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Loss and resiliency of social amoeba symbiosis under simulated warming

Anthropogenic global change is increasingly raising concerns about collapses of symbiotic interactions worldwide. Therefore, understanding how climate change affects symbioses remains a challenge and demands more study. Here, we look at how simulated warming affects the social ameba Dictyostelium di...

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Autores principales: Shu, Longfei, Qian, Xinye, Brock, Debra A., Geist, Katherine S., Queller, David C., Strassmann, Joan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713973/
https://www.ncbi.nlm.nih.gov/pubmed/33304528
http://dx.doi.org/10.1002/ece3.6909
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author Shu, Longfei
Qian, Xinye
Brock, Debra A.
Geist, Katherine S.
Queller, David C.
Strassmann, Joan E.
author_facet Shu, Longfei
Qian, Xinye
Brock, Debra A.
Geist, Katherine S.
Queller, David C.
Strassmann, Joan E.
author_sort Shu, Longfei
collection PubMed
description Anthropogenic global change is increasingly raising concerns about collapses of symbiotic interactions worldwide. Therefore, understanding how climate change affects symbioses remains a challenge and demands more study. Here, we look at how simulated warming affects the social ameba Dictyostelium discoideum and its relationship with its facultative bacterial symbionts, Paraburkholderia hayleyella and Paraburkholderia agricolaris. We cured and cross‐infected ameba hosts with different symbionts. We found that warming significantly decreased D. discoideum's fitness, and we found no sign of local adaptation in two wild populations. Experimental warming had complex effects on these symbioses with responses determined by both symbiont and host. Neither of these facultative symbionts increases its hosts’ thermal tolerance. The nearly obligate symbiont with a reduced genome, P. hayleyella, actually decreases D. discoideum's thermal tolerance and even causes symbiosis breakdown. Our study shows how facultative symbioses may have complex responses to global change.
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spelling pubmed-77139732020-12-09 Loss and resiliency of social amoeba symbiosis under simulated warming Shu, Longfei Qian, Xinye Brock, Debra A. Geist, Katherine S. Queller, David C. Strassmann, Joan E. Ecol Evol Original Research Anthropogenic global change is increasingly raising concerns about collapses of symbiotic interactions worldwide. Therefore, understanding how climate change affects symbioses remains a challenge and demands more study. Here, we look at how simulated warming affects the social ameba Dictyostelium discoideum and its relationship with its facultative bacterial symbionts, Paraburkholderia hayleyella and Paraburkholderia agricolaris. We cured and cross‐infected ameba hosts with different symbionts. We found that warming significantly decreased D. discoideum's fitness, and we found no sign of local adaptation in two wild populations. Experimental warming had complex effects on these symbioses with responses determined by both symbiont and host. Neither of these facultative symbionts increases its hosts’ thermal tolerance. The nearly obligate symbiont with a reduced genome, P. hayleyella, actually decreases D. discoideum's thermal tolerance and even causes symbiosis breakdown. Our study shows how facultative symbioses may have complex responses to global change. John Wiley and Sons Inc. 2020-10-20 /pmc/articles/PMC7713973/ /pubmed/33304528 http://dx.doi.org/10.1002/ece3.6909 Text en © 2020 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Shu, Longfei
Qian, Xinye
Brock, Debra A.
Geist, Katherine S.
Queller, David C.
Strassmann, Joan E.
Loss and resiliency of social amoeba symbiosis under simulated warming
title Loss and resiliency of social amoeba symbiosis under simulated warming
title_full Loss and resiliency of social amoeba symbiosis under simulated warming
title_fullStr Loss and resiliency of social amoeba symbiosis under simulated warming
title_full_unstemmed Loss and resiliency of social amoeba symbiosis under simulated warming
title_short Loss and resiliency of social amoeba symbiosis under simulated warming
title_sort loss and resiliency of social amoeba symbiosis under simulated warming
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713973/
https://www.ncbi.nlm.nih.gov/pubmed/33304528
http://dx.doi.org/10.1002/ece3.6909
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