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Pervasive Prophage Recombination Occurs During Evolution of Spore-forming Bacilli

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Journal ISME J
Date 2020 Dec 21
PMID 33343000
Citations 19
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Abstract

Phages are the main source of within-species bacterial diversity and drivers of horizontal gene transfer, but we know little about the mechanisms that drive genetic diversity of these mobile genetic elements (MGEs). Recently, we showed that a sporulation selection regime promotes evolutionary changes within SPβ prophage of Bacillus subtilis, leading to direct antagonistic interactions within the population. Herein, we reveal that under a sporulation selection regime, SPβ recombines with low copy number phi3Ts phage DNA present within the B. subtilis population. Recombination results in a new prophage occupying a different integration site, as well as the spontaneous release of virulent phage hybrids. Analysis of Bacillus sp. strains suggests that SPβ and phi3T belong to a distinct cluster of unusually large phages inserted into sporulation-related genes that are equipped with a spore-related genetic arsenal. Comparison of Bacillus sp. genomes indicates that similar diversification of SPβ-like phages takes place in nature. Our work is a stepping stone toward empirical studies on phage evolution, and understanding the eco-evolutionary relationships between bacteria and their phages. By capturing the first steps of new phage evolution, we reveal striking relationship between survival strategy of bacteria and evolution of their phages.

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References
1.
Knowles B, Silveira C, Bailey B, Barott K, Cantu V, Cobian-Guemes A . Lytic to temperate switching of viral communities. Nature. 2016; 531(7595):466-70. DOI: 10.1038/nature17193. View

2.
Koskella B, Brockhurst M . Bacteria-phage coevolution as a driver of ecological and evolutionary processes in microbial communities. FEMS Microbiol Rev. 2014; 38(5):916-31. PMC: 4257071. DOI: 10.1111/1574-6976.12072. View

3.
Azam A, Tanji Y . Bacteriophage-host arm race: an update on the mechanism of phage resistance in bacteria and revenge of the phage with the perspective for phage therapy. Appl Microbiol Biotechnol. 2019; 103(5):2121-2131. DOI: 10.1007/s00253-019-09629-x. View

4.
Howard-Varona C, Hargreaves K, Abedon S, Sullivan M . Lysogeny in nature: mechanisms, impact and ecology of temperate phages. ISME J. 2017; 11(7):1511-1520. PMC: 5520141. DOI: 10.1038/ismej.2017.16. View

5.
Kim M, Bae J . Lysogeny is prevalent and widely distributed in the murine gut microbiota. ISME J. 2018; 12(4):1127-1141. PMC: 5864201. DOI: 10.1038/s41396-018-0061-9. View