78 resultados para Sclerotinia sclerotiorum


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A preservação de fungos fitopatogênicos por longos períodos de tempo é importante para que pesquisas possam ser realizadas a qualquer momento. Os fungos habitantes do solo são organismos que podem produzir estruturas de resistência em face de situações adversas, tais como ausência de hospedeiros e ou condições climáticas desfavoráveis para a sua sobrevivência. O objetivo deste trabalho foi desenvolver metodologias de preservação de estruturas de resistência para os fungos Fusarium oxysporum f.sp. lycopersici raça 2, Macrophomina phaseolina, Rhizoctonia solani AG4 HGI, Sclerotium rolfsii, Sclerotinia sclerotiorum e Verticillium dahliae. O delineamento foi inteiramente casualizado, com um método de produção de estruturas para cada fungo, submetido a três tratamentos [temperatura ambiente de laboratório (28±2ºC), de geladeira (5ºC) e de freezer (-20ºC)] e com dois frascos por temperatura. Mensalmente, e por um período de um ano, a sobrevivência e o vigor das colônias de cada patógeno foram avaliadas em meios de cultura específicos. Testes de patogenicidade foram realizados após um ano de preservação, com as estruturas que sobreviveram aos melhores tratamentos (temperatura) para todos os fungos. As melhores temperaturas (tratamentos) para preservar os fungos foram: a) F. oxysporum f.sp. lycopersici em temperatura de refrigeração e de freezer (5,2 e 2,9 x 10³ufc.g-1 de talco, respectivamente); b) M. phaseolina em temperatura de refrigeração [100% de sobrevivência (S) e índice 3 de vigor (V)] e S. rolfsii em temperatura ambiente (74,4% S e 1 V) e c) S. sclerotiorum e V. dahliae, ambos em temperatura de freezer (100% S e 3 V). Após um ano de preservação, somente V. dahliae perdeu a patogenicidade na metodologia desenvolvida.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

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The biofertilizer was produced through anaerobic fermentation of cow manure adding milk, sugar, salts, cow liver parts and bone powder. After 73 days of fermentation it was evaluated the effect on micelial growth of Pythium aphanidermatum, Alternaria solani, Stemphylium solani, Septoria licopersici, Sclerotinia sclerotiorum, Botrytis cinerea, Rhizoctonia solani, Fusarium oxysporum f. sp. phaseoli and spores germination of B. cinerea, A. solani, Hemileia vastatrix and Coleosporium plumierae. In relation to micelial growth inhibition, the growth rate was calculated and it was found that, in general, concentrations over 10% caused a total inhibition of growth for the majority of fungi assayed. In case of spores germination, biofertilizer concentration over 20% has inhibited completely the germination of B. cinerea, over 10% inhibited A. solani, 5 and 1% of C. plumierae and H. vastatrix, respectively. Three different biofertilizers were also tested and one of them was less effective, which was the one produced with manure from confined cows opposed to the others produced with grazing cows.

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The common beans (Phaseolus vulgaris L.) is a fabacea sufficiently spread out in all domestic territory. However, the quality of its seeds represents one of the main causes of low productivity in the beans farmings in Brazil. The objective of this work was to evaluate physiological and sanitary seed qualities of eleven bean cultivars. The physiological seed quality was evaluated trough standard germination and vigor tests. The sanitary seed quality was evaluated through two tests: blotter test was employed to evaluate fungi incidence and Koch & Menten method was employed to observe Sclerotinia sclerotiorum (Lib) de Bary occurrence. Xamego, BRS Valente, Bambu and Pérola had the best results of physiological tests. Jalo Precoce, Roxo 90, Corrente and Aporé had no good results of vigor and germination, besides presenting the lowest indices of died seeds. Fusarium sp., Aspergillus spp., Penicillium sp., Phoma sp., Rhizopus sp. and Botrytis sp. were the fungi detected in the sanity tests.

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The aim of this research was to evaluate the white mold severity (Sclerotinia sclerotiorum (Lib.) of Bary), bean production components and yield (Phaseolus vulgaris L.), variety Perola, according to the application of procimidone fungicide (Sialex 500), through fungigation (center pivot) and automotive sprayer (Uniport). The study was carried under field production commercial conditions, in Primavera do Leste - MT - Brazil. The experiment consisted of 5 treatments (with 4 repetitions of 4 ha each), all with two procimidone applications (1.2 kg ha-1 each application, same as, 0.6 kg a.i. per hectare) to the 42 and 52 days after seeding. The water depths of 5.5 and 11.0 mm were tested in the application through central pivot (this had your checked uniformity), providing volumes of 55.000 and 110.000 L ha-1, respectively, and the volumes of 120 and 200 L ha-1 in the automotive sprayer. The severity of disease was evaluated by the percentage of the area affected by plant damage using diagramatic grade scale of white mold severity, as described by Azevedo (1998). The values were used to calculate the area under the disease progress curve (AUDPC). They were also analyzed, the number of the fungus apothecia during the crop cycle and the residual sclerotias weight in harvest. On this occasion, it was also evaluated the crop yield parameters: number of plants per plot (final stand), pods per plant, grains per pod, medium weight of 200 grains and productivity of grains. The AUDPC values, apothecia to 42, 49 and 56 days after seeding, sclerotias in 2 soil kg and the crop productivity parameters were submitted to the variance analysis and Tukey Test at 0.05 of probability. This test was also applied in the comparison among the different fungicide application methods, independent of spray volumes in each one. The statistical processing was accomplished by STAT program. The results showed that weren't differences among application techniques studied in relation to productivity parameters, however, best white mold control, smaller apothecia number to 49 and 56 days after seeding and smaller weight of residual sclerotias in the harvest were obtained with the fungigation, independently of the spray volume used.

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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Pós-graduação em Agronomia (Proteção de Plantas) - FCA

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Fungi are disease-causing agents in plants and affect crops of economic importance. One control method is to induce resistance in the host by using biological control with hypovirulent phytopathogenic fungi. Here, we report the detection of a mycovirus in a strain of Colletotrichum gloeosporioides causing anthracnose of cashew tree. The strain C. gloeosporioides URM 4903 was isolated from a cashew tree (Anacardium occidentale) in Igarassu, PE, Brazil. After nucleic acid extraction and electrophoresis, the band corresponding to a possible double-stranded RNA (dsRNA) was purified by cellulose column chromatography. Nine extrachromosomal bands were obtained. Enzymatic digestion with DNAse I and Nuclease S1 had no effect on these bands, indicating their dsRNA nature. Transmission electron microscopic examination of extracts from this strain showed the presence of isometric particles (30-35 nm in diameter). These data strongly suggest the infection of this C. gloeosporioides strain by a dsRNA mycovirus. Once the hypovirulence of this strain is confirmed, the strain may be used for the biological control of cashew anthracnose.

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The sugarcane root endophyte Trichoderma virens 223 holds enormous potential as a sustainable alternative to chemical pesticides in the control of sugarcane diseases. Its efficacy as a biocontrol agent is thought to be associated with its production of chitinase enzymes, including N-acetyl-beta-D-glucosaminidases, chitobiosidases and endochitinases. We used targeted gene deletion and RNA-dependent gene silencing strategies to disrupt N-acetyl-beta-D-glucosaminidase and endochitinase activities of the fungus, and to determine their roles in the biocontrol of soil-borne plant pathogens. The loss of N-acetyl-beta-D-glucosaminidase activities was dispensable for biocontrol of the plurivorous damping-off pathogens Rhizoctonia solani and Sclerotinia sclerotiorum, and of the sugarcane pathogen Ceratocystis paradoxa, the causal agent of pineapple disease. Similarly, suppression of endochitinase activities had no effect on R. solani and S. sclerotiorum disease control, but had a pronounced effect on the ability of T. virens 223 to control pineapple disease. Our work demonstrates a critical requirement for T. virens 223 endochitinase activity in the biocontrol of C. paradoxa sugarcane disease, but not for general antagonism of other soil pathogens. This may reflect its lifestyle as a sugarcane root endophyte.

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Botrytis cinerea ist einer der wichtigsten Phytopathogene, der im Bereich der Weinbereitung als Erreger des Edel- bzw. des Grauschimmels von Trauben eine zentrale Stellung einnimmt. Taxonomisch gehört dieser Organismus zur Familie der Sclerotiniaceae, die ausnahmslos Phytopathogene sind und weltweit große Schäden bei verschiedenen Pflanzen verursachen. Die molekularbiologische Identifikation von Vertretern dieser wichtigen Gruppe von Pflanzenpathogenen ist jedoch bis heute ein Problem. Aus diesem Grund wurde in der vorliegenden Arbeit als Themenschwerpunkt die zweifelsfreie Identifikation einiger Vertreter der Sclerotiniaceae bearbeitet. Hier konnte von neun verschiedenen Organismen die ‚Internal Transcribed Spacer Region’ identifiziert und zusätzlich zur 18S rDNA für eine sichere Identifikation ausgeschlossen werden. Die Unterscheidung der einzelnen Gattungen und verschiedener B. cinerea-Stämme wurde mit Hilfe der neuartigen nSAPD-PCR Technologie erfolgreich überprüft. Hier konnten die drei Gattungen Botrytis, Monilinia sowie Sclerotinia zweifelsfrei differenziert werden. Ferner konnten von Monilinia fructigena, Sclerotinia minor und Sclerotinia sclerotiorum neue Laccase-Gene identifiziert und komplett sequenziert werden, die homolog zur Laccase2 (lcc2) von B. cinerea sind. Auf Basis dieser Sequenzen bzw. Sequenzunterschiede konnte eine Multiplex-PCR zur zweifelsfreien Identifi-kation dieser Spezies etabliert werden. Im Folgenden konnte dieses System auch an Umweltproben aus der Umgebung von Mainz und Wiesbaden, aus Flomborn (Rheinhessen) sowie aus Stollberg (Sachsen) überprüft werden. Anhand dieser Proben konnte gleichzeitig ein konstantes Vorkommen dieses Gens in allen über-prüften Organismen gezeigt werden. Somit ist es zum ersten Mal möglich, ver-schiedene Spezies der Sclerotiniaceae in einer Probe simultan nachzuweisen und zu differenzieren. Anschließend wurde die Laccase-Expression der jeweiligen Sclerotiniaceae überprüft. Für M. fructigena konnte mindestens eine konstitutiv exprimierte Laccase im Kulturüberstand detektiert werden. Im Gegensatz dazu zeigten weder S. minor noch S. sclerotiorum eine derartige Aktivität. Da B. cinerea lcc2 expri-miert, wurde dies auch für M. fructigena angenommen. Die reverse Transkription der codierenden mRNA konnte jedoch nicht erfolgreich durchgeführt werden. Die Analyse des Genoms von B. cinerea und S. sclerotiorum zeigte zudem 13 bzw. 8 mögliche Laccase-Gene. Somit ist es wahrscheinlich, dass M. fructigena mehr als einen codierenden Bereich für ein derartiges Enzym besitzt und somit eine oder mehrere andere Laccasen exprimiert. Auf Basis der codierenden DNA-Sequenzen konnten EDV-gestützte Prote-incharakterisierungen mit allen neu entdeckten Laccase-Sequenzen durchgeführt werden. Die hier ermittelten Eigenschaften legen den Schluss nahe, dass es sich ausnahmslos um Proteine handelt, die extrazellulär lokalisiert sind. So besitzen alle drei eine identisch lange Signalsequenz, die für die Translokation in die extra-zelluläre Matrix nötig ist. Des Weiteren zeigen alle Laccasen eine schwache Hydrophobizität, so dass davon ausgegangen werden kann, dass diese Enzyme keine membranständigen Proteine sind. Auch konnten zahlreiche Glykosylie-rungspositionen ermittelt werden und bei M. fructigena die Glykosylierung der akti-ven Laccase nachgewiesen werden. Des Weiteren konnten alle konservierten Kupferbindepositionen ermittelt werden. Der Vergleich zur mRNA der Lcc2 von B. cinerea offenbarte die lcc2 von M. fructigena drei nicht-codierende Intronse-quenzen, für S. minor und S. sclerotiorum jedoch lediglich die ersten beiden. Somit bleibt für alle neu identifizierten Sequenzen die Frage nach der Expression offen. Es wurden weder Deletionen von Nukleotiden noch frame-shift Mutationen in den einzelnen Genen gefunden. Auch geben die Signalsequenzen bzw. die ent-haltenen Kupferbindepositionen keine Aufschluss über das Ausbleiben der Ex-pression dieser Gene. Da das von B. cinerea synthetisierte ß-1,3-1,6-Glucan in der Kellerwirtschaft große Filtrationsprobleme verursacht, wurde als ein zusätzlicher Themenschwerpunkt die Lyse dieses Polymers mit symbiontischen Mikroorganismen aus Termitendär-men untersucht. Da Termiten auf den Abbau von Polymeren, wie Cellulose und Hemicellulosen spezialisiert sind, lag die Vermutung nahe, dass auch das ß-Glucan von symbiontischen Mikroorganismen hydrolysiert werden kann. In der hier vorliegenden Arbeit konnte zwar das ß-Glucan erfolgreich herge-stellt und in pulverisierter Form 5 verschiedenen Termitenspezies als Futter ange-boten werden, die anschließende Isolierung der Darmflora und die Untersuchung der isolierten Mikroorganismen auf ein mögliche glucanolytische Aktivität erbrach-te jedoch nicht den erhofften Erfolg. Hier wurden acht verschiedene filamentöse Ascomyceten bzw. Zygomyceten isoliert, eine lytische Aktivität konnte jedoch bei keiner dieser Spezies gezeigt werden.

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The crops are affected by pests and diseases that decrease productivity. Among them are the damping off of seedlings that can occur in pre and post-emergence. In bean crops, cucumber and beet these diseases occur, being caused by various pathogens, especialy fitopathogenic fungi. Several measures are used for the controle of such diseases, among them, is the chemical seed treatment fungicides. However, society has become increasingly concerned about the quality and food and environmental contamination, generation a growting search for sensitive products to humans and the environment. The use of essential oils to control plant pathogens is an example of alternative tested by science in the search for less aggressive technologies. This study aimed to evaluate the efficiency of the use of essential oil Aloysia citriodora, in control of pathogens causing damping off in beans, cucumber and beet. This thesis was divided in four chapters, the introductory first, and the other addressing the control of Pythium sp. in beans, Sclerotinia sclerotiorum on cucumber, and Fusarium sp. on beet. The methodology consisted of four experiments in each pathosystem, with all the work done at the Federal Technological University of Parana, Campus Dois Vizinhos. In the first experiment evaluated the fungistatic and fungicidal effect of the essential oil of A. citriodora on PDA in vitro in mycelial growth of pathogens studied. In the second experiment evaluated the in vitro effect of essential oil concentrations of A. citriodora in BD medium on microscope slides, on the germination of sporangia Pythium sp. and conidia Fusarium sp., and in Petri dishes with PDA medium, the sclerotia germination speed index of S. sclerotiorum. In the third experiment, we evaluated in germination test in paper roll (PR), the phytotoxic effect or not the use of essential oil concentrations of A. citriodora in dry bean seed, cucumber and beet. The variables used to assess this experiment were the germination percentage, mediun green mass per plant and average length of seedlings. In the fourth experiment we assessed the effect of treating bean seeds, cucumber and beet with essential oil contents of A. citriodora, seeds in their subsequent substrates contamined with pathogens studied, Pythium sp., S. sclerotiorum and Fusarium sp. In this experiment we used the following variables: percentage of emergence, percentage of post-emergence damping off, green average mass per plant, average length per plant and biochemical analyzes. The biochemistry of plant tissues evaluated were as follows: protein content, enzymatic activities of peroxidases, phenylalanine ammonia-liase (PAL), chitinases and β-1,3-glucanases. The in vitro results show that the essential oil has fungistatic and fungicidal effect on mycelial growth, on sporangia germination, conidia and sclerotia of the pathogens studied in this work, wich may be related to its major components, citral and limonene. The oil also exhibits low phytotoxicity to seeds of the species studied, only in beans decreases germination in most studied dosage (0,25%), cucumber also in the higher dosage (0,25%) reduce the length of seedlings, and beet there were no negative effects to the seedlings. In the test in substrate contaminated with the pathogens, the use of essential oil: increased germination and decreased post emergence damping off of beans seedlings; at a concentration of 0,0625% decreases post emergence damping off in cucumber. In biochemical analyzes found an increase in the enzymatic activity of peroxidases and β-1,3-glucanases on beans, and glucanases on cucumber, and increased enzyme activity of peroxidases on beet, showing action in resistance induction at damping off.

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Soybean plays an important role in the Brazilian agriculture being one of the products most exported by the country. Its yield may be affected by diseases such as white mold, caused by the fungus Sclerotinia sclerotiorum Lib. de Bary, which, under favorable field conditions prevents the crop of expressing all its productive potential. The fungus is cosmopolitan and infects more than 400 species of plants. This disease is difficult to control, and the use of chemicals has not been sufficient to avoid significant losses, thus, this products are expensive and may cause environmental damage. Alternative methods, such as foliar fertilizers based on potassium phosphite, can also be used in the management of this disease. In this context, this work aimed to study different sources of potassium phosphite and its effects in the control of white mold in soybeans, as well as the time of application in culture, its action in inducing plants defense responses and/or its influence over the seeds quality. The effect of phosphites, over the pathogen, was evaluated in vitro, on mycelial inhibition, the mass of dry mycelium and germination of sclerotia. In all tests, the following phosphites were utilized: Phosphite A (P2O5-40%; K2O-20% - 1 L/ha); Phosphite B (P2O5-40%; K2O-28% - 1 L/ha); Phosphite C (P2O5-40%; K2O-20% - 1 L/ha) e Phosphite D (P2O5-30%; K2O-20% - 2,4 L/ha). At the induction of resistance tests were evaluated the synthesis of phytoalexin in soybean cotyledons and the enzymes FAL and POX evaluated in seedlings in growing chamber, sprayed with phosphites and the fungicide fluazinam. Field experiment was carried out at Coronel Domingos Soares-PR, in the 2012/2013 season, in an area with natural infestation of the pathogen. Soybean cultivar BMX Active was no-till seeded with 0,5m between rows. The experimental was laid out as a factorial 5 x 4 scheme (treatment x application time). Phosphites sources were used, as described above, and water was sprayed in the control treatment. Treatments were applied at four different growth stages: V4, V4 + R1, R1 and R2 at the rates recommended by the manufacturer. Soybean yield components and seeds and health and physiological quality were evaluated after harvesting. None of the tested phosphites affected mycelial growth and sclerotia germination or influenced phytoalexin synthesis. Phosphites C and D stood out due to an increasing in the phenylalanine ammonia-lyase activity 48 hours after its inoculation. These same products also induced the synthesis and peroxidases and phosphite C kept the levels of this enzyme elevated up to 72 hours after inoculation. At the field trials, phosphites C and D stood out in the control of white mold. There was no significant interaction of potassium phosphite on physiological and sanitary quality of the seeds.

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The use of inputs containing phosphites have been presenting results in many studies, taking on importance to the control of diseases in some cultures and demonstrating the resistance induction in seedlings, with ability to activate defense mechanisms, conferring protection to plants against microorganisms. The soybean crop is recognized for its importance in providing grains and derivatives for human consumption, animal, production of biofuels, pharmaceuticals, among others. Positive results obtained through studies based on resistance inducers in some cultures arouse the interest for further study. The objective of this study was to evaluate the effect of potassium phosphites on the resistance induction and treatment of soybean seeds. Therefore were conducted four laboratory studies at the Federal Technological University of Paraná, Campus of Dois Vizinhos. In the first study it was evaluated the quality attributes of the seeds and the resistance induction as seed treatment. Then it was verified that phosphites have action upon the seedlings metabolism in due to seed treatment, having the phosphite Reforce® contributed to seed quality attributes and phosphites FitofosK® and Fitofos K Plus® induced the resistance increasing the activity of β-1,3-glucanase. In the second study it was evaluated the the resistance induction in soybean cotyledons, in which the phosphites demonstrated induction potential of phytoalexin gliceolin. In the third study It was evaluated the soybean seed health treated with potassium phosphites.. it was observed that the phosphites reduced the incidence of many fungi on seeds, especially of storage fungi like Aspergillus sp. and Fusarium semitectum. In the fourth study it was evaluated the in vitro effect of potassium phosphites on pathogenic fungi of the culture. And it was found direct action of phosphites on the mycelial growth of Fusarium semitectum, Pythium sp. and Sclerotinia sclerotiorum. Based on these results, we concluded that potassium phosphites have potential in seeds treatment, as resistance inducer and on in vitro control of phytopathogens.