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Shuang Feng

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Open access Aug 2026

Bacillus velezensis B313-6 as a Potential Biocontrol Strain Against Anthracnose of Panax quinquefolius, and Its Fermentation Optimization, and Field Efficacy on American Ginseng

Anthracnose of American ginseng is caused by Colletotrichum panacicola. In this study, Bacillus velezensis B313-6, isolated from the rhizosphere soil of American ginseng, was identified based on morphological, physiological, biochemical, 16S rRNA, and the gyrase subunit A protein (gyrA) regions’ analyses. B. velezensis B313-6 showed strong antagonistic activity against C. panacicola with an inhibition rate of 94.4% in dual culture assay, and exhibited broad-spectrum antifungal activity against eight other plant pathogenic fungi (inhibition rates 70–94%). Using single-factor experiments combined with response surface methodology, the fermentation conditions were optimized, increasing the inhibition rate against C. panacicola from 93.9% to 97.4%. In field trials, the B. velezensis B313-6 fermentation broth at a low dose (33.3 mL/m2) provided a control efficacy of 67.6% after the third spray, comparable to a commercial B. subtilis product used as a positive control. The low-dose treatment also significantly promoted American ginseng growth, increasing plant height, root length, shoot fresh weight and root fresh weight by 9.7%, 11.3%, 10.5% and 15.5%, respectively, compared to the treatment of water. These results indicate that B. velezensis B313-6 has great potential as a biocontrol agent against the anthracnose of Panax quinquefolius and also promotes the growth of American ginseng.

Shuang Feng, Yue Shi, Ruijie Liu et al. · 0 citations
Jul 2026

Design, Synthesis, and Antifungal Activity of Thiazolidinedione Derivatives Incorporating Thioamide and Piperidine Moieties.

A series of thiazolidinedione derivatives containing thioamide and piperidine moieties were designed, synthesized, and evaluated for antifungal activity against plant pathogenic fungi. Several compounds exhibited potent antifungal activity, among which Z17 was the most active against Rhizoctonia solani (EC50 = 1.8 μg/mL), with substantially greater activity than azoxystrobin (Az; EC50 = 42.6 μg/mL). Physiological analyses indicated that Z17 disrupted membrane integrity and cellular energy metabolism, as reflected by increased malondialdehyde levels and decreased pyruvate kinase activity and pyruvate content. Density functional theory calculations, molecular docking, and molecular dynamics simulations suggested that Z17 forms favorable interactions with the cytochrome bc1 complex. Preliminary safety assessments showed no significant effects on rice seed germination or earthworm viability. These findings suggest Z17 as a promising lead for the development of antifungal agents against crop pathogens.

Junrong Song, Shuang Feng, Miaohe Zhang et al. · 0 citations

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