Lateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22
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Accepted version
Author(s)
Type
Journal Article
Abstract
Lysogenic 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 wildtype 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 selfpreservation.
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 wildtype 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 selfpreservation.
Date Issued
2021-11-08
Date Acceptance
2021-10-01
Citation
Nature Communications, 2021, 12 (6510), pp.1-11
ISSN
2041-1723
Publisher
Nature Research
Start Page
1
End Page
11
Journal / Book Title
Nature Communications
Volume
12
Issue
6510
Copyright Statement
© The Author(s) 2021. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
License URL
Sponsor
Biotechnology and Biological Sciences Research Council (BBSRC)
Medical Research Council (MRC)
Identifier
https://www.nature.com/articles/s41467-021-26520-4
Grant Number
BB/V002376/1
MR/S00940X/2
Subjects
Science & Technology
Multidisciplinary Sciences
Science & Technology - Other Topics
SOS REGULATORY SYSTEM
GENE-EXPRESSION
DNA
LAMBDA
CHROMOSOME
CLEAVAGE
SEQUENCE
IDENTIFICATION
INACTIVATION
REPLICATION
Publication Status
Published
Date Publish Online
2021-11-08