Cargando…
Hi-C metagenome sequencing reveals soil phage–host interactions
Bacteriophages are abundant in soils. However, the majority are uncharacterized, and their hosts are unknown. Here, we apply high-throughput chromosome conformation capture (Hi–C) to directly capture phage-host relationships. Some hosts have high centralities in bacterial community co-occurrence net...
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/PMC10667309/ https://www.ncbi.nlm.nih.gov/pubmed/37996432 http://dx.doi.org/10.1038/s41467-023-42967-z |
_version_ | 1785149032911339520 |
---|---|
author | Wu, Ruonan Davison, Michelle R. Nelson, William C. Smith, Montana L. Lipton, Mary S. Jansson, Janet K. McClure, Ryan S. McDermott, Jason E. Hofmockel, Kirsten S. |
author_facet | Wu, Ruonan Davison, Michelle R. Nelson, William C. Smith, Montana L. Lipton, Mary S. Jansson, Janet K. McClure, Ryan S. McDermott, Jason E. Hofmockel, Kirsten S. |
author_sort | Wu, Ruonan |
collection | PubMed |
description | Bacteriophages are abundant in soils. However, the majority are uncharacterized, and their hosts are unknown. Here, we apply high-throughput chromosome conformation capture (Hi–C) to directly capture phage-host relationships. Some hosts have high centralities in bacterial community co-occurrence networks, suggesting phage infections have an important impact on the soil bacterial community interactions. We observe increased average viral copies per host (VPH) and decreased viral transcriptional activity following a two-week soil-drying incubation, indicating an increase in lysogenic infections. Soil drying also alters the observed phage host range. A significant negative correlation between VPH and host abundance prior to drying indicates more lytic infections result in more host death and inversely influence host abundance. This study provides empirical evidence of phage-mediated bacterial population dynamics in soil by directly capturing specific phage-host interactions. |
format | Online Article Text |
id | pubmed-10667309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106673092023-11-23 Hi-C metagenome sequencing reveals soil phage–host interactions Wu, Ruonan Davison, Michelle R. Nelson, William C. Smith, Montana L. Lipton, Mary S. Jansson, Janet K. McClure, Ryan S. McDermott, Jason E. Hofmockel, Kirsten S. Nat Commun Article Bacteriophages are abundant in soils. However, the majority are uncharacterized, and their hosts are unknown. Here, we apply high-throughput chromosome conformation capture (Hi–C) to directly capture phage-host relationships. Some hosts have high centralities in bacterial community co-occurrence networks, suggesting phage infections have an important impact on the soil bacterial community interactions. We observe increased average viral copies per host (VPH) and decreased viral transcriptional activity following a two-week soil-drying incubation, indicating an increase in lysogenic infections. Soil drying also alters the observed phage host range. A significant negative correlation between VPH and host abundance prior to drying indicates more lytic infections result in more host death and inversely influence host abundance. This study provides empirical evidence of phage-mediated bacterial population dynamics in soil by directly capturing specific phage-host interactions. Nature Publishing Group UK 2023-11-23 /pmc/articles/PMC10667309/ /pubmed/37996432 http://dx.doi.org/10.1038/s41467-023-42967-z Text en © Battelle Memorial Institute 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wu, Ruonan Davison, Michelle R. Nelson, William C. Smith, Montana L. Lipton, Mary S. Jansson, Janet K. McClure, Ryan S. McDermott, Jason E. Hofmockel, Kirsten S. Hi-C metagenome sequencing reveals soil phage–host interactions |
title | Hi-C metagenome sequencing reveals soil phage–host interactions |
title_full | Hi-C metagenome sequencing reveals soil phage–host interactions |
title_fullStr | Hi-C metagenome sequencing reveals soil phage–host interactions |
title_full_unstemmed | Hi-C metagenome sequencing reveals soil phage–host interactions |
title_short | Hi-C metagenome sequencing reveals soil phage–host interactions |
title_sort | hi-c metagenome sequencing reveals soil phage–host interactions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667309/ https://www.ncbi.nlm.nih.gov/pubmed/37996432 http://dx.doi.org/10.1038/s41467-023-42967-z |
work_keys_str_mv | AT wuruonan hicmetagenomesequencingrevealssoilphagehostinteractions AT davisonmicheller hicmetagenomesequencingrevealssoilphagehostinteractions AT nelsonwilliamc hicmetagenomesequencingrevealssoilphagehostinteractions AT smithmontanal hicmetagenomesequencingrevealssoilphagehostinteractions AT liptonmarys hicmetagenomesequencingrevealssoilphagehostinteractions AT janssonjanetk hicmetagenomesequencingrevealssoilphagehostinteractions AT mcclureryans hicmetagenomesequencingrevealssoilphagehostinteractions AT mcdermottjasone hicmetagenomesequencingrevealssoilphagehostinteractions AT hofmockelkirstens hicmetagenomesequencingrevealssoilphagehostinteractions |