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Lateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22

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 i...

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Autores principales: Fillol-Salom, Alfred, Bacigalupe, Rodrigo, Humphrey, Suzanne, Chiang, Yin Ning, Chen, John, Penadés, José R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8575938/
https://www.ncbi.nlm.nih.gov/pubmed/34751192
http://dx.doi.org/10.1038/s41467-021-26520-4
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author Fillol-Salom, Alfred
Bacigalupe, Rodrigo
Humphrey, Suzanne
Chiang, Yin Ning
Chen, John
Penadés, José R.
author_facet Fillol-Salom, Alfred
Bacigalupe, Rodrigo
Humphrey, Suzanne
Chiang, Yin Ning
Chen, John
Penadés, José R.
author_sort Fillol-Salom, Alfred
collection PubMed
description 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 tsc(2)29 heat-inducible mutant, and that wild-type P22 actually follows the replication-packaging-excision (RPE) program. We find that P22 tsc(2)29 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.
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spelling pubmed-85759382021-11-19 Lateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22 Fillol-Salom, Alfred Bacigalupe, Rodrigo Humphrey, Suzanne Chiang, Yin Ning Chen, John Penadés, José R. Nat Commun Article 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 tsc(2)29 heat-inducible mutant, and that wild-type P22 actually follows the replication-packaging-excision (RPE) program. We find that P22 tsc(2)29 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. Nature Publishing Group UK 2021-11-08 /pmc/articles/PMC8575938/ /pubmed/34751192 http://dx.doi.org/10.1038/s41467-021-26520-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Fillol-Salom, Alfred
Bacigalupe, Rodrigo
Humphrey, Suzanne
Chiang, Yin Ning
Chen, John
Penadés, José R.
Lateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22
title Lateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22
title_full Lateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22
title_fullStr Lateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22
title_full_unstemmed Lateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22
title_short Lateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22
title_sort lateral transduction is inherent to the life cycle of the archetypical salmonella phage p22
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8575938/
https://www.ncbi.nlm.nih.gov/pubmed/34751192
http://dx.doi.org/10.1038/s41467-021-26520-4
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