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Sensitivity of Soybean (Glycine max) Pathogens Diaporthe aspalathi, D. caulivora, and D. longicolla to Difenoconazole and Fluopyram Fungicides

  • Karthika Mohan
  • , Sarah Barnes
  • , Dilorom Rasuleva
  • , Taofeek Mukaila
  • , Tom W. Allen
  • , Gary C. Bergstrom
  • , Alyssa K. Betts
  • , Kaitlyn M. Bissonnette
  • , John Bonkowski
  • , Carl A. Bradley
  • , James W. Buck
  • , Martin I. Chilvers
  • , Anne E. Dorrance
  • , Loren J. Giesler
  • , Heather M. Kelly
  • , Nathan Kleczewski
  • , Horacio D. Lopez-Nicora
  • , Dean K. Malvick
  • , Dylan J. Mangel
  • , Samuel G. Markell
  • Daren S. Mueller, Madalyn Shires, Edward J. Sikora, Damon L. Smith, Terry N. Spurlock, Darcy E.P. Telenko, Kiersten A. Wise, Dalitso Yabwalo, Febina M. Mathew

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

Abstract

Diseases of soybean (Glycine max L.) caused by species of Diaporthe have resulted in estimated yield losses totaling $248.2 million in the United States over the past 10 years. To effectively manage species of Diaporthe, it is important to use an integrated approach. In this study, we evaluated the in vitro sensitivity of isolates of the soybean pathogens D. aspalathi, D. caulivora, and D. longicolla from 18 U.S. states to difenoconazole (a demethylation inhibitor fungicide) and fluopyram (a succinate dehydrogenase inhibitor fungicide). The fungicides were incorporated into 2% water agar (WA) in Petri dishes at various concentrations. A mycelial plug of each isolate (n = 59 for difenoconazole and n=55 for fluopyram) obtained froma 7-dayold culture was placed at the center of the WA and incubated in the dark. After 5 days for D. caulivora and D. longicolla and 8 days for D. aspalathi, the colony diameter was measured, and the corresponding percent inhibition and effective concentration at which 50%mycelial growthwas inhibited (EC50)were determined. Significant differences in EC50 values (P < 0.0001) were observed among the isolates of D. aspalathi (0.227 μg/ml), D. caulivora (0.130 μg/ml), and D. longicolla (1.860 μg/ml) for difenoconazole. Similarly, for fluopyram, the EC50 values varied significantly (P < 0.001) among the D. aspalathi (2.233 μg/ml), D. caulivora (1.610 μg/ml), and D. longicolla (0.347 μg/ml) isolates. This study established sensitivity profiles for difenoconazole and fluopyram fungicides for D. aspalathi, D. caulivora, and D. longicolla and provides valuable information that may help in the development of a Diaporthe disease management program.

Original languageEnglish
Pages (from-to)62-69
Number of pages8
JournalPlant Health Progress
Volume26
Issue number1
DOIs
StatePublished - 2025

Bibliographical note

Publisher Copyright:
© 2025 The American Phytopathological Society

Funding

Funding: Support was provided by the United States Department of Agriculture-National Institute of Food and Agriculture (Hatch project number ND02250), the North Central Soybean Research Program, and the United Soybean Board (project number 2411-209-0203).

FundersFunder number
US Department of Agriculture National Institute of Food and Agriculture, Agriculture and Food Research InitiativeND02250
United Soybean Board2411-209-0203

    Keywords

    • Phomopsis
    • pod and stem blight
    • seed decay
    • stem canker

    ASJC Scopus subject areas

    • Plant Science
    • Horticulture

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