Ocimum basilicum (sweet basil) is an economically important aromatic herb; in Italy, approximately 1000 ha of “Genovese-type” basil are grown annually in greenhouses and open fields and are subjected to Downy Mildew (DM) disease, caused by Peronospora belbahrii, leading to huge crop losses. Mutation of the Susceptibility (S) gene DMR6 (Downy Mildew Resistant 6) has been proven to confer a broad-spectrum resistance to DM. In this work, an effective Genome Editing (GE) approach mediated by CRISPR/Cas9 in O. basilicum ‘Italiko’, the élite cultivar used to produce “Pesto Genovese D.O.P”, was developed. A highly efficient genetic transformation method mediated by A. tumefaciens has been optimized from cotyledonary nodes, obtaining 82.2% of regenerated shoots, 84.6% of which resulted in Cas9+ plants. Eleven T0 lines presented different type of mutations in ObDMR6; 60% were indel frameshift mutations with knock-out of ObDMR6 of ‘FT Italiko’. Analysis of six T1 transgene-free seedlings revealed that the mutations of T0 plants were inherited and segregated. Based on infection trials conducted on T0 plants, clone 22B showed a very low percentage of disease incidence after 14 days post infection. The aromatic profile of all in vitro edited plants was also reported; all of them showed oxygenated monoterpenes as the major fraction.

The aims of the present study were (i) to characterize the dichloromethane extract of the fresh aerial parts of S. somalensis, cultivated in Liguria (Italy), (ii) to quantify carnosic acid production and (iii) to find an eco-friendly alternative approach to control diseases caused by phytopathogenic fungi. The phytochemical investigation yielded several known terpenoids, as well as a diterpene, 4α,9α-epoxy-2H-dibenzo[a,d]cyclohepten-7(5H)-one, not previously described as a plant metabolite before. The results showed a noteworthy quantity of carnosic acid (113.90 µg/mg of dried extract). The potential antifungal activity of the plant surface extract and carnosic acid against five phytopathogenic fungi (Colletotrichum coccodes, Fusarium oxysporum, Sclerotinia sclerotiorum, Botrytis cinerea and Rhizoctonia solani) was considered. A complete inhibition of C. coccodes, S. sclerotiorum and R. solani mycelium growth was observed by carnosic acid at 500 µg/mL. High inhibition values were observed against B. cinerea and F. oxysporum compared to reference active ingredients. Four different B. cinerea strains exhibited a pronounced sensitivity to carnosic acid, as well as those originating from agricultural crop scenarios where a high load of active ingredient for gray mold control was historically adopted. Additionally, the formation and development of the germinative tube in B. cinerea were greatly slowed down.

The Italian garlic ecotype “Vessalico” possesses distinct characteristics compared to its French parent cultivars Messidor and Messidrôme, used for sowing, as well as other ecotypes in neighboring regions. However, due to the lack of a standardized seed supply method and cultivation protocol among farmers in the Vessalico area, a need to identify garlic products that align with the Vessalico ecotype arises. In this study, an NMR-based approach followed by multivariate analysis to analyze the chemical composition of Vessalico garlic sourced from 17 different farms, along with its two French parent cultivars, was employed. Self-organizing maps allowed to identify a homogeneous subset of representative samples of the Vessalico ecotype. Through the OPLS-DA model, the most discriminant metabolites based on values of VIP (Variable Influence on Projections) were selected. Among them, S-allylcysteine emerged as a potential marker for distinguishing the Vessalico garlic from the French parent cultivars by NMR screening. Additionally, to promote sustainable agricultural practices, the potential of Vessalico garlic extracts and its main components as agrochemicals against Xanthomonas campestris pv. campestris, responsible for black rot disease, was explored. The crude extract exhibited a MIC of 125 μg/mL, and allicin demonstrated the highest activity among the tested compounds (MIC value of 31.25 μg/mL).

Phytopathogenic fungi and bacteria pose a serious threat to global agriculture, leading to significant economic losses and potential health risks. Consequently, the search for natural alternatives to synthetic agrochemicals has garnered increasing scientific attention, with plant extracts emerging as promising environmentally friendly solutions. In this context, the surface extract of Salvia discolor, obtained using dichloromethane, was analyzed for its bioactive potential. Chemical profiling revealed a rich composition of terpenoids and flavonoids. The antimicrobial potential of the ground extract was evaluated against nine phytopathogenic fungi (Alternaria solani, Botrytis cinerea, Colletotrichum lindemuthianum, Fusarium solani, Fusarium oxysporum f. sp. lactucae race 1, Phoma betae, Phaeomoniella chlamydospora, Pythium dissotocum, and Stemphylium sp.), and two phytopathogenic bacteria (Clavibacter michiganesis subsp. michiganesis and Pectobacterium carotovorum subsp. carotovorum), selected from common pathogens of agricultural interest. Complete inhibition of P. chlamydospora at 1000 µg mL⁻¹ and strong activity against P. dissotocum, F. solani and B. cinerea was observed, and low inhibition (<40%) against C. lindemuthianum and F. oxysporum f. sp. lactucae race 1. However, the extract showed promising results in the post-harvest protection of tomatoes against gray mold. Moderate antibacterial activity was seen against C. michiganensis subsp. michiganensis. These findings indicate that S. discolor extract has the potential to serve as an effective natural crop protection agent, though further optimization may be needed for broader application.

The tomato leaf miner (Tuta absoluta) is recognized as a highly destructive pest affecting members of the Solanaceae family, particularly tomato crops, where infestations may cause total crop loss. Its rapid spread and increasing resistance to chemical insecticides underscore the urgent need for innovative, environmentally compatible control strategies. In this context, the present study investigates the bioactivity of surface extracts derived from four Salvia species (S. buchananii, S. corrugata, S. discolor, and S. namaensis) against T. absoluta larvae, focusing on their insecticidal and feeding-deterrent effects. Chemical characterization through LC–MS analysis demonstrated that these Salvia species contain diverse secondary metabolites, including diterpenoids, triterpenoids, and flavonoids. Initial screening using a leaf-dip bioassay at a concentration of 2.50 mg/mL showed that S. discolor was particularly effective among the Salvia extracts tested. Subsequent dose–response assays with S. discolor extracts (0.16–5.00 mg/mL) confirmed strong larvicidal and feeding inhibitory effects, with LC₅₀ and FI₅₀ values of 0.12 and 0.13 mg/mL, respectively. Additionally, weak inhibition of acetylcholinesterase (AChE) was observed, suggesting a minor contribution of neurotoxic effects to the overall activity of the extract. The findings suggest that S. discolor extracts may be useful for managing T. absoluta infestations, pending evaluation of their effects on non-target organisms.

Salvia somalensis Vatke is a source of specialized metabolites with potential biological and agrochemical applications. Previous studies on the dichloromethane plant surface extract demonstrated strong antifungal activity associated with abietane diterpenoids. Building on these findings, the present study aimed to characterize the methanolic extract of S. somalensis and evaluate its antifungal potential against major phytopathogenic fungi, with the broader goal of exploring the extract as a sustainable source of antifungal metabolites for crop protection. LC-MS analysis of the methanolic extract revealed a diverse phytochemical profile comprising phenolic acids, including caffeic acid, ferulic acid, and rosmarinic acid, as well as abietane-type diterpenoids such as carnosol, rosmanol, and carnosic acid. Quantitative analysis showed that carnosic acid was present only at low levels (0.09% w/w of fresh biomass). The extract exhibited antifungal activity against Botrytis cinerea, Colletotrichum coccodes, Fusarium oxysporum, Rhizoctonia solani, and Sclerotinia sclerotiorum. More than 80% inhibition of mycelial growth was observed against B. cinerea and C. coccodes at 1000 μg/mL. In addition, as in vitro cultivation of this species has not previously been explored, micropropagated plants and callus culture were established. Phytochemical profiling revealed distinct chemical compositions in the in vitro biomass. Extracts obtained from micropropagated plants inhibited mycelial growth of the tested phytopathogens by 60–70% at 1000 μg/mL, except for F. oxysporum, which showed 35.29% inhibition at the same concentration. Collectively, these findings highlight S. somalensis as a source of bioactive metabolites with antifungal potential.