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Unexpected host dependency of Antarctic Nanohaloarchaeota
In hypersaline environments, Nanohaloarchaeota (Diapherotrites, Parvarchaeota, Aenigmarchaeota, Nanoarchaeota, Nanohaloarchaeota [DPANN] superphylum) are thought to be free-living microorganisms. We report cultivation of 2 strains of Antarctic Nanohaloarchaeota and show that they require the haloarc...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642349/ https://www.ncbi.nlm.nih.gov/pubmed/31253704 http://dx.doi.org/10.1073/pnas.1905179116 |
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author | Hamm, Joshua N. Erdmann, Susanne Eloe-Fadrosh, Emiley A. Angeloni, Allegra Zhong, Ling Brownlee, Christopher Williams, Timothy J. Barton, Kirston Carswell, Shaun Smith, Martin A. Brazendale, Sarah Hancock, Alyce M. Allen, Michelle A. Raftery, Mark J. Cavicchioli, Ricardo |
author_facet | Hamm, Joshua N. Erdmann, Susanne Eloe-Fadrosh, Emiley A. Angeloni, Allegra Zhong, Ling Brownlee, Christopher Williams, Timothy J. Barton, Kirston Carswell, Shaun Smith, Martin A. Brazendale, Sarah Hancock, Alyce M. Allen, Michelle A. Raftery, Mark J. Cavicchioli, Ricardo |
author_sort | Hamm, Joshua N. |
collection | PubMed |
description | In hypersaline environments, Nanohaloarchaeota (Diapherotrites, Parvarchaeota, Aenigmarchaeota, Nanoarchaeota, Nanohaloarchaeota [DPANN] superphylum) are thought to be free-living microorganisms. We report cultivation of 2 strains of Antarctic Nanohaloarchaeota and show that they require the haloarchaeon Halorubrum lacusprofundi for growth. By performing growth using enrichments and fluorescence-activated cell sorting, we demonstrated successful cultivation of Candidatus Nanohaloarchaeum antarcticus, purification of Ca. Nha. antarcticus away from other species, and growth and verification of Ca. Nha. antarcticus with Hrr. lacusprofundi; these findings are analogous to those required for fulfilling Koch’s postulates. We use fluorescent in situ hybridization and transmission electron microscopy to assess cell structures and interactions; metagenomics to characterize enrichment taxa, generate metagenome assembled genomes, and interrogate Antarctic communities; and proteomics to assess metabolic pathways and speculate about the roles of certain proteins. Metagenome analysis indicates the presence of a single species, which is endemic to Antarctic hypersaline systems that support the growth of haloarchaea. The presence of unusually large proteins predicted to function in attachment and invasion of hosts plus the absence of key biosynthetic pathways (e.g., lipids) in metagenome assembled genomes of globally distributed Nanohaloarchaeota indicate that all members of the lineage have evolved as symbionts. Our work expands the range of archaeal symbiotic lifestyles and provides a genetically tractable model system for advancing understanding of the factors controlling microbial symbiotic relationships. |
format | Online Article Text |
id | pubmed-6642349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-66423492019-07-25 Unexpected host dependency of Antarctic Nanohaloarchaeota Hamm, Joshua N. Erdmann, Susanne Eloe-Fadrosh, Emiley A. Angeloni, Allegra Zhong, Ling Brownlee, Christopher Williams, Timothy J. Barton, Kirston Carswell, Shaun Smith, Martin A. Brazendale, Sarah Hancock, Alyce M. Allen, Michelle A. Raftery, Mark J. Cavicchioli, Ricardo Proc Natl Acad Sci U S A PNAS Plus In hypersaline environments, Nanohaloarchaeota (Diapherotrites, Parvarchaeota, Aenigmarchaeota, Nanoarchaeota, Nanohaloarchaeota [DPANN] superphylum) are thought to be free-living microorganisms. We report cultivation of 2 strains of Antarctic Nanohaloarchaeota and show that they require the haloarchaeon Halorubrum lacusprofundi for growth. By performing growth using enrichments and fluorescence-activated cell sorting, we demonstrated successful cultivation of Candidatus Nanohaloarchaeum antarcticus, purification of Ca. Nha. antarcticus away from other species, and growth and verification of Ca. Nha. antarcticus with Hrr. lacusprofundi; these findings are analogous to those required for fulfilling Koch’s postulates. We use fluorescent in situ hybridization and transmission electron microscopy to assess cell structures and interactions; metagenomics to characterize enrichment taxa, generate metagenome assembled genomes, and interrogate Antarctic communities; and proteomics to assess metabolic pathways and speculate about the roles of certain proteins. Metagenome analysis indicates the presence of a single species, which is endemic to Antarctic hypersaline systems that support the growth of haloarchaea. The presence of unusually large proteins predicted to function in attachment and invasion of hosts plus the absence of key biosynthetic pathways (e.g., lipids) in metagenome assembled genomes of globally distributed Nanohaloarchaeota indicate that all members of the lineage have evolved as symbionts. Our work expands the range of archaeal symbiotic lifestyles and provides a genetically tractable model system for advancing understanding of the factors controlling microbial symbiotic relationships. National Academy of Sciences 2019-07-16 2019-06-28 /pmc/articles/PMC6642349/ /pubmed/31253704 http://dx.doi.org/10.1073/pnas.1905179116 Text en Copyright © 2019 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | PNAS Plus Hamm, Joshua N. Erdmann, Susanne Eloe-Fadrosh, Emiley A. Angeloni, Allegra Zhong, Ling Brownlee, Christopher Williams, Timothy J. Barton, Kirston Carswell, Shaun Smith, Martin A. Brazendale, Sarah Hancock, Alyce M. Allen, Michelle A. Raftery, Mark J. Cavicchioli, Ricardo Unexpected host dependency of Antarctic Nanohaloarchaeota |
title | Unexpected host dependency of Antarctic Nanohaloarchaeota |
title_full | Unexpected host dependency of Antarctic Nanohaloarchaeota |
title_fullStr | Unexpected host dependency of Antarctic Nanohaloarchaeota |
title_full_unstemmed | Unexpected host dependency of Antarctic Nanohaloarchaeota |
title_short | Unexpected host dependency of Antarctic Nanohaloarchaeota |
title_sort | unexpected host dependency of antarctic nanohaloarchaeota |
topic | PNAS Plus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642349/ https://www.ncbi.nlm.nih.gov/pubmed/31253704 http://dx.doi.org/10.1073/pnas.1905179116 |
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