A novel uncultured marine cyanophage lineage with lysogenic potential linked to a putative marine Synechococcus 'relic' prophage
Abstract
Marine cyanobacteria are important contributors to primary production in the ocean and their viruses (cyanophages) affect the ocean microbial communities. Despite reports of lysogeny in marine cyanobacteria, a genome sequence of such temperate cyanophages remains unknown although genomic analysis indicate potential for lysogeny in certain marine cyanophages. Using assemblies from Red Sea and Tara Oceans metagenomes, we recovered genomes of a novel uncultured marine cyanophage lineage, which contain, in addition to common cyanophage genes, a phycobilisome degradation protein NblA, an integrase and a split DNA polymerase. The DNA polymerase forms a monophyletic clade with a DNA polymerase from a genomic island in Synechococcus WH8016. The island contains a relic prophage that does not resemble any previously reported cyanophage but shares several genes with the newly identified cyanophages reported here. Metagenomic recruitment indicates that the novel cyanophages are widespread, albeit at low abundance. Here, we describe a novel potentially lysogenic cyanophage family, their abundance and distribution in the marine environment.
Additional Information
© 2019 Wiley-Blackwell. Issue Online: 02 July 2019; Version of Record online: 17 June 2019; Accepted manuscript online: 24 May 2019; Manuscript accepted: 23 May 2019; Manuscript received: 21 October 2018. Author Contributions: J.F.-U. and O.B conceived the project. J.F.-U., A.P., I.S., and O.B. performed bioinformatic analyses. J.F.-U., S.F. and S.L. performed mitomycin C experiments. J.F.-U. and O.B. wrote the manuscript with contributions from all authors to data analysis, figure generation, and the final manuscript. We thank Laurence Garczarek for sharing unpublished data for Synechococcus WH8016, and Curtis Suttle and Caroline Chénard for sharing DNA polymerase sequences. This work was funded by a European Commission (ERC Advanced Grant no. 321647), and the Louis and Lyra Richmond Memorial Chair in Life Sciences (to O.B.). The authors declare no conflict of interest.Attached Files
Accepted Version - 1758-2229.12773.pdf
Submitted - 325100.full.pdf
Supplemental Material - emi412773-sup-0001-supinfo01.txt
Supplemental Material - emi412773-sup-0002-supinfo02.xls
Supplemental Material - emi412773-sup-0003-supinfo03.txt
Supplemental Material - emi412773-sup-0004-supinfo04.txt
Supplemental Material - emi412773-sup-0005-supinfo05.xls
Supplemental Material - emi412773-sup-0006-supinfo06.pdf
Supplemental Material - emi412773-sup-0007-supinfo07.xls
Supplemental Material - emi412773-sup-0008-supinfo08.xlsx
Supplemental Material - emi412773-sup-0009-supinfo09.txt
Supplemental Material - emi412773-sup-0010-supinfo10.txt
Supplemental Material - emi412773-sup-0011-supinfo11.txt
Supplemental Material - emi412773-sup-0012-supinfo12.docx
Supplemental Material - emi412773-sup-0013-figures1.eps
Supplemental Material - emi412773-sup-0014-figures2.eps
Supplemental Material - emi412773-sup-0015-figures3.pdf
Supplemental Material - emi412773-sup-0016-figures4.pdf
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Additional details
- Eprint ID
- 95017
- Resolver ID
- CaltechAUTHORS:20190426-093153891
- European Research Council (ERC)
- 321647
- Louis and Lyra Richmond Memorial Chair
- Created
-
2019-04-26Created from EPrint's datestamp field
- Updated
-
2023-06-01Created from EPrint's last_modified field