Biological and molecular characterization of pydiflumetofen and phenamacril dual-resistant Fusarium graminearum strains

被引:0
|
作者
Liu, Chang [1 ]
Shao, Wenyong [1 ]
Duan, Yabin [2 ]
Zhao, Youfu [3 ]
Liu, Zunyong [1 ]
Ma, Zhonghua [1 ]
机构
[1] Zhejiang Univ, Inst Biotechnol, State Key Lab Rice Biol, Key Lab Mol Biol Crop Pathogens & Insects, Hangzhou 310058, Peoples R China
[2] Nanjing Agr Univ, Coll Plant Protect, Key Lab Pesticide, Nanjing, Peoples R China
[3] Washington State Univ, Irrigated Agr Res & Extens Ctr, Dept Plant Pathol, Prosser, WA USA
基金
中国国家自然科学基金;
关键词
Fusarium graminearum; fungicides resistance; Fusarium head blight; pydiflumetofen; phenamacril; SPECIES COMPLEX; SDHI FUNGICIDES; WHEAT; MECHANISMS; EVOLUTION;
D O I
10.1002/ps.8226
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
BACKGROUND: Fusarium head blight (FHB) caused by Fusarium graminearum species complex (FGSG) remains a major challenge to cereal crops and resistance to key fungicides by the pathogen threatens control efficacy. Pydiflumetofen, a succinate dehydrogenase inhibitor, and phenamacril, a cyanoacrylate fungicide targeting myosin I, have been applied to combat this disease. Nonetheless, emergence of pydiflumetofen resistance in a subset of field isolates alongside laboratory-induced facile generation of phenamacril-resistant isolates signals a critical danger of resistance proliferation. RESULTS: Our study investigates the development of dual resistance to these fungicides in F. graminearum. Utilizing pydiflumetofen-resistant (Py (R)) and -sensitive (Py-S) isolates, we obtained dual-resistant (Py (R) Ph (R)) and phenamacril-resistant ((PyPh)-Ph-S (R)) mutants on potato sucrose agar containing phenamacril. Mutation rates for phenamacril resistance were comparable between pydiflumetofen-resistant and -sensitive isolates, implying independent pathways for resistance development. The mutants compromised in fungal growth, competitive viability and deoxynivalenol production, suggesting fitness penalties for the dual-resistant mutants. However, no cross-resistance was found with tebuconazole or fludioxonil. In addition, we characterized four critical amino acid changes (S217L, C423R, K537T, E420G) in the Myo1 that were verified to confer phenamacril resistance in F. graminearum. CONCLUSION: This research indicates the possibility of resistance development for both pydiflumetofen and phenamacril in F. graminearum and emphasizes the need for fungicide resistance management for FHB. (c) 2024 Society of Chemical Industry.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] Physiological and molecular responses of resistant and susceptible wheat cultivars to Fusarium graminearum mycotoxin extract
    Sorahinobar, Mona
    Soltanloo, Hassan
    Niknam, Vahid
    Ebrahimzadeh, Hassan
    Moradi, Babak
    Safaie, Naser
    Behmanesh, Mehrdad
    Bahram, Mohammad
    CANADIAN JOURNAL OF PLANT PATHOLOGY, 2017, 39 (04) : 444 - 453
  • [22] Molecular characterization of insertional mutant 8B5 of Fusarium graminearum
    Catlett, S. M.
    Stamey, E. M.
    Shychuk, A. J.
    Armentrout, R. S.
    Flaherty, J. E.
    PHYTOPATHOLOGY, 2009, 99 (06) : S20 - S20
  • [23] Molecular characterization of a cutinase gene (CUT2) from Fusarium graminearum
    Hwang, R.
    Feng, J.
    Hwang, S. F.
    Strelkov, S. E.
    CANADIAN JOURNAL OF PLANT PATHOLOGY-REVUE CANADIENNE DE PHYTOPATHOLOGIE, 2009, 31 (01): : 123 - 123
  • [24] Molecular characterization of a novel hypovirus from the plant pathogenic fungus Fusarium graminearum
    Li, Pengfei
    Zhang, Hailong
    Chen, Xiaoguang
    Qiu, Dewen
    Guo, Lihua
    VIROLOGY, 2015, 481 : 151 - 160
  • [25] Phylogenetic analyses of Fusarium graminearum strains from cereals in Italy, and characterisation of their molecular and chemical chemotypes
    Somma, S.
    Petruzzella, A. L.
    Logrieco, A. F.
    Meca, G.
    Cacciola, O. S.
    Moretti, A.
    CROP & PASTURE SCIENCE, 2014, 65 (01): : 52 - 60
  • [26] Characterization of the interaction between biological control agent ZJU60 and Fusarium graminearum
    Wang, J.
    Chen, Y.
    Yang, N.
    Ma, Z.
    PHYTOPATHOLOGY, 2017, 107 (12) : 23 - 24
  • [27] Phenotypic and molecular characterization of the resistance to azoxystrobin and pyraclostrobin in Fusarium graminearum populations from Brazil
    Andrade, Sheila M. P.
    Augusti, Guilherme R.
    Paiva, Gabriel F.
    Feksa, Heraldo R.
    Tessmann, Dauri J.
    Machado, Franklin J.
    Mizubuti, Eduardo S. G.
    Del Ponte, Emerson M.
    PLANT PATHOLOGY, 2022, 71 (05) : 1152 - 1163
  • [28] Searching molecular determinants of sensitivity differences towards four demethylase inhibitors in Fusarium graminearum field strains
    Pasquali, Matias
    Pallez-Barthel, Marine
    Beyer, Marco
    PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 2020, 164 : 209 - 220
  • [29] Molecular Phylogenetic Relationships, Trichothecene Chemotype Diversity and Aggressiveness of Strains in a Global Collection of Fusarium graminearum Species
    Amarasinghe, Chami
    Sharanowski, Barbara
    Fernando, W. G. Dilantha
    TOXINS, 2019, 11 (05)
  • [30] Biochemical Characterization of the Fusarium graminearum Candidate ACC-Deaminases and Virulence Testing of Knockout Mutant Strains
    Svoboda, Thomas
    Parich, Alexandra
    Gueldener, Ulrich
    Schoefbeck, Denise
    Twaruschek, Krisztian
    Vaclavikova, Marta
    Hellinger, Roland
    Wiesenberger, Gerlinde
    Schuhmacher, Rainer
    Adam, Gerhard
    FRONTIERS IN PLANT SCIENCE, 2019, 10