Language

English

Publication Date

1-7-2025

Journal

Microbiology Spectrum

DOI

10.1128/spectrum.00998-24

PMID

39656008

PMCID

PMC11705802

PubMedCentral® Posted Date

12-10-2024

PubMedCentral® Full Text Version

Post-print

Abstract

This study compared intestinal DNA phage dynamics and gut microbiota changes observed at the onset of coronavirus disease 2019 (COVID-19). The study participants included 19 healthy individuals and 19 patients with severe acute respiratory syndrome coronavirus 2 infection. Significant differences were observed in the diversity of the intestinal DNA virome after the onset of COVID-19 compared with that in healthy individuals. Classification by their tail morphology resulted in the order Caudovirales, a double-stranded DNA phage, accounting for >95% of all participants. In classifying phages based on host bacteria, a decreased number of phages infecting mainly the Clostridia class was observed immediately after the onset of COVID-19 and recovered over time. After the onset of COVID-19, two distinct movement patterns of intestinal phages and their host bacteria were observed: phage- and bacteria-predominant. The abundance of obligate anaerobes, such as Clostridium_sense_strict_1, Fusicatenibacter, and Romboutsia, and the phages hosting these bacteria decreased immediately after the onset of COVID-19, and faster phage recovery was observed compared with bacterial recovery. In contrast, the genus Staphylococcus, a facultative anaerobic bacterium, increased immediately after the onset of COVID-19, whereas the phages infecting Staphylococcus decreased. Furthermore, immediately after the onset of COVID-19, the percentage of lytic phages increased, whereas that of temperate phages decreased. These observations suggest that the gut microbiota dysbiosis observed immediately after the onset of COVID-19 may be linked to phage dynamics that control gut microbiota and may also affect the recovery from dysbiosis.

Keywords

Humans, Gastrointestinal Microbiome, Dysbiosis, COVID-19, Bacteriophages, SARS-CoV-2, Adult, Bacteria, Female, Male, Middle Aged, Lysogeny, Virome, Aged, Feces, Intestines, DNA, Viral, COVID-19, SARS-CoV-2, gut microbiome, bacteriophages

Published Open-Access

yes

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