Journal Article

Zearalenone and ß-Zearalenol But Not Their Glucosides Inhibit Heat Shock Protein 90 ATPase Activity

Werner, Ulrike, Hauser, Marie-Theres, Mitterbauer, Rudolf, Merz, David, Berthiller, Franz, Michlmayr, Herbert, Schweiger, Wolfgang, Torres Acosta, Juan Antonio, Wiesenberger, Gerlinde, Adam, Gerhard, Hametner, Christian, Krska, Rudolf, Shams, Mehrdad, Varga, Elisabeth

2019

Overview

The mycotoxin zearalenone (ZEN) is produced by many plant pathogenic Fusarium species. It is well known for its estrogenic activity in humans and animals, but whether ZEN has a role in plant–pathogen interaction and which process it is targeting in planta was so far unclear. We found that treatment of Arabidopsis thaliana seedlings with ZEN induced transcription of the AtHSP90.1 gene. This heat shock protein (HSP) plays an important role in plant–pathogen interaction, assisting in stability and functionality of various disease resistance gene products. Inhibition of HSP90 ATPase activity impairs functionality. Because HSP90 inhibitors are known to induce HSP90 gene expression and due to the structural similarity with the known HSP90 inhibitor radicicol (RAD), we tested whether ZEN and its phase I metabolites α- and ß-zearalenol are also HSP90 ATPase inhibitors. Indeed, At HSP90.1 and wheat Ta HSP90-2 were inhibited by ZEN and ß-zearalenol, while α-zearalenol was almost inactive. Plants can efficiently glycosylate ZEN and α/ß-zearalenol. We therefore tested whether glucosylation has an effect on the inhibitory activity of these metabolites. Expression of the A. thaliana glucosyltransferase UGT73C6 conferred RAD resistance to a sensitive yeast strain. Glucosylation of RAD, ZEN, and α/ß-zearalenol abolished the in vitro inhibitory activity with recombinant HSP90 purified from Escherichia coli . In conclusion, the mycotoxin ZEN has a very prominent target in plants, HSP90, but it can be inactivated by glycosylation. This may explain why there is little evidence for a virulence function of ZEN in host plants.

• Publisher: Frontiers Media SA,Frontiers Media S.A
• Subject: Adenosine triphosphatase / Arabidopsis / Barley / Binding sites / Disease resistance / Enzymes / Estrogenic activity / Fusarium / Gene expression / Glucosides / Glucosyltransferase / Glycosylation / Heat shock proteins / Host plants / HSP90 / Hsp90 protein / Kinases / Metabolites / Mycotoxins / Pathogens / Pharmacology / Proteins / radicicol / Seeds / Signal transduction / Virulence / wheat / Xenoestrogens / Zearalenone