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Experimental evolution can enhance benefits of rhizobia to novel legume hosts

Legumes preferentially associate with and reward beneficial rhizobia in root nodules, but the processes by which rhizobia evolve to provide benefits to novel hosts remain poorly understood. Using cycles of in planta and in vitro evolution, we experimentally simulated lifestyles where rhizobia repeat...

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Autores principales: Quides, Kenjiro W., Weisberg, Alexandra J., Trinh, Jerry, Salaheldine, Fathi, Cardenas, Paola, Lee, Hsu-Han, Jariwala, Ruchi, Chang, Jeff H., Sachs, Joel L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150021/
https://www.ncbi.nlm.nih.gov/pubmed/34034525
http://dx.doi.org/10.1098/rspb.2021.0812
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author Quides, Kenjiro W.
Weisberg, Alexandra J.
Trinh, Jerry
Salaheldine, Fathi
Cardenas, Paola
Lee, Hsu-Han
Jariwala, Ruchi
Chang, Jeff H.
Sachs, Joel L.
author_facet Quides, Kenjiro W.
Weisberg, Alexandra J.
Trinh, Jerry
Salaheldine, Fathi
Cardenas, Paola
Lee, Hsu-Han
Jariwala, Ruchi
Chang, Jeff H.
Sachs, Joel L.
author_sort Quides, Kenjiro W.
collection PubMed
description Legumes preferentially associate with and reward beneficial rhizobia in root nodules, but the processes by which rhizobia evolve to provide benefits to novel hosts remain poorly understood. Using cycles of in planta and in vitro evolution, we experimentally simulated lifestyles where rhizobia repeatedly interact with novel plant genotypes with which they initially provide negligible benefits. Using a full-factorial replicated design, we independently evolved two rhizobia strains in associations with each of two Lotus japonicus genotypes that vary in regulation of nodule formation. We evaluated phenotypic evolution of rhizobia by quantifying fitness, growth effects and histological features on hosts, and molecular evolution via genome resequencing. Rhizobia evolved enhanced host benefits and caused changes in nodule development in one of the four host–symbiont combinations, that appeared to be driven by reduced costs during symbiosis, rather than increased nitrogen fixation. Descendant populations included genetic changes that could alter rhizobial infection or proliferation in host tissues, but lack of evidence for fixation of these mutations weakens the results. Evolution of enhanced rhizobial benefits occurred only in a subset of experiments, suggesting a role for host–symbiont genotype interactions in mediating the evolution of enhanced benefits from symbionts.
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spelling pubmed-81500212021-07-06 Experimental evolution can enhance benefits of rhizobia to novel legume hosts Quides, Kenjiro W. Weisberg, Alexandra J. Trinh, Jerry Salaheldine, Fathi Cardenas, Paola Lee, Hsu-Han Jariwala, Ruchi Chang, Jeff H. Sachs, Joel L. Proc Biol Sci Evolution Legumes preferentially associate with and reward beneficial rhizobia in root nodules, but the processes by which rhizobia evolve to provide benefits to novel hosts remain poorly understood. Using cycles of in planta and in vitro evolution, we experimentally simulated lifestyles where rhizobia repeatedly interact with novel plant genotypes with which they initially provide negligible benefits. Using a full-factorial replicated design, we independently evolved two rhizobia strains in associations with each of two Lotus japonicus genotypes that vary in regulation of nodule formation. We evaluated phenotypic evolution of rhizobia by quantifying fitness, growth effects and histological features on hosts, and molecular evolution via genome resequencing. Rhizobia evolved enhanced host benefits and caused changes in nodule development in one of the four host–symbiont combinations, that appeared to be driven by reduced costs during symbiosis, rather than increased nitrogen fixation. Descendant populations included genetic changes that could alter rhizobial infection or proliferation in host tissues, but lack of evidence for fixation of these mutations weakens the results. Evolution of enhanced rhizobial benefits occurred only in a subset of experiments, suggesting a role for host–symbiont genotype interactions in mediating the evolution of enhanced benefits from symbionts. The Royal Society 2021-05-26 2021-05-26 /pmc/articles/PMC8150021/ /pubmed/34034525 http://dx.doi.org/10.1098/rspb.2021.0812 Text en © 2021 The Authors. https://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/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Quides, Kenjiro W.
Weisberg, Alexandra J.
Trinh, Jerry
Salaheldine, Fathi
Cardenas, Paola
Lee, Hsu-Han
Jariwala, Ruchi
Chang, Jeff H.
Sachs, Joel L.
Experimental evolution can enhance benefits of rhizobia to novel legume hosts
title Experimental evolution can enhance benefits of rhizobia to novel legume hosts
title_full Experimental evolution can enhance benefits of rhizobia to novel legume hosts
title_fullStr Experimental evolution can enhance benefits of rhizobia to novel legume hosts
title_full_unstemmed Experimental evolution can enhance benefits of rhizobia to novel legume hosts
title_short Experimental evolution can enhance benefits of rhizobia to novel legume hosts
title_sort experimental evolution can enhance benefits of rhizobia to novel legume hosts
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150021/
https://www.ncbi.nlm.nih.gov/pubmed/34034525
http://dx.doi.org/10.1098/rspb.2021.0812
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