Potencial de herbicidas para o controle de patógenos de solo do feijão

Pouco se conhece sobre os efeitos de herbicidas em fungos patogênicos habitantes do solo que infectam os feijoeiros. Foi avaliado o efeito de herbicidas no crescimento micelial de Fusarium solani f. sp. phaseoli, F. oxysporum f. sp. phaseoli, Macrophomina phaseolina, Rhizoctonia solani, Sclerotium rolfsii e Sclerotinia sclerotiorum. Esses fungos causam as doenças de solo mais danosas do feijão. Avaliou-se, em placas de Petri, o crescimento radial desses fungos em meio batata-dextrose-ágar com cinco concentrações (0, 1, 10, 100 e 1.000 mg L-1) dos herbicidas imazamox, fomesafen, fluazifop-p-butyl, bentazon, glyphosate e S-metolachlor. O crescimento micelial de todos os fungos decresceu acentuadamente apenas com o S-metolachlor na concentração de 1.000 mg L-1. Por isso, o efeito desse herbicida também foi testado em duas concentrações (1.000 ou 12.000 mg L-1) na germinação de escleródios de S. rolfsi e S. sclerotiorum (miceliogênica) ou de S. sclerotiorum (carpogênica). Não houve efeito significativo de S-metolachlor na germinação miceliogênica de escleródios desses dois fungos. Entretanto, o S-metolachlor retardou a germinação carpogênica de escleródios de S. sclerotiorum. Os resultados sugerem que o herbicida S-metolachlor tem potencial de uso no manejo de doenças do feijão causadas por fungos de solo.

Molecular Identification of Trichoderma spp. in Garlic and Onion Fields and In Vitro Antagonism Trials on Sclerotium cepivorum

ABSTRACT Trichoderma species are non-pathogenic microorganisms that protect against fungal diseases and contribute to increased crop yields. However, not all Trichoderma species have the same effects on crop or a pathogen, whereby the characterization and identification of strains at the species level is the first step in the use of a microorganism. The aim of this study was the identification – at species level – of five strains of Trichoderma isolated from soil samples obtained from garlic and onion fields located in Costa Rica, through the analysis of the ITS1, 5.8S, and ITS2 ribosomal RNA regions; as well as the determination of their individual antagonistic ability over S. cepivorum Berkeley. In order to distinguish the strains, the amplified products were analyzed using MEGA v6.0 software, calculating the genetic distances through the Tamura-Nei model and building the phylogenetic tree using the Maximum Likelihood method. We established that the evaluated strains belonged to the species T. harzianum and T. asperellum; however it was not possible to identify one of the analyzed strains based on the species criterion. To evaluate their antagonistic ability, the dual culture technique, Bell’s scale, and the percentage inhibition of radial growth (PIRG) were used, evidencing that one of the T. asperellum isolates presented the best yields under standard, solid fermentation conditions.

Macrophomina phaseolina: density and longevity of microsclerotia in soybean root tissues and free on the soil, and competitive saprophytic ability

In field experiments, the density of Macrophomina phaseolina microsclerotia in root tissues of naturally colonized soybean cultivars was quantified. The density of free sclerotia on the soil was determined for plots of crop rotation (soybean-corn) and soybean monoculture soon after soybean harvest. M. phaseolina natural infection was also determined for the roots of weeds grown in the experimental area. To verify the ability of M. phaseolina to colonize dead substrates, senesced stem segments from the main plant species representing the agricultural system of southern Brazil were exposed on naturally infested soil for 30 and 60 days. To quantify the sclerotia, the methodology of Cloud and Rupe (1991) and Mengistu et al. (2007) was employed. Sclerotium density, assessed based on colony forming units (CFU), ranged from 156 to 1,108/g root tissue. Sclerotium longevity, also assessed according to CFU, was 157 days for the rotation and 163 days for the monoculture system. M. phaseolina did not colonize saprophytically any dead stem segment of Avena strigosa,Avena sativa,Hordeum vulgare,Brassica napus,Gossypium hirsutum,Secale cereale,Helianthus annus,Triticosecalerimpaui, and Triticum aestivum. Mp was isolated from infected root tissues of Amaranthus viridis,Bidens pilosa,Cardiospermum halicacabum,Euphorbia heterophylla,Ipomoea sp., and Richardia brasiliensis. The survival mechanisms of M. phaseolina studied in this paper met the microsclerotium longevity in soybean root tissues, free on the soil, as well as asymptomatic colonization of weeds.