Cargando…
Highly host-linked viromes in the built environment possess habitat-dependent diversity and functions for potential virus-host coevolution
Viruses in built environments (BEs) raise public health concerns, yet they are generally less studied than bacteria. To better understand viral dynamics in BEs, this study assesses viromes from 11 habitats across four types of BEs with low to high occupancy. The diversity, composition, metabolic fun...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10169181/ https://www.ncbi.nlm.nih.gov/pubmed/37160974 http://dx.doi.org/10.1038/s41467-023-38400-0 |
_version_ | 1785038999961731072 |
---|---|
author | Du, Shicong Tong, Xinzhao Lai, Alvin C. K. Chan, Chak K. Mason, Christopher E. Lee, Patrick K. H. |
author_facet | Du, Shicong Tong, Xinzhao Lai, Alvin C. K. Chan, Chak K. Mason, Christopher E. Lee, Patrick K. H. |
author_sort | Du, Shicong |
collection | PubMed |
description | Viruses in built environments (BEs) raise public health concerns, yet they are generally less studied than bacteria. To better understand viral dynamics in BEs, this study assesses viromes from 11 habitats across four types of BEs with low to high occupancy. The diversity, composition, metabolic functions, and lifestyles of the viromes are found to be habitat dependent. Caudoviricetes species are ubiquitous on surface habitats in the BEs, and some of them are distinct from those present in other environments. Antimicrobial resistance genes are identified in viruses inhabiting surfaces frequently touched by occupants and in viruses inhabiting occupants’ skin. Diverse CRISPR/Cas immunity systems and anti-CRISPR proteins are found in bacterial hosts and viruses, respectively, consistent with the strongly coupled virus–host links. Evidence of viruses potentially aiding host adaptation in a specific-habitat manner is identified through a unique gene insertion. This work illustrates that virus–host interactions occur frequently in BEs and that viruses are integral members of BE microbiomes. |
format | Online Article Text |
id | pubmed-10169181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101691812023-05-11 Highly host-linked viromes in the built environment possess habitat-dependent diversity and functions for potential virus-host coevolution Du, Shicong Tong, Xinzhao Lai, Alvin C. K. Chan, Chak K. Mason, Christopher E. Lee, Patrick K. H. Nat Commun Article Viruses in built environments (BEs) raise public health concerns, yet they are generally less studied than bacteria. To better understand viral dynamics in BEs, this study assesses viromes from 11 habitats across four types of BEs with low to high occupancy. The diversity, composition, metabolic functions, and lifestyles of the viromes are found to be habitat dependent. Caudoviricetes species are ubiquitous on surface habitats in the BEs, and some of them are distinct from those present in other environments. Antimicrobial resistance genes are identified in viruses inhabiting surfaces frequently touched by occupants and in viruses inhabiting occupants’ skin. Diverse CRISPR/Cas immunity systems and anti-CRISPR proteins are found in bacterial hosts and viruses, respectively, consistent with the strongly coupled virus–host links. Evidence of viruses potentially aiding host adaptation in a specific-habitat manner is identified through a unique gene insertion. This work illustrates that virus–host interactions occur frequently in BEs and that viruses are integral members of BE microbiomes. Nature Publishing Group UK 2023-05-09 /pmc/articles/PMC10169181/ /pubmed/37160974 http://dx.doi.org/10.1038/s41467-023-38400-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Du, Shicong Tong, Xinzhao Lai, Alvin C. K. Chan, Chak K. Mason, Christopher E. Lee, Patrick K. H. Highly host-linked viromes in the built environment possess habitat-dependent diversity and functions for potential virus-host coevolution |
title | Highly host-linked viromes in the built environment possess habitat-dependent diversity and functions for potential virus-host coevolution |
title_full | Highly host-linked viromes in the built environment possess habitat-dependent diversity and functions for potential virus-host coevolution |
title_fullStr | Highly host-linked viromes in the built environment possess habitat-dependent diversity and functions for potential virus-host coevolution |
title_full_unstemmed | Highly host-linked viromes in the built environment possess habitat-dependent diversity and functions for potential virus-host coevolution |
title_short | Highly host-linked viromes in the built environment possess habitat-dependent diversity and functions for potential virus-host coevolution |
title_sort | highly host-linked viromes in the built environment possess habitat-dependent diversity and functions for potential virus-host coevolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10169181/ https://www.ncbi.nlm.nih.gov/pubmed/37160974 http://dx.doi.org/10.1038/s41467-023-38400-0 |
work_keys_str_mv | AT dushicong highlyhostlinkedviromesinthebuiltenvironmentpossesshabitatdependentdiversityandfunctionsforpotentialvirushostcoevolution AT tongxinzhao highlyhostlinkedviromesinthebuiltenvironmentpossesshabitatdependentdiversityandfunctionsforpotentialvirushostcoevolution AT laialvinck highlyhostlinkedviromesinthebuiltenvironmentpossesshabitatdependentdiversityandfunctionsforpotentialvirushostcoevolution AT chanchakk highlyhostlinkedviromesinthebuiltenvironmentpossesshabitatdependentdiversityandfunctionsforpotentialvirushostcoevolution AT masonchristophere highlyhostlinkedviromesinthebuiltenvironmentpossesshabitatdependentdiversityandfunctionsforpotentialvirushostcoevolution AT leepatrickkh highlyhostlinkedviromesinthebuiltenvironmentpossesshabitatdependentdiversityandfunctionsforpotentialvirushostcoevolution |