English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

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

MPS-Authors
/persons/resource/persons295852

Mercier,  Coraline
Research Group Archaeal Virology, Max Planck Institute for Marine Microbiology, Max Planck Society;

/persons/resource/persons256590

Thies,  Daniela
Research Group Archaeal Virology, Max Planck Institute for Marine Microbiology, Max Planck Society;

/persons/resource/persons276362

Erdmann,  Susanne
Research Group Archaeal Virology, Max Planck Institute for Marine Microbiology, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

fmicb-14-1274068.pdf
(Publisher version), 3MB

Supplementary Material (public)
There is no public supplementary material available
Citation

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.


Cite as: https://hdl.handle.net/21.11116/0000-000E-5EB0-2
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.