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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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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. |
format | Online Article Text |
id | pubmed-6336404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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