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Isolation of phages infecting the abundant freshwater Actinobacteriota order ‘Ca. Nanopelagicales’

Low-GC Actinobacteriota of the order ‘Ca. Nanopelagicales’ (also known as acI or hgcI clade) are abundant in freshwaters around the globe. Extensive predation pressure by phages has been assumed to be the reason for their high levels of microdiversity. So far, however, only a few metagenome-assemble...

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Autores principales: Kavagutti, Vinicius S., Chiriac, Maria-Cecilia, Ghai, Rohit, Salcher, Michaela M., Haber, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202952/
https://www.ncbi.nlm.nih.gov/pubmed/36964199
http://dx.doi.org/10.1038/s41396-023-01400-5
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author Kavagutti, Vinicius S.
Chiriac, Maria-Cecilia
Ghai, Rohit
Salcher, Michaela M.
Haber, Markus
author_facet Kavagutti, Vinicius S.
Chiriac, Maria-Cecilia
Ghai, Rohit
Salcher, Michaela M.
Haber, Markus
author_sort Kavagutti, Vinicius S.
collection PubMed
description Low-GC Actinobacteriota of the order ‘Ca. Nanopelagicales’ (also known as acI or hgcI clade) are abundant in freshwaters around the globe. Extensive predation pressure by phages has been assumed to be the reason for their high levels of microdiversity. So far, however, only a few metagenome-assembled phages have been proposed to infect them and no phages have been isolated. Taking advantage of recent advances in the cultivation of ‘Ca. Nanopelagicales’ we isolated a novel species of its genus ‘Ca. Planktophila’. Using this isolate as bait, we cultivated the first two phages infecting this abundant bacterial order. Both genomes contained a whiB-like transcription factor and a RNA polymerase sigma-70 factor, which might aid in manipulating their host’s metabolism. Both phages encoded a glycosyltransferase and one an anti-restriction protein, potential means to evade degradation of their DNA by nucleases present in the host genome. The two phage genomes shared only 6% of their genome with their closest relatives, with whom they form a previously uncultured family of actinophages within the Caudoviricetes. Read recruitment analyses against globally distributed metagenomes revealed the endemic distribution of this group of phages infecting ‘Ca. Nanopelagicales’. The recruitment pattern against metagenomes from the isolation site and the modular distribution of shared genes between the two phages indicate high levels of horizontal gene transfer, likely mirroring the microdiversity of their host in the evolutionary arms race between host and phage.
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spelling pubmed-102029522023-05-24 Isolation of phages infecting the abundant freshwater Actinobacteriota order ‘Ca. Nanopelagicales’ Kavagutti, Vinicius S. Chiriac, Maria-Cecilia Ghai, Rohit Salcher, Michaela M. Haber, Markus ISME J Brief Communication Low-GC Actinobacteriota of the order ‘Ca. Nanopelagicales’ (also known as acI or hgcI clade) are abundant in freshwaters around the globe. Extensive predation pressure by phages has been assumed to be the reason for their high levels of microdiversity. So far, however, only a few metagenome-assembled phages have been proposed to infect them and no phages have been isolated. Taking advantage of recent advances in the cultivation of ‘Ca. Nanopelagicales’ we isolated a novel species of its genus ‘Ca. Planktophila’. Using this isolate as bait, we cultivated the first two phages infecting this abundant bacterial order. Both genomes contained a whiB-like transcription factor and a RNA polymerase sigma-70 factor, which might aid in manipulating their host’s metabolism. Both phages encoded a glycosyltransferase and one an anti-restriction protein, potential means to evade degradation of their DNA by nucleases present in the host genome. The two phage genomes shared only 6% of their genome with their closest relatives, with whom they form a previously uncultured family of actinophages within the Caudoviricetes. Read recruitment analyses against globally distributed metagenomes revealed the endemic distribution of this group of phages infecting ‘Ca. Nanopelagicales’. The recruitment pattern against metagenomes from the isolation site and the modular distribution of shared genes between the two phages indicate high levels of horizontal gene transfer, likely mirroring the microdiversity of their host in the evolutionary arms race between host and phage. Nature Publishing Group UK 2023-03-24 2023-06 /pmc/articles/PMC10202952/ /pubmed/36964199 http://dx.doi.org/10.1038/s41396-023-01400-5 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 Brief Communication
Kavagutti, Vinicius S.
Chiriac, Maria-Cecilia
Ghai, Rohit
Salcher, Michaela M.
Haber, Markus
Isolation of phages infecting the abundant freshwater Actinobacteriota order ‘Ca. Nanopelagicales’
title Isolation of phages infecting the abundant freshwater Actinobacteriota order ‘Ca. Nanopelagicales’
title_full Isolation of phages infecting the abundant freshwater Actinobacteriota order ‘Ca. Nanopelagicales’
title_fullStr Isolation of phages infecting the abundant freshwater Actinobacteriota order ‘Ca. Nanopelagicales’
title_full_unstemmed Isolation of phages infecting the abundant freshwater Actinobacteriota order ‘Ca. Nanopelagicales’
title_short Isolation of phages infecting the abundant freshwater Actinobacteriota order ‘Ca. Nanopelagicales’
title_sort isolation of phages infecting the abundant freshwater actinobacteriota order ‘ca. nanopelagicales’
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202952/
https://www.ncbi.nlm.nih.gov/pubmed/36964199
http://dx.doi.org/10.1038/s41396-023-01400-5
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