TY - JOUR
T1 - Cryptococcus neoformans UGT1 encodes a UDP-Galactose/UDP-GalNAc transporter
AU - Li, Lucy X.
AU - Ashikov, Angel
AU - Liu, Hong
AU - Griffith, Cara L.
AU - Bakker, Hans
AU - Doering, Tamara L.
N1 - Funding Information:
This work was supported by National Institutes of Health grants GM071007 and AI109623. LXL was partly supported by a Sondra Schlesinger Graduate Fellowship, and National Institute of Health grants F30 AI120339 and T32 GM007200.
Publisher Copyright:
© The Author 2016.
PY - 2017/1
Y1 - 2017/1
N2 - Cryptococcus neoformans, an opportunistic fungal pathogen, produces a glycan capsule to evade the immune system during infection. This definitive virulence factor is composed mainly of complex polysaccharides, which are made in the secretory pathway by reactions that utilize activated nucleotide sugar precursors. Although the pathways that synthesize these precursors are known, the identity and the regulation of the nucleotide sugar transporters (NSTs) responsible for importing them into luminal organelles remain elusive. The UDP-galactose transporter, Ugt1, was initially identified by homology to known UGTs and glycan composition analysis of ugt1Δ mutants. However, sequence is an unreliable predictor of NST substrate specificity, cells may express multiple NSTs with overlapping specificities, and NSTs may transport multiple substrates. Determining NST activity thus requires biochemical demonstration of function. We showed that Ugt1 transports both UDP-galactose and UDP-N-acetylgalactosamine in vitro. Deletion of UGT1 resulted in growth and mating defects along with altered capsule and cellular morphology. The mutant was also phagocytosed more readily by macrophages than wild-type cells and cleared more quickly in vivo and in vitro, suggesting a mechanism for the lack of virulence observed in mouse models of infection.
AB - Cryptococcus neoformans, an opportunistic fungal pathogen, produces a glycan capsule to evade the immune system during infection. This definitive virulence factor is composed mainly of complex polysaccharides, which are made in the secretory pathway by reactions that utilize activated nucleotide sugar precursors. Although the pathways that synthesize these precursors are known, the identity and the regulation of the nucleotide sugar transporters (NSTs) responsible for importing them into luminal organelles remain elusive. The UDP-galactose transporter, Ugt1, was initially identified by homology to known UGTs and glycan composition analysis of ugt1Δ mutants. However, sequence is an unreliable predictor of NST substrate specificity, cells may express multiple NSTs with overlapping specificities, and NSTs may transport multiple substrates. Determining NST activity thus requires biochemical demonstration of function. We showed that Ugt1 transports both UDP-galactose and UDP-N-acetylgalactosamine in vitro. Deletion of UGT1 resulted in growth and mating defects along with altered capsule and cellular morphology. The mutant was also phagocytosed more readily by macrophages than wild-type cells and cleared more quickly in vivo and in vitro, suggesting a mechanism for the lack of virulence observed in mouse models of infection.
KW - Cryptococcus neoformans
KW - Nucleotide sugar transporters
KW - Polysaccharide capsule
KW - UDP-galactose
KW - Udp-galnac
UR - http://www.scopus.com/inward/record.url?scp=85014399712&partnerID=8YFLogxK
U2 - 10.1093/glycob/cww078
DO - 10.1093/glycob/cww078
M3 - Article
C2 - 27496760
AN - SCOPUS:85014399712
SN - 0959-6658
VL - 27
SP - 87
EP - 98
JO - Glycobiology
JF - Glycobiology
IS - 1
ER -