Methee ChayakulkeereeTania C. SorrellA. Rosemary SiafakasChristabel F. WilsonNamfon PantaratKimberly J. GerikRoss BoadleJulianne T. DjordjevicThe University of SydneyMahidol UniversitySt. Louis University2018-07-122018-07-122008-08-01Molecular Microbiology. Vol.69, No.4 (2008), 809-826136529580950382X2-s2.0-47749156040https://repository.li.mahidol.ac.th/handle/20.500.14594/18885Phospholipase B1 (Plb1) is secreted after release from its glycosylphosphatidylinositol anchor and is implicated in initiation and dissemination of infection of the pathogenic fungus, Cryptococcus neoformans. To investigate the role of phosphatidylinositol-specific phospholipase C (PI-PLC) in Plb1 secretion, we identified two putative PI-PLC-encoding genes in C. neoformans var. grubii (PLC1 and PLC2), and created Δplc1 and Δplc2 deletion mutants. In Δplc1, which expressed less PI-PLC activity than wild type (WT), three major cryptococcal virulence traits, Plb1 secretion, melanin production and growth at host temperature (37°C) were abolished and absence of Plb1 secretion coincided with Plb1 accumulation in plasma membranes. In addition, Δplc1 cell walls were defective, as indicated by cell clumping and irregular morphology, slower growth and an inability to activate mitogen-activated protein kinase (MAPK) in the presence of cell wall-perturbing agents. In contrast to Δplc2, which was as virulent as WT, Δplc1 was avirulent in mice and exhibited attenuated killing of Caenorhabditis elegans at 25°C, demonstrating that mechanism(s) independent of the 37°C growth defect contribute to the virulence composite. We conclude that Plc1 is a central regulator of cryptococcal virulence, acting through the protein kinase C/MAPK pathway, that it regulates release of Plb1 from the plasma membrane and is a candidate antifungal drug target. © 2008 The Authors.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyImmunology and MicrobiologyArticleSCOPUS10.1111/j.1365-2958.2008.06310.x