Exposure of <i>Aspergillus fumigatus</i> to <i>Klebsiella pneumoniae</i> Culture Filtrate Inhibits Growth and Stimulates Gliotoxin Production

<i>Aspergillus fumigatus</i> is an opportunistic fungal pathogen capable of inducing chronic and acute infection in susceptible patients. <i>A. fumigatus</i> interacts with numerous bacteria that compose the microbiota of the lung, including <i>Pseudomonas aeruginosa<...

Full description

Bibliographic Details
Main Authors: Aaron Curtis, Michelle Ryan, Kevin Kavanagh
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Journal of Fungi
Subjects:
Online Access:https://www.mdpi.com/2309-608X/9/2/222
_version_ 1797620005922144256
author Aaron Curtis
Michelle Ryan
Kevin Kavanagh
author_facet Aaron Curtis
Michelle Ryan
Kevin Kavanagh
author_sort Aaron Curtis
collection DOAJ
description <i>Aspergillus fumigatus</i> is an opportunistic fungal pathogen capable of inducing chronic and acute infection in susceptible patients. <i>A. fumigatus</i> interacts with numerous bacteria that compose the microbiota of the lung, including <i>Pseudomonas aeruginosa</i> and <i>Klebsiella pneumoniae</i>, both of which are common isolates from cystic fibrosis sputum. Exposure of <i>A. fumigatus</i> to <i>K. pneumoniae</i> culture filtrate reduced fungal growth and increased gliotoxin production. Qualitative proteomic analysis of the <i>K. pneumoniae</i> culture filtrate identified proteins associated with metal sequestering, enzymatic degradation and redox activity, which may impact fungal growth and development. Quantitative proteomic analysis of <i>A. fumigatus</i> following exposure to <i>K. pneumoniae</i> culture filtrate (25% <i>v</i>/<i>v</i>) for 24 h revealed a reduced abundance of 1,3-beta-glucanosyltransferase (−3.97 fold), methyl sterol monooxygenase erg25B (−2.9 fold) and calcium/calmodulin-dependent protein kinase (−4.2 fold) involved in fungal development, and increased abundance of glutathione S-transferase GliG (+6.17 fold), non-ribosomal peptide synthase GliP (+3.67 fold), O-methyltransferase GliM (+3.5 fold), gamma-glutamyl acyltransferase GliK (+2.89 fold) and thioredoxin reductase GliT (+2.33 fold) involved in gliotoxin production. These results reveal that exposure of <i>A. fumigatus</i> to <i>K. pneumoniae</i> in vivo could exacerbate infection and negatively impact patient prognosis.
first_indexed 2024-03-11T08:36:07Z
format Article
id doaj.art-d15c7dc5aa5d49cbbba39ce7cc739764
institution Directory Open Access Journal
issn 2309-608X
language English
last_indexed 2024-03-11T08:36:07Z
publishDate 2023-02-01
publisher MDPI AG
record_format Article
series Journal of Fungi
spelling doaj.art-d15c7dc5aa5d49cbbba39ce7cc7397642023-11-16T21:30:46ZengMDPI AGJournal of Fungi2309-608X2023-02-019222210.3390/jof9020222Exposure of <i>Aspergillus fumigatus</i> to <i>Klebsiella pneumoniae</i> Culture Filtrate Inhibits Growth and Stimulates Gliotoxin ProductionAaron Curtis0Michelle Ryan1Kevin Kavanagh2Medical Mycology Unit, Department of Biology, Maynooth University, W23 F2H6 Co. Kildare, IrelandMedical Mycology Unit, Department of Biology, Maynooth University, W23 F2H6 Co. Kildare, IrelandMedical Mycology Unit, Department of Biology, Maynooth University, W23 F2H6 Co. Kildare, Ireland<i>Aspergillus fumigatus</i> is an opportunistic fungal pathogen capable of inducing chronic and acute infection in susceptible patients. <i>A. fumigatus</i> interacts with numerous bacteria that compose the microbiota of the lung, including <i>Pseudomonas aeruginosa</i> and <i>Klebsiella pneumoniae</i>, both of which are common isolates from cystic fibrosis sputum. Exposure of <i>A. fumigatus</i> to <i>K. pneumoniae</i> culture filtrate reduced fungal growth and increased gliotoxin production. Qualitative proteomic analysis of the <i>K. pneumoniae</i> culture filtrate identified proteins associated with metal sequestering, enzymatic degradation and redox activity, which may impact fungal growth and development. Quantitative proteomic analysis of <i>A. fumigatus</i> following exposure to <i>K. pneumoniae</i> culture filtrate (25% <i>v</i>/<i>v</i>) for 24 h revealed a reduced abundance of 1,3-beta-glucanosyltransferase (−3.97 fold), methyl sterol monooxygenase erg25B (−2.9 fold) and calcium/calmodulin-dependent protein kinase (−4.2 fold) involved in fungal development, and increased abundance of glutathione S-transferase GliG (+6.17 fold), non-ribosomal peptide synthase GliP (+3.67 fold), O-methyltransferase GliM (+3.5 fold), gamma-glutamyl acyltransferase GliK (+2.89 fold) and thioredoxin reductase GliT (+2.33 fold) involved in gliotoxin production. These results reveal that exposure of <i>A. fumigatus</i> to <i>K. pneumoniae</i> in vivo could exacerbate infection and negatively impact patient prognosis.https://www.mdpi.com/2309-608X/9/2/222<i>Aspergillus fumigatus</i><i>Klebsiella pneumoniae</i>fungal–bacterial interactiongliotoxinproteomics
spellingShingle Aaron Curtis
Michelle Ryan
Kevin Kavanagh
Exposure of <i>Aspergillus fumigatus</i> to <i>Klebsiella pneumoniae</i> Culture Filtrate Inhibits Growth and Stimulates Gliotoxin Production
Journal of Fungi
<i>Aspergillus fumigatus</i>
<i>Klebsiella pneumoniae</i>
fungal–bacterial interaction
gliotoxin
proteomics
title Exposure of <i>Aspergillus fumigatus</i> to <i>Klebsiella pneumoniae</i> Culture Filtrate Inhibits Growth and Stimulates Gliotoxin Production
title_full Exposure of <i>Aspergillus fumigatus</i> to <i>Klebsiella pneumoniae</i> Culture Filtrate Inhibits Growth and Stimulates Gliotoxin Production
title_fullStr Exposure of <i>Aspergillus fumigatus</i> to <i>Klebsiella pneumoniae</i> Culture Filtrate Inhibits Growth and Stimulates Gliotoxin Production
title_full_unstemmed Exposure of <i>Aspergillus fumigatus</i> to <i>Klebsiella pneumoniae</i> Culture Filtrate Inhibits Growth and Stimulates Gliotoxin Production
title_short Exposure of <i>Aspergillus fumigatus</i> to <i>Klebsiella pneumoniae</i> Culture Filtrate Inhibits Growth and Stimulates Gliotoxin Production
title_sort exposure of i aspergillus fumigatus i to i klebsiella pneumoniae i culture filtrate inhibits growth and stimulates gliotoxin production
topic <i>Aspergillus fumigatus</i>
<i>Klebsiella pneumoniae</i>
fungal–bacterial interaction
gliotoxin
proteomics
url https://www.mdpi.com/2309-608X/9/2/222
work_keys_str_mv AT aaroncurtis exposureofiaspergillusfumigatusitoiklebsiellapneumoniaeiculturefiltrateinhibitsgrowthandstimulatesgliotoxinproduction
AT michelleryan exposureofiaspergillusfumigatusitoiklebsiellapneumoniaeiculturefiltrateinhibitsgrowthandstimulatesgliotoxinproduction
AT kevinkavanagh exposureofiaspergillusfumigatusitoiklebsiellapneumoniaeiculturefiltrateinhibitsgrowthandstimulatesgliotoxinproduction