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  Characterization of an archaeal virus-host system reveals massive genomic rearrangements in a laboratory strain

Mercier, C., Thies, D., Zhong, L., Raftery, M. J., & Erdmann, S. (2023). Characterization of an archaeal virus-host system reveals massive genomic rearrangements in a laboratory strain. FRONTIERS IN MICROBIOLOGY, 14: 1274068. doi:10.3389/fmicb.2023.1274068.

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Mercier, Coraline1, Author           
Thies, Daniela1, Author           
Zhong, Ling2, Author
Raftery, Mark J.2, Author
Erdmann, Susanne1, Author           
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1Research Group Archaeal Virology, Max Planck Institute for Marine Microbiology, Max Planck Society, ou_3282403              
2external, ou_persistent22              

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Free keywords: DNA-REPLICATION; EVOLUTION; BACTERIA; DEFENSE; PROTEIN; CDC6; BACTERIOPHAGES; DOMAINSMicrobiology; Halorubrum lacusprofundi; secondary chromosome; haloarchaea; archaeal virus; virus defense; genome plasticity;
 Abstract: 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.

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Language(s): eng - English
 Dates: 2023-09-18
 Publication Status: Published online
 Pages: 16
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 Table of Contents: -
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Title: FRONTIERS IN MICROBIOLOGY
Source Genre: Journal
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Publ. Info: AVENUE DU TRIBUNAL FEDERAL 34, LAUSANNE, CH-1015, SWITZERLAND : FRONTIERS MEDIA SA
Pages: - Volume / Issue: 14 Sequence Number: 1274068 Start / End Page: - Identifier: -