The putative phospholipase Lip2 counteracts oxidative damage and influences the virulence of Ustilago maydis. (21st April 2016)

• Record Type: Journal Article
• Authors: Lambie, Scott C.; Kretschmer, Matthias; Croll, Daniel; Haslam, Tegan M.; Kunst, Ljerka; Klose, Jana; Kronstad, James W.
• Is Part Of: Molecular plant pathology. Volume 18:Number 2(2017)
• Page Start: 210
• Page End: 221
• Publication Date: 2016-04-21
• Subjects: corn -- fungal pathogenesis -- maize -- mitochondria -- smut disease; Plant diseases -- Molecular aspects -- Periodicals; Plant-pathogen relationships -- Molecular aspects -- Periodicals; 571.936
• DOI: 10.1111/mpp.12391
• Languages: English
• ISSNs: 1464-6722

Abstract

Summary: Ustilago maydis is an obligate biotrophic fungal pathogen which causes common smut disease of corn. To proliferate in host tissue, U. maydis must gain access to nutrients and overcome plant defence responses, such as the production of reactive oxygen species. The elucidation of the mechanisms by which U. maydis meets these challenges is critical for the development of strategies to combat smut disease. In this study, we focused on the contributions of phospholipases (PLs) to the pathogenesis of corn smut disease. We identified 11 genes encoding putative PLs and characterized the transcript levels for these genes in the fungus grown in culture and during infection of corn tissue. To assess the contributions of specific PLs, we focused on two genes, lip1 and lip2, which encode putative phospholipase A2 (PLA2 ) enzymes with similarity to platelet‐activating factor acetylhydrolases. PLA2 enzymes are known to counteract oxidative damage to lipids in other organisms. Consistent with a role in the mitigation of oxidative damage, lip2 mutants were sensitive to oxidative stress provoked by hydrogen peroxide and by increased production of reactive oxygen species caused by inhibitors of mitochondrial functions. Importantly, mutants defective in lip2, but not lip1, were attenuated for virulence in corn seedlings. Finally, a comparative analysis of fatty acid and cardiolipin profiles in the wild‐type strain and a lip2 mutant revealed differences consistent with a protective role for Lip2 in maintaining lipid homeostasis and mitochondrial health during proliferation in the hostile host environment.