4.6 Article

Characterization of the Field Fludioxonil Resistance and Its Molecular Basis in Botrytis cinerea from Shanghai Province in China

期刊

MICROORGANISMS
卷 9, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/microorganisms9020266

关键词

Botrytis cinerea; fludioxonil; fungicide resistance; biological characteristics; osmotic sensitivity; molecular mechanism; mutation

资金

  1. National Key Research and Development Program of China [2016YFD0201305]
  2. National Natural Science Foundation of China [31772192]

向作者/读者索取更多资源

Botrytis cinerea shows varying degrees of resistance to fludioxonil, with most resistant isolates also developing resistance to other fungicides. However, the fitness of resistant isolates is lower than that of sensitive ones. Further investigation into the molecular resistance mechanisms revealed specific amino acid mutations in the resistant isolates.
Botrytis cinerea is a destructive necrotrophic pathogen that can infect many plant species. The control of gray mold mainly relies on the application of fungicides, and the fungicide fludioxonil is widely used in China. However, the field fungicide resistance of B. cinerea to this compound is largely unknown. In this study, B. cinerea isolates were collected from different districts of Shanghai province in 2015-2017, and their sensitivity to fludioxonil was determined. A total of 65 out of 187 field isolates (34.76%) were found to be resistant to fludioxonil, with 36 (19.25%) showing high resistance and 29 (15.51%) showing moderate resistance. Most of these resistant isolates also showed resistance to iprodione, and some developed resistance to fungicides of other modes of action. AtrB gene expression, an indicator of MDR1 and MDR1h phenotypes, was not dramatically increased in the tested resistant isolates. Biological characteristics and osmotic sensitivity investigations showed that the fitness of resistant isolates was lower than that of sensitive ones. To investigate the molecular resistance mechanisms of B. cinerea to fludioxonil, the Bos1 amino acid sequences were compared between resistant and sensitive isolates. Resistant isolates revealed either no amino acid variations or the mutations I365S, I365N, Q369P/N373S, and N373S.

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