Abstract
Background:
The upper respiratory tract (URT) is an important site for the predisposition and multiplication of the SARS-CoV-2 virus. Therefore, URT is a critical site for investigating the changes in the microbiome caused by the SARS-CoV-2 infection. This study aims to compare phageome diversity and investigate the correlation of the phageome profiles with the sample type (SARS-CoV-2 or control) to determine the nature of phage–host interactions in the human URT microbiome and to assess the effect of SARS-CoV-2 viral load on host and phage abundance.
Materials and Methods:
In this study, we have used the whole-genome shotgun metagenomic approach to investigate URT swab samples (
Results:
The results revealed distinct phageome profiles among the groups;
Conclusion:
SARS-CoV-2 infection alters URT microbiome composition, increasing microbial diversity but disrupting host–phage dynamics. SARS-CoV-2 Viral load correlates with the shifts in microbial abundance, indicating infection-driven shifts in microbiome stability compared to healthy controls.
Get full access to this article
View all access options for this article.
References
Supplementary Material
Please find the following supplemental material available below.
For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.
For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.
