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Functional differentiation determines the molecular basis of the symbiotic lifestyle of Ca. Nanohaloarchaeota
BACKGROUND: Candidatus Nanohaloarchaeota, an archaeal phylum within the DPANN superphylum, is characterized by limited metabolic capabilities and limited phylogenetic diversity and until recently has been considered to exclusively inhabit hypersaline environments due to an obligate association with...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563170/ https://www.ncbi.nlm.nih.gov/pubmed/36242054 http://dx.doi.org/10.1186/s40168-022-01376-y |
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author | Xie, Yuan-Guo Luo, Zhen-Hao Fang, Bao-Zhu Jiao, Jian-Yu Xie, Qi-Jun Cao, Xing-Ru Qu, Yan-Ni Qi, Yan-Lin Rao, Yang-Zhi Li, Yu-Xian Liu, Yong-Hong Li, Andrew Seymour, Cale Palmer, Marike Hedlund, Brian P. Li, Wen-Jun Hua, Zheng-Shuang |
author_facet | Xie, Yuan-Guo Luo, Zhen-Hao Fang, Bao-Zhu Jiao, Jian-Yu Xie, Qi-Jun Cao, Xing-Ru Qu, Yan-Ni Qi, Yan-Lin Rao, Yang-Zhi Li, Yu-Xian Liu, Yong-Hong Li, Andrew Seymour, Cale Palmer, Marike Hedlund, Brian P. Li, Wen-Jun Hua, Zheng-Shuang |
author_sort | Xie, Yuan-Guo |
collection | PubMed |
description | BACKGROUND: Candidatus Nanohaloarchaeota, an archaeal phylum within the DPANN superphylum, is characterized by limited metabolic capabilities and limited phylogenetic diversity and until recently has been considered to exclusively inhabit hypersaline environments due to an obligate association with Halobacteria. Aside from hypersaline environments, Ca. Nanohaloarchaeota can also have been discovered from deep-subsurface marine sediments. RESULTS: Three metagenome-assembled genomes (MAGs) representing a new order within the Ca. Nanohaloarchaeota were reconstructed from a stratified salt crust and proposed to represent a novel order, Nucleotidisoterales. Genomic features reveal them to be anaerobes capable of catabolizing nucleotides by coupling nucleotide salvage pathways with lower glycolysis to yield free energy. Comparative genomics demonstrated that these and other Ca. Nanohaloarchaeota inhabiting saline habitats use a “salt-in” strategy to maintain osmotic pressure based on the high proportion of acidic amino acids. In contrast, previously described Ca. Nanohaloarchaeota MAGs from geothermal environments were enriched with basic amino acids to counter heat stress. Evolutionary history reconstruction revealed that functional differentiation of energy conservation strategies drove diversification within Ca. Nanohaloarchaeota, further leading to shifts in the catabolic strategy from nucleotide degradation within deeper lineages to polysaccharide degradation within shallow lineages. CONCLUSIONS: This study provides deeper insight into the ecological functions and evolution of the expanded phylum Ca. Nanohaloarchaeota and further advances our understanding on the functional and genetic associations between potential symbionts and hosts. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01376-y. |
format | Online Article Text |
id | pubmed-9563170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95631702022-10-15 Functional differentiation determines the molecular basis of the symbiotic lifestyle of Ca. Nanohaloarchaeota Xie, Yuan-Guo Luo, Zhen-Hao Fang, Bao-Zhu Jiao, Jian-Yu Xie, Qi-Jun Cao, Xing-Ru Qu, Yan-Ni Qi, Yan-Lin Rao, Yang-Zhi Li, Yu-Xian Liu, Yong-Hong Li, Andrew Seymour, Cale Palmer, Marike Hedlund, Brian P. Li, Wen-Jun Hua, Zheng-Shuang Microbiome Research BACKGROUND: Candidatus Nanohaloarchaeota, an archaeal phylum within the DPANN superphylum, is characterized by limited metabolic capabilities and limited phylogenetic diversity and until recently has been considered to exclusively inhabit hypersaline environments due to an obligate association with Halobacteria. Aside from hypersaline environments, Ca. Nanohaloarchaeota can also have been discovered from deep-subsurface marine sediments. RESULTS: Three metagenome-assembled genomes (MAGs) representing a new order within the Ca. Nanohaloarchaeota were reconstructed from a stratified salt crust and proposed to represent a novel order, Nucleotidisoterales. Genomic features reveal them to be anaerobes capable of catabolizing nucleotides by coupling nucleotide salvage pathways with lower glycolysis to yield free energy. Comparative genomics demonstrated that these and other Ca. Nanohaloarchaeota inhabiting saline habitats use a “salt-in” strategy to maintain osmotic pressure based on the high proportion of acidic amino acids. In contrast, previously described Ca. Nanohaloarchaeota MAGs from geothermal environments were enriched with basic amino acids to counter heat stress. Evolutionary history reconstruction revealed that functional differentiation of energy conservation strategies drove diversification within Ca. Nanohaloarchaeota, further leading to shifts in the catabolic strategy from nucleotide degradation within deeper lineages to polysaccharide degradation within shallow lineages. CONCLUSIONS: This study provides deeper insight into the ecological functions and evolution of the expanded phylum Ca. Nanohaloarchaeota and further advances our understanding on the functional and genetic associations between potential symbionts and hosts. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01376-y. BioMed Central 2022-10-14 /pmc/articles/PMC9563170/ /pubmed/36242054 http://dx.doi.org/10.1186/s40168-022-01376-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Xie, Yuan-Guo Luo, Zhen-Hao Fang, Bao-Zhu Jiao, Jian-Yu Xie, Qi-Jun Cao, Xing-Ru Qu, Yan-Ni Qi, Yan-Lin Rao, Yang-Zhi Li, Yu-Xian Liu, Yong-Hong Li, Andrew Seymour, Cale Palmer, Marike Hedlund, Brian P. Li, Wen-Jun Hua, Zheng-Shuang Functional differentiation determines the molecular basis of the symbiotic lifestyle of Ca. Nanohaloarchaeota |
title | Functional differentiation determines the molecular basis of the symbiotic lifestyle of Ca. Nanohaloarchaeota |
title_full | Functional differentiation determines the molecular basis of the symbiotic lifestyle of Ca. Nanohaloarchaeota |
title_fullStr | Functional differentiation determines the molecular basis of the symbiotic lifestyle of Ca. Nanohaloarchaeota |
title_full_unstemmed | Functional differentiation determines the molecular basis of the symbiotic lifestyle of Ca. Nanohaloarchaeota |
title_short | Functional differentiation determines the molecular basis of the symbiotic lifestyle of Ca. Nanohaloarchaeota |
title_sort | functional differentiation determines the molecular basis of the symbiotic lifestyle of ca. nanohaloarchaeota |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563170/ https://www.ncbi.nlm.nih.gov/pubmed/36242054 http://dx.doi.org/10.1186/s40168-022-01376-y |
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