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Stress Responses Elicited by Glucose Withdrawal in Aspergillus fumigatus
Glucose is a widely used carbon source in laboratory practice to culture Aspergillus fumigatus, however, glucose availability is often low in its “natural habitats”, including the human body. We used a physiological–transcriptomical approach to reveal differences between A. fumigatus Af293 cultures...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692504/ https://www.ncbi.nlm.nih.gov/pubmed/36422047 http://dx.doi.org/10.3390/jof8111226 |
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author | Emri, Tamás Antal, Károly Gila, Barnabás Jónás, Andrea P. Pócsi, István |
author_facet | Emri, Tamás Antal, Károly Gila, Barnabás Jónás, Andrea P. Pócsi, István |
author_sort | Emri, Tamás |
collection | PubMed |
description | Glucose is a widely used carbon source in laboratory practice to culture Aspergillus fumigatus, however, glucose availability is often low in its “natural habitats”, including the human body. We used a physiological–transcriptomical approach to reveal differences between A. fumigatus Af293 cultures incubated on glucose, glucose and peptone, peptone (carbon limitation), or without any carbon source (carbon starvation). Autolytic cell wall degradation was upregulated by both carbon starvation and limitation. The importance of autolytic cell wall degradation in the adaptation to carbon stress was also highlighted by approximately 12.4% of the A. fumigatus genomes harboring duplication of genes involved in N-acetyl glucosamine utilization. Glucose withdrawal increased redox imbalance, altered both the transcription of antioxidative enzyme genes and oxidative stress tolerance, and downregulated iron acquisition, but upregulated heme protein genes. Transcriptional activity of the Gliotoxin cluster was low in all experiments, while the Fumagillin cluster showed substantial activity both on glucose and under carbon starvation, and the Hexadehydro-astechrome cluster only on glucose. We concluded that glucose withdrawal substantially modified the physiology of A. fumigatus, including processes that contribute to virulence. This may explain the challenge of predicting the in vivo behavior of A. fumigatus based on data from glucose rich cultures. |
format | Online Article Text |
id | pubmed-9692504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96925042022-11-26 Stress Responses Elicited by Glucose Withdrawal in Aspergillus fumigatus Emri, Tamás Antal, Károly Gila, Barnabás Jónás, Andrea P. Pócsi, István J Fungi (Basel) Article Glucose is a widely used carbon source in laboratory practice to culture Aspergillus fumigatus, however, glucose availability is often low in its “natural habitats”, including the human body. We used a physiological–transcriptomical approach to reveal differences between A. fumigatus Af293 cultures incubated on glucose, glucose and peptone, peptone (carbon limitation), or without any carbon source (carbon starvation). Autolytic cell wall degradation was upregulated by both carbon starvation and limitation. The importance of autolytic cell wall degradation in the adaptation to carbon stress was also highlighted by approximately 12.4% of the A. fumigatus genomes harboring duplication of genes involved in N-acetyl glucosamine utilization. Glucose withdrawal increased redox imbalance, altered both the transcription of antioxidative enzyme genes and oxidative stress tolerance, and downregulated iron acquisition, but upregulated heme protein genes. Transcriptional activity of the Gliotoxin cluster was low in all experiments, while the Fumagillin cluster showed substantial activity both on glucose and under carbon starvation, and the Hexadehydro-astechrome cluster only on glucose. We concluded that glucose withdrawal substantially modified the physiology of A. fumigatus, including processes that contribute to virulence. This may explain the challenge of predicting the in vivo behavior of A. fumigatus based on data from glucose rich cultures. MDPI 2022-11-21 /pmc/articles/PMC9692504/ /pubmed/36422047 http://dx.doi.org/10.3390/jof8111226 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Emri, Tamás Antal, Károly Gila, Barnabás Jónás, Andrea P. Pócsi, István Stress Responses Elicited by Glucose Withdrawal in Aspergillus fumigatus |
title | Stress Responses Elicited by Glucose Withdrawal in Aspergillus fumigatus |
title_full | Stress Responses Elicited by Glucose Withdrawal in Aspergillus fumigatus |
title_fullStr | Stress Responses Elicited by Glucose Withdrawal in Aspergillus fumigatus |
title_full_unstemmed | Stress Responses Elicited by Glucose Withdrawal in Aspergillus fumigatus |
title_short | Stress Responses Elicited by Glucose Withdrawal in Aspergillus fumigatus |
title_sort | stress responses elicited by glucose withdrawal in aspergillus fumigatus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692504/ https://www.ncbi.nlm.nih.gov/pubmed/36422047 http://dx.doi.org/10.3390/jof8111226 |
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