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The Salmonella type-3 secretion system-1 and flagellar motility influence the neutrophil respiratory burst

Neutrophils are innate immune response cells designed to kill invading microorganisms. One of the mechanisms neutrophils use to kill bacteria is generation of damaging reactive oxygen species (ROS) via the respiratory burst. However, during enteric salmonellosis, neutrophil-derived ROS actually faci...

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Autores principales: Westerman, Trina L., Bogomolnaya, Lydia, Andrews-Polymenis, Helene L., Sheats, M. Katherine, Elfenbein, Johanna R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133356/
https://www.ncbi.nlm.nih.gov/pubmed/30204776
http://dx.doi.org/10.1371/journal.pone.0203698
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author Westerman, Trina L.
Bogomolnaya, Lydia
Andrews-Polymenis, Helene L.
Sheats, M. Katherine
Elfenbein, Johanna R.
author_facet Westerman, Trina L.
Bogomolnaya, Lydia
Andrews-Polymenis, Helene L.
Sheats, M. Katherine
Elfenbein, Johanna R.
author_sort Westerman, Trina L.
collection PubMed
description Neutrophils are innate immune response cells designed to kill invading microorganisms. One of the mechanisms neutrophils use to kill bacteria is generation of damaging reactive oxygen species (ROS) via the respiratory burst. However, during enteric salmonellosis, neutrophil-derived ROS actually facilitates Salmonella expansion and survival in the gut. This seeming paradox led us to hypothesize that Salmonella may possess mechanisms to influence the neutrophil respiratory burst. In this work, we used an in vitro Salmonella-neutrophil co-culture model to examine the impact of enteric infection relevant virulence factors on the respiratory burst of human neutrophils. We report that neutrophils primed with granulocyte-macrophage colony stimulating factor and suspended in serum containing complement produce a robust respiratory burst when stimulated with viable STm. The magnitude of the respiratory burst increases when STm are grown under conditions to induce the expression of the type-3 secretion system-1. STm mutants lacking the type-3 secretion system-1 induce less neutrophil ROS than the virulent WT. In addition, we demonstrate that flagellar motility is a significant agonist of the neutrophil respiratory burst. Together our data demonstrate that both the type-3 secretion system-1 and flagellar motility, which are established virulence factors in enteric salmonellosis, also appear to directly influence the magnitude of the neutrophil respiratory burst in response to STm in vitro.
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spelling pubmed-61333562018-09-27 The Salmonella type-3 secretion system-1 and flagellar motility influence the neutrophil respiratory burst Westerman, Trina L. Bogomolnaya, Lydia Andrews-Polymenis, Helene L. Sheats, M. Katherine Elfenbein, Johanna R. PLoS One Research Article Neutrophils are innate immune response cells designed to kill invading microorganisms. One of the mechanisms neutrophils use to kill bacteria is generation of damaging reactive oxygen species (ROS) via the respiratory burst. However, during enteric salmonellosis, neutrophil-derived ROS actually facilitates Salmonella expansion and survival in the gut. This seeming paradox led us to hypothesize that Salmonella may possess mechanisms to influence the neutrophil respiratory burst. In this work, we used an in vitro Salmonella-neutrophil co-culture model to examine the impact of enteric infection relevant virulence factors on the respiratory burst of human neutrophils. We report that neutrophils primed with granulocyte-macrophage colony stimulating factor and suspended in serum containing complement produce a robust respiratory burst when stimulated with viable STm. The magnitude of the respiratory burst increases when STm are grown under conditions to induce the expression of the type-3 secretion system-1. STm mutants lacking the type-3 secretion system-1 induce less neutrophil ROS than the virulent WT. In addition, we demonstrate that flagellar motility is a significant agonist of the neutrophil respiratory burst. Together our data demonstrate that both the type-3 secretion system-1 and flagellar motility, which are established virulence factors in enteric salmonellosis, also appear to directly influence the magnitude of the neutrophil respiratory burst in response to STm in vitro. Public Library of Science 2018-09-11 /pmc/articles/PMC6133356/ /pubmed/30204776 http://dx.doi.org/10.1371/journal.pone.0203698 Text en © 2018 Westerman 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Westerman, Trina L.
Bogomolnaya, Lydia
Andrews-Polymenis, Helene L.
Sheats, M. Katherine
Elfenbein, Johanna R.
The Salmonella type-3 secretion system-1 and flagellar motility influence the neutrophil respiratory burst
title The Salmonella type-3 secretion system-1 and flagellar motility influence the neutrophil respiratory burst
title_full The Salmonella type-3 secretion system-1 and flagellar motility influence the neutrophil respiratory burst
title_fullStr The Salmonella type-3 secretion system-1 and flagellar motility influence the neutrophil respiratory burst
title_full_unstemmed The Salmonella type-3 secretion system-1 and flagellar motility influence the neutrophil respiratory burst
title_short The Salmonella type-3 secretion system-1 and flagellar motility influence the neutrophil respiratory burst
title_sort salmonella type-3 secretion system-1 and flagellar motility influence the neutrophil respiratory burst
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133356/
https://www.ncbi.nlm.nih.gov/pubmed/30204776
http://dx.doi.org/10.1371/journal.pone.0203698
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