A method based on restriction analysis of polymerase chain reaction (PCR)-amplified ribosomal DNA was developed for the rapid characterization of large populations of Rhizoctonia solani at the anastomosis group (AG) level. The restriction maps of the internal transcribed spacers (ITS) sequences were compared for 219 isolates of R. solani belonging to AG-1 to AG-12 and AG-BI, representing diverse geographic and host range origins. Four discriminant restriction enzymes (MseI, AvaII, HincII, and MunI) resolved 40 restriction fragment length polymorphism (RFLP) types among the 219 ITS sequences of R. solani. Each RFLP type could be assigned to a single AG except for two RFLP types, which were common to two AG. A fifth enzyme allowed the discrimination of AG-6 and AG-12. In addition, the combination of four enzymes allowed the discrimination of subsets within AG-1, AG-2, AG-3, and AG-4. The efficiency of the typing method was confirmed by analyzing PCR-amplified ITS sequences of 30 reference strains. Furthermore, the PCR-RFLP method was used to characterize at the AG level 307 isolates of R. solani originating from ten sugar beet fields exhibiting patches of diseased plants in France. The PCR-based procedure described in this paper provides a rapid method for AG typing in R. solani.

Pour Trichoderma, dont la systématique est assez aléatoire, les modes d'action antagoniste, bien étudiés par DE NNI S & WE BSTER (1971, a, b, c) peuvent servir

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Field experiments were carried out at two different forest nurseries during the summer of 1994 to examine the efficacy of soil solarization for the control of damping-off. Both soils hosted Pythium spp., Fusarium spp. and Rhizoctonia solani as damping-off agents. Soil samples from solarized, steamed, fumigated and untreated plots were periodically collected and assayed for soil infectivity. Solarization with a double layer of polyethylene film was as effective as steaming or fumigation in reducing soil infectivity in the uppermost layer. During July the temperature of covered beds rose as high as 50 °C at a soil depth of 5 cm. The method achieved good control of Pythium spp., the main cause of damping-off at both nurseries, whereas Fusarium spp. were more tolerant. The association of Trichoderma spp. with a reduction of soil infectivity at the last sampling date strongly suggested that biocontrol processes were induced after solarization. Soil solarization provides a suitable method for control of damping-off.