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Microbial evolution and transitions along the parasite–mutualist continuum

Virtually all plants and animals, including humans, are home to symbiotic microorganisms. Symbiotic interactions can be neutral, harmful or have beneficial effects on the host organism. However, growing evidence suggests that microbial symbionts can evolve rapidly, resulting in drastic transitions a...

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Detalles Bibliográficos
Autores principales: Drew, Georgia C., Stevens, Emily J., King, Kayla C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054256/
https://www.ncbi.nlm.nih.gov/pubmed/33875863
http://dx.doi.org/10.1038/s41579-021-00550-7
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author Drew, Georgia C.
Stevens, Emily J.
King, Kayla C.
author_facet Drew, Georgia C.
Stevens, Emily J.
King, Kayla C.
author_sort Drew, Georgia C.
collection PubMed
description Virtually all plants and animals, including humans, are home to symbiotic microorganisms. Symbiotic interactions can be neutral, harmful or have beneficial effects on the host organism. However, growing evidence suggests that microbial symbionts can evolve rapidly, resulting in drastic transitions along the parasite–mutualist continuum. In this Review, we integrate theoretical and empirical findings to discuss the mechanisms underpinning these evolutionary shifts, as well as the ecological drivers and why some host–microorganism interactions may be stuck at the end of the continuum. In addition to having biomedical consequences, understanding the dynamic life of microorganisms reveals how symbioses can shape an organism’s biology and the entire community, particularly in a changing world.
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spelling pubmed-80542562021-04-19 Microbial evolution and transitions along the parasite–mutualist continuum Drew, Georgia C. Stevens, Emily J. King, Kayla C. Nat Rev Microbiol Review Article Virtually all plants and animals, including humans, are home to symbiotic microorganisms. Symbiotic interactions can be neutral, harmful or have beneficial effects on the host organism. However, growing evidence suggests that microbial symbionts can evolve rapidly, resulting in drastic transitions along the parasite–mutualist continuum. In this Review, we integrate theoretical and empirical findings to discuss the mechanisms underpinning these evolutionary shifts, as well as the ecological drivers and why some host–microorganism interactions may be stuck at the end of the continuum. In addition to having biomedical consequences, understanding the dynamic life of microorganisms reveals how symbioses can shape an organism’s biology and the entire community, particularly in a changing world. Nature Publishing Group UK 2021-04-19 2021 /pmc/articles/PMC8054256/ /pubmed/33875863 http://dx.doi.org/10.1038/s41579-021-00550-7 Text en © Springer Nature Limited 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Article
Drew, Georgia C.
Stevens, Emily J.
King, Kayla C.
Microbial evolution and transitions along the parasite–mutualist continuum
title Microbial evolution and transitions along the parasite–mutualist continuum
title_full Microbial evolution and transitions along the parasite–mutualist continuum
title_fullStr Microbial evolution and transitions along the parasite–mutualist continuum
title_full_unstemmed Microbial evolution and transitions along the parasite–mutualist continuum
title_short Microbial evolution and transitions along the parasite–mutualist continuum
title_sort microbial evolution and transitions along the parasite–mutualist continuum
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054256/
https://www.ncbi.nlm.nih.gov/pubmed/33875863
http://dx.doi.org/10.1038/s41579-021-00550-7
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