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Structural Dynamics of Bacteriophage P22 Virions During the Initiation of Infection

For successful infection, bacteriophages must overcome multiple barriers to transport the genome and proteins across the bacterial cell envelope. We use cryo-electron tomography to study infection initiation of phage P22 in Salmonella enterica sv. Typhimurium, revealing how a channel forms to allow...

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Autores principales: Wang, Chunyan, Tu, Jiagang, Liu, Jun, Molineux, Ian J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533119/
https://www.ncbi.nlm.nih.gov/pubmed/30886360
http://dx.doi.org/10.1038/s41564-019-0403-z
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author Wang, Chunyan
Tu, Jiagang
Liu, Jun
Molineux, Ian J.
author_facet Wang, Chunyan
Tu, Jiagang
Liu, Jun
Molineux, Ian J.
author_sort Wang, Chunyan
collection PubMed
description For successful infection, bacteriophages must overcome multiple barriers to transport the genome and proteins across the bacterial cell envelope. We use cryo-electron tomography to study infection initiation of phage P22 in Salmonella enterica sv. Typhimurium, revealing how a channel forms to allow genome translocation into the cytoplasm. Our results show free phages initially attaching obliquely to the cell through interactions between the O antigen and two of the six tailspikes; the tail needle also abuts the cell surface. The virion then orients to the perpendicular and the needle penetrates the outer membrane. The needle is released and the internal head protein gp7* is ejected and assembles into an extra-cellular channel extending from the gp10 baseplate to the cell surface. A second protein, gp20, is ejected and assembles into a structure that extends the extra-cellular channel across the outer membrane into the periplasm. Insertion of the third ejected protein gp16 into the cytoplasmic membrane likely completes the overall trans-envelope channel into the cytoplasm. Construction of a trans-envelope channel is an essential step during infection by all short-tailed phages of Gram-negative bacteria because such virions cannot directly deliver their genome into the cell cytoplasm.
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spelling pubmed-65331192019-09-18 Structural Dynamics of Bacteriophage P22 Virions During the Initiation of Infection Wang, Chunyan Tu, Jiagang Liu, Jun Molineux, Ian J. Nat Microbiol Article For successful infection, bacteriophages must overcome multiple barriers to transport the genome and proteins across the bacterial cell envelope. We use cryo-electron tomography to study infection initiation of phage P22 in Salmonella enterica sv. Typhimurium, revealing how a channel forms to allow genome translocation into the cytoplasm. Our results show free phages initially attaching obliquely to the cell through interactions between the O antigen and two of the six tailspikes; the tail needle also abuts the cell surface. The virion then orients to the perpendicular and the needle penetrates the outer membrane. The needle is released and the internal head protein gp7* is ejected and assembles into an extra-cellular channel extending from the gp10 baseplate to the cell surface. A second protein, gp20, is ejected and assembles into a structure that extends the extra-cellular channel across the outer membrane into the periplasm. Insertion of the third ejected protein gp16 into the cytoplasmic membrane likely completes the overall trans-envelope channel into the cytoplasm. Construction of a trans-envelope channel is an essential step during infection by all short-tailed phages of Gram-negative bacteria because such virions cannot directly deliver their genome into the cell cytoplasm. 2019-03-18 2019-06 /pmc/articles/PMC6533119/ /pubmed/30886360 http://dx.doi.org/10.1038/s41564-019-0403-z Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Wang, Chunyan
Tu, Jiagang
Liu, Jun
Molineux, Ian J.
Structural Dynamics of Bacteriophage P22 Virions During the Initiation of Infection
title Structural Dynamics of Bacteriophage P22 Virions During the Initiation of Infection
title_full Structural Dynamics of Bacteriophage P22 Virions During the Initiation of Infection
title_fullStr Structural Dynamics of Bacteriophage P22 Virions During the Initiation of Infection
title_full_unstemmed Structural Dynamics of Bacteriophage P22 Virions During the Initiation of Infection
title_short Structural Dynamics of Bacteriophage P22 Virions During the Initiation of Infection
title_sort structural dynamics of bacteriophage p22 virions during the initiation of infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533119/
https://www.ncbi.nlm.nih.gov/pubmed/30886360
http://dx.doi.org/10.1038/s41564-019-0403-z
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