Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1783618655977734144 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7713973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT shulongfei lossandresiliencyofsocialamoebasymbiosisundersimulatedwarming AT qianxinye lossandresiliencyofsocialamoebasymbiosisundersimulatedwarming AT brockdebraa lossandresiliencyofsocialamoebasymbiosisundersimulatedwarming AT geistkatherines lossandresiliencyofsocialamoebasymbiosisundersimulatedwarming AT quellerdavidc lossandresiliencyofsocialamoebasymbiosisundersimulatedwarming AT strassmannjoane lossandresiliencyofsocialamoebasymbiosisundersimulatedwarming |