Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-021-26520-4
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dc.titleLateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22
dc.contributor.authorFillol-Salom, Alfred
dc.contributor.authorBacigalupe, Rodrigo
dc.contributor.authorHumphrey, Suzanne
dc.contributor.authorChiang, Yin Ning
dc.contributor.authorChen, John
dc.contributor.authorPenadés, José R.
dc.date.accessioned2022-10-13T06:42:39Z
dc.date.available2022-10-13T06:42:39Z
dc.date.issued2021-11-08
dc.identifier.citationFillol-Salom, Alfred, Bacigalupe, Rodrigo, Humphrey, Suzanne, Chiang, Yin Ning, Chen, John, Penadés, José R. (2021-11-08). Lateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22. Nature Communications 12 (1) : 6510. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-021-26520-4
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/233019
dc.description.abstractLysogenic induction ends the stable association between a bacteriophage and its host, and the transition to the lytic cycle begins with early prophage excision followed by DNA replication and packaging (ERP). This temporal program is considered universal for P22-like temperate phages, though there is no direct evidence to support the timing and sequence of these events. Here we report that the long-standing ERP program is an observation of the experimentally favored Salmonella phage P22 tsc229 heat-inducible mutant, and that wild-type P22 actually follows the replication-packaging-excision (RPE) program. We find that P22 tsc229 excises early after induction, but P22 delays excision to just before it is detrimental to phage production. This allows P22 to engage in lateral transduction. Thus, at minimal expense to itself, P22 has tuned the timing of excision to balance propagation with lateral transduction, powering the evolution of its host through gene transfer in the interest of self-preservation. © 2021, The Author(s).
dc.publisherNature Research
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.typeArticle
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.description.doi10.1038/s41467-021-26520-4
dc.description.sourcetitleNature Communications
dc.description.volume12
dc.description.issue1
dc.description.page6510
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