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Filamentous phages reduce bacterial growth in low salinities
Being non-lytic, filamentous phages can replicate at high frequencies and often carry virulence factors, which are important in the evolution and emergence of novel pathogens. However, their net effect on bacterial fitness remains unknown. To understand the ecology and evolution between filamentous...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6936277/ https://www.ncbi.nlm.nih.gov/pubmed/31903215 http://dx.doi.org/10.1098/rsos.191669 |
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author | Goehlich, Henry Roth, Olivia Wendling, Carolin C. |
author_facet | Goehlich, Henry Roth, Olivia Wendling, Carolin C. |
author_sort | Goehlich, Henry |
collection | PubMed |
description | Being non-lytic, filamentous phages can replicate at high frequencies and often carry virulence factors, which are important in the evolution and emergence of novel pathogens. However, their net effect on bacterial fitness remains unknown. To understand the ecology and evolution between filamentous phages and their hosts, it is important to assess (i) fitness effects of filamentous phages on their hosts and (ii) how these effects depend on the environment. To determine how the net effect on bacterial fitness by filamentous phages changes across environments, we constructed phage–bacteria infection networks at ambient 15 practical salinity units (PSU) and stressful salinities (11 and 7 PSU) using the marine bacterium, Vibrio alginolyticus and its derived filamentous phages as model system. We observed no significant difference in network structure at 15 and 11 PSU. However, at 7 PSU phages significantly reduced bacterial growth changing network structure. This pattern was mainly driven by a significant increase in bacterial susceptibility. Our findings suggest that filamentous phages decrease bacterial growth, an indirect measure of fitness in stressful environmental conditions, which might impact bacterial communities, alter horizontal gene transfer events and possibly favour the emergence of novel pathogens in environmental Vibrios. |
format | Online Article Text |
id | pubmed-6936277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-69362772020-01-03 Filamentous phages reduce bacterial growth in low salinities Goehlich, Henry Roth, Olivia Wendling, Carolin C. R Soc Open Sci Biology (Whole Organism) Being non-lytic, filamentous phages can replicate at high frequencies and often carry virulence factors, which are important in the evolution and emergence of novel pathogens. However, their net effect on bacterial fitness remains unknown. To understand the ecology and evolution between filamentous phages and their hosts, it is important to assess (i) fitness effects of filamentous phages on their hosts and (ii) how these effects depend on the environment. To determine how the net effect on bacterial fitness by filamentous phages changes across environments, we constructed phage–bacteria infection networks at ambient 15 practical salinity units (PSU) and stressful salinities (11 and 7 PSU) using the marine bacterium, Vibrio alginolyticus and its derived filamentous phages as model system. We observed no significant difference in network structure at 15 and 11 PSU. However, at 7 PSU phages significantly reduced bacterial growth changing network structure. This pattern was mainly driven by a significant increase in bacterial susceptibility. Our findings suggest that filamentous phages decrease bacterial growth, an indirect measure of fitness in stressful environmental conditions, which might impact bacterial communities, alter horizontal gene transfer events and possibly favour the emergence of novel pathogens in environmental Vibrios. The Royal Society 2019-12-11 /pmc/articles/PMC6936277/ /pubmed/31903215 http://dx.doi.org/10.1098/rsos.191669 Text en © 2019 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Biology (Whole Organism) Goehlich, Henry Roth, Olivia Wendling, Carolin C. Filamentous phages reduce bacterial growth in low salinities |
title | Filamentous phages reduce bacterial growth in low salinities |
title_full | Filamentous phages reduce bacterial growth in low salinities |
title_fullStr | Filamentous phages reduce bacterial growth in low salinities |
title_full_unstemmed | Filamentous phages reduce bacterial growth in low salinities |
title_short | Filamentous phages reduce bacterial growth in low salinities |
title_sort | filamentous phages reduce bacterial growth in low salinities |
topic | Biology (Whole Organism) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6936277/ https://www.ncbi.nlm.nih.gov/pubmed/31903215 http://dx.doi.org/10.1098/rsos.191669 |
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