Cargando…

The Aspergillus fumigatus Secretome Alters the Proteome of Pseudomonas aeruginosa to Stimulate Bacterial Growth: Implications for Co-infection

Individuals with cystic fibrosis are susceptible to co-infection by Aspergillus fumigatus and Pseudomonas aeruginosa. Despite the persistence of A. fumigatus in the cystic fibrosis lung P. aeruginosa eventually predominates as the primary pathogen. Several factors are likely to facilitate P. aerugin...

Descripción completa

Detalles Bibliográficos
Autores principales: Margalit, Anatte, Carolan, James C., Sheehan, David, Kavanagh, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015003/
https://www.ncbi.nlm.nih.gov/pubmed/32447284
http://dx.doi.org/10.1074/mcp.RA120.002059
_version_ 1783673597008543744
author Margalit, Anatte
Carolan, James C.
Sheehan, David
Kavanagh, Kevin
author_facet Margalit, Anatte
Carolan, James C.
Sheehan, David
Kavanagh, Kevin
author_sort Margalit, Anatte
collection PubMed
description Individuals with cystic fibrosis are susceptible to co-infection by Aspergillus fumigatus and Pseudomonas aeruginosa. Despite the persistence of A. fumigatus in the cystic fibrosis lung P. aeruginosa eventually predominates as the primary pathogen. Several factors are likely to facilitate P. aeruginosa colonization in the airways, including alterations to the microbial environment. The cystic fibrosis airways are hypoxic, nitrate-rich environments, and the sputum has higher amino acid concentrations than normal. In this study, significant growth proliferation was observed in P. aeruginosa when the bacteria were exposed to A. fumigatus culture filtrates (CuF) containing a high nitrate content. Proteomic analysis of the A. fumigatus CuF identified a significant number of environment-altering proteases and peptidases. The molecular mechanisms promoting bacterial growth were investigated using label-free quantitative (LFQ) proteomics to compare the proteome of P. aeruginosa grown in the A. fumigatus CuF and in CuF produced by a P. aeruginosa-A. fumigatus co-culture, to that cultured in P. aeruginosa CuF. LFQ proteomics revealed distinct changes in the proteome of P. aeruginosa when cultured in the different CuFs, including increases in the levels of proteins involved in denitrification, stress response, replication, amino acid metabolism and efflux pumps, and a down-regulation of pathways involving ABC transporters. These findings offer novel insights into the complex dynamics that exist between P. aeruginosa and A. fumigatus. Understanding the molecular strategies that enable P. aeruginosa to predominate in an environment where A. fumigatus exists is important in the context of therapeutic development to target this pathogen.
format Online
Article
Text
id pubmed-8015003
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Society for Biochemistry and Molecular Biology
record_format MEDLINE/PubMed
spelling pubmed-80150032021-04-12 The Aspergillus fumigatus Secretome Alters the Proteome of Pseudomonas aeruginosa to Stimulate Bacterial Growth: Implications for Co-infection Margalit, Anatte Carolan, James C. Sheehan, David Kavanagh, Kevin Mol Cell Proteomics Research Individuals with cystic fibrosis are susceptible to co-infection by Aspergillus fumigatus and Pseudomonas aeruginosa. Despite the persistence of A. fumigatus in the cystic fibrosis lung P. aeruginosa eventually predominates as the primary pathogen. Several factors are likely to facilitate P. aeruginosa colonization in the airways, including alterations to the microbial environment. The cystic fibrosis airways are hypoxic, nitrate-rich environments, and the sputum has higher amino acid concentrations than normal. In this study, significant growth proliferation was observed in P. aeruginosa when the bacteria were exposed to A. fumigatus culture filtrates (CuF) containing a high nitrate content. Proteomic analysis of the A. fumigatus CuF identified a significant number of environment-altering proteases and peptidases. The molecular mechanisms promoting bacterial growth were investigated using label-free quantitative (LFQ) proteomics to compare the proteome of P. aeruginosa grown in the A. fumigatus CuF and in CuF produced by a P. aeruginosa-A. fumigatus co-culture, to that cultured in P. aeruginosa CuF. LFQ proteomics revealed distinct changes in the proteome of P. aeruginosa when cultured in the different CuFs, including increases in the levels of proteins involved in denitrification, stress response, replication, amino acid metabolism and efflux pumps, and a down-regulation of pathways involving ABC transporters. These findings offer novel insights into the complex dynamics that exist between P. aeruginosa and A. fumigatus. Understanding the molecular strategies that enable P. aeruginosa to predominate in an environment where A. fumigatus exists is important in the context of therapeutic development to target this pathogen. American Society for Biochemistry and Molecular Biology 2020-11-23 /pmc/articles/PMC8015003/ /pubmed/32447284 http://dx.doi.org/10.1074/mcp.RA120.002059 Text en © 2020 © 2020 Margalit et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research
Margalit, Anatte
Carolan, James C.
Sheehan, David
Kavanagh, Kevin
The Aspergillus fumigatus Secretome Alters the Proteome of Pseudomonas aeruginosa to Stimulate Bacterial Growth: Implications for Co-infection
title The Aspergillus fumigatus Secretome Alters the Proteome of Pseudomonas aeruginosa to Stimulate Bacterial Growth: Implications for Co-infection
title_full The Aspergillus fumigatus Secretome Alters the Proteome of Pseudomonas aeruginosa to Stimulate Bacterial Growth: Implications for Co-infection
title_fullStr The Aspergillus fumigatus Secretome Alters the Proteome of Pseudomonas aeruginosa to Stimulate Bacterial Growth: Implications for Co-infection
title_full_unstemmed The Aspergillus fumigatus Secretome Alters the Proteome of Pseudomonas aeruginosa to Stimulate Bacterial Growth: Implications for Co-infection
title_short The Aspergillus fumigatus Secretome Alters the Proteome of Pseudomonas aeruginosa to Stimulate Bacterial Growth: Implications for Co-infection
title_sort aspergillus fumigatus secretome alters the proteome of pseudomonas aeruginosa to stimulate bacterial growth: implications for co-infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015003/
https://www.ncbi.nlm.nih.gov/pubmed/32447284
http://dx.doi.org/10.1074/mcp.RA120.002059
work_keys_str_mv AT margalitanatte theaspergillusfumigatussecretomealterstheproteomeofpseudomonasaeruginosatostimulatebacterialgrowthimplicationsforcoinfection
AT carolanjamesc theaspergillusfumigatussecretomealterstheproteomeofpseudomonasaeruginosatostimulatebacterialgrowthimplicationsforcoinfection
AT sheehandavid theaspergillusfumigatussecretomealterstheproteomeofpseudomonasaeruginosatostimulatebacterialgrowthimplicationsforcoinfection
AT kavanaghkevin theaspergillusfumigatussecretomealterstheproteomeofpseudomonasaeruginosatostimulatebacterialgrowthimplicationsforcoinfection
AT margalitanatte aspergillusfumigatussecretomealterstheproteomeofpseudomonasaeruginosatostimulatebacterialgrowthimplicationsforcoinfection
AT carolanjamesc aspergillusfumigatussecretomealterstheproteomeofpseudomonasaeruginosatostimulatebacterialgrowthimplicationsforcoinfection
AT sheehandavid aspergillusfumigatussecretomealterstheproteomeofpseudomonasaeruginosatostimulatebacterialgrowthimplicationsforcoinfection
AT kavanaghkevin aspergillusfumigatussecretomealterstheproteomeofpseudomonasaeruginosatostimulatebacterialgrowthimplicationsforcoinfection