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Endogenous membrane stress induces T6SS activity in Pseudomonas aeruginosa
The type 6 secretion system (T6SS) is a dynamic organelle encoded by many gram-negative bacteria that can be used to kill competing bacterial prey species in densely occupied niches. Some predatory species, such as Vibrio cholerae, use their T6SS in an untargeted fashion while in contrast, Pseudomon...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817224/ https://www.ncbi.nlm.nih.gov/pubmed/33443205 http://dx.doi.org/10.1073/pnas.2018365118 |
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author | Stolle, Anne-Sophie Meader, Bradley Thomas Toska, Jonida Mekalanos, John J. |
author_facet | Stolle, Anne-Sophie Meader, Bradley Thomas Toska, Jonida Mekalanos, John J. |
author_sort | Stolle, Anne-Sophie |
collection | PubMed |
description | The type 6 secretion system (T6SS) is a dynamic organelle encoded by many gram-negative bacteria that can be used to kill competing bacterial prey species in densely occupied niches. Some predatory species, such as Vibrio cholerae, use their T6SS in an untargeted fashion while in contrast, Pseudomonas aeruginosa assembles and fires its T6SS apparatus only after detecting initial attacks by other bacterial prey cells; this targeted attack strategy has been termed the T6SS tit-for-tat response. Molecules that interact with the P. aeruginosa outer membrane such as polymyxin B can also trigger assembly of T6SS organelles via a signal transduction pathway that involves protein phosphorylation. Recent work suggests that a phospholipase T6SS effector (TseL) of V. cholerae can induce T6SS dynamic activity in P. aeruginosa when delivered to or expressed in the periplasmic space of this organism. Here, we report that inhibiting expression of essential genes involved in outer membrane biogenesis can also trigger T6SS activation in P. aeruginosa. Specifically, we developed a CRISPR interference (CRISPRi) system to knock down expression of bamA, tolB, and lptD and found that these knockdowns activated T6SS activity. This increase in T6SS activity was dependent on the same signal transduction pathway that was previously shown to be required for the tit-for-tat response. We conclude that outer membrane perturbation can be sensed by P. aeruginosa to activate the T6SS even when the disruption is generated by aberrant cell envelope biogenesis. |
format | Online Article Text |
id | pubmed-7817224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-78172242021-01-28 Endogenous membrane stress induces T6SS activity in Pseudomonas aeruginosa Stolle, Anne-Sophie Meader, Bradley Thomas Toska, Jonida Mekalanos, John J. Proc Natl Acad Sci U S A Biological Sciences The type 6 secretion system (T6SS) is a dynamic organelle encoded by many gram-negative bacteria that can be used to kill competing bacterial prey species in densely occupied niches. Some predatory species, such as Vibrio cholerae, use their T6SS in an untargeted fashion while in contrast, Pseudomonas aeruginosa assembles and fires its T6SS apparatus only after detecting initial attacks by other bacterial prey cells; this targeted attack strategy has been termed the T6SS tit-for-tat response. Molecules that interact with the P. aeruginosa outer membrane such as polymyxin B can also trigger assembly of T6SS organelles via a signal transduction pathway that involves protein phosphorylation. Recent work suggests that a phospholipase T6SS effector (TseL) of V. cholerae can induce T6SS dynamic activity in P. aeruginosa when delivered to or expressed in the periplasmic space of this organism. Here, we report that inhibiting expression of essential genes involved in outer membrane biogenesis can also trigger T6SS activation in P. aeruginosa. Specifically, we developed a CRISPR interference (CRISPRi) system to knock down expression of bamA, tolB, and lptD and found that these knockdowns activated T6SS activity. This increase in T6SS activity was dependent on the same signal transduction pathway that was previously shown to be required for the tit-for-tat response. We conclude that outer membrane perturbation can be sensed by P. aeruginosa to activate the T6SS even when the disruption is generated by aberrant cell envelope biogenesis. National Academy of Sciences 2021-01-05 2020-12-28 /pmc/articles/PMC7817224/ /pubmed/33443205 http://dx.doi.org/10.1073/pnas.2018365118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access 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 Stolle, Anne-Sophie Meader, Bradley Thomas Toska, Jonida Mekalanos, John J. Endogenous membrane stress induces T6SS activity in Pseudomonas aeruginosa |
title | Endogenous membrane stress induces T6SS activity in Pseudomonas aeruginosa |
title_full | Endogenous membrane stress induces T6SS activity in Pseudomonas aeruginosa |
title_fullStr | Endogenous membrane stress induces T6SS activity in Pseudomonas aeruginosa |
title_full_unstemmed | Endogenous membrane stress induces T6SS activity in Pseudomonas aeruginosa |
title_short | Endogenous membrane stress induces T6SS activity in Pseudomonas aeruginosa |
title_sort | endogenous membrane stress induces t6ss activity in pseudomonas aeruginosa |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817224/ https://www.ncbi.nlm.nih.gov/pubmed/33443205 http://dx.doi.org/10.1073/pnas.2018365118 |
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