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Symbiont location, host fitness, and possible coadaptation in a symbiosis between social amoebae and bacteria

Recent symbioses, particularly facultative ones, are well suited for unravelling the evolutionary give and take between partners. Here we look at variation in natural isolates of the social amoeba Dictyostelium discoideum and their relationships with bacterial symbionts, Burkholderia hayleyella and...

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Autores principales: Shu, Longfei, Brock, Debra A, Geist, Katherine S, Miller, Jacob W, Queller, David C, Strassmann, Joan E, DiSalvo, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336404/
https://www.ncbi.nlm.nih.gov/pubmed/30596477
http://dx.doi.org/10.7554/eLife.42660
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author Shu, Longfei
Brock, Debra A
Geist, Katherine S
Miller, Jacob W
Queller, David C
Strassmann, Joan E
DiSalvo, Susanne
author_facet Shu, Longfei
Brock, Debra A
Geist, Katherine S
Miller, Jacob W
Queller, David C
Strassmann, Joan E
DiSalvo, Susanne
author_sort Shu, Longfei
collection PubMed
description Recent symbioses, particularly facultative ones, are well suited for unravelling the evolutionary give and take between partners. Here we look at variation in natural isolates of the social amoeba Dictyostelium discoideum and their relationships with bacterial symbionts, Burkholderia hayleyella and Burkholderia agricolaris. Only about a third of field-collected amoebae carry a symbiont. We cured and cross-infected amoebae hosts with different symbiont association histories and then compared host responses to each symbiont type. Before curing, field-collected clones did not vary significantly in overall fitness, but infected hosts produced morphologically different multicellular structures. After curing and reinfecting, host fitness declined. However, natural B. hayleyella hosts suffered fewer fitness costs when reinfected with B. hayleyella, indicating that they have evolved mechanisms to tolerate their symbiont. Our work suggests that amoebae hosts have evolved mechanisms to tolerate specific acquired symbionts; exploring host-symbiont relationships that vary within species may provide further insights into disease dynamics.
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spelling pubmed-63364042019-01-24 Symbiont location, host fitness, and possible coadaptation in a symbiosis between social amoebae and bacteria Shu, Longfei Brock, Debra A Geist, Katherine S Miller, Jacob W Queller, David C Strassmann, Joan E DiSalvo, Susanne eLife Evolutionary Biology Recent symbioses, particularly facultative ones, are well suited for unravelling the evolutionary give and take between partners. Here we look at variation in natural isolates of the social amoeba Dictyostelium discoideum and their relationships with bacterial symbionts, Burkholderia hayleyella and Burkholderia agricolaris. Only about a third of field-collected amoebae carry a symbiont. We cured and cross-infected amoebae hosts with different symbiont association histories and then compared host responses to each symbiont type. Before curing, field-collected clones did not vary significantly in overall fitness, but infected hosts produced morphologically different multicellular structures. After curing and reinfecting, host fitness declined. However, natural B. hayleyella hosts suffered fewer fitness costs when reinfected with B. hayleyella, indicating that they have evolved mechanisms to tolerate their symbiont. Our work suggests that amoebae hosts have evolved mechanisms to tolerate specific acquired symbionts; exploring host-symbiont relationships that vary within species may provide further insights into disease dynamics. eLife Sciences Publications, Ltd 2018-12-31 /pmc/articles/PMC6336404/ /pubmed/30596477 http://dx.doi.org/10.7554/eLife.42660 Text en © 2018, Shu et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Evolutionary Biology
Shu, Longfei
Brock, Debra A
Geist, Katherine S
Miller, Jacob W
Queller, David C
Strassmann, Joan E
DiSalvo, Susanne
Symbiont location, host fitness, and possible coadaptation in a symbiosis between social amoebae and bacteria
title Symbiont location, host fitness, and possible coadaptation in a symbiosis between social amoebae and bacteria
title_full Symbiont location, host fitness, and possible coadaptation in a symbiosis between social amoebae and bacteria
title_fullStr Symbiont location, host fitness, and possible coadaptation in a symbiosis between social amoebae and bacteria
title_full_unstemmed Symbiont location, host fitness, and possible coadaptation in a symbiosis between social amoebae and bacteria
title_short Symbiont location, host fitness, and possible coadaptation in a symbiosis between social amoebae and bacteria
title_sort symbiont location, host fitness, and possible coadaptation in a symbiosis between social amoebae and bacteria
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336404/
https://www.ncbi.nlm.nih.gov/pubmed/30596477
http://dx.doi.org/10.7554/eLife.42660
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