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Characterization of an archaeal virus-host system reveals massive genomic rearrangements in a laboratory strain
Halophilic archaea (haloarchaea) are known to exhibit multiple chromosomes, with one main chromosome and one or several smaller secondary chromosomes or megaplasmids. Halorubrum lacusprofundi, a model organism for studying cold adaptation, exhibits one secondary chromosome and one megaplasmid that i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10544981/ https://www.ncbi.nlm.nih.gov/pubmed/37789858 http://dx.doi.org/10.3389/fmicb.2023.1274068 |
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author | Mercier, Coraline Thies, Daniela Zhong, Ling Raftery, Mark J. Erdmann, Susanne |
author_facet | Mercier, Coraline Thies, Daniela Zhong, Ling Raftery, Mark J. Erdmann, Susanne |
author_sort | Mercier, Coraline |
collection | PubMed |
description | Halophilic archaea (haloarchaea) are known to exhibit multiple chromosomes, with one main chromosome and one or several smaller secondary chromosomes or megaplasmids. Halorubrum lacusprofundi, a model organism for studying cold adaptation, exhibits one secondary chromosome and one megaplasmid that include a large arsenal of virus defense mechanisms. We isolated a virus (Halorubrum tailed virus DL1, HRTV-DL1) infecting Hrr. lacusprofundi, and present an in-depth characterization of the virus and its interactions with Hrr. lacusprofundi. While studying virus-host interactions between Hrr. lacusprofundi and HRTV-DL1, we uncover that the strain in use (ACAM34_UNSW) lost the entire megaplasmid and about 38% of the secondary chromosome. The loss included the majority of virus defense mechanisms, making the strain sensitive to HRTV-DL1 infection, while the type strain (ACAM34_DSMZ) appears to prevent virus replication. Comparing infection of the type strain ACAM34_DSMZ with infection of the laboratory derived strain ACAM34_UNSW allowed us to identify host responses to virus infection that were only activated in ACAM34_UNSW upon the loss of virus defense mechanisms. We identify one of two S-layer proteins as primary receptor for HRTV-DL1 and conclude that the presence of two different S-layer proteins in one strain provides a strong advantage in the arms race with viruses. Additionally, we identify archaeal homologs to eukaryotic proteins potentially being involved in the defense against virus infection. |
format | Online Article Text |
id | pubmed-10544981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105449812023-10-03 Characterization of an archaeal virus-host system reveals massive genomic rearrangements in a laboratory strain Mercier, Coraline Thies, Daniela Zhong, Ling Raftery, Mark J. Erdmann, Susanne Front Microbiol Microbiology Halophilic archaea (haloarchaea) are known to exhibit multiple chromosomes, with one main chromosome and one or several smaller secondary chromosomes or megaplasmids. Halorubrum lacusprofundi, a model organism for studying cold adaptation, exhibits one secondary chromosome and one megaplasmid that include a large arsenal of virus defense mechanisms. We isolated a virus (Halorubrum tailed virus DL1, HRTV-DL1) infecting Hrr. lacusprofundi, and present an in-depth characterization of the virus and its interactions with Hrr. lacusprofundi. While studying virus-host interactions between Hrr. lacusprofundi and HRTV-DL1, we uncover that the strain in use (ACAM34_UNSW) lost the entire megaplasmid and about 38% of the secondary chromosome. The loss included the majority of virus defense mechanisms, making the strain sensitive to HRTV-DL1 infection, while the type strain (ACAM34_DSMZ) appears to prevent virus replication. Comparing infection of the type strain ACAM34_DSMZ with infection of the laboratory derived strain ACAM34_UNSW allowed us to identify host responses to virus infection that were only activated in ACAM34_UNSW upon the loss of virus defense mechanisms. We identify one of two S-layer proteins as primary receptor for HRTV-DL1 and conclude that the presence of two different S-layer proteins in one strain provides a strong advantage in the arms race with viruses. Additionally, we identify archaeal homologs to eukaryotic proteins potentially being involved in the defense against virus infection. Frontiers Media S.A. 2023-09-18 /pmc/articles/PMC10544981/ /pubmed/37789858 http://dx.doi.org/10.3389/fmicb.2023.1274068 Text en Copyright © 2023 Mercier, Thies, Zhong, Raftery and Erdmann. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Mercier, Coraline Thies, Daniela Zhong, Ling Raftery, Mark J. Erdmann, Susanne Characterization of an archaeal virus-host system reveals massive genomic rearrangements in a laboratory strain |
title | Characterization of an archaeal virus-host system reveals massive genomic rearrangements in a laboratory strain |
title_full | Characterization of an archaeal virus-host system reveals massive genomic rearrangements in a laboratory strain |
title_fullStr | Characterization of an archaeal virus-host system reveals massive genomic rearrangements in a laboratory strain |
title_full_unstemmed | Characterization of an archaeal virus-host system reveals massive genomic rearrangements in a laboratory strain |
title_short | Characterization of an archaeal virus-host system reveals massive genomic rearrangements in a laboratory strain |
title_sort | characterization of an archaeal virus-host system reveals massive genomic rearrangements in a laboratory strain |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10544981/ https://www.ncbi.nlm.nih.gov/pubmed/37789858 http://dx.doi.org/10.3389/fmicb.2023.1274068 |
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