Effect of isofetamid on SDHI-resistant isolates of Botrytis cinerea

Yuzuka Abe1, Yoshitake Desaki1, Nanami Kuwahara1

  • 1Central Research Institute, Ishihara Sangyo Kaisha, Ltd.

PubMed

Insights

Isofetamid remains effective against Botrytis cinerea, showing no reduced sensitivity in recent Japanese isolates. While some mutations confer resistance to other succinate dehydrogenase inhibitors (SDHIs), these mutations do not affect isofetamid sensitivity, though specific mutations can cause resistance.

Area of Science:

  • Agricultural Science
  • Plant Pathology
  • Mycology

Background:

  • Botrytis cinerea is a significant plant pathogen causing gray mold disease.
  • Succinate dehydrogenase inhibitors (SDHIs) are crucial fungicides for controlling B. cinerea.
  • Monitoring fungicide resistance in plant pathogens is essential for sustainable agriculture.

Purpose of the Study:

  • To assess the sensitivity of Botrytis cinerea isolates to isofetamid.
  • To investigate the impact of specific SDHI resistance mutations on isofetamid sensitivity.
  • To evaluate the fitness of isofetamid-resistant B. cinerea isolates.

Main Methods:

  • Fungicide sensitivity testing of B. cinerea isolates from Japan and Germany.
  • Molecular analysis of sdhB gene mutations (H272Y/R, P225F, H272L).
  • Competitive assays under in vitro and in vivo conditions.

Main Results:

  • No reduced sensitivity to isofetamid was observed in Japanese B. cinerea isolates (2011-2018).
  • SDHIs resistance mutations (H272Y/R) did not confer cross-resistance to isofetamid.
  • Specific mutations (P225F, H272L) caused moderate to high resistance to isofetamid.
  • Resistant isolates exhibited reduced fitness, disappearing in competitive assays.

Conclusions:

  • Isofetamid maintains efficacy against B. cinerea, even in isolates resistant to other SDHIs.
  • Specific mutations conferring isofetamid resistance also reduce fungal fitness.
  • Isofetamid is a valuable tool for managing B. cinerea, with resistance development unlikely to be rapid.

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