Metabolic reconstruction of the human pathogen Candida auris: using a cross-species approach for drug target prediction

dc.commentsCEB56548por
dc.contributor.authorViana, Romeupor
dc.contributor.authorCarreiro, Tiagopor
dc.contributor.authorCouceiro, Diogopor
dc.contributor.authorDias, Oscarpor
dc.contributor.authorRocha, I.por
dc.contributor.authorTeixeira, Miguel Cachopor
dc.date.accessioned2024-09-12T16:17:02Z
dc.date.available2024-09-12T16:17:02Z
dc.date.issued2023-10-18
dc.date.updated2024-09-12T11:02:12Z
dc.description.abstractCandida auris is an emerging human pathogen, associated with antifungal drug resistance and hospital candidiasis outbreaks. In this work, we present iRV973, the first reconstructed Genome-scale metabolic model (GSMM) for C. auris. The model was manually curated and experimentally validated, being able to accurately predict the specific growth rate of C. auris and the utilization of several sole carbon and nitrogen sources. The model was compared to GSMMs available for other pathogenic Candida species and exploited as a platform for cross-species comparison, aiming the analysis of their metabolic features and the identification of potential new antifungal targets common to the most prevalent pathogenic Candida species. From a metabolic point of view, we were able to identify unique enzymes in C. auris in comparison with other Candida species, which may represent unique metabolic features. Additionally, 50 enzymes were identified as potential drug targets, given their essentiality in conditions mimicking human serum, common to all four different Candida models analysed. These enzymes represent interesting drug targets for antifungal therapy, including some known targets of antifungal agents used in clinical practice, but also new potential drug targets without any human homolog or drug association in Candida species.por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersion
dc.description.sponsorshipThis work was supported by “Fundação para a Ciência e a Tecnologia” (FCT) (Contract PTDC/BII-BIO/28216/2017 and AEM PhD grant to RV). Funding received from project LISBOA-01- 0145-FEDER-022231-the BioData.pt Research Infrastructure is acknowledged. This work was further financed by national funds from FCT in the scope of the project UIDB/04565/2020 and UIDP/04565/2020 of the Research Unit Institute for Bioengineering and Biosciences—iBB, project UIDB/04469/2020 for the Centre of Biological Engineering —CEB, and the project LA/P/0140/2020 of the Associate Laboratory Institute for Health and Bioeconomy — i4HB.por
dc.distributioninternationalpor
dc.identifier.citationViana, R., Carreiro, T., Couceiro, D., Dias, O., Rocha, I., & Teixeira, M. C. (2023). Metabolic reconstruction of the human pathogen Candida auris: using a cross-species approach for drug target prediction. FEMS Yeast Research. Oxford University Press (OUP). http://doi.org/10.1093/femsyr/foad045por
dc.identifier.doi10.1093/femsyr/foad045por
dc.identifier.isbn1567-1364
dc.identifier.issn1567-1356por
dc.identifier.pmid37852663por
dc.identifier.urihttps://hdl.handle.net/1822/93044
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherOxford University Presspor
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04565%2F2020/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F04565%2F2020/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04469%2F2020/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FBII-BIO%2F28216%2F2017/PTpor
dc.relation.publisherversionhttps://academic.oup.com/femsyr/article/doi/10.1093/femsyr/foad045/7321573por
dc.rightsopenAccesspor
dc.subjectC. aurispor
dc.subjectGlobal stoichiometric modelpor
dc.subjectgene essentialitypor
dc.subjectdrug targetpor
dc.subjectmetabolic featurespor
dc.titleMetabolic reconstruction of the human pathogen Candida auris: using a cross-species approach for drug target predictionpor
dc.typearticle
dspace.entity.typePublicationen
oaire.citationConferencePlaceUnited Kingdom
oaire.citationIssuefoad045por
oaire.citationVolume23por
sdum.journalFEMS Yeast Researchpor

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