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The conserved nematode pheromone ascr#18 primes plant immunity

  • Murli Manohar
  • , Andrea Sistenich
  • , Shoashuai Liu
  • , Shine Baby
  • , Shiyan Chen
  • , Wim Dejonghe
  • , Anshu Kumari
  • , Emily Luna
  • , Sophie Levecque
  • , Patricia M. Manosalva
  • , Jan E. Leach
  • , Xiaohong Wang
  • , Aardra Kachroo
  • , Karl Heinz Kogel
  • , Uwe Conrath
  • , Frank C. Schroeder
  • , Daniel F. Klessig

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Plants sense a diverse array of small molecules and macromolecules derived from their natural environment, including diverse microbe-associated molecular patterns (MAMPs) that can trigger defense responses. Several MAMPs have been shown to prime plants for enhanced defense, providing extended protection against pathogens with minimal fitness costs. However, the extent to which conserved small molecule signatures of other phyla contribute to priming of plant defenses is unclear. Here, we demonstrate that exposure of seeds or plants to the ascaroside ascr#18, a pheromone secreted by plant-parasitic and free-living soil nematodes, primes immune genes for enhanced expression upon pathogen challenge, thereby increasing resistance to diverse microbial pathogens. We further show that ascr#18-induced priming is associated with the formation of open chromatin in the regulatory regions of defense genes. Defense priming and disease protection by ascr#18 is compromised in Arabidopsis mutants defective in the receptor of ascr#18, the leucine-rich repeat receptor-like kinase NILR1. Defense priming by ascr#18 is retained under field conditions, demonstrating potential of ascaroside treatment as a crop protection strategy to reduce pesticide usage. Our findings provide insight into the molecular basis of defense priming by ascr#18 and demonstrate how evolutionarily conserved small molecule signatures of plant-associated macrobiota modulate immunity.

Original languageEnglish
Article number936
Number of pages13
JournalCommunications Biology
Volume9
Issue number1
DOIs
StatePublished - Dec 2026

Bibliographical note

Publisher Copyright:
© The Author(s) 2026.

Funding

This research was supported in part by the National Institutes of Health (R35GM131877 to F.C.S.) and the Howard Hughes Medical Institute (Faculty Scholar grant to F.C.S.), USDA (AFRI 2011- 68004- 30154 to D.F.K.), the Foundation for Food and Agriculture Research (FFAR G-20011-01 to J.E.L.), the German Research Foundation (271511104 to U.C.), USDA (ARS 8062-22000-023-000D to X.W.) and the Federal Ministry of Research, Technology and Space of Germany (BMFTR), project Wheat Interference to K.H.K. We thank Goncalo Gouveia for assistance with data analysis, and Fangming Xiao, University of Idaho, for providing Arabidopsis nilr1 -1 and nilr1 -2 mutant seeds. We thank the staff of Ascribe Bioscience Inc. for providing field trial data in corn and soybean. These trials were contracted by Ascribe Bioscience and supported in part by funds from the National Science Foundation (SBIR 1951164).

FundersFunder number
Ascribe Bioscience
Bundesministerium für Forschung, Technologie und Raumfahrt
Brigham Young University—Idaho
BMFTR
Howard Hughes Medical Institute
National Science Foundation Arctic Social Science ProgramSBIR 1951164
Foundation for Food and Agriculture ResearchFFAR G-20011-01
National Institutes of Health (NIH)R35GM131877
Deutsche Forschungsgemeinschaft271511104, ARS 8062-22000-023-000D
U.S. Department of AgricultureAFRI 2011- 68004- 30154

    ASJC Scopus subject areas

    • Medicine (miscellaneous)
    • General Biochemistry, Genetics and Molecular Biology
    • General Agricultural and Biological Sciences

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