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Bacteriophage P22 SieA mediated superinfection exclusion

Many temperate phages encode prophage-expressed functions that interfere with superinfection of the host bacterium by external phages. Salmonella phage P22 has four such systems that are expressed from the prophage in a lysogen that are encoded by the c2 (repressor), gtrABC, sieA, and sieB genes. He...

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Autores principales: Leavitt, Justin C., Woodbury, Brianna M., Gilcrease, Eddie B., Bridges, Charles M., Teschke, Carolyn M., Casjens, Sherwood R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461980/
https://www.ncbi.nlm.nih.gov/pubmed/37645741
http://dx.doi.org/10.1101/2023.08.15.553423
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author Leavitt, Justin C.
Woodbury, Brianna M.
Gilcrease, Eddie B.
Bridges, Charles M.
Teschke, Carolyn M.
Casjens, Sherwood R.
author_facet Leavitt, Justin C.
Woodbury, Brianna M.
Gilcrease, Eddie B.
Bridges, Charles M.
Teschke, Carolyn M.
Casjens, Sherwood R.
author_sort Leavitt, Justin C.
collection PubMed
description Many temperate phages encode prophage-expressed functions that interfere with superinfection of the host bacterium by external phages. Salmonella phage P22 has four such systems that are expressed from the prophage in a lysogen that are encoded by the c2 (repressor), gtrABC, sieA, and sieB genes. Here we report that the P22-encoded SieA protein is the only phage protein required for exclusion by the SieA system, and that it is an inner membrane protein that blocks DNA injection by P22 and its relatives, but has no effect on infection by other tailed phage types. The P22 virion injects its DNA through the host cell membranes and periplasm via a conduit assembled from three “ejection proteins” after their release from the virion. Phage P22 mutants were isolated that overcome the SieA block, and they have amino acid changes in the C-terminal regions of the gene 16 and 20 encoded ejection proteins. Three different single amino acid changes in these proteins are required to obtain nearly full resistance to SieA. Hybrid P22 phages that have phage HK620 ejection protein genes are also partially resistant to SieA. There are three sequence types of extant phage-encoded SieA proteins that are less than 30% identical to one another, yet comparison of two of these types found no differences in target specificity. Our data are consistent with a model in which the inner membrane protein SieA interferes with the assembly or function of the periplasmic gp20 and membrane-bound gp16 DNA delivery conduit.
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spelling pubmed-104619802023-08-29 Bacteriophage P22 SieA mediated superinfection exclusion Leavitt, Justin C. Woodbury, Brianna M. Gilcrease, Eddie B. Bridges, Charles M. Teschke, Carolyn M. Casjens, Sherwood R. bioRxiv Article Many temperate phages encode prophage-expressed functions that interfere with superinfection of the host bacterium by external phages. Salmonella phage P22 has four such systems that are expressed from the prophage in a lysogen that are encoded by the c2 (repressor), gtrABC, sieA, and sieB genes. Here we report that the P22-encoded SieA protein is the only phage protein required for exclusion by the SieA system, and that it is an inner membrane protein that blocks DNA injection by P22 and its relatives, but has no effect on infection by other tailed phage types. The P22 virion injects its DNA through the host cell membranes and periplasm via a conduit assembled from three “ejection proteins” after their release from the virion. Phage P22 mutants were isolated that overcome the SieA block, and they have amino acid changes in the C-terminal regions of the gene 16 and 20 encoded ejection proteins. Three different single amino acid changes in these proteins are required to obtain nearly full resistance to SieA. Hybrid P22 phages that have phage HK620 ejection protein genes are also partially resistant to SieA. There are three sequence types of extant phage-encoded SieA proteins that are less than 30% identical to one another, yet comparison of two of these types found no differences in target specificity. Our data are consistent with a model in which the inner membrane protein SieA interferes with the assembly or function of the periplasmic gp20 and membrane-bound gp16 DNA delivery conduit. Cold Spring Harbor Laboratory 2023-08-16 /pmc/articles/PMC10461980/ /pubmed/37645741 http://dx.doi.org/10.1101/2023.08.15.553423 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Leavitt, Justin C.
Woodbury, Brianna M.
Gilcrease, Eddie B.
Bridges, Charles M.
Teschke, Carolyn M.
Casjens, Sherwood R.
Bacteriophage P22 SieA mediated superinfection exclusion
title Bacteriophage P22 SieA mediated superinfection exclusion
title_full Bacteriophage P22 SieA mediated superinfection exclusion
title_fullStr Bacteriophage P22 SieA mediated superinfection exclusion
title_full_unstemmed Bacteriophage P22 SieA mediated superinfection exclusion
title_short Bacteriophage P22 SieA mediated superinfection exclusion
title_sort bacteriophage p22 siea mediated superinfection exclusion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461980/
https://www.ncbi.nlm.nih.gov/pubmed/37645741
http://dx.doi.org/10.1101/2023.08.15.553423
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