Evidence of Pyricularia oryzae adaptability to tricyclazole.

Pyricularia oryzae is the etiological agent of rice blast, the most destructive disease in rice crops and chemical control based on fungicide is the main method used in its management. The aim of this study was characterize pathogenicity and identify P. oryzae isolates adapted to tricyclazole. P. oryzae monosporic isolates were collected in the state of Tocantins and inoculated in international differentiating series of rice cultivars for determination of pathotypes. After, the same isolates were inoculated in the rice cultivar IRGA 424 to evaluate resistance to fungicide Bim® 750 BR (Tricyclazole - 250 g/ha) that was applied 24 and 48 hours after pathogen inoculation (hai). Leaf blast severity and infection efficiency were evaluated 9 days after inoculation (dai), latency period (2 dai) and sporulation intensity (7 dai). Nine different pathotypes were identified, predominantly as IA group. The latent period of isolates occurred between from 48 to 120 h. The application of tricyclazole, 24 hai reduced disease severity with the exception of the isolate Py 7.1. The great variability of the pathogen allowed for adaptation to this molecule and can increase its aggressiveness and should be considered to guide the integrated management of the disease.

Molecular identification of Trichoderma sp. isolates and biochemical characterization of antagonistic interaction against rice blast.

This study aimed to identify four isolates of Trichoderma sp. (Ufra.T06, Ufra.T09, Ufra.T12, and Ufra.T52) and characterize their interaction with Magnaporthe oryzae in vitro and in vivo conditions. The four isolates of Trichoderma sp. were sequenced, investigated as an antagonist against M. oryzae in five Petri plate assays, and as an inhibitor of conidial germination appressoria formation. Finally, were quantified the lytic activity of chitinase (CHI), glucanase (GLU), and protease (PRO) during co-cultivation of Trichoderma sp. and M. oryzae. In vivo, leaf blast suppression was evaluated in two assays: simultaneous and curative application. Both in vitro and in vivo assays were scanned by electron microscopy (SEM). All isolates were identified as Trichoderma asperellum. All in vitro Petri plates assays reduced M. oryzae colony growth (paired-91.18% by Ufra.T09, volatile metabolites-all isolates equally reduced, non-volatile-68.33% by Ufra.T06, thermostability-99.77% by Ufra.T52 and co-cultivate-64.25% by Ufra.T52). The filtrates and conidia suspensions for T. asperellum isolates inhibited the conidia germination and appressoria formation significantly. In co-cultivate (mycelial or cell wall), all enzymes (GLU, CHI, and PRO) and times (24, 48, and 72 h) showed increased activity. In vivo, reduced leaf blast severity until 94.64% (Ufra.T52cs) in a simultaneous and until 85% (Ufra.T09 24 and 48 hasi) in a curative application. T. asperellum isolates showed efficient control of M. oryzae by mycoparasitism, and antibiosis mechanisms were interfered with by the M. oryzae infection process.