The present study aimed to chemically profile the hydroalcoholic extracts from the microalgae (MEs) Nannochloropsis oculata, Phaeodactylum tricornutum, Tetradesmus obliquus, and Tetraselmis tetrathele and evaluate their effects on the development of Colletotrichum lindemuthianum and anthracnose symptoms, as well as on the initial growth of bean plants. For this, MEs were analyzed using UPLC coupled with a mass spectrometer, allowing the identification of peaks and annotation of potential metabolites. Fungal mycelial growth was assessed seven days after inoculation, and conidial germination was measured 72 h after incubation, using ME concentrations of 0, 0.1, 0.5, and 1.0 mg·mL⁻¹. Bean seeds of the IPR Uirapuru cultivar were sown and treated with 3 mL of extracts at four time points: at sowing and 72 h after each previous treatment. After 11 days of cultivation in a growth chamber, the plants were divided into two groups: one for anthracnose control assessment and the other for evaluating growth promotion by MEs. Plant length as well as fresh and dry weights of shoots and roots were determined, leaf pigments were quantified, and anthracnose severity was assessed using a diagrammatic scale. The UPLC analysis identified 32 compounds in the extracts of the four microalgae, belonging to different chemical and functional groups, with lipids being the most significant fraction. The extracts exhibited variability and diversity in chemical composition depending on the microalgal species. MEs did not affect mycelial growth yet increased the germination of C. lindemuthianum conidia, regardless of the dose or species used. Anthracnose severity was not affected by the microalgae extracts. Regarding growth promotion, the extracts showed varying effects but generally increased shoot and root length, fresh biomass, and leaf pigment content.

The present study aimed to evaluate the effect of silver nanoparticles (AgNPs) on the development of Colletotrichum lindemuthianum, the progression of anthracnose symptoms, and the growth of common bean plants. For this purpose, the fungal mycelial growth and conidial germination were assessed at AgNP concentrations of 0, 10, 30, and 50 mg·L⁻¹ after seven days of incubation, as well as at 0, 0.1, 0.5, 1, 10, 30, and 50 mg·L⁻¹ after 72 h, respectively. Bean plants of the IPR Uirapuru cultivar were sprayed at the V3 growth stage with AgNPs at 0, 10, 30, or 50 mg·L⁻¹, either two days before, on the day of, or two days after inoculation. Conidial germination and appressoria melanization were measured on the leaf discs collected 24, 48, and 72 h after inoculation, and disease severity was assessed at 7 and 12 days post-inoculation. Another set of bean plants grown under the same conditions was used to evaluate growth promotion by AgNPs. For this, the plants were sprayed twice (with a seven-day interval), starting at the V3 growth stage, with AgNPs at 0, 10, 30, or 50 mg·L⁻¹. Seven days after the second treatment, plant length and the fresh and dry weights of shoots and roots were measured, and the foliar pigments were quantified. The AgNPs did not reduce mycelial growth but completely inhibited the germination of C. lindemuthianum conidia. The severity of anthracnose decreased with the AgNPs in a dose- and application time-dependent manner, with the highest reduction (90%) observed when applied on the same day as an inoculation at 50 mg·L⁻¹. This was strongly linked to a 70% decline in conidia germination and appressorium melanization on bean leaves. AgNPs at 50 mg·L⁻¹ promoted plant growth by increasing the total length by 3%, as well as the fresh weights of bean shoots and roots by 17% and 90%, respectively, but did not affect the content of leaf pigments.

As plantas cultivadas estão em constante contato com microrganismos e animais que, se não manejados de acordo, podem ameaçar a segurança alimentar regional e causar sérios prejuízos econômicos. Assim, o acesso a um diagnóstico rápido e preciso do agente causal é fundamental para a elaboração de estratégias de manejo adequadas e efetivas. Neste contexto, criou-se em 2002 a Clínica de Doenças de Plantas da UFSC. Nesses 20 anos de atuação, a Clínica recebeu um total de 404 amostras para análise provenientes dos estados de Santa Catarina, Paraná, Rio Grande do Sul e Mato Grosso. Estas foram agrupadas em: outras (substratos, ração animal, água, etc; 147 amostras), plantas ornamentais (106), hortaliças (83), frutíferas (6) e grãos (7) e apresentavam, principalmente, doenças causadas por fungos. Além disso, o trabalho realizado pela Clínica contribuiu para a capacitação profissional na área de fitopatologia e para a criação e fortalecimento de laços entre a academia e o setor produtivo.