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Pseudomonas aeruginosa biofilm is a potent inducer of phagocyte hyperinflammation

OBJECTIVE: Pseudomonas aeruginosa effectively facilitate resistance to phagocyte killing by biofilm formation. However, the cross talk between biofilm components and phagocytes is still unclear. We hypothesize that a biofilm provides a concentrated extracellular source of LPS, DNA and exopolysacchar...

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Autores principales: Ciszek-Lenda, Marta, Strus, Magdalena, Walczewska, Maria, Majka, Grzegorz, Machul-Żwirbla, Agnieszka, Mikołajczyk, Diana, Górska, Sabina, Gamian, Andrzej, Chain, Benjamin, Marcinkiewicz, Janusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450861/
https://www.ncbi.nlm.nih.gov/pubmed/30887082
http://dx.doi.org/10.1007/s00011-019-01227-x
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author Ciszek-Lenda, Marta
Strus, Magdalena
Walczewska, Maria
Majka, Grzegorz
Machul-Żwirbla, Agnieszka
Mikołajczyk, Diana
Górska, Sabina
Gamian, Andrzej
Chain, Benjamin
Marcinkiewicz, Janusz
author_facet Ciszek-Lenda, Marta
Strus, Magdalena
Walczewska, Maria
Majka, Grzegorz
Machul-Żwirbla, Agnieszka
Mikołajczyk, Diana
Górska, Sabina
Gamian, Andrzej
Chain, Benjamin
Marcinkiewicz, Janusz
author_sort Ciszek-Lenda, Marta
collection PubMed
description OBJECTIVE: Pseudomonas aeruginosa effectively facilitate resistance to phagocyte killing by biofilm formation. However, the cross talk between biofilm components and phagocytes is still unclear. We hypothesize that a biofilm provides a concentrated extracellular source of LPS, DNA and exopolysaccharides (EPS), which polarize neighbouring phagocytes into an adverse hyperinflammatory state of activation. METHODS: We measured the release of a panel of mediators produced in vitro by murine neutrophils and macrophages exposed to various biofilm components of P. aeruginosa cultures. RESULTS: We found that conditioned media from a high biofilm-producing strain of P. aeruginosa, PAR5, accumulated high concentrations of extracellular bacterial LPS, DNA and EPS by 72 h. These conditioned media induced phagocytes to release a hyperinflammatory pattern of mediators, with enhanced levels of TNF-α, IL-6, IL12p40, PGE(2) and NO. Moreover, the phagocytes also upregulated COX-2 and iNOS with no influence on the expression of arginase-1. CONCLUSIONS: Phagocytes exposed to biofilm microenvironment, called by us biofilm-associated neutrophils/macrophages (BANs/BAMs), display secretory properties similar to that of N1/M1-type phagocytes. These results suggest that in vivo high concentrations of LPS and DNA, trapped in biofilm by EPS, might convert infiltrating phagocytes into cells responsible for tissue injury without direct contact with bacteria and phagocytosis.
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spelling pubmed-64508612019-04-17 Pseudomonas aeruginosa biofilm is a potent inducer of phagocyte hyperinflammation Ciszek-Lenda, Marta Strus, Magdalena Walczewska, Maria Majka, Grzegorz Machul-Żwirbla, Agnieszka Mikołajczyk, Diana Górska, Sabina Gamian, Andrzej Chain, Benjamin Marcinkiewicz, Janusz Inflamm Res Original Research Paper OBJECTIVE: Pseudomonas aeruginosa effectively facilitate resistance to phagocyte killing by biofilm formation. However, the cross talk between biofilm components and phagocytes is still unclear. We hypothesize that a biofilm provides a concentrated extracellular source of LPS, DNA and exopolysaccharides (EPS), which polarize neighbouring phagocytes into an adverse hyperinflammatory state of activation. METHODS: We measured the release of a panel of mediators produced in vitro by murine neutrophils and macrophages exposed to various biofilm components of P. aeruginosa cultures. RESULTS: We found that conditioned media from a high biofilm-producing strain of P. aeruginosa, PAR5, accumulated high concentrations of extracellular bacterial LPS, DNA and EPS by 72 h. These conditioned media induced phagocytes to release a hyperinflammatory pattern of mediators, with enhanced levels of TNF-α, IL-6, IL12p40, PGE(2) and NO. Moreover, the phagocytes also upregulated COX-2 and iNOS with no influence on the expression of arginase-1. CONCLUSIONS: Phagocytes exposed to biofilm microenvironment, called by us biofilm-associated neutrophils/macrophages (BANs/BAMs), display secretory properties similar to that of N1/M1-type phagocytes. These results suggest that in vivo high concentrations of LPS and DNA, trapped in biofilm by EPS, might convert infiltrating phagocytes into cells responsible for tissue injury without direct contact with bacteria and phagocytosis. Springer International Publishing 2019-03-18 2019 /pmc/articles/PMC6450861/ /pubmed/30887082 http://dx.doi.org/10.1007/s00011-019-01227-x Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research Paper
Ciszek-Lenda, Marta
Strus, Magdalena
Walczewska, Maria
Majka, Grzegorz
Machul-Żwirbla, Agnieszka
Mikołajczyk, Diana
Górska, Sabina
Gamian, Andrzej
Chain, Benjamin
Marcinkiewicz, Janusz
Pseudomonas aeruginosa biofilm is a potent inducer of phagocyte hyperinflammation
title Pseudomonas aeruginosa biofilm is a potent inducer of phagocyte hyperinflammation
title_full Pseudomonas aeruginosa biofilm is a potent inducer of phagocyte hyperinflammation
title_fullStr Pseudomonas aeruginosa biofilm is a potent inducer of phagocyte hyperinflammation
title_full_unstemmed Pseudomonas aeruginosa biofilm is a potent inducer of phagocyte hyperinflammation
title_short Pseudomonas aeruginosa biofilm is a potent inducer of phagocyte hyperinflammation
title_sort pseudomonas aeruginosa biofilm is a potent inducer of phagocyte hyperinflammation
topic Original Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450861/
https://www.ncbi.nlm.nih.gov/pubmed/30887082
http://dx.doi.org/10.1007/s00011-019-01227-x
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