Lysogeny in the oceans: Lessons from cultivated model systems and a reanalysis of its prevalence
- PMID: 32935433
- DOI: 10.1111/1462-2920.15233
Lysogeny in the oceans: Lessons from cultivated model systems and a reanalysis of its prevalence
Abstract
In the oceans, viruses that infect bacteria (phages) influence a variety of microbially mediated processes that drive global biogeochemical cycles. The nature of their influence is dependent upon infection mode, be it lytic or lysogenic. Temperate phages are predicted to be prevalent in marine systems where they are expected to execute both types of infection modes. Understanding the range and outcomes of temperate phage-host interactions is fundamental for evaluating their ecological impact. Here, we (i) review phage-mediated rewiring of host metabolism, with a focus on marine systems, (ii) consider the range and nature of temperate phage-host interactions, and (iii) draw on studies of cultivated model systems to examine the consequences of lysogeny among several dominant marine bacterial lineages. We also readdress the prevalence of lysogeny among marine bacteria by probing a collection of 1239 publicly available bacterial genomes, representing cultured and uncultivated strains, for evidence of complete prophages. Our conservative analysis, anticipated to underestimate true prevalence, predicts 18% of the genomes examined contain at least one prophage, the majority (97%) were found within genomes of cultured isolates. These results highlight the need for cultivation of additional model systems to better capture the diversity of temperate phage-host interactions in the oceans.
© 2020 Society for Applied Microbiology and John Wiley & Sons Ltd.
Similar articles
-
Lysogenic host-virus interactions in SAR11 marine bacteria.Nat Microbiol. 2020 Aug;5(8):1011-1015. doi: 10.1038/s41564-020-0725-x. Epub 2020 May 18. Nat Microbiol. 2020. PMID: 32424337 Free PMC article.
-
The Life Cycle Transitions of Temperate Phages: Regulating Factors and Potential Ecological Implications.Viruses. 2022 Aug 28;14(9):1904. doi: 10.3390/v14091904. Viruses. 2022. PMID: 36146712 Free PMC article. Review.
-
Targeting of temperate phages drives loss of type I CRISPR-Cas systems.Nature. 2020 Feb;578(7793):149-153. doi: 10.1038/s41586-020-1936-2. Epub 2020 Jan 22. Nature. 2020. PMID: 31969710 Free PMC article.
-
Prophages in marine bacteria: dangerous molecular time bombs or the key to survival in the seas?ISME J. 2008 Jun;2(6):579-89. doi: 10.1038/ismej.2008.35. ISME J. 2008. PMID: 18521076 Review.
-
Bacteriophage tRNA-dependent lysogeny: requirement of phage-encoded tRNA genes for establishment of lysogeny.mBio. 2024 Feb 14;15(2):e0326023. doi: 10.1128/mbio.03260-23. Epub 2024 Jan 18. mBio. 2024. PMID: 38236026 Free PMC article.
Cited by
-
Ligand cross-feeding resolves bacterial vitamin B12 auxotrophies.Nature. 2024 May;629(8013):886-892. doi: 10.1038/s41586-024-07396-y. Epub 2024 May 8. Nature. 2024. PMID: 38720071
-
Community Structure, Drivers, and Potential Functions of Different Lifestyle Viruses in Chaohu Lake.Viruses. 2024 Apr 11;16(4):590. doi: 10.3390/v16040590. Viruses. 2024. PMID: 38675931 Free PMC article.
-
Prophage enhances the ability of deep-sea bacterium Shewanella psychrophila WP2 to utilize D-amino acid.Microbiol Spectr. 2024 Feb 6;12(2):e0326323. doi: 10.1128/spectrum.03263-23. Epub 2024 Jan 3. Microbiol Spectr. 2024. PMID: 38170979 Free PMC article.
-
A systematic analysis of marine lysogens and proviruses.Nat Commun. 2023 Sep 27;14(1):6013. doi: 10.1038/s41467-023-41699-4. Nat Commun. 2023. PMID: 37758717 Free PMC article.
-
Four Novel Caudoviricetes Bacteriophages Isolated from Baltic Sea Water Infect Colonizers of Aurelia aurita.Viruses. 2023 Jul 9;15(7):1525. doi: 10.3390/v15071525. Viruses. 2023. PMID: 37515211 Free PMC article.
References
-
- Alonso-Sáez, L., and Gasol, J.M. (2007) Seasonal variations in the contributions of different bacterial groups to the uptake of low-molecular-weight compounds in northwestern Mediterranean coastal waters. Appl Environ Microbiol 73: 3528-3535.
-
- Alrasheed, H., Jin, R., and Weitz, J.S. (2019) Caution in inferring viral strategies from abundance correlations in marine metagenomes. Nat Commun 10: 501.
-
- Ankrah, N.Y.D., May, A.L., Middleton, J.L., Jones, D.R., Hadden, M.K., Gooding, J.R., et al. (2014) Phage infection of an environmentally relevant marine bacterium alters host metabolism and lysate composition. ISME J 8: 1089-1100.
-
- Basso, J.T.R., Ankrah, N.Y.D., Tuttle, M.J., Grossman, A.S., Sandaa, R.-A., and Buchan, A. (2020) Genetically similar temperate phages form coalitions with their shared host that lead to niche-specific fitness effects. ISME J 14: 1688-1700.
-
- Beleneva, I.A. (2008) Distribution and characteristics of Bacillus bacteria associated with hydrobionts and the waters of the Peter the Great Bay, sea of Japan. Microbiology 77: 497-503.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources