TY - JOUR
T1 - Metabolic reconstruction of the human pathogen Candida auris
T2 - using a cross-species approach for drug target prediction
AU - Viana, Romeu
AU - Carreiro, Tiago
AU - Couceiro, Diogo
AU - Dias, Oscar
AU - Rocha, Isabel
AU - Teixeira, Miguel Cacho
N1 - Funding Information:
This 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.
Publisher Copyright:
© The Author(s) 2023. Published by Oxford University Press on behalf of FEMS. All rights reserved.
PY - 2023
Y1 - 2023
N2 - Candida 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.
AB - Candida 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.
KW - C. auris
KW - drug target
KW - gene essentiality
KW - Global stoichiometric model
KW - metabolic features
UR - http://www.scopus.com/inward/record.url?scp=85176977712&partnerID=8YFLogxK
U2 - 10.1093/femsyr/foad045
DO - 10.1093/femsyr/foad045
M3 - Article
C2 - 37852663
AN - SCOPUS:85176977712
SN - 1567-1356
VL - 23
JO - FEMS Yeast Research
JF - FEMS Yeast Research
M1 - foad045
ER -