Resistance risk asssement and molecular basis of metconazole in Fusarium pseudograminearum

The fungicide metconazole, which acts as a sterol 14α-demethylation inhibitor (DMI), can exhibit strong inhibitory effects on Fusarium pseudograminearum. However, the resistance mechanism as well as the risk that F. pseudograminearum develops resistance to metconazole is yet to be fully assessed. In this study, metconazole displayed a mean EC<sub>50</sub> value of 0.0559 μg/mL against 105 F. pseudograminearum isolates. Ten sensitive parental isolates were then subjected to fungicide adaptation to generate resistant mutants, with in vitro experiments subsequently highlighting the inferior fitness of the mutants. In addition, metconazole exhibited positive cross-resistance with both mefentrifluconazole and tebuconazole. Altogether, the results confirmed the low risk that F. pseudograminearum develops resistance to metconazole. Finally, a mutation genotype (M151T) was identified in FpCYP51B, with the mutants also overexpressing the FpCYP51 genes. Subsequent molecular docking and transformation-based experiments indicated that M151T substitution and overexpression in FpCYP51 genes conferred resistance to metconazole in F. pseudograminearum.

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Publication Details

Journal
Stress Biology
Published
2025-05-01
DOI
https://doi.org/10.1007/s44154-025-00221-0
Citations
3
Primary Topic
Plant Pathogens and Fungal Diseases
Type
article
Field-Weighted Citation Impact
3.45

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article

Resistance risk asssement and molecular basis of metconazole in Fusarium pseudograminearum

Jianqiang Miao, Kang Yuan, Guixiang Li, Han Jiang et al.
3 citations
Stress Biology
Plant Pathogens and Fungal Diseases
3.45
article

Resistance risk asssement and molecular basis of metconazole in Fusarium pseudograminearum

Jianqiang Miao, Kang Yuan, Guixiang Li, Han Jiang, Yiwen Li, Ling Zhang, Xili Liu
article en
3 citations

Abstract

The fungicide metconazole, which acts as a sterol 14α-demethylation inhibitor (DMI), can exhibit strong inhibitory effects on Fusarium pseudograminearum. However, the resistance mechanism as well as the risk that F. pseudograminearum develops resistance to metconazole is yet to be fully assessed. In this study, metconazole displayed a mean EC<sub>50</sub> value of 0.0559 μg/mL against 105 F. pseudograminearum isolates. Ten sensitive parental isolates were then subjected to fungicide adaptation to generate resistant mutants, with in vitro experiments subsequently highlighting the inferior fitness of the mutants. In addition, metconazole exhibited positive cross-resistance with both mefentrifluconazole and tebuconazole. Altogether, the results confirmed the low risk that F. pseudograminearum develops resistance to metconazole. Finally, a mutation genotype (M151T) was identified in FpCYP51B, with the mutants also overexpressing the FpCYP51 genes. Subsequent molecular docking and transformation-based experiments indicated that M151T substitution and overexpression in FpCYP51 genes conferred resistance to metconazole in F. pseudograminearum.

Stress BiologyVol. 5(1)
North West Agriculture and Forestry University (CN), China Agricultural University (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 9%
Plant Pathogens and Fungal Diseases
3.45
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Resistance risk asssement and molecular basis of metconazole in Fusarium pseudograminearum — Jianqiang Miao, Kang Yuan, et al. · Stress Biology (2025) | TGRS Research Map | TGRS