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Bacteriophage Crosstalk: Coordination of Prophage Induction by Trans-Acting Antirepressors

Many species of bacteria harbor multiple prophages in their genomes. Prophages often carry genes that confer a selective advantage to the bacterium, typically during host colonization. Prophages can convert to infectious viruses through a process known as induction, which is relevant to the spread o...

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Autores principales: Lemire, Sébastien, Figueroa-Bossi, Nara, Bossi, Lionello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121763/
https://www.ncbi.nlm.nih.gov/pubmed/21731505
http://dx.doi.org/10.1371/journal.pgen.1002149
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author Lemire, Sébastien
Figueroa-Bossi, Nara
Bossi, Lionello
author_facet Lemire, Sébastien
Figueroa-Bossi, Nara
Bossi, Lionello
author_sort Lemire, Sébastien
collection PubMed
description Many species of bacteria harbor multiple prophages in their genomes. Prophages often carry genes that confer a selective advantage to the bacterium, typically during host colonization. Prophages can convert to infectious viruses through a process known as induction, which is relevant to the spread of bacterial virulence genes. The paradigm of prophage induction, as set by the phage Lambda model, sees the process initiated by the RecA-stimulated self-proteolysis of the phage repressor. Here we show that a large family of lambdoid prophages found in Salmonella genomes employs an alternative induction strategy. The repressors of these phages are not cleaved upon induction; rather, they are inactivated by the binding of small antirepressor proteins. Formation of the complex causes the repressor to dissociate from DNA. The antirepressor genes lie outside the immunity region and are under direct control of the LexA repressor, thus plugging prophage induction directly into the SOS response. GfoA and GfhA, the antirepressors of Salmonella prophages Gifsy-1 and Gifsy-3, each target both of these phages' repressors, GfoR and GfhR, even though the latter proteins recognize different operator sites and the two phages are heteroimmune. In contrast, the Gifsy-2 phage repressor, GtgR, is insensitive to GfoA and GfhA, but is inactivated by an antirepressor from the unrelated Fels-1 prophage (FsoA). This response is all the more surprising as FsoA is under the control of the Fels-1 repressor, not LexA, and plays no apparent role in Fels-1 induction, which occurs via a Lambda CI-like repressor cleavage mechanism. The ability of antirepressors to recognize non-cognate repressors allows coordination of induction of multiple prophages in polylysogenic strains. Identification of non-cleavable gfoR/gtgR homologues in a large variety of bacterial genomes (including most Escherichia coli genomes in the DNA database) suggests that antirepression-mediated induction is far more common than previously recognized.
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spelling pubmed-31217632011-06-30 Bacteriophage Crosstalk: Coordination of Prophage Induction by Trans-Acting Antirepressors Lemire, Sébastien Figueroa-Bossi, Nara Bossi, Lionello PLoS Genet Research Article Many species of bacteria harbor multiple prophages in their genomes. Prophages often carry genes that confer a selective advantage to the bacterium, typically during host colonization. Prophages can convert to infectious viruses through a process known as induction, which is relevant to the spread of bacterial virulence genes. The paradigm of prophage induction, as set by the phage Lambda model, sees the process initiated by the RecA-stimulated self-proteolysis of the phage repressor. Here we show that a large family of lambdoid prophages found in Salmonella genomes employs an alternative induction strategy. The repressors of these phages are not cleaved upon induction; rather, they are inactivated by the binding of small antirepressor proteins. Formation of the complex causes the repressor to dissociate from DNA. The antirepressor genes lie outside the immunity region and are under direct control of the LexA repressor, thus plugging prophage induction directly into the SOS response. GfoA and GfhA, the antirepressors of Salmonella prophages Gifsy-1 and Gifsy-3, each target both of these phages' repressors, GfoR and GfhR, even though the latter proteins recognize different operator sites and the two phages are heteroimmune. In contrast, the Gifsy-2 phage repressor, GtgR, is insensitive to GfoA and GfhA, but is inactivated by an antirepressor from the unrelated Fels-1 prophage (FsoA). This response is all the more surprising as FsoA is under the control of the Fels-1 repressor, not LexA, and plays no apparent role in Fels-1 induction, which occurs via a Lambda CI-like repressor cleavage mechanism. The ability of antirepressors to recognize non-cognate repressors allows coordination of induction of multiple prophages in polylysogenic strains. Identification of non-cleavable gfoR/gtgR homologues in a large variety of bacterial genomes (including most Escherichia coli genomes in the DNA database) suggests that antirepression-mediated induction is far more common than previously recognized. Public Library of Science 2011-06-23 /pmc/articles/PMC3121763/ /pubmed/21731505 http://dx.doi.org/10.1371/journal.pgen.1002149 Text en Lemire et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lemire, Sébastien
Figueroa-Bossi, Nara
Bossi, Lionello
Bacteriophage Crosstalk: Coordination of Prophage Induction by Trans-Acting Antirepressors
title Bacteriophage Crosstalk: Coordination of Prophage Induction by Trans-Acting Antirepressors
title_full Bacteriophage Crosstalk: Coordination of Prophage Induction by Trans-Acting Antirepressors
title_fullStr Bacteriophage Crosstalk: Coordination of Prophage Induction by Trans-Acting Antirepressors
title_full_unstemmed Bacteriophage Crosstalk: Coordination of Prophage Induction by Trans-Acting Antirepressors
title_short Bacteriophage Crosstalk: Coordination of Prophage Induction by Trans-Acting Antirepressors
title_sort bacteriophage crosstalk: coordination of prophage induction by trans-acting antirepressors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121763/
https://www.ncbi.nlm.nih.gov/pubmed/21731505
http://dx.doi.org/10.1371/journal.pgen.1002149
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