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Backround: Grapevine is among the most economically important cultivated crops worldwide, yet it is increasingly threatened by the grapevine trunk disease (GTD) complex. Due to the lack of effective curative treatments for GTDs and the growing need to reduce chemical pesticide use, alternative strategies, such as the application of nanoparticles, are being investigated. In a 2-year in planta study, the inhibitory effects of four chemical compounds and one nanoparticle formulation were evaluated against three serious pathogens associated with GTD complex: Diaporthe eres Nitschke, Diplodia seriata De Not., and Eutypa lata (Pers.) Tul. & C. Tul. Selection of the chemical compounds and nanoparticles was based on their inhibitory effects observed under in vitro conditions, as previously reported.
Results: All chemical treatments demonstrated antifungal activity, with inhibition rates ranging from 33.6% to 93.7%. Silver-selenium nanoparticles exhibited inhibitory effects specifically against D. eres and E. lata, with inhibition rates between 55.0% and 86.9%. The absence of phytotoxic effects at the applied concentrations was also confirmed for the nanoparticles used in this study.
Conclusion: The experimental results demonstrate that the nanoparticles exhibit strong antifungal activity against pathogenic fungi, without causing any detectable phytotoxic effects on grapevines. These findings highlight their potential as a viable alternative to conventional chemical plant protection methods in viticulture. © 2025 The Author(s). Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.
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http://dx.doi.org/10.1002/ps.70110 | DOI Listing |
Chem Biodivers
September 2025
Instituto De Química, Universidade Federal de Mato Grosso Do Sul, Campo Grande, Brazil.
Mezilaurus duckei, a Brazilian endemic tree species found exclusively in the Amazon Rainforest, is primarily exploited for timber in construction. Due to its endangered status, this study aimed to investigate the chemical profile and biological properties of the ethanolic extract and its phases derived from M. duckei leaves.
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September 2025
Department of Clinical Pharmacy, College of Pharmacy, University of Sulaimani, Sulaimani, Iraq.
The global rise in antibiotic resistance demands the urgent development of new antibacterial agents. This study investigated the antibacterial potential of four synthesized methoxy and thiophene chalcone derivatives (designated 3a, 4a, 3b, and 4b) against clinically relevant bacterial pathogens. These compounds were prepared through Claisen-Schmidt condensation, while their chemical structures were verified through applying Fourier-transform infrared, mass spectrometry, H nuclear magnetic resonance (NMR), and C NMR.
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September 2025
Zhejiang Provincial Engineering Research Center of New Technologies and Applications for Targeted Therapy of Major Diseases, Laboratory of Anti-Allergy Functional Compounds, College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Autoimmune diseases (AIDs), defined by irregularities in immune system function, pose a substantial health challenge worldwide, impacting millions with persistent and frequently debilitating conditions. Conventional treatments, such as glucocorticoid-based immunosuppressive therapies, are associated with notable drawbacks and limitations. In response to these difficulties, recent scientific efforts have increasingly focused on natural compounds as potential therapeutic agents.
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September 2025
Department of Biology, Faculty of Science, Selçuk University, Konya, Turkey.
Hippophae salicifolia, commonly known as sea buckthorn, is native to the Indian Himalayan region. This study is the first to comprehensively assess the phytochemical profile and biological activities of H. salicifolia leaves extracted through maceration, infusion, and percolation (Soxhlet apparatus) methods.
View Article and Find Full Text PDFJ Agric Food Chem
September 2025
College of Materials and Chemistry & School of Plant Protection, Anhui Agricultural University, Hefei, 230036, P. R. China.
In recent years, the hydrazide skeleton, as a pivotal class of nitrogen-containing structures, has garnered considerable attention in medicinal chemistry and organic synthesis owing to its unique chemical versatility and broad-spectrum biological activities. In this study, a series of thiazole-containing benzoylhydrazine derivatives -, -, and - with structural divergence from conventional hydrazide-based molecular frameworks were designed, synthesized, and evaluated for their antifungal/antioomycete activities. The antifungal/antioomycete assay showed that some of the targeted compounds exhibited remarkable and broad-spectrum antifungal activities.
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