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High speciation rate of niche specialists in hot springs
Ecological and evolutionary processes simultaneously regulate microbial diversity, but the evolutionary processes and their driving forces remain largely unexplored. Here we investigated the ecological and evolutionary characteristics of microbiota in hot springs spanning a broad temperature range (...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356836/ https://www.ncbi.nlm.nih.gov/pubmed/37286739 http://dx.doi.org/10.1038/s41396-023-01447-4 |
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author | He, Qing Wang, Shang Feng, Kai Michaletz, Sean T. Hou, Weiguo Zhang, Wenhui Li, Fangru Zhang, Yidi Wang, Danrui Peng, Xi Yang, Xingsheng Deng, Ye |
author_facet | He, Qing Wang, Shang Feng, Kai Michaletz, Sean T. Hou, Weiguo Zhang, Wenhui Li, Fangru Zhang, Yidi Wang, Danrui Peng, Xi Yang, Xingsheng Deng, Ye |
author_sort | He, Qing |
collection | PubMed |
description | Ecological and evolutionary processes simultaneously regulate microbial diversity, but the evolutionary processes and their driving forces remain largely unexplored. Here we investigated the ecological and evolutionary characteristics of microbiota in hot springs spanning a broad temperature range (54.8–80 °C) by sequencing the 16S rRNA genes. Our results demonstrated that niche specialists and niche generalists are embedded in a complex interaction of ecological and evolutionary dynamics. On the thermal tolerance niche axis, thermal (T) sensitive (at a specific temperature) versus T-resistant (at least in five temperatures) species were characterized by different niche breadth, community abundance and dispersal potential, consequently differing in potential evolutionary trajectory. The niche-specialized T-sensitive species experienced strong temperature barriers, leading to completely species shift and high fitness but low abundant communities at each temperature (“home niche”), and such trade-offs thus reinforced peak performance, as evidenced by high speciation across temperatures and increasing diversification potential with temperature. In contrast, T-resistant species are advantageous of niche expansion but with poor local performance, as shown by wide niche breadth with high extinction, indicating these niche generalists are “jack-of-all-trades, master-of-none”. Despite of such differences, the T-sensitive and T-resistant species are evolutionarily interacted. Specifically, the continuous transition from T-sensitive to T-resistant species insured the exclusion probability of T-resistant species at a relatively constant level across temperatures. The co-evolution and co-adaptation of T-sensitive and T-resistant species were in line with the red queen theory. Collectively, our findings demonstrate that high speciation of niche specialists could alleviate the environmental-filtering-induced negative effect on diversity. |
format | Online Article Text |
id | pubmed-10356836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103568362023-07-21 High speciation rate of niche specialists in hot springs He, Qing Wang, Shang Feng, Kai Michaletz, Sean T. Hou, Weiguo Zhang, Wenhui Li, Fangru Zhang, Yidi Wang, Danrui Peng, Xi Yang, Xingsheng Deng, Ye ISME J Article Ecological and evolutionary processes simultaneously regulate microbial diversity, but the evolutionary processes and their driving forces remain largely unexplored. Here we investigated the ecological and evolutionary characteristics of microbiota in hot springs spanning a broad temperature range (54.8–80 °C) by sequencing the 16S rRNA genes. Our results demonstrated that niche specialists and niche generalists are embedded in a complex interaction of ecological and evolutionary dynamics. On the thermal tolerance niche axis, thermal (T) sensitive (at a specific temperature) versus T-resistant (at least in five temperatures) species were characterized by different niche breadth, community abundance and dispersal potential, consequently differing in potential evolutionary trajectory. The niche-specialized T-sensitive species experienced strong temperature barriers, leading to completely species shift and high fitness but low abundant communities at each temperature (“home niche”), and such trade-offs thus reinforced peak performance, as evidenced by high speciation across temperatures and increasing diversification potential with temperature. In contrast, T-resistant species are advantageous of niche expansion but with poor local performance, as shown by wide niche breadth with high extinction, indicating these niche generalists are “jack-of-all-trades, master-of-none”. Despite of such differences, the T-sensitive and T-resistant species are evolutionarily interacted. Specifically, the continuous transition from T-sensitive to T-resistant species insured the exclusion probability of T-resistant species at a relatively constant level across temperatures. The co-evolution and co-adaptation of T-sensitive and T-resistant species were in line with the red queen theory. Collectively, our findings demonstrate that high speciation of niche specialists could alleviate the environmental-filtering-induced negative effect on diversity. Nature Publishing Group UK 2023-06-07 2023-08 /pmc/articles/PMC10356836/ /pubmed/37286739 http://dx.doi.org/10.1038/s41396-023-01447-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article He, Qing Wang, Shang Feng, Kai Michaletz, Sean T. Hou, Weiguo Zhang, Wenhui Li, Fangru Zhang, Yidi Wang, Danrui Peng, Xi Yang, Xingsheng Deng, Ye High speciation rate of niche specialists in hot springs |
title | High speciation rate of niche specialists in hot springs |
title_full | High speciation rate of niche specialists in hot springs |
title_fullStr | High speciation rate of niche specialists in hot springs |
title_full_unstemmed | High speciation rate of niche specialists in hot springs |
title_short | High speciation rate of niche specialists in hot springs |
title_sort | high speciation rate of niche specialists in hot springs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356836/ https://www.ncbi.nlm.nih.gov/pubmed/37286739 http://dx.doi.org/10.1038/s41396-023-01447-4 |
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