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Genomic variation and biogeography of Antarctic haloarchaea
BACKGROUND: The genomes of halophilic archaea (haloarchaea) often comprise multiple replicons. Genomic variation in haloarchaea has been linked to viral infection pressure and, in the case of Antarctic communities, can be caused by intergenera gene exchange. To expand understanding of genome variati...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011602/ https://www.ncbi.nlm.nih.gov/pubmed/29925429 http://dx.doi.org/10.1186/s40168-018-0495-3 |
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author | Tschitschko, Bernhard Erdmann, Susanne DeMaere, Matthew Z. Roux, Simon Panwar, Pratibha Allen, Michelle A. Williams, Timothy J. Brazendale, Sarah Hancock, Alyce M. Eloe-Fadrosh, Emiley A. Cavicchioli, Ricardo |
author_facet | Tschitschko, Bernhard Erdmann, Susanne DeMaere, Matthew Z. Roux, Simon Panwar, Pratibha Allen, Michelle A. Williams, Timothy J. Brazendale, Sarah Hancock, Alyce M. Eloe-Fadrosh, Emiley A. Cavicchioli, Ricardo |
author_sort | Tschitschko, Bernhard |
collection | PubMed |
description | BACKGROUND: The genomes of halophilic archaea (haloarchaea) often comprise multiple replicons. Genomic variation in haloarchaea has been linked to viral infection pressure and, in the case of Antarctic communities, can be caused by intergenera gene exchange. To expand understanding of genome variation and biogeography of Antarctic haloarchaea, here we assessed genomic variation between two strains of Halorubrum lacusprofundi that were isolated from Antarctic hypersaline lakes from different regions (Vestfold Hills and Rauer Islands). To assess variation in haloarchaeal populations, including the presence of genomic islands, metagenomes from six hypersaline Antarctic lakes were characterised. RESULTS: The sequence of the largest replicon of each Hrr. lacusprofundi strain (primary replicon) was highly conserved, while each of the strains’ two smaller replicons (secondary replicons) were highly variable. Intergenera gene exchange was identified, including the sharing of a type I-B CRISPR system. Evaluation of infectivity of an Antarctic halovirus provided experimental evidence for the differential susceptibility of the strains, bolstering inferences that strain variation is important for modulating interactions with viruses. A relationship was found between genomic structuring and the location of variation within replicons and genomic islands, demonstrating that the way in which haloarchaea accommodate genomic variability relates to replicon structuring. Metagenome read and contig mapping and clustering and scaling analyses demonstrated biogeographical patterning of variation consistent with environment and distance effects. The metagenome data also demonstrated that specific haloarchaeal species dominated the hypersaline systems indicating they are endemic to Antarctica. CONCLUSION: The study describes how genomic variation manifests in Antarctic-lake haloarchaeal communities and provides the basis for future assessments of Antarctic regional and global biogeography of haloarchaea. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0495-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6011602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60116022018-07-05 Genomic variation and biogeography of Antarctic haloarchaea Tschitschko, Bernhard Erdmann, Susanne DeMaere, Matthew Z. Roux, Simon Panwar, Pratibha Allen, Michelle A. Williams, Timothy J. Brazendale, Sarah Hancock, Alyce M. Eloe-Fadrosh, Emiley A. Cavicchioli, Ricardo Microbiome Research BACKGROUND: The genomes of halophilic archaea (haloarchaea) often comprise multiple replicons. Genomic variation in haloarchaea has been linked to viral infection pressure and, in the case of Antarctic communities, can be caused by intergenera gene exchange. To expand understanding of genome variation and biogeography of Antarctic haloarchaea, here we assessed genomic variation between two strains of Halorubrum lacusprofundi that were isolated from Antarctic hypersaline lakes from different regions (Vestfold Hills and Rauer Islands). To assess variation in haloarchaeal populations, including the presence of genomic islands, metagenomes from six hypersaline Antarctic lakes were characterised. RESULTS: The sequence of the largest replicon of each Hrr. lacusprofundi strain (primary replicon) was highly conserved, while each of the strains’ two smaller replicons (secondary replicons) were highly variable. Intergenera gene exchange was identified, including the sharing of a type I-B CRISPR system. Evaluation of infectivity of an Antarctic halovirus provided experimental evidence for the differential susceptibility of the strains, bolstering inferences that strain variation is important for modulating interactions with viruses. A relationship was found between genomic structuring and the location of variation within replicons and genomic islands, demonstrating that the way in which haloarchaea accommodate genomic variability relates to replicon structuring. Metagenome read and contig mapping and clustering and scaling analyses demonstrated biogeographical patterning of variation consistent with environment and distance effects. The metagenome data also demonstrated that specific haloarchaeal species dominated the hypersaline systems indicating they are endemic to Antarctica. CONCLUSION: The study describes how genomic variation manifests in Antarctic-lake haloarchaeal communities and provides the basis for future assessments of Antarctic regional and global biogeography of haloarchaea. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0495-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-20 /pmc/articles/PMC6011602/ /pubmed/29925429 http://dx.doi.org/10.1186/s40168-018-0495-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Tschitschko, Bernhard Erdmann, Susanne DeMaere, Matthew Z. Roux, Simon Panwar, Pratibha Allen, Michelle A. Williams, Timothy J. Brazendale, Sarah Hancock, Alyce M. Eloe-Fadrosh, Emiley A. Cavicchioli, Ricardo Genomic variation and biogeography of Antarctic haloarchaea |
title | Genomic variation and biogeography of Antarctic haloarchaea |
title_full | Genomic variation and biogeography of Antarctic haloarchaea |
title_fullStr | Genomic variation and biogeography of Antarctic haloarchaea |
title_full_unstemmed | Genomic variation and biogeography of Antarctic haloarchaea |
title_short | Genomic variation and biogeography of Antarctic haloarchaea |
title_sort | genomic variation and biogeography of antarctic haloarchaea |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011602/ https://www.ncbi.nlm.nih.gov/pubmed/29925429 http://dx.doi.org/10.1186/s40168-018-0495-3 |
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