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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
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.
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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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