TY - JOUR
T1 - Genome-scale metabolic model of the human pathogen candida albicans
T2 - A promising platform for drug target prediction
AU - Viana, Romeu
AU - Dias, Oscar
AU - Lagoa, Davide
AU - Galocha, Mónica
AU - Rocha, Isabel
AU - Teixeira, Miguel Cacho
PY - 2020/9
Y1 - 2020/9
N2 - Candida albicans is one of the most impactful fungal pathogens and the most common cause of invasive candidiasis, which is associated with very high mortality rates. With the rise in the frequency of multidrug-resistant clinical isolates, the identification of new drug targets and new drugs is crucial in overcoming the increase in therapeutic failure. In this study, the first validated genome-scale metabolic model for Candida albicans, iRV781, is presented. The model consists of 1221 reactions, 926 metabolites, 781 genes, and four compartments. This model was reconstructed using the open-source software tool merlin 4.0.2. It is provided in the well-established systems biology markup language (SBML) format, thus, being usable in most metabolic engineering platforms, such as OptFlux or COBRA. The model was validated, proving accurate when predicting the capability of utilizing different carbon and nitrogen sources when compared to experimental data. Finally, this genome-scale metabolic reconstruction was tested as a platform for the identification of drug targets, through the comparison between known drug targets and the prediction of gene essentiality in conditions mimicking the human host. Altogether, this model provides a promising platform for global elucidation of the metabolic potential of C. albicans, possibly guiding the identification of new drug targets to tackle human candidiasis.
AB - Candida albicans is one of the most impactful fungal pathogens and the most common cause of invasive candidiasis, which is associated with very high mortality rates. With the rise in the frequency of multidrug-resistant clinical isolates, the identification of new drug targets and new drugs is crucial in overcoming the increase in therapeutic failure. In this study, the first validated genome-scale metabolic model for Candida albicans, iRV781, is presented. The model consists of 1221 reactions, 926 metabolites, 781 genes, and four compartments. This model was reconstructed using the open-source software tool merlin 4.0.2. It is provided in the well-established systems biology markup language (SBML) format, thus, being usable in most metabolic engineering platforms, such as OptFlux or COBRA. The model was validated, proving accurate when predicting the capability of utilizing different carbon and nitrogen sources when compared to experimental data. Finally, this genome-scale metabolic reconstruction was tested as a platform for the identification of drug targets, through the comparison between known drug targets and the prediction of gene essentiality in conditions mimicking the human host. Altogether, this model provides a promising platform for global elucidation of the metabolic potential of C. albicans, possibly guiding the identification of new drug targets to tackle human candidiasis.
KW - Candida albicans
KW - Drug targets
KW - Gene essentiality
KW - Global stoichiometric model
KW - Metabolic reconstruction
UR - http://www.scopus.com/inward/record.url?scp=85091159109&partnerID=8YFLogxK
U2 - 10.3390/jof6030171
DO - 10.3390/jof6030171
M3 - Article
AN - SCOPUS:85091159109
SN - 2309-608X
VL - 6
SP - 1
EP - 19
JO - Journal of Fungi
JF - Journal of Fungi
IS - 3
M1 - 171
ER -