Nanoparticles are implemented in different biotechnological fields, and there is interest in their use in plant biology. Nanotechnology can help overcome the persistent limitations of using conventional fungicides in the management of plant diseases, contributing to a safer environment. Hence, this study is focused on evaluating the behavior of nanoparticles on two different strains of Fusarium oxysporum, which have a wide-ranging occurrence in tomato production and account for important economic losses. Fusarium oxysporum is an ascomycetous fungus that is well-known as a soilborne plant pathogen, adapted to any soil type, and it lives in different forms on organic materials. Gold–chitosan and carbon nanoparticles were suspended in potato dextrose agar growth media, and their antifungal activity was evaluated at 1, 3, 5, and 7 days after incubation by measuring the diameter of fungal colonies. The results showed that the nanoparticles have antifungal properties against F. oxysporum, the fungal colony growth diameter being reduced. Likewise, it was observed that the colony diameter was smaller when the nanoparticle concentration increased. However, in the case of one F. oxysporum strain, the highest nanoparticle concentration applied during the experiment’s execution was not able to completely inhibit fungal growth.

The study presents the preparation and characterization of new scaffolds based on bacterial cellulose and keratin hydrogel which were seeded with adipose stem cells. The bacterial cellulose was obtained by developing an Acetobacter xylinum culture and was visualized using SEM (scanning electron microscopy) and elementally determined through EDAX (dispersive X-ray analysis) tests. Keratin species (β–keratose and γ-keratose) was extracted by hydrolytic degradation from non-dyed human hair. SEM, EDAX and conductometric titration tests were performed for physical–chemical and morphological evaluation. Cytocompatibility tests performed in vitro confirmed the material non-toxic effect on cells. The scaffolds, with and without stem cells, were grafted on the burned wounds on the rabbit’s dorsal region and the grafts were monitored for 21 days after the application on the wounds. The clinical monitoring of the grafts and the histopathological examination demonstrated the regenerative potential of the bacterial cellulose–keratin scaffolds, under the test conditions.

Sclerotinia sclerotiorum (Lib.) de Bary (1884) is a fungal plant pathogen with worldwide distribution and a varying host range from different botanical families. It can cause damage to a large variety of crops such as sunflower, soybean, dry bean, canola, some vegetables, and ornamental plants. This article reports the occurrence of twig blight on the forsythia plant from the NE region of Romania. The disease was observed on Forsythia × intermedia Zab. plants from the Arboretum Park of the Iasi University of Life Sciences (IULS), located in Iasi City, Romania. Infected tissue was investigated through morphological characteristics using Sanger sequencing. Genomic DNA was extracted from the isolate obtained from naturally infected plants, and the ribosomal internal transcribed spacer region was amplified using the ITS1, ITS2, and LSU D1 and D2. Based on the results of this study, molecular and morphological data suggest that Forsythia twig blight can be caused by S. sclerotiorum. Constant monitoring of Sclerotinia sclerotiorum across multiple hosts and time intervals will reduce potential spread and future economic losses in cultivated species.