TY - CHAP
T1 - Integration of Metabolism with Virulence in Candida albicans
AU - Ene, Iuliana V.
AU - Brown, Alistair J.P.
N1 - We are grateful to many colleagues for stimulating debates about Candida genomics, especially our friends in the Aberdeen Fungal Group and the European FINSysB Consortium and Ken Haynes and Jan Quinn. IVE and AJPB were supported by a grant from the European Commission (PITN-GA-2008-214004). AJPB was also supported by the European Research Council (ERC-2009-AdG-249793), the U.K. Biotechnology and Biological Sciences Research Council (BBS/B/06679; BB/C510391/1; BB/D009308/1; BB/F000111/1; BB/F010826/1; BB/F00513X/1), and the Wellcome Trust (080088; 097377).
PY - 2014/3/1
Y1 - 2014/3/1
N2 - The genome of the model pathogenic fungus Candida albicans was sequenced about a decade ago, facilitating unbiased genome-wide explorations of its pathobiology. These studies, in combination with the molecular and biochemical dissection of specific pathways and networks, have revealed that metabolic adaptation is intimately linked with the virulence of C. albicans. This fungus tunes its metabolic activity to specific host niches, and its virulence depends on the functionality of certain metabolic pathways. Also, its pathogenicity and antifungal drug susceptibility are modulated by growth on nutrients found in such niches. Specific regulators appear to coordinate the expression of metabolic functions with virulence factors such as yeast-hypha morphogenesis, thereby promoting host colonisation. It has become clear that the regulatory networks controlling certain metabolic pathways in C. albicans have undergone transcriptional rewiring in comparison with Saccharomyces cerevisiae, reflecting the evolutionary tuning of C. albicans to mammalian host niches.
AB - The genome of the model pathogenic fungus Candida albicans was sequenced about a decade ago, facilitating unbiased genome-wide explorations of its pathobiology. These studies, in combination with the molecular and biochemical dissection of specific pathways and networks, have revealed that metabolic adaptation is intimately linked with the virulence of C. albicans. This fungus tunes its metabolic activity to specific host niches, and its virulence depends on the functionality of certain metabolic pathways. Also, its pathogenicity and antifungal drug susceptibility are modulated by growth on nutrients found in such niches. Specific regulators appear to coordinate the expression of metabolic functions with virulence factors such as yeast-hypha morphogenesis, thereby promoting host colonisation. It has become clear that the regulatory networks controlling certain metabolic pathways in C. albicans have undergone transcriptional rewiring in comparison with Saccharomyces cerevisiae, reflecting the evolutionary tuning of C. albicans to mammalian host niches.
UR - http://www.scopus.com/inward/record.url?scp=85014463117&partnerID=8YFLogxK
U2 - 10.1007/978-3-642-45218-5_14
DO - 10.1007/978-3-642-45218-5_14
M3 - Chapter
AN - SCOPUS:85014463117
SN - 9783642452178
T3 - The Mycota
SP - 349
EP - 370
BT - Fungal Genomics
A2 - Nowrousian, Minou
PB - Springer
ER -