well-designed human cohort studies are essential to elucidate the complex interplay between respiratory infections and gut microbial ecology.
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