Cargando…

Review of Potential Pseudomonas Weaponry, Relevant to the Pseudomonas–Aspergillus Interplay, for the Mycology Community

Pseudomonas aeruginosa is one of the most prominent opportunistic bacteria in airways of cystic fibrosis patients and in immunocompromised patients. These bacteria share the same polymicrobial niche with other microbes, such as the opportunistic fungus Aspergillus fumigatus. Their inter-kingdom inte...

Descripción completa

Detalles Bibliográficos
Autores principales: Chatterjee, Paulami, Sass, Gabriele, Swietnicki, Wieslaw, Stevens, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345761/
https://www.ncbi.nlm.nih.gov/pubmed/32517271
http://dx.doi.org/10.3390/jof6020081
_version_ 1783556259173105664
author Chatterjee, Paulami
Sass, Gabriele
Swietnicki, Wieslaw
Stevens, David A.
author_facet Chatterjee, Paulami
Sass, Gabriele
Swietnicki, Wieslaw
Stevens, David A.
author_sort Chatterjee, Paulami
collection PubMed
description Pseudomonas aeruginosa is one of the most prominent opportunistic bacteria in airways of cystic fibrosis patients and in immunocompromised patients. These bacteria share the same polymicrobial niche with other microbes, such as the opportunistic fungus Aspergillus fumigatus. Their inter-kingdom interactions and diverse exchange of secreted metabolites are responsible for how they both fare in competition for ecological niches. The outcomes of their contests likely determine persistent damage and degeneration of lung function. With a myriad of virulence factors and metabolites of promising antifungal activity, P. aeruginosa products or their derivatives may prove useful in prophylaxis and therapy against A. fumigatus. Quorum sensing underlies the primary virulence strategy of P. aeruginosa, which serves as cell–cell communication and ultimately leads to the production of multiple virulence factors. Understanding the quorum-sensing-related pathogenic mechanisms of P. aeruginosa is a first step for understanding intermicrobial competition. In this review, we provide a basic overview of some of the central virulence factors of P. aeruginosa that are regulated by quorum-sensing response pathways and briefly discuss the hitherto known antifungal properties of these virulence factors. This review also addresses the role of the bacterial secretion machinery regarding virulence factor secretion and maintenance of cell–cell communication.
format Online
Article
Text
id pubmed-7345761
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-73457612020-07-09 Review of Potential Pseudomonas Weaponry, Relevant to the Pseudomonas–Aspergillus Interplay, for the Mycology Community Chatterjee, Paulami Sass, Gabriele Swietnicki, Wieslaw Stevens, David A. J Fungi (Basel) Review Pseudomonas aeruginosa is one of the most prominent opportunistic bacteria in airways of cystic fibrosis patients and in immunocompromised patients. These bacteria share the same polymicrobial niche with other microbes, such as the opportunistic fungus Aspergillus fumigatus. Their inter-kingdom interactions and diverse exchange of secreted metabolites are responsible for how they both fare in competition for ecological niches. The outcomes of their contests likely determine persistent damage and degeneration of lung function. With a myriad of virulence factors and metabolites of promising antifungal activity, P. aeruginosa products or their derivatives may prove useful in prophylaxis and therapy against A. fumigatus. Quorum sensing underlies the primary virulence strategy of P. aeruginosa, which serves as cell–cell communication and ultimately leads to the production of multiple virulence factors. Understanding the quorum-sensing-related pathogenic mechanisms of P. aeruginosa is a first step for understanding intermicrobial competition. In this review, we provide a basic overview of some of the central virulence factors of P. aeruginosa that are regulated by quorum-sensing response pathways and briefly discuss the hitherto known antifungal properties of these virulence factors. This review also addresses the role of the bacterial secretion machinery regarding virulence factor secretion and maintenance of cell–cell communication. MDPI 2020-06-06 /pmc/articles/PMC7345761/ /pubmed/32517271 http://dx.doi.org/10.3390/jof6020081 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Chatterjee, Paulami
Sass, Gabriele
Swietnicki, Wieslaw
Stevens, David A.
Review of Potential Pseudomonas Weaponry, Relevant to the Pseudomonas–Aspergillus Interplay, for the Mycology Community
title Review of Potential Pseudomonas Weaponry, Relevant to the Pseudomonas–Aspergillus Interplay, for the Mycology Community
title_full Review of Potential Pseudomonas Weaponry, Relevant to the Pseudomonas–Aspergillus Interplay, for the Mycology Community
title_fullStr Review of Potential Pseudomonas Weaponry, Relevant to the Pseudomonas–Aspergillus Interplay, for the Mycology Community
title_full_unstemmed Review of Potential Pseudomonas Weaponry, Relevant to the Pseudomonas–Aspergillus Interplay, for the Mycology Community
title_short Review of Potential Pseudomonas Weaponry, Relevant to the Pseudomonas–Aspergillus Interplay, for the Mycology Community
title_sort review of potential pseudomonas weaponry, relevant to the pseudomonas–aspergillus interplay, for the mycology community
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345761/
https://www.ncbi.nlm.nih.gov/pubmed/32517271
http://dx.doi.org/10.3390/jof6020081
work_keys_str_mv AT chatterjeepaulami reviewofpotentialpseudomonasweaponryrelevanttothepseudomonasaspergillusinterplayforthemycologycommunity
AT sassgabriele reviewofpotentialpseudomonasweaponryrelevanttothepseudomonasaspergillusinterplayforthemycologycommunity
AT swietnickiwieslaw reviewofpotentialpseudomonasweaponryrelevanttothepseudomonasaspergillusinterplayforthemycologycommunity
AT stevensdavida reviewofpotentialpseudomonasweaponryrelevanttothepseudomonasaspergillusinterplayforthemycologycommunity