Submitted by Cássia Santos (cassia.bcufg@gmail.com) on 2017-01-10T09:15:32Z No. of bitstreams: 2 Dissertação - Nayane Oliveira Almeida - 2016.pdf: 4246837 bytes, checksum: 2ee0e2f0ece0d114ea4032c91be4556f (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2017-01-10T10:58:54Z (GMT) No. of bitstreams: 2 Dissertação - Nayane Oliveira Almeida - 2016.pdf: 4246837 bytes, checksum: 2ee0e2f0ece0d114ea4032c91be4556f (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Made available in DSpace on 2017-01-10T10:58:54Z (GMT). No. of bitstreams: 2 Dissertação - Nayane Oliveira Almeida - 2016.pdf: 4246837 bytes, checksum: 2ee0e2f0ece0d114ea4032c91be4556f (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2016-03-22 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES / The problems caused by nematodes and by the Panama disease on banana plantations are responsible for production losses and limiting to its cultivation. In the state of Goiás there is few information about the nematode genus that affect this crop, and its relationship with the incidence of the fungus Fusarium oxysporum f. sp. cubense (Foc). This research aimed to survey the occurrence of plant parasitic nematodes, the incidence of Foc and soil attributes, and determine if there is a correlation among these factors. In January 2015, twelve banana producing regions in the state of Goiás were sampled: Anápolis, Caiapônia, Goiatuba, Itaguaru, Itumbiara (two areas), Jataí, Morrinhos, Ouro Verde, Palestina, Taquaral and Uruana. All sampled areas, except Morrinhos, revealed contamination with Foc, and all had different genus of nematodes. Meloidogyne sp., Helicotylenchus sp. and Rotylenchus sp. were the main genus of plant parasitic nematodes present in the banana plantations, with Meloidogyne sp. and Rotylenchus sp. the most dominant and abundant genus. We found that Pratylenchus sp. increases the population levels of F. oxysporum and that Helicotylenchus sp. has been affected by the concentration of P, Ca, Mn and the soil pH. / Os problemas fitossanitários causados por nematoides e pela doença mal-do-Panamá, na cultura da banana, são responsáveis por grandes perdas de produção ou são fatores limitantes de seu cultivo. Em Goiás, são escassas as informações sobre os gêneros de nematoides que afetam a bananicultura, bem como sua relação com a incidência do fungo Fusarium oxysporum f. sp. cubense (Foc), agente causal do mal-do-Panamá. Assim, esse trabalho teve por objetivo fazer levantamento da ocorrência de fitonematoides, da incidência de Foc e dos atributos dos solos, e determinar se há correlação entre estes fatores. Em janeiro de 2015, foram amostradas doze regiões produtoras de banana no estado de Goiás, distribuídas em onze municípios: Anápolis, Caiapônia, Goiatuba, Itaguaru, Itumbiara, Jataí, Morrinhos, Ouro Verde, Palestina, Taquaral e Uruana. Todas as áreas amostradas, exceto a do município de Morrinhos, apresentaram-se contaminadas com Foc, e todas apresentaram diversos gêneros de fitonematoides. Meloidogyne sp., Helicotylenchus sp. e Rotylenchus sp. foram os principais gêneros de fitonematoides presentes nos bananais no estado de Goiás, sendo Meloidogyne sp. e Rotylenchus sp. os gêneros mais dominantes e abundantes. Foi constatado que a presença de Pratylenchus sp. aumenta o nível populacional de F. oxysporum e que Helicotylenchus sp. é afetado pelos teores de P, Ca, Mn e pelo pH do solo.

Nas últimas décadas, tem sido relatado o aumento de casos de infecções fúngicas invasivas por agentes oportunistas, tais como Aspergillus spp., Fusarium spp. e fungos da ordem Mucorales, em pacientes hospitalizados, particularmente os imunocomprometidos. Como os sintomas são frequentemente inespecíficos, esses patógenos não são identificados inicialmente como agentes causais. Além disso, muitas vezes o diagnóstico só é estabelecido em estágios tardios da infecção, pois as metodologias diagnósticas de rotina, como cultura e microscopia, apresentam limitações caracterizadas, sobretudo, por baixa sensibilidade e especificidade. Os métodos moleculares, incluindo as amplificações de material genômico por PCR, em tecidos a fresco e parafinados, têm sido mais aplicados para a melhoria na detecção e identificação desses patógenos. A técnica de PCR em tempo real apresenta a vantagem de fornecer resultados com rapidez e elevada sensibilidade, além de minimizar os riscos de contaminação ambiental das amostras. Para aprimorar o conhecimento sobre a eficácia desta técnica na detecção e identificação dos patógenos, neste estudo foram utilizados camundongos da linhagem BALB/c para o desenvolvimento de modelos de infecção invasiva por Aspergillus fumigatus, Rhizopus arrhizus e Fusarium solani. Após inoculação dos fungos por via intravenosa, os órgãos (pulmão, fígado, rins, cérebro e coração) foram retirados para realização dos exames de cultura, histopatologia, PCR semi-nested e PCR em tempo real. As culturas foram realizadas em ágar Sabouraud dextrose e incubadas por 3 a 5 dias à temperatura ambiente. Para as análises histopatológicas, uma parte dos órgãos foi emblocada em parafina e cortes foram submetidos às colorações por hematoxilina-eosina e Gomori-Grocott. Para as análises moleculares, foram realizadas clonagens dos amplicons obtidos com os mesmos primers gênero-específicos (Aspergillus spp. e Fusarium spp.) e ordem-específicos (mucoráceos) empregados nas reações de PCR. Os clones foram empregados na técnica de PCR em tempo real para avaliação da sensibilidade analítica dos ensaios e como controles positivos. Os tecidos a fresco e parafinados foram submetidos a extrações de DNA, e as amostras foram avaliadas por PCR do tipo semi-nested, e por PCR em tempo real, empregando-se os primers gênero e ordem-específicos. Após 48-72 horas, observou-se crescimento fúngico nas culturas, porém a identificação macroscópica foi possível somente após 96 horas. Nos exames histopatológicos foram observadas presença de estruturas fúngicas e alterações na morfologia tecidual, confirmando a disseminação da infecção nos três modelos experimentais. Os dois métodos de PCR (convencional e tempo real) empregando os primers para Aspergillus e mucoráceos demonstraram 100% de especificidade. Além disso, os primers para mucoráceos amplificaram amostras de DNA dos gêneros Rhizopus, Mucor e Lichtheimia, confirmando serem ordem-específicos. Por outro lado, os testes moleculares com emprego de diversos primers de Fusarium apresentaram reatividade cruzada, principalmente com amostras de DNA de Aspergillus e Rhizopus. O limiar de detecção (LD) das PCR semi-nested para Aspergillus e Rhizopus foi de 50 fentogramas de DNA, enquanto na PCR em tempo real o LD foi de 20 fentogramas de DNA e 2x102 plasmídios/ul. Os dois métodos moleculares detectaram DNA de Aspergillus e Rhizopus, em 100% das amostras de tecido a fresco e parafinado, corroborando com os resultados de cultura e histopatologia. Os resultados do estudo demonstraram que a PCR em tempo real foi capaz de detectar e diferenciar Aspergillus e Rhizopus nos tecidos a fresco e parafinados, com 100% de especificidade e maior sensibilidade analítica quando comparada à PCR semi-nested. Entretanto, os resultados obtidos com diversos primers de Fusarium utilizados nos ensaios de PCR foram inconsistentes em relação à especificidade das amplificações. A PCR em tempo real constituiu um método rápido para diagnosticar, com acurácia, aspergilose e mucormicose em tecidos, podendo ser implementada como alternativa na rotina diagnóstica de laboratórios de patologia ou microbiologia. Por outro lado, a técnica apresentou baixa especificidade com os primers de Fusarium selecionados neste estudo. Outras sequências gênicas deste fungo deverão ser avaliadas na técnica molecular para se atingir resultados precisos / Increase of invasive fungal infections by opportunistic agents, such as Aspergillus sp., Fusarium sp. and fungi from the order Mucorales, in immunocompromised patients has been reported in the last decades. As the symptoms are often non-specific, diagnosis are only established in late stages of infection. Routine diagnostic methodologies, such as culture and direct microscopy, have limitations due to their low sensitivity and specificity. Molecular methods, including amplifications of nucleic acids by PCR in fresh and paraffined tissues, have been more frequently applied to improve the detection and identification of these pathogens. The real-time PCR (qPCR) technique has the advantage of providing fast results with high sensitivity, as well as minimizing the risks of environmental contamination of the samples. This study aimed to evaluate the effectiveness of this technique for detection and discrimination of the fungal pathogens in tissues taken from BALB/c mice intravenously inoculated with Aspergillus fumigatus, Rhizopus arrhizus and Fusarium solani. The organs (lung, liver, kidneys, brain and heart) were removed from animals and analysed by culture, histopathology, semi-nested PCR and qPCR. Recombinant plasmid clones containing small sequences of Aspergillus, Fusarium and mucoraceous were used to draw qPCR standard curves and to evaluate the analytical sensitivity of the assays. The fresh and paraffined tissues were submitted to DNA extractions, and samples were evaluated by semi-nested PCR and qPCR with genus-specific primers for Aspergillus and Fusarium, and order-specific primers for mucoraceous. Cultures were positive for all fresh tissue samples. Presence of typical fungal structures and alterations in tissue morphology were observed in the histopathological examinations, confirming the dissemination of infection in the three experimental models. Both PCR assays employing Aspergillus and mucoraceous primers demonstrated 100% specificity. On the other hand, molecular tests using at least six different Fusarium primers showed cross reactivity, mainly with Aspergillus and Rhizopus DNA samples. The limit of detection (LD) of the semi-nested PCR for Aspergillus and Rhizopus was 50 femtograms of DNA, while for the qPCR it was 20 femtograms of DNA, and 2x102 plasmids/?l. Both molecular methods detected Aspergillus and Rhizopus DNA in 100% of fresh and paraffined tissue samples, corroborating the results with cultures and histopathology. The results of the study demonstrated that qPCR assay was able to detect and differentiate Aspergillus and Rhizopus in fresh and paraffined tissues, with 100% of specificity and higher analytical sensitivity when compared to semi-nested PCR assay. However, the results obtained with several Fusarium primers in the PCR assays were inconsistent regarding specificity of the amplifications. Real-time PCR assay is a fast and accurate method to diagnose aspergillosis and mucormycosis in tissues, and could be implemented as an alternative tool for diagnostic routine in pathology or microbiology laboratories. On the other hand, the technique showed low specificity with the Fusarium primers selected in this study. Other gene sequences should be evaluated by PCR assays techniques to achieve accurate results

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In the genus Fusarium are many important plant pathogens. The diversity of hosts the genus attacks, the number of pathogenic taxa and the range of habitats in which they cause disease are the greatest in plant pathology. One important species complex within the genus Fusarium is Fusarium oxysporum Schlecht. This species complex consists more than 80 pathogenic forma specialis and is particularly difficult to control. The fungi can survive in soil for decades as specialized spores, known as chlamydospores. Interestingly, however, this species complex also contains beneficial non-pathogenic forms that can be exploited to manage Fusarium wilt diseases. In this study, the ability of non-pathogenic F. oxysporum strains, Trichoderma harzianum Rifai Eco-T®, soluble silicon, and their combination was evaluated on two important crops, banana (Musa sp. L.) and beans (Phaseolus vulgaris L.), for their potential to suppress pathogenic strains of F. oxysporum. The ability of these crops to take up and accumulate silicon in their organs, and its effect on low temperature stress was also investigated. Several endophytic fungi, mainly Fusarium spp. and bacteria, were isolated from healthy mature banana plants. After preliminary and secondary in vivo screening tests against F. oxysporum f.sp. phaseoli on beans (Phaseolus vulgaris L.) cv. Outeniqua, two non-pathogenic F. oxysporum strains were selected for further testing. These two non-pathogenic F. oxysporum strains were found to colonize banana (Musa sp.) cv. Cavendish Williams and bean plants, and to suppress Fusarium wilt of these crops. In order to improve the efficacy of these biocontrol fungi, soluble silicon was introduced. The relationship between plant mineral nutrition and plant diseases have been reported by several authors. Plants take up silicon equivalent to some macronutrients, although it is not widely recognized as an essential element. In this study, we established that roots, the target plant organ for soilborne plant pathogens, accumulated the greatest quantity of silicon of any plant organs when fertilized with high concentrations of silicon. On the other hand, the corm and stem accumulated the least silicon. Such observations contradict the concept of passive uptake of silicon via the transpiration stream in these plants as the only uptake mechanism. The prophylactic properties of silicon have been documented for many crops against a variety of diseases. In vitro bioassay tests of silicon against these wilt pathogens showed that silicon can be toxic to Fusarium wilt fungi at high concentrations (>7840 mg .-1), resulting in complete inhibition of hyphal growth, spore germination and sporulation. However, low concentrations of silicon (<490 mg .-1) encouraged hyphal growth. Silicon fertilization of banana and beans significantly reduced disease severity of these crops by reducing the impact of the Fusarium wilt pathogens on these crops. However, it could not prevent infection of plants from the wilt pathogens on its own. Synergistic responses were obtained from combined applications of silicon and non-pathogenic F. oxysporum strains against Fusarium wilt of banana. Combinations of silicon with the non-pathogenic F. oxysporum strains significantly suppressed disease severity of Fusarium wilt of banana, caused by F. oxysporum f.sp. cubense (E.F. Smith) Snyder & Hansen, better than applications of either control measure on their own. Banana production in the subtropical regions frequently suffer from chilling injury, and from extreme variations between night and day temperatures. Such stress predisposes banana plants to Fusarium wilt disease. Silicon, on the other hand, is emerging as important mineral in the physiology of many plants, ameliorating a variety of biotic and abiotic stress factors. We established that silicon fertilization of banana plants significantly reduced chilling injury of banana plants. Membrane permeability, lipid peroxidation (MDA level) and proline levels were higher in silicon-untreated plants than the treated ones, all of which demonstrated the stress alleviating effect of silicon. Low temperatures damage the cell membrane of susceptible plants and cause desiccation or dehydration of these cells. Levels of sucrose and raffinose, recognized as cryoprotectants, were significantly higher in silicon-amended banana plants than unamended plants. / Thesis (Ph.D.)-University of KwaZulu-Natal, Pietermaritzburg, 2008.

Responses from pedigree selection for resistance to gibberella ear rot were assessed in four maize (Zea mays L.) populations, two selected after inoculation of Fusarium graminearum (Schwabe) macroconidia into the silk channel and two selected after inoculation into developing kernels. Responses were significant in both populations selected for silk resistance and in one of the populations selected for kernel resistance. Selection was more effective in later generations and genetic gains were associated with among-family selection but not with within-family selection. Results obtained here indicate that responses to selection could be more efficiently obtained by applying high selection intensities in advanced generations, by managing earlier generations as bulks and by reducing the number of plants per family. In another experiment, a wide sample of Argentine maize germplasm was evaluated for silk and kernel resistance to gibberella ear rot and to fusarium ear rot (caused by F. verticillioides (Saccardo) Nirenberg [=F. moniliforme (Sheldon)]. Several entries exhibited disease resistance in comparison with local check hybrids, particularly for fusarium ear rot, the most prevalent ear rot in Argentina. Results obtained in this study suggested the presence of general mechanisms controlling silk and kernel resistance to both diseases. In a supplementary study, viral diseases were surveyed in maize fields from the provinces of Ontario and Quebec in 1999 and 2000. Barley yellow dwarf was found in 1999. Sugarcane mosaic, maize dwarf mosaic and wheat streak mosaic were found in 2000. These diseases were not important for grain-maize planted in May, the most prevalent kind of maize crop in these provinces. Some of these diseases, such as sugarcane maize mosaic and maize dwarf mosaic were found important only in maize fields planted during or after the month of June, and this is of commercial relevance only for sweet corn.

Les mycotoxines sont des molécules toxiques produites par de nombreuses espèces fongiques. Les seules mycotoxines avérées aujourd’hui cancérigènes pour l’homme sont les aflatoxines. Elles sont produites par le genre Aspergillus principalement et sont retrouvées tout au long de la chaine alimentaire (champs, stockage, transformation, etc.). A cause du réchauffement climatique, la France devient de plus en plus exposée à la présence de ces mycotoxines. Afin de limiter l’exposition des consommateurs, de nombreuses stratégies de prévention ou de décontamination sont développées. Dans ce contexte, nous avons recherché à mettre au point un système de lutte biologique permettant de prévenir la production d’aflatoxines sur le maïs au champ. Pour cela, nous avons choisi des bactéries issues du sol et déjà connues pour être commercialisées pour la lutte biologique, les actinomycètes. Nous avons étudié l’interaction in vitro sur boites de Pétri entre Aspergillus flavus, principal producteur d’aflatoxines, et certains actinomycètes. Nous avons démontré que l’interaction peut réduire la concentration en aflatoxines mesurée par HPLC. De plus, certains isolats bactériens sont aussi capables de réduire, en culture pure, la concentration d’aflatoxine B1 dans le milieu. Des premiers tests d’adsorption ont été réalisés pour comprendre la nature de ce mécanisme. Par ailleurs, une étude approfondie via RT-qPCR sur 6 souches bactériennes du genre Streptomyces sp. A montré que celles-ci étaient capables d’impacter l’expression de différents gènes impliqués dans la voie de biosynthèse chez A. flavus et A. parasiticus. Enfin, nous avons complété les données déjà existantes sur l’impact de facteurs environnementaux (température, disponibilité en eau et du temps d’incubation) sur la production d’aflatoxines. / Mycotoxins are toxic contaminants of foodstuffs produced by a wide range of fungal species. Aflatoxins are the only mycotoxins carcinogenic for humans. They are mainly produced by the Aspergillus genus and can be found at each step of the agrofood chain (e.g. field, storage, process). Due to climate changes, France is starting to be exposed to aflatoxins. In order to limit the consumer exposure, many prevention or decontamination techniques have been developed. To this aim, we started the development of a biocontrol against aflatoxins accumulation for maize field application. Actinomycetes, are soil-borne bacteria that has already been commercialized as biocontrol. In Petri dishes, we studied the in vitro interaction between some actinomycetes and Aspergillus flavus, the main aflatoxins producer. We revealed that the interaction reduced the aflatoxins content (monitored by HPLC). Moreover, some bacterial isolates were able to reduce pure-aflatoxin B1 added in the medium. To understand this mechanism, adsorption tests has been conducted. Otherwise, RT-qPCR methodology was used to study the impact of Streptomyces-Aspergillus sp. on aflatoxin gene expression. Finally, the current knowledge of the impact of environmental factors (temperature, water activity and incubation time) on aflatoxins production was supplemented.

Made available in DSpace on 2014-06-11T19:35:01Z (GMT). No. of bitstreams: 0 Previous issue date: 2009-12-16Bitstream added on 2014-06-13T19:44:47Z : No. of bitstreams: 1 pinto_zv_dr_botfca.pdf: 894968 bytes, checksum: 522dc825bbc64c7631c86fa63430a259 (MD5) / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / A murcha de Fusarium spp. em crisântemo é responsável por sérios prejuízos à cultura no Brasil. Uma alternativa para o seu controle é o uso de substrato supressivo, o qual pode ser obtido pela adição de fontes de matérias orgânicas. Dessa forma, o presente trabalho teve por objetivo desenvolver um substrato supressivo à murcha do Fusarium em crisântemo com a introdução de matéria orgânica em substratos comerciais. Para tanto, lodo de esgoto e lodo de esgoto compostado; torta de mamona; esterco suíno; cama aviária; compostos comerciais Lanzi®; casca de camarão, biofertilizante e hidrolisado de peixe foram incorporados a substratos à base de casca de Pinus e de turfa em diferentes concentrações e combinações. Os experimentos foram realizados em propriedade produtora de crisântemo Bola-belga com problemas de Fusarium. Em todos os experimentos o número mínimo de repetições foi de 20 vasos por tratamento. Transcorridas 8, 12, 15 e 20 semanas do transplantio foi avaliada a severidade da doença por uma escala de notas de 0 para planta sadia a 5 para planta morta. Com os dados foram calculadas as áreas abaixo da curva de progresso da severidade da murcha de Fusarium. Além disso, foram realizadas análises dos atributos químicos e da atividade microbiana dos substratos bem como do desenvolvimento das plantas. O lodo de esgoto, lodo de esgoto compostado, cama aviária, casca de camarão e o composto Lanzi® induziram a supressividade do substrato à base de casca se Pinus e/ou de turfa, controlando a murcha de Fusarium. Por outro lado, esterco suíno, torta de mamona, hidrolisado de peixe, quitosana e Trichoderma asperellum não interferiram na supressividade à doença. Substratos obtidos com lodo de esgoto e cama aviária, em mistura ou não, nas concentrações de 10, 20 e 30% (v/v) foram os mais adequados do ponto de vista de indução de supressividade... / Fusarium spp. wilt causes serious damages to chrysanthemum crops in Brazil. An alternative for its control is the use of suppressive plant growth media, which can be obtained by the addition of organic matter to container media. The objective of the present work was to develop a plant growth media suppressive to the Fusarium spp. in chrysanthemum with the introduction of organic matter to commercial container media. Sewage sludge and sewage sludge compost; castorbean presscake, swine manure; poultry litter; shrimp peel, biofertilizer, chitosan and fish hydrolyzed were incorporated to pine-bark and turf container media in different concentrations and combinations. The experiments were conducted in a Belgianchrysanthemum variety producing property with a Fusarium problem. In all experiments the minimum number of repetitions was 20 containers per treatment. Eight, 12, 15 and 20 weeks following transplanting the severity of the disease was evaluated according to a progressive scale from 0 (healthy plant) to 5 (dead plant). Areas under the disease progress curve for disease severity of Fusarium wilt were calculated. Chemical and microbiological attributes of container media and plant development were analyzed. The sewage sludge, sewage sludge compost, poultry litter, shrimp peel and the Lanzi® compost induced the suppressiveness of pine bark and/or turf container media, controlling the wilt. On the other hand, swine manure, castorbean presscake, fish hydrolyzed, chitosan and Trichoderma asperellum did not affect the suppressiveness to the disease. Plant growth media with sewage sludge and poultry litter, in mixture or alone, in the concentrations of 10, 20 and 30% (v/v) were the most appropriate from the point of view of induction of suppressiveness and product quality, being the plant growth media recommended... (Complete abstract click electronic access below)

The present work aims to determine the physiological and sanitary quality of Sweet sorghum (Sorghum bicolor (L.) Moench) seeds, as well as to identify pathogens associated with seed, their transmission to seedlings and the subsequent pathogenicity of isolates obtained, In addition, molecularly identify the fungal species pathogenic to this crop. The experiments were carried out in the Teaching and Seed Research Laboratory (TSRL), of the Plant Engineering Department; In the Elocy Minussi Phytopathology Laboratory, Department of Plant Protection, and at the Biological Institute of São Paulo. Sweet sorghum seeds were used, all without chemical treatment. Sanitary quality was evaluated by sanity test, and physiological characteristics by germination and vigor tests (seedling length, dry mass, emergence, rate of emergence and accelerated aging). It was performed the test of transmission of the pathogens associated to the seeds and the subsequent pathogenicity of the obtained isolates, culminating with the molecular characterization of the identified pathogens, in which were sequenced the Internal Transcribed Spacer (ITS) genomic regions and the Elongation Factor 1 - alpha (TEF1-α) gene. The design used was the completely randomized design, with four cultivars of Sweet sorghum (BRS 506, F19, BRS 511 and BRS 509); For the evaluation of pathogenicity, the factorial scheme is represented by four cultivars and three isolates of Fusarium spp., besides the witness. The seeds of the BRS 509 cultivar were considered to have lower physiological quality than the other cultivars. The DNA sequencing allowed identifying the Fusarium thapsinum species as a pathogenic agent in the sweet sorghum crop, and proven its transmission via seeds. / O presente trabalho teve como objetivo determinar a qualidade fisiológica e sanitária de sementes de cultivares de sorgo sacarino (Sorghum bicolor (L.) Moench), bem como identificar os patógenos associados à semente, sua transmissão às plântulas e a posterior patogenicidade de isolados obtidos, além disso, identificar molecularmente as espécies fúngicas patogênicas a esta cultura. Os experimentos foram realizados no Laboratório Didático e de Pesquisas em Sementes (LDPS), do Departamento de Fitotecnia; no Laboratório de Fitopatologia Elocy Minussi, do Departamento de Defesa Fitossanitária e, no Instituto Biológico de São Paulo. Foram utilizadas sementes de sorgo sacarino, todas sem tratamento químico. A qualidade sanitária foi avaliada pelo teste de sanidade, e as características fisiológicas por meio dos testes de germinação e de vigor (comprimento de plântulas, massa seca, emergência, índice de velocidade de emergência e envelhecimento acelerado). Foi realizado o teste de transmissão dos patógenos associados à semente e a posterior patogenicidade dos isolados fúngicos obtidos, culminando com a caracterização molecular dos patógenos identificados, na qual foram sequenciadas as regiões genômicas Internal Transcribed Spacer (ITS) e o gene do fator de elongação 1-α (TEF1α). O delineamento utilizado foi o inteiramente casualizado com quatro cultivares de sorgo sacarino (BRS 506, Fepagro 19, BRS 511 e BRS 509); já para a avaliação da patogenicidade, o esquema fatorial foi representado pelas quatro cultivares e três isolados de Fusarium sp., além da testemunha. As sementes da cultivar BRS 509 foram consideradas de qualidade fisiológica inferior as demais cultivares. O sequenciamento de DNA permitiu identificar a espécie Fusarium thapsinum como agente patogênico na cultura do sorgo sacarino, sendo comprovada sua transmissão via sementes.