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Facing lethal temperatures: Heat‐shock response in desert and temperate ants
Global climate changes may cause profound effects on species adaptation, particularly in ectotherms for whom even moderate warmer temperatures can lead to disproportionate heat failure. Still, several organisms evolved to endure high desert temperatures. Here, we describe the thermal tolerance survi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500329/ https://www.ncbi.nlm.nih.gov/pubmed/37720060 http://dx.doi.org/10.1002/ece3.10438 |
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author | Araujo, Natalia de Souza Perez, Rémy Willot, Quentin Defrance, Matthieu Aron, Serge |
author_facet | Araujo, Natalia de Souza Perez, Rémy Willot, Quentin Defrance, Matthieu Aron, Serge |
author_sort | Araujo, Natalia de Souza |
collection | PubMed |
description | Global climate changes may cause profound effects on species adaptation, particularly in ectotherms for whom even moderate warmer temperatures can lead to disproportionate heat failure. Still, several organisms evolved to endure high desert temperatures. Here, we describe the thermal tolerance survival and the transcriptomic heat stress response of three genera of desert (Cataglyphis, Melophorus, and Ocymyrmex) and two of temperate ants (Formica and Myrmica) and explore convergent and specific adaptations. We found heat stress led to either a reactive or a constitutive response in desert ants: Cataglyphis holgerseni and Melophorus bagoti differentially regulated very few transcripts in response to heat (0.12% and 0.14%, respectively), while Cataglyphis bombycina and Ocymyrmex robustior responded with greater expression alterations (respectively affecting 0.6% and 1.53% of their transcriptomes). These two responsive mechanisms—reactive and constitutive—were related to individual thermal tolerance survival and convergently evolved in distinct desert ant genera. Moreover, in comparison with desert species, the two temperate ants differentially expressed thousands of transcripts more in response to heat stress (affecting 8% and 12.71% of F. fusca and Myr. sabuleti transcriptomes). In summary, we show that heat adaptation in thermophilic ants involved changes in the expression response. Overall, desert ants show reduced transcriptional alterations even when under high thermal stress, and their expression response may be either constitutive or reactive to temperature increase. |
format | Online Article Text |
id | pubmed-10500329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105003292023-09-15 Facing lethal temperatures: Heat‐shock response in desert and temperate ants Araujo, Natalia de Souza Perez, Rémy Willot, Quentin Defrance, Matthieu Aron, Serge Ecol Evol Research Articles Global climate changes may cause profound effects on species adaptation, particularly in ectotherms for whom even moderate warmer temperatures can lead to disproportionate heat failure. Still, several organisms evolved to endure high desert temperatures. Here, we describe the thermal tolerance survival and the transcriptomic heat stress response of three genera of desert (Cataglyphis, Melophorus, and Ocymyrmex) and two of temperate ants (Formica and Myrmica) and explore convergent and specific adaptations. We found heat stress led to either a reactive or a constitutive response in desert ants: Cataglyphis holgerseni and Melophorus bagoti differentially regulated very few transcripts in response to heat (0.12% and 0.14%, respectively), while Cataglyphis bombycina and Ocymyrmex robustior responded with greater expression alterations (respectively affecting 0.6% and 1.53% of their transcriptomes). These two responsive mechanisms—reactive and constitutive—were related to individual thermal tolerance survival and convergently evolved in distinct desert ant genera. Moreover, in comparison with desert species, the two temperate ants differentially expressed thousands of transcripts more in response to heat stress (affecting 8% and 12.71% of F. fusca and Myr. sabuleti transcriptomes). In summary, we show that heat adaptation in thermophilic ants involved changes in the expression response. Overall, desert ants show reduced transcriptional alterations even when under high thermal stress, and their expression response may be either constitutive or reactive to temperature increase. John Wiley and Sons Inc. 2023-09-14 /pmc/articles/PMC10500329/ /pubmed/37720060 http://dx.doi.org/10.1002/ece3.10438 Text en © 2023 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Araujo, Natalia de Souza Perez, Rémy Willot, Quentin Defrance, Matthieu Aron, Serge Facing lethal temperatures: Heat‐shock response in desert and temperate ants |
title | Facing lethal temperatures: Heat‐shock response in desert and temperate ants |
title_full | Facing lethal temperatures: Heat‐shock response in desert and temperate ants |
title_fullStr | Facing lethal temperatures: Heat‐shock response in desert and temperate ants |
title_full_unstemmed | Facing lethal temperatures: Heat‐shock response in desert and temperate ants |
title_short | Facing lethal temperatures: Heat‐shock response in desert and temperate ants |
title_sort | facing lethal temperatures: heat‐shock response in desert and temperate ants |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500329/ https://www.ncbi.nlm.nih.gov/pubmed/37720060 http://dx.doi.org/10.1002/ece3.10438 |
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