Wheat pathogen -myristoyltransferase inhibitors: on-target antifungal activity and an unusual metabolic defense mechanism
Zymoseptoria tritici is the causative agent of Septoria tritici blotch (STB), which costs billions of dollars annually to major wheat-producing countries in terms of both fungicide use and crop loss. Agricultural pathogenic fungi have acquired resistance to most commercially available fungicide clas...
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Veröffentlicht in: | RSC chemical biology 2020-06, Vol.1 (2), p.68-78 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Zymoseptoria tritici
is the causative agent of
Septoria tritici
blotch (STB), which costs billions of dollars annually to major wheat-producing countries in terms of both fungicide use and crop loss. Agricultural pathogenic fungi have acquired resistance to most commercially available fungicide classes, and the rate of discovery and development of new fungicides has stalled, demanding new approaches and insights. Here we investigate a potential mechanism of targeting an important wheat pathogen
Z. tritici via
inhibition of
N
-myristoyltransferase (NMT). We characterize
Z. tritici
NMT biochemically for the first time, profile the
in vivo Z. tritici
myristoylated proteome and identify and validate the first
Z. tritici
NMT inhibitors. Proteomic investigation of the downstream effects of NMT inhibition identified an unusual and novel mechanism of defense against chemical toxicity in
Z. tritici
through the application of comparative bioinformatics to deconvolute function from the previously largely unannotated
Z. tritici
proteome. Research into novel fungicidal modes-of-action is essential to satisfy an urgent unmet need for novel fungicide targets, and we anticipate that this study will serve as a useful proteomics and bioinformatics resource for researchers studying
Z. tritici
.
Investigation of the downstream effects of NMT inhibition identified novel defense mechanism against chemical toxicity in fungal pathogen
Z. tritici. |
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ISSN: | 2633-0679 |
DOI: | 10.1039/d0cb00020e |