HUBEI AGRICULTURAL SCIENCES ›› 2024, Vol. 63 ›› Issue (9): 89-94.doi: 10.14088/j.cnki.issn0439-8114.2024.09.016

• Plant Protection • Previous Articles     Next Articles

Identification of pathogen of sclerotinia on Sophora tonkinensis Radix and screening of laboratory agents

SONG Li-sha, JIANG Ni, ZHANG Zhan-jiang, WEI Shu-gen, QIU Zhuo-qiu, HUANG Qi, ZHAN Xin-jie, PAN Li-mei   

  1. Guangxi Botanical Garden of Medicinal Plants/Guangxi Key Laboratory of High-Quality Formation and Utilization of Dao-Di Herbs/Guangxi Traditional Chinese Medicine Breeding Technology Innovation Center/ National Center for Traditional Chinese Medicine Inheritance and Innovation, Nanning 530023, China
  • Received:2023-06-19 Online:2024-09-25 Published:2024-09-30

Abstract: The pathogens from Sophora tonkinensis Radix were isolated by conventional tissue separation method, the pathogenicity was determined by Koch's formula, and the pathogens were identified based on morphological characteristics, mycelium fusion group determination, nuclear fluorescence staining and rDNA-ITS sequence analysis. The inhibitory activities of 5 fungicides against pathogens were measured by the mycelium growth rate method. The results showed that the pathogen was Rhizoctonia solani, belonging to the fusion group AG-1. 98% hymexazol soluble power (SP), 75% oxime ·pentazolol water dispersible granule (WG), 250 g/L pyraclostrobin emulsifiable concentrate (EC), 1 billion /g Trichoderma harziana suspension concentrate (SC), and 50% carbendazim wettable power (WP) all had good inhibitory effects on the growth of pathogenic fungi mycelia. The inhibitory medium effective concentrations (EC50) were 0.061 1, 0.575 7, 0.074 8, 0.284 3, 0.740 5 mg/L, respectively.

Key words: Sophora tonkinensis Radix, sclerotinia, identification of pathogen, screening of laboratory agents, Rhizoctonia solani

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