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Immune-mediated competition benefits protective microbes over pathogens in a novel host species

Microbes that protect against infection inhabit hosts across the tree of life. It is unclear whether and how the host immune system may affect the formation of new protective symbioses. We investigated the transcriptomic response of Caenorhabditis elegans following novel interactions with a protecti...

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Autores principales: Ford, Suzanne A., Drew, Georgia C., King, Kayla C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708653/
https://www.ncbi.nlm.nih.gov/pubmed/36352206
http://dx.doi.org/10.1038/s41437-022-00569-3
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author Ford, Suzanne A.
Drew, Georgia C.
King, Kayla C.
author_facet Ford, Suzanne A.
Drew, Georgia C.
King, Kayla C.
author_sort Ford, Suzanne A.
collection PubMed
description Microbes that protect against infection inhabit hosts across the tree of life. It is unclear whether and how the host immune system may affect the formation of new protective symbioses. We investigated the transcriptomic response of Caenorhabditis elegans following novel interactions with a protective microbe (Enterococcus faecalis) able to defend against infection by pathogenic Staphylococcus aureus. We have previously shown that E. faecalis can directly limit pathogen growth within hosts. In this study, we show that colonisation by protective E. faecalis caused the differential expression of 1,557 genes in pathogen infected hosts, including the upregulation of immune genes such as lysozymes and C-type lectins. The most significantly upregulated host lysozyme gene, lys-7, impacted the competitive abilities of E. faecalis and S. aureus when knocked out. E. faecalis has an increased ability to resist lysozyme activity compared to S. aureus, suggesting that the protective microbe could gain a competitive advantage from this host response. Our finding that protective microbes can benefit from immune-mediated competition after introduction opens up new possibilities for biocontrol design and our understanding of symbiosis evolution. Crosstalk between the host immune response and microbe-mediated protection should favour the continued investment in host immunity and avoid the potentially risky evolution of host dependence.
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spelling pubmed-97086532022-12-01 Immune-mediated competition benefits protective microbes over pathogens in a novel host species Ford, Suzanne A. Drew, Georgia C. King, Kayla C. Heredity (Edinb) Article Microbes that protect against infection inhabit hosts across the tree of life. It is unclear whether and how the host immune system may affect the formation of new protective symbioses. We investigated the transcriptomic response of Caenorhabditis elegans following novel interactions with a protective microbe (Enterococcus faecalis) able to defend against infection by pathogenic Staphylococcus aureus. We have previously shown that E. faecalis can directly limit pathogen growth within hosts. In this study, we show that colonisation by protective E. faecalis caused the differential expression of 1,557 genes in pathogen infected hosts, including the upregulation of immune genes such as lysozymes and C-type lectins. The most significantly upregulated host lysozyme gene, lys-7, impacted the competitive abilities of E. faecalis and S. aureus when knocked out. E. faecalis has an increased ability to resist lysozyme activity compared to S. aureus, suggesting that the protective microbe could gain a competitive advantage from this host response. Our finding that protective microbes can benefit from immune-mediated competition after introduction opens up new possibilities for biocontrol design and our understanding of symbiosis evolution. Crosstalk between the host immune response and microbe-mediated protection should favour the continued investment in host immunity and avoid the potentially risky evolution of host dependence. Springer International Publishing 2022-11-09 2022-12 /pmc/articles/PMC9708653/ /pubmed/36352206 http://dx.doi.org/10.1038/s41437-022-00569-3 Text en © The Author(s) 2022 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
Ford, Suzanne A.
Drew, Georgia C.
King, Kayla C.
Immune-mediated competition benefits protective microbes over pathogens in a novel host species
title Immune-mediated competition benefits protective microbes over pathogens in a novel host species
title_full Immune-mediated competition benefits protective microbes over pathogens in a novel host species
title_fullStr Immune-mediated competition benefits protective microbes over pathogens in a novel host species
title_full_unstemmed Immune-mediated competition benefits protective microbes over pathogens in a novel host species
title_short Immune-mediated competition benefits protective microbes over pathogens in a novel host species
title_sort immune-mediated competition benefits protective microbes over pathogens in a novel host species
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708653/
https://www.ncbi.nlm.nih.gov/pubmed/36352206
http://dx.doi.org/10.1038/s41437-022-00569-3
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