This work describes a green synthesis, the characterization, and biological evaluation of silver nanoparticles (AgNPs). The AgNPs suspension was synthesized using aqueous leaf extract of Eucalyptus grandis, which presented a characteristic band at 407 nm in the UV-Vis spectrum. The AgNPs presented a spherical shape and size of 9.7 ± 0.3 nm. The nanoparticles were stable over a month, indicating that E. grandis’ extract is suitable for their preparation and stabilization. The X-ray analysis showed that the crystallinity of AgNPs corresponded to the centered face phase of silver. The antibacterial and leishmanicidal activities of AgNPs were evaluated. The AgNPs presented antibacterial activity on the Gram-negative bacteria Escherichia coli at 53.9 µg mL-1. The leishmanicidal activity evaluation against promastigote forms of Leishmania infantum, Leishmania amazonensis, and Leishmania braziliensis showed that the biological response is dependent on the volume of AgNP suspension. It was demonstrated that L. infantum was more sensitive to the nanoparticle’s treatment than L. amazonensis and L. braziliensis. The treatment of L infantum promastigotes with 150 µL of AgNP suspension reduced parasite growth by 67.9%, a result which was similar to the treatment with 1 (66.7%) or 2 µL (70.6%) of amphotericin B used as a positive control.

Calonectria pteridis is one of the most important causal agents of Calonectria leaf blight (CLB) of Eucalyptus spp. in Brazil, which is a limiting factor for growth of Eucalyptus plantations. In this study we developed standard procedures for in vitro mass spore production and inoculation of C. pteridis for screening plant species and clones for resistance to CLB. The isolates used in this study were identified using similarity in DNA sequence to reference strains. Among six media tested, glucose asparagine agar induced the highest sporulation production and a significantly enhanced sporulation was found by scraping the aerial mycelium and temporarily submersing the cultures in tap water, followed by drying and additional incubation of the culture. We also demonstrated that the severity of CLB on excised leaves of two Eucalyptus spp. clones increased significantly when the inoculated leaves were incubated in the dark. The optimal temperature for infection was 26ºC when plants were incubated for 48 hours post-inoculation in a mist chamber and then maintained in a greenhouse (25ºC±5ºC) for 50 days. This study identifies environmental conditions to improve spore production and inoculation procedures of C. pteridis for selection of resistant Eucalyptus spp.