RESUMO

The fungus Rhizoctonia oryzae-sativae is an important pathogen that causes the aggregated sheath spot disease on rice. In this study, we investigated the genetic structure of rice-adapted populations of R. oryzae-sativae sampled from traditional rice-cropping areas from the Paraíba Valley, São Paulo, Brazil, and from Meta, in the Colombian Llanos, in South America. We used five microsatellite loci to measure population differentiation and infer the pathogen's reproductive system. Gene flow was detected among the three populations of R. oryzae-sativae from lowland rice in Brazil and Colombia. In contrast, a lack of gene flow was observed between the lowland and the upland rice populations of the pathogen. Evidence of sexual reproduction including low clonality, Hardy-Weinberg equilibrium within loci and gametic equilibrium between loci, indicated the predominance of a mixed reproductive system in all populations. In addition, we assessed the adaptive potential of the Brazilian populations of R. oryzae-sativae to emerge as a pathogen to Urochloa spp. (signalgrass) based on greenhouse aggressiveness assays. The Brazilian populations of R. oryzae-sativae were probably only incipiently adapted as a pathogen to Urochloa spp. Comparison between RST and QST showed the predominance of diversifying selection in the divergence between the two populations of R. oryzae-sativae from Brazil.

Assuntos

RESUMO

Rhizoctonia solani Kühn, es un patógeno de suelo, que causa enfermedades en un amplio rango de hospedantes de cultivos agrícolas. Las necesidades de reducir el uso indiscriminado de fungicidas químicos conllevan al estudio de otras alternativas menos agresivas al medio ambiente. Los monoterpenos presentes en los aceites esenciales de plantas, presentan una marcada actividad biocida y son compuestos que resultan menos perjudiciales desde el punto de vista ambiental. Se prepararon cuatro mezclas de monoterpenos (timol-entol, timolalcanfor, timol-citronelal y timol-1,8 cineol) con el objetivo de evaluar la actividad antifúngica in vitro sobre R. solani, mediante su efecto sinérgico. Se empleó el método de adición al medio de cultivo de cada una de las mezclas a concentraciones de: 0,5; 0,1; 0,05; 0,03 y 0,01 por ciento, partiendo de una solución madre al 10 por ciento en dimetilsufóxido (DMSO) al 5 por ciento. Se calcularon los porcentajes de inhibición y los resultados se analizaron estadísticamente. Se determinaron las dosis inhibitorias medias y se clasificaron la toxicidad de cada una de las mezclas en: inocua, ligera, moderada y tóxica a cada concentración. Las cuatro mezclas mostraron 100 por ciento de inhibición a las concentraciones de: 0, 5; 0, 1; 0,05 y 0,03 por ciento. A la menor concentración las mezclas de timol-mentol y timol-cineol fueron las de mayor efecto inhibitorio del crecimiento micelial de R. solani.

Rhizoctonia solani Kühn is a soil pathogen that causes diseases in a wide host range from agricultural crops. The need to reduce the indiscriminate use of chemical fungicide it has led to the study of other less aggressive environment alternatives. Monoterpenes, common components in plants essential oils, shows a maked biocide activity and are compounds less harmful from an environmental point of view. With the objective of evaluate the in vitro antifungal activity against R. solani, four binary monoterpenes mixtures (thymol-menthol, thymol-camphor, thymol-citronellal and thymol-1,8 cineol) with the objective of evaluate the in vitro antifungal activity against R. solani, four monoterpenes mixtures were prepared. The method of addition to culture media of each of the mixtures in concentrations of: 0, 5; 0, 1; 0, 05; 0, 03 and 0, 01 percent, from a stock solution to 10 percent in dimethylsulfoxide (DMSO) to 5 percent were used. The inhibition percentages were calculated and the results were statistically analyzed. Median inhibitory dose was determined and the toxicity of each mixture were classified in: harmless, light, moderate and toxic in each concentration. The four mixtures showed 100 percent of micelial growth inhibition in concentrations of 0, 5; 0, 1; 0,05 and 0,03 percent. The thymol-cineol and thymol-menthol mixtures had the higher inhibitory effect on micelial growth of R. solani at the lower concentration.

Assuntos

Assuntos

RESUMO

Rice sheath blight (ShB), which is caused by Rhizoctonia solani, has become the most serious rice disease in China. Yangdao 4, a cultivar with partial resistance to ShB, was crossed with Lemont, a susceptible cultivar, to develop mapping populations that were used to analyze quantitative trait loci (QTL) that confer resistance to ShB. QTL analysis were performed in 3 environments (E1-E3) using 2 F2 and 1 F2:3 populations, respectively. Three traits were recorded to evaluate ShB resistance, including disease rating (DR), lesion height (LH), and percentage of lesion height (PLH). Based on field evaluation of ShB resistance and the 2 genetic maps constructed, we identified a total of 8 QTLs for DR (4 in E1, 4 in E2, and 3 in E3), 6 QTLs for LH (1 in E1, 3 in E2, and 2 in E3), and 7 QTLs for PLH (1 in E1, 4 in E2, and 2 in E3). Sixteen of the ShB-QTLs co-localized as 6 clusters on chromosomes 3, 7, 11, and 12. Four of the 6 clusters contained ShB-QTLs that were detected in 2 environments, while the other 2 clusters with ShB-QTLs were detected in 1 environment. Three ShB-QTLs (qSBD-3-2, qSBL-3-1, and qSBPL-3-1) were delimited to a 581-kb region flanked by markers D333B and D334 on chromosome 3. The resistance alleles of Yangdao 4 at the qSBD-3-2 locus decreased DR by 0.68 and 0.79 in E2 and E3, respectively.

Assuntos

RESUMO

The soilborne fungus Rhizoctonia solani anastomosis group 3 (AG-3PT) is a globally important potato pathogen. However, little is known about the population genetic processes affecting field populations of R. solani AG-3PT, especially in the South American Colombian Andes, which is near the center of diversity of the two most common groups of cultivated potato, Solanum tuberosum and S. phureja. We analyzed the genetic structure of 15 populations of R. solani AG-3PT infecting potato in Colombia using 11 simple-sequence repeat (SSR) markers. In total, 288 different multilocus genotypes were identified among 349 fungal isolates. Clonal fractions within field populations were 7 to 33%. RST statistics indicated a very low level of population differentiation overall, consistent with high contemporary gene flow, though moderate differentiation was found for the most distant southern populations. Genotype flow was also detected, with the most common genotype found widely distributed among field populations. All populations showed evidence of a mixed reproductive mode, including both asexual and sexual reproduction, but two populations displayed evidence of inbreeding.

Assuntos

RESUMO

Twenty-one isolates of Rhizoctonia solani were categorized into three anastomosis groups consisting of AG-4-HG-I (eight isolates), AG-2-2 (nine isolates) and AG-5 (four isolates). Their pathogenic capacities were tested on cotton cultivar Giza 86. Pre-emergence damping-off varied in response to the different isolates; however, the differences were not significant. Soluble proteins of the fungal isolates were electrophoresed using SDS-PAGE and gel electrophoreses. A dendrogram of the protein banding patterns by the UPGMA of arithmetic means placed the fungal isolates into distinct groups. There was no evidence of a relationship between protein dendrogram, anastomosis grouping or level of virulence or geographic origin. The dendrogram generated from these isolates based on PCR analysis with five RAPD-PCR primers showed high levels of genetic similarity among the isolates from the same geographical locations. There was partially relationship between the genetic similarity and AGs or level of virulence or geographic origin based on RAPD dendrogram. These results demonstrate that RAPD technique is a useful tool in determining the genetic characterization among isolates of R. solani.

Assuntos

RESUMO

The interface between plants and pathogens plays an important role in their interaction. Studies of fungal cell walls are scarce and previous results show the existence of alpha-1,3-glucans in addition to ss-glucans. In addition, alpha-1,3-glucans are not present in plant cell walls, and alpha-glucanase activity in plants has not been described before. In a previous work, we purified and characterized an alpha-1,3-glucan from a binucleated, non-pathogenic Rhizoctonia isolate, which induces plant defence responses. Therefore, in order to study the architecture of the fungal cell wall, and the accessibility and localization of the alpha-glucan elicitor, we prepared an antibody against the alpha-1,3-glucan and analysed its localization by TEM. Immunolocalization showed the presence of the alpha-1,3-glucan in the intercellular spaces and along the cell walls, mainly on the inner layers. This result, and the presence of the alpha-1,3-glucan in the liquid culture medium in which binucleated non-pathogenic Rhizoctonia was grown, confirmed that the alpha-glucan had been secreted. The alpha-1,3-glucan was also immunocytolocalized on potato sprouts tissue elicited with the glucan; gold particles were observed in vacuoles and close to the plasmalemma. In addition, alpha-glucanase activity in potato sprouts was detected using cell wall glucans from the pathogenic isolate R. solani AG-3 as substrates; whereas, when cell wall glucans from non-pathogenic isolates were used, no alpha-glucanase activity was detected. Our results suggest that the presence of alpha-1,3-glucans could be associated with the formation and integrity of the cell wall and also with plant-fungi interactions. This is the first report to describe alpha-glucanolytic activity in plants.

Assuntos

RESUMO

Binucleate Rhizoctonia (BNR) isolate (232-C6) is an effective biocontrol agent for protection of potato from Rhizoctonia canker, a disease caused by Rhizoctonia solani. Production of hydrolytic enzymes is one of the best known inducible defense responses following microbial infection. We isolated and characterized a cell wall alpha-glucan from BNR, which induces beta-1,3 glucanase activities in potato sprouts, the primary site of infection by R. solani. An autoclaving method, previously reported for isolation of oligosaccharide elicitors was used, and the glucan purified by chromatographic techniques. Maximal induction of beta-1,3 glucanase activity in potato sprouts was obtained with 250 microg of the alpha-glucan elicitor after 6 days from inoculation time. Both, BNR mycelium and the alpha-glucan produced a similar kinetic response of beta-1,3 glucanase. However, the alpha-glucan did not induce phytoalexin accumulation, previously correlated with the defense response. Uronic acids (approximately 10% with respect to total neutral sugars) were determined and identified as glucuronic acid by high-pH anion-exchange chromatography. Methylation analysis showed that the glucan consists of (1-->3) and (1-->4)-linked glucose units with preponderance of the first ones. Some of the (1-->4) linkages were branched at position 6. The glucan was partially degraded with amyloglucosidase. This, together with the NMR spectra data and the high optical rotation of the original (+195 degrees ) and degraded glucans (+175 degrees ) proved the alpha configuration. Further methylation of the amyloglucosidase degraded glucans indicated that they consist of (1-->3)-linked glucoses. The present study is the first report on the isolation and characterization of an alpha-glucan from Rhizoctonia, that may be important as a biocontrol factor.

Assuntos

Assuntos

RESUMO

Pre-and post-emergence damping-off of canola seedlings caused by Rhizoctonia solani is a serious disease in Western Canada. Other fungi such as Fusarium spp. and Pythium spp. are also related to seedling damping-off. To-day, the search of soil bacteria is becoming a tool to use microorganisms as potential biocontrol agents for several plant diseases. The purpose of this research was to detect bacteria to biologically control R. solani, Pyrhium spp., and Fusarium spp. Soil samples were collected throughout Alberta during 1987 to isolate bacteria. Canola seedlings were also used to obtain bacteria from the same samples. Plant pathogenic fungi were tested to detect the antagonistic activity of the isolates. Tests were made with coated canola seeds, amendments and fresh of freeze-dried cells. Three hundred forty-one bacterial cultures were isolated. Only 16 inhibited fungal growth: 7 showed the same effects against R. solani and 9 showed uneven effects. Some isolates showed a weak action to Pythium spp. and Fusarium spp. three isolated showed inhibitory effect on R. solani and Pythium spp. isolate F1 improved by about 50% the germination of canola seeds in inoculated pots when compared with the inoculated control. Coated seeds had low germination and emergence was below the inoculated control. the emergence of vanola seedlings was very much improved when isolate 147 was delivered as an amendment in inoculated pots. Identification showed that 3 bacterial belonged to Bacillus spp., 4 to green fluorescent Pseudomonas spp. and 2 were Streptomyces spp

Assuntos