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dc.contributor.authorRies, LNA
dc.contributor.authorSteenwyk, JL
dc.contributor.authorde Castro, PA
dc.contributor.authorde Lima, PBA
dc.contributor.authorAlmeida, F
dc.contributor.authorde Assis, LJ
dc.contributor.authorManfiolli, AO
dc.contributor.authorTakahashi-Nakaguchi, A
dc.contributor.authorKusuya, Y
dc.contributor.authorHagiwara, D
dc.contributor.authorTakahashi, H
dc.contributor.authorWang, X
dc.contributor.authorObar, JJ
dc.contributor.authorRokas, A
dc.contributor.authorGoldman, GH
dc.date.accessioned2024-02-27T13:48:46Z
dc.date.available2024-02-27T13:48:46Z
dc.date.issued2019
dc.identifier.issn1664-302X
dc.identifier.issn1664-302X
dc.identifier.otherARTN 854
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/22098
dc.description.abstract

Acquisition and subsequent metabolism of different carbon and nitrogen sources have been shown to play an important role in virulence attributes of the fungal pathogen Aspergillus fumigatus, such as the secretion of host tissue-damaging proteases and fungal cell wall integrity. We examined the relationship between the metabolic processes of carbon catabolite repression (CCR), nitrogen catabolite repression (NCR) and virulence in a variety of A. fumigatus clinical isolates. A considerable amount of heterogeneity with respect to the degree of CCR and NCR was observed and a positive correlation between NCR and virulence in a neutropenic mouse model of pulmonary aspergillosis (PA) was found. Isolate Afs35 was selected for further analysis and compared to the reference strain A1163, with both strains presenting the same degree of virulence in a neutropenic mouse model of PA. Afs35 metabolome analysis in physiological-relevant carbon sources indicated an accumulation of intracellular sugars that also serve as cell wall polysaccharide precursors. Genome analysis showed an accumulation of missense substitutions in the regulator of protease secretion and in genes encoding enzymes required for cell wall sugar metabolism. Based on these results, the virulence of strains Afs35 and A1163 was assessed in a triamcinolone murine model of PA and found to be significantly different, confirming the known importance of using different mouse models to assess strain-specific pathogenicity. These results highlight the importance of nitrogen metabolism for virulence and provide a detailed example of the heterogeneity that exists between A. fumigatus isolates with consequences for virulence in a strain-specific and host-dependent manner.

dc.format.extent854-
dc.format.mediumElectronic-eCollection
dc.languageeng
dc.publisherFrontiers Media SA
dc.subjectAspergillus fumigatus
dc.subjectclinical isolates
dc.subjectcarbon and nitrogen catabolite repression
dc.subjectgenome comparison
dc.subjectcell wall
dc.subjectvirulence
dc.titleNutritional Heterogeneity Among Aspergillus fumigatus Strains Has Consequences for Virulence in a Strain- and Host-Dependent Manner
dc.typejournal-article
dc.typeArticle
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/31105662
plymouth.issueAPR
plymouth.volume10
plymouth.publication-statusPublished online
plymouth.journalFrontiers in Microbiology
dc.identifier.doi10.3389/fmicb.2019.00854
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Academics
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA01 Clinical Medicine
plymouth.organisational-group|Plymouth|Faculty of Health|Peninsula Medical School
plymouth.organisational-group|Plymouth|Faculty of Health|School of Biomedical Sciences
plymouth.organisational-group|Plymouth|REF 2028 Researchers by UoA
plymouth.organisational-group|Plymouth|REF 2028 Researchers by UoA|UoA01 Clinical Medicine
dc.publisher.placeSwitzerland
dcterms.dateAccepted2019-04-03
dc.date.updated2024-02-27T13:48:45Z
dc.identifier.eissn1664-302X
dc.rights.embargoperiodforever
rioxxterms.versionofrecord10.3389/fmicb.2019.00854


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