Hypogin‐derived N‐cinnamoylated peptide as a promising green fungicide against peanut southern blight caused by <scp> <i>S</i> </scp> <i>clerotium rolfsii</i>
BACKGROUND: Peanut southern blight, caused by Sclerotium rolfsii, severely reduces yield and quality. The overuse of chemical fungicides accelerates resistance development and raises environmental concerns, highlighting the necessity for eco-friendly alternatives. Hypogin is an endogenous peanut peptide with broad-spectrum antifungal activity. This study aims to identify the active centers of hypogin and evaluate the antifungal activity and preliminary mechanisms of its derived peptides. RESULTS: ) demonstrated the highest in vitro activity against S. rolfsii, with a half-maximal effective concentration value of 257.93 mg/L. In vivo studies revealed that II-1 provided superior curative efficacy (66.47%) against peanut southern blight, surpassing the commercial fungicide polyoxin (57.33%), and also promoted root growth in peanuts. Both I-7 and II-1 exhibited low cytotoxicity toward human LO2 liver cells, with inhibition rates of 5.05% and 17.44%, respectively, at a concentration of 400 mg/L. Preliminary mechanistic investigations indicated that I-7 specifically targets the Vps34 signaling pathway in S. rolfsii. CONCLUSION: Hypogin-derived peptide II-1 exhibits significant antifungal activity and low toxicity, making it a promising candidate for a green fungicide in the management of peanut southern blight. © 2026 Society of Chemical Industry.
Authors
- Guangyao Li
- Meizi Wang (ORCID: https://orcid.org/0000-0001-9591-5753)
- Q Wang
- Lin Zhou (ORCID: https://orcid.org/0000-0002-7374-4620)
- Xicheng Mao (ORCID: https://orcid.org/0009-0008-9972-5998)
- Yayu Ren
- Yaru Song
Institutions
- Nanjing Agricultural University (CN)
- Henan Agricultural University (CN)
Publication Details
- Journal
- Pest Management Science
- Published
- 2026-06-29
- DOI
- https://doi.org/10.1002/ps.71059
- Primary Topic
- Antimicrobial Peptides and Activities
- Type
- article
- Field-Weighted Citation Impact
- 0.00