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Efficient dilution-to-extinction isolation of novel virus–host model systems for fastidious heterotrophic bacteria

Microbes and their associated viruses are key drivers of biogeochemical processes in marine and soil biomes. While viruses of phototrophic cyanobacteria are well-represented in model systems, challenges of isolating marine microbial heterotrophs and their viruses have hampered experimental approache...

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Autores principales: Buchholz, Holger H., Michelsen, Michelle L., Bolaños, Luis M., Browne, Emily, Allen, Michael J., Temperton, Ben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163748/
https://www.ncbi.nlm.nih.gov/pubmed/33495565
http://dx.doi.org/10.1038/s41396-020-00872-z
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author Buchholz, Holger H.
Michelsen, Michelle L.
Bolaños, Luis M.
Browne, Emily
Allen, Michael J.
Temperton, Ben
author_facet Buchholz, Holger H.
Michelsen, Michelle L.
Bolaños, Luis M.
Browne, Emily
Allen, Michael J.
Temperton, Ben
author_sort Buchholz, Holger H.
collection PubMed
description Microbes and their associated viruses are key drivers of biogeochemical processes in marine and soil biomes. While viruses of phototrophic cyanobacteria are well-represented in model systems, challenges of isolating marine microbial heterotrophs and their viruses have hampered experimental approaches to quantify the importance of viruses in nutrient recycling. A resurgence in cultivation efforts has improved the availability of fastidious bacteria for hypothesis testing, but this has not been matched by similar efforts to cultivate their associated bacteriophages. Here, we describe a high-throughput method for isolating important virus–host systems for fastidious heterotrophic bacteria that couples advances in culturing of hosts with sequential enrichment and isolation of associated phages. Applied to six monthly samples from the Western English Channel, we first isolated one new member of the globally dominant bacterial SAR11 clade and three new members of the methylotrophic bacterial clade OM43. We used these as bait to isolate 117 new phages, including the first known siphophage-infecting SAR11, and the first isolated phage for OM43. Genomic analyses of 13 novel viruses revealed representatives of three new viral genera, and infection assays showed that the viruses infecting SAR11 have ecotype-specific host ranges. Similar to the abundant human-associated phage ɸCrAss001, infection dynamics within the majority of isolates suggested either prevalent lysogeny or chronic infection, despite a lack of associated genes, or host phenotypic bistability with lysis putatively maintained within a susceptible subpopulation. Broader representation of important virus–host systems in culture collections and genomic databases will improve both our understanding of virus–host interactions, and accuracy of computational approaches to evaluate ecological patterns from metagenomic data.
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spelling pubmed-81637482021-06-10 Efficient dilution-to-extinction isolation of novel virus–host model systems for fastidious heterotrophic bacteria Buchholz, Holger H. Michelsen, Michelle L. Bolaños, Luis M. Browne, Emily Allen, Michael J. Temperton, Ben ISME J Article Microbes and their associated viruses are key drivers of biogeochemical processes in marine and soil biomes. While viruses of phototrophic cyanobacteria are well-represented in model systems, challenges of isolating marine microbial heterotrophs and their viruses have hampered experimental approaches to quantify the importance of viruses in nutrient recycling. A resurgence in cultivation efforts has improved the availability of fastidious bacteria for hypothesis testing, but this has not been matched by similar efforts to cultivate their associated bacteriophages. Here, we describe a high-throughput method for isolating important virus–host systems for fastidious heterotrophic bacteria that couples advances in culturing of hosts with sequential enrichment and isolation of associated phages. Applied to six monthly samples from the Western English Channel, we first isolated one new member of the globally dominant bacterial SAR11 clade and three new members of the methylotrophic bacterial clade OM43. We used these as bait to isolate 117 new phages, including the first known siphophage-infecting SAR11, and the first isolated phage for OM43. Genomic analyses of 13 novel viruses revealed representatives of three new viral genera, and infection assays showed that the viruses infecting SAR11 have ecotype-specific host ranges. Similar to the abundant human-associated phage ɸCrAss001, infection dynamics within the majority of isolates suggested either prevalent lysogeny or chronic infection, despite a lack of associated genes, or host phenotypic bistability with lysis putatively maintained within a susceptible subpopulation. Broader representation of important virus–host systems in culture collections and genomic databases will improve both our understanding of virus–host interactions, and accuracy of computational approaches to evaluate ecological patterns from metagenomic data. Nature Publishing Group UK 2021-01-25 2021-06 /pmc/articles/PMC8163748/ /pubmed/33495565 http://dx.doi.org/10.1038/s41396-020-00872-z Text en © The Author(s) 2021 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
Buchholz, Holger H.
Michelsen, Michelle L.
Bolaños, Luis M.
Browne, Emily
Allen, Michael J.
Temperton, Ben
Efficient dilution-to-extinction isolation of novel virus–host model systems for fastidious heterotrophic bacteria
title Efficient dilution-to-extinction isolation of novel virus–host model systems for fastidious heterotrophic bacteria
title_full Efficient dilution-to-extinction isolation of novel virus–host model systems for fastidious heterotrophic bacteria
title_fullStr Efficient dilution-to-extinction isolation of novel virus–host model systems for fastidious heterotrophic bacteria
title_full_unstemmed Efficient dilution-to-extinction isolation of novel virus–host model systems for fastidious heterotrophic bacteria
title_short Efficient dilution-to-extinction isolation of novel virus–host model systems for fastidious heterotrophic bacteria
title_sort efficient dilution-to-extinction isolation of novel virus–host model systems for fastidious heterotrophic bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163748/
https://www.ncbi.nlm.nih.gov/pubmed/33495565
http://dx.doi.org/10.1038/s41396-020-00872-z
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