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Polyamines and linear DNA mediate bacterial threat assessment of bacteriophage infection

Monitoring the extracellular environment for danger signals is a critical aspect of cellular survival. However, the danger signals released by dying bacteria and the mechanisms bacteria use for threat assessment remain largely unexplored. Here, we show that lysis of Pseudomonas aeruginosa cells rele...

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Autores principales: de Mattos, Camilla D., Faith, Dominick R., Nemudryi, Artem A., Schmidt, Amelia K., Bublitz, DeAnna C., Hammond, Lauren, Kinnersley, Margie A., Schwartzkopf , Caleb M., Robinson, Autumn J., Joyce, Alex, Michaels, Lia A., Brzozowski, Robert S., Coluccio, Alison, Xing, Denghui David, Uchiyama, Jumpei, Jennings, Laura K., Eswara, Prahathees, Wiedenheft, Blake, Secor, Patrick R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992862/
https://www.ncbi.nlm.nih.gov/pubmed/36802441
http://dx.doi.org/10.1073/pnas.2216430120
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author de Mattos, Camilla D.
Faith, Dominick R.
Nemudryi, Artem A.
Schmidt, Amelia K.
Bublitz, DeAnna C.
Hammond, Lauren
Kinnersley, Margie A.
Schwartzkopf , Caleb M.
Robinson, Autumn J.
Joyce, Alex
Michaels, Lia A.
Brzozowski, Robert S.
Coluccio, Alison
Xing, Denghui David
Uchiyama, Jumpei
Jennings, Laura K.
Eswara, Prahathees
Wiedenheft, Blake
Secor, Patrick R.
author_facet de Mattos, Camilla D.
Faith, Dominick R.
Nemudryi, Artem A.
Schmidt, Amelia K.
Bublitz, DeAnna C.
Hammond, Lauren
Kinnersley, Margie A.
Schwartzkopf , Caleb M.
Robinson, Autumn J.
Joyce, Alex
Michaels, Lia A.
Brzozowski, Robert S.
Coluccio, Alison
Xing, Denghui David
Uchiyama, Jumpei
Jennings, Laura K.
Eswara, Prahathees
Wiedenheft, Blake
Secor, Patrick R.
author_sort de Mattos, Camilla D.
collection PubMed
description Monitoring the extracellular environment for danger signals is a critical aspect of cellular survival. However, the danger signals released by dying bacteria and the mechanisms bacteria use for threat assessment remain largely unexplored. Here, we show that lysis of Pseudomonas aeruginosa cells releases polyamines that are subsequently taken up by surviving cells via a mechanism that relies on Gac/Rsm signaling. While intracellular polyamines spike in surviving cells, the duration of this spike varies according to the infection status of the cell. In bacteriophage-infected cells, intracellular polyamines are maintained at high levels, which inhibits replication of the bacteriophage genome. Many bacteriophages package linear DNA genomes and linear DNA is sufficient to trigger intracellular polyamine accumulation, suggesting that linear DNA is sensed as a second danger signal. Collectively, these results demonstrate how polyamines released by dying cells together with linear DNA allow P. aeruginosa to make threat assessments of cellular injury.
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spelling pubmed-99928622023-08-21 Polyamines and linear DNA mediate bacterial threat assessment of bacteriophage infection de Mattos, Camilla D. Faith, Dominick R. Nemudryi, Artem A. Schmidt, Amelia K. Bublitz, DeAnna C. Hammond, Lauren Kinnersley, Margie A. Schwartzkopf , Caleb M. Robinson, Autumn J. Joyce, Alex Michaels, Lia A. Brzozowski, Robert S. Coluccio, Alison Xing, Denghui David Uchiyama, Jumpei Jennings, Laura K. Eswara, Prahathees Wiedenheft, Blake Secor, Patrick R. Proc Natl Acad Sci U S A Biological Sciences Monitoring the extracellular environment for danger signals is a critical aspect of cellular survival. However, the danger signals released by dying bacteria and the mechanisms bacteria use for threat assessment remain largely unexplored. Here, we show that lysis of Pseudomonas aeruginosa cells releases polyamines that are subsequently taken up by surviving cells via a mechanism that relies on Gac/Rsm signaling. While intracellular polyamines spike in surviving cells, the duration of this spike varies according to the infection status of the cell. In bacteriophage-infected cells, intracellular polyamines are maintained at high levels, which inhibits replication of the bacteriophage genome. Many bacteriophages package linear DNA genomes and linear DNA is sufficient to trigger intracellular polyamine accumulation, suggesting that linear DNA is sensed as a second danger signal. Collectively, these results demonstrate how polyamines released by dying cells together with linear DNA allow P. aeruginosa to make threat assessments of cellular injury. National Academy of Sciences 2023-02-21 2023-02-28 /pmc/articles/PMC9992862/ /pubmed/36802441 http://dx.doi.org/10.1073/pnas.2216430120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
de Mattos, Camilla D.
Faith, Dominick R.
Nemudryi, Artem A.
Schmidt, Amelia K.
Bublitz, DeAnna C.
Hammond, Lauren
Kinnersley, Margie A.
Schwartzkopf , Caleb M.
Robinson, Autumn J.
Joyce, Alex
Michaels, Lia A.
Brzozowski, Robert S.
Coluccio, Alison
Xing, Denghui David
Uchiyama, Jumpei
Jennings, Laura K.
Eswara, Prahathees
Wiedenheft, Blake
Secor, Patrick R.
Polyamines and linear DNA mediate bacterial threat assessment of bacteriophage infection
title Polyamines and linear DNA mediate bacterial threat assessment of bacteriophage infection
title_full Polyamines and linear DNA mediate bacterial threat assessment of bacteriophage infection
title_fullStr Polyamines and linear DNA mediate bacterial threat assessment of bacteriophage infection
title_full_unstemmed Polyamines and linear DNA mediate bacterial threat assessment of bacteriophage infection
title_short Polyamines and linear DNA mediate bacterial threat assessment of bacteriophage infection
title_sort polyamines and linear dna mediate bacterial threat assessment of bacteriophage infection
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992862/
https://www.ncbi.nlm.nih.gov/pubmed/36802441
http://dx.doi.org/10.1073/pnas.2216430120
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