Pantoea stewartii subsp. stewartii is a bacterial phytopathogen that causes the disease Stewart's wilt in corn. The insect vector Chaetocnema pulicaria, the corn flea beetle, transmits P. stewartii into corn plants through wounds in the leaves. The bacteria can then move to the xylem of the plant where they form a biofilm that inhibits the flow of water. A previous in planta RNA-Seq study resulted in the selection of lrp as a gene of interest for further analyses. A reverse genetics approach was used for the creation of a strain containing the in-frame deletion of lrp, as well as a revertant strain. The strain with the deletion of the lrp gene showed reduced motility and capsule formation when in vitro assays were conducted. It has previously been demonstrated that these characteristics are both important for the bacteria's ability to form a biofilm in the xylem of corn plants and produce disease symptoms. The in planta virulence and competition assays demonstrated that the lrp gene deletion also results in reduced disease symptoms in infected corn plants, as well as an inability to outcompete wildtype P. stewartii in xylem colonization. In a bioinformatics approach, the transcriptional regulator Lrp of P. stewartii was present in the same node of the phylogeny as homologues from other closely related phytopathogens. This demonstrates that Lrp from P. stewartii and such homologues have evolved from a recent common ancestral gene. Examining the genomic islands present in P. stewartii, it is possible to begin to predict where some of the genes which have functions involved in plant colonization may have originated. Overall, the results collected from the studies in this thesis contribute to improving understanding of how P. stewartii is successful at colonizing the xylem of corn plants and cause disease. This research could result in the development of methods to decrease crop susceptibility to infection with P. stewartii. / Master of Science / Stewart's wilt is a disease of corn plants caused by the bacterium Pantoea stewartii subsp. stewartii via the insect vector Chaetocnema pulicaria, the corn flea beetle. This infection has proven to be costly as it impacts the health of corn crops and impedes the export of corn seeds from varieties that are susceptible to infection by P. stewartii. The focus of the research conducted for this thesis has been on learning more about how specific P. stewartii genes impact the ability of the bacterium to colonize corn plants and cause Stewart's wilt disease symptoms. The information collected from this study is important for developing a better understanding of how wilt disease-causing pathogens are able to successfully infect plants, as well as for developing future treatments to prevent further infection of corn plants. In addition, preliminary bioinformatics work has shown that some of the P. stewartii genes of interest share a common ancestor with select genes from other known plant pathogens. Additional preliminary bioinformatics work on regions of the DNA called genomic islands has revealed where some genes of importance to the bacterium's ability to colonize plants may have originated. Overall, the work presented in this thesis contributes to improving our understanding of the roles that different parts of the P. stewartii genome have in allowing the bacterium to successfully colonize and cause disease in corn plants.

Thesis (M.Sc. (Agriculture)) --University of Limpopo, 2018 / Tomato is second most cultivated crop globally and in South Africa it is planted by both commercial and smallholder farmers. However, the crop is susceptible to a number of diseases including those caused by fungal pathogens. Fusarium wilt caused by Fusarium oxysporum f. sp. lycopersici and seedling damping-off caused by Rhizoctonia solani, are known to cause serious yield loss in tomato production. Their management is mainly based on the application of synthetic fungicides and cultural practices. However, both methods have limitations which result in their inefficiency. Synthetic fungicides also have negative impact on the environment and human health. The ability of fungal pathogens to develop resistance to fungicides has also resulted in their reduced application. These challenges have led to a need to identify novel methods using plant extracts and biological control agents which can be used to manage these diseases. The objectives of this study were therefore to, firstly determine the efficacy of both plant extracts on mycelial growth of F. oxysporum f. sp. lycopersici and R. solani under laboratory conditions and secondly, to evaluate the effectiveness of both plant extracts as well as antagonistic fungi Trichoderma harzianum against Fusarium wilt and damping-off of tomato under greenhouse conditions. Food poisoning assay was used to investigate the efficacy of M. burkeana and M. oleifera extracts in vitro. Six (0, 2, 4, 6, 8, 10 g/ml) treatments were arranged in a completely randomised design and replicated four times. After 7 days of incubation at 25 °C, radial growth colony was measured. For the greenhouse xp im nt, Fusa ium wilt was t st d on cv. ‘HTX14’ as th most susc ptibl cultiva whilst seedling damping-off was t st d on cv. ‘Mon y-make ’. Aqu ous xt acts were prepared by decocting different concentrations of M. burkeana (4, 6, 8 g/ml) xiv and M. oleifera (2, 4 and 6 g/ml) in 100 ml of distilled water at 100 °C for 15 minutes then left to cool before filtering and applying as a treatment. Trichoderma harzianum as a treatment was applied 7 days after inoculating the soil-borne pathogens. In-vitro M. burkeana treatments concentrations had the highest mycelia growth suppression against both F. oxysporum f. sp. lycopersici at 10 g/ml (76 %) whilst suppression on R. solani was at 8 g/ml (71 %) relative to control. Moringa oleifera xt acts’ highest pathogen suppression for both F. oxysporum f. sp. lycopersici and R. solani were respectively 35 % and 60 % relative to control at concentration 6 g/ml. Under greenhouse conditions shoot disease severity had highest suppression at 0.6 g/ml of M. burkeana and 0.4 g/ml of M. oleifera treatment concentrations resulting to 32 and 49 % relative to control. Whereas, treatment 0.8 g/ml of M. burkeana and 0.4 g/ml of M. oleifera suppressed stem and root discoloration by 39 and 54 % respectively. Trichoderma harzianum significantly (P ≤ 0.05) reduced shoot severity and root and stem discolouration contributing the highest suppression of 49 % relative to control. In damping-off treatments, both plant extracts and T. harzianum also significantly duc d (P ≤ 0.05) pre- and post-emergence damping-off incidence with M.burkeana recording the highest suppression at 78 % followed by M. oleifera at 64 %. Trichoderma harzianum reduced incidence of damping-off by 60 % relative to untreated control on both M. burkeana and M. oleifera experiments. The results of this study showed that M. burkeana, M. oleifera extracts and T. harzianum can be highly suppressive to both tested plant diseases. However, further studies should be conducted to determine their mode of action, application method and their effect on other soil microorganisms. Keywords: Damping-off, Fusarium wilt, Plant extracts, T. harzianum, Tomato plant

Surveys of the four major soilborne pathogens of strawberry (Fusarium oxysporum f. sp. fragariae, Macrophomina phaseolina, Phytophthora spp., and Verticillium dahliae) to determine their relative prevalence were conducted in Watsonville-Salinas, CA in 2021 and in Santa Maria, CA in 2022. All four major pathogens were detected at relatively similar prevalence in Watsonville-Salinas, between 22% and 31% of sampled fields. In Santa Maria, M. phaseolina was far more prevalent at 52% of sampled fields, the other three falling between 14% and 17%. Additionally replicated greenhouse and field trials were conducted to evaluate the effects of wheat as a single season cover crop on Macrophomina root rot of strawberry and the soil microbiome. Greenhouse trials and the first year of the field trial are described here and demonstrate a lack of substantial disease mitigation or pathogen reduction in the soil following wheat growth compared to no-treatment control. Significant changes were seen in the soil microbiome following wheat growth, including the significant amplification of several bacterial species known to be antagonistic to plant-pathogenic fungi.

Submitted by Marlene Santos (marlene.bc.ufg@gmail.com) on 2018-08-01T17:33:51Z No. of bitstreams: 2 Dissertação - Maythsulene Inácio de Sousa Oliveira - 2015.pdf: 3135445 bytes, checksum: a08e11c7f2df635f3ff7726cfde58f49 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2018-08-02T11:09:15Z (GMT) No. of bitstreams: 2 Dissertação - Maythsulene Inácio de Sousa Oliveira - 2015.pdf: 3135445 bytes, checksum: a08e11c7f2df635f3ff7726cfde58f49 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Made available in DSpace on 2018-08-02T11:09:15Z (GMT). No. of bitstreams: 2 Dissertação - Maythsulene Inácio de Sousa Oliveira - 2015.pdf: 3135445 bytes, checksum: a08e11c7f2df635f3ff7726cfde58f49 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2015-04-11 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES / Common bean (Phaseolus vulgaris L.) is grown in Brazil in three different cropping seasons, and in diverse agroecosystems. In such different environments, the crop is exposed to several constraints responsible for yield losses, such as pathogenic organisms. Among common bean relevant diseases, fusarium wilt (Fusarium oxysporum f. sp. phaseoli), dry root-rot (Fusarium solani) and Curtobacterium wilt (Curtobacterium flaccumfaciens pv. flaccumfaciens) have similar symptoms, hindering diagnosis in the field, and whose identification in seed health testing is also limited. In both cases, identification at species level is an important step to manage this root pathogen complex, whose detection can be improved by molecular biology tools. Therefore, this study aimed to: 1) to develop and validate a multiplex PCR (m-PCR) method for simultaneous identification of three common bean pathogens, F. oxysporum f. sp. phaseoli, F. solani and C. flaccumfaciens pv. flaccumfaciens; and 2) develop an isothermal amplification of DNA (LAMP) method to detect of F. oxysporum f. sp. phaseoli on seeds. M-PCR method was developed for identification of isolated colonies, as well as infected seeds. In seeds, total DNA was obtained by alkaline lysis method, which inactivates nucleases during the extraction process. M-PCR allowed the identification of all pathogens, with detection of C. flaccumfaciens pv. flaccumfaciens, F. oxysporum f. sp. phaseoli and F. solani amplicons in agarose gel with respectively 306, 609 and 143 base pairs. Furthermore, m-PCR also reduced costs and time to detect Fusarium oxysporum f. sp. phaseoli from 10 days to three hours. It was not possible to develop an optimized protocol for detection of F. oxysporum f. sp. phaseoli by the LAMP method, using only the tf1 gene for design of primers, since such primers were functional only for amplifying large amounts of target DNA. Based on the negative results with LAMP, it is suggested that further studies should be performed using other DNA sequences available in GenBank database. / O feijoeiro-comum (Phaseolus vulgaris L.) é cultivado durante todo o ano no território brasileiro, em três épocas distintas e em vários agroecosistemas. Nestes ambientes distintos, a cultura está exposta a diversos fatores que causam perdas de rendimento, como o ataque de patógenos. Dentre as doenças do feijoeiro-comum encontram-se a murcha-de-fusarium (Fusarium oxysporum f. sp. phaseoli), a podridão-radicular-seca (Fusarium solani) e a murcha-de-curtobacterium (Curtobacterium flaccumfaciens pv. flaccumfaciens) que apresentam sintomas semelhantes, dificultando seu diagnóstico no campo, e cuja identificação em testes de sanidade de sementes também é limitada. Em ambos os casos, a identificação em nível de espécie é uma importante etapa do manejo deste complexo de patógenos, cuja detecção pode ser aperfeiçoada com a adoção de ferramentas de biologia molecular. Portanto, este estudo teve como objetivos: 1) Desenvolver e validar um método de multiplex PCR (m-PCR) para identificação simultânea de três espécies de patógenos do feijoeiro-comum, F. oxysporum f. sp. phaseoli, F. solani e C. flaccumfaciens pv. flaccumfaciens; e 2) desenvolver a técnica de amplificação isotérmica de DNA (LAMP) para detecção de F. oxysporum f. sp. phaseoli em sementes. O método de m-PCR foi desenvolvido para identificação de colônias isoladas bem como sementes infectadas. Nas sementes, o DNA total foi obtido pela lise alcalina, método que inativa nucleases durante o processo de extração. A m-PCR possibilitou a identificação de todos os patógenos, com detecção de C. flaccumfaciens pv. flaccumfaciens, F. oxysporum f. sp. phaseoli e F. solani em bandas formadas em gel de agarose respectivamente com 306, 609 e 143 pares de base. Além disso, a extração do DNA total das sementes pela lise alcalina em combinação com a m-PCR também possibilitou redução de custos e tempo de realização do diagnóstico de Fusarium oxysporum f. sp. phaseoli, de 10 dias para três horas. Não foi possível estabelecer um protocolo otimizado para detecção de F. oxysporum f. sp. phaseoli pelo método LAMP, utilizando somente o gene tf1 para desenho dos iniciadores, uma vez que, os iniciadores revelaram-se funcionais apenas para a amplificação com grandes quantidades de DNA alvo. Diante dos resultados obtidos com LAMP, sugere-se que estudos posteriores sejam realizados empregando outras sequências de DNA disponíveis no banco de dados GenBank.

El género Fabavirus pertenece a la familia Comoviridae e incluye tres especies: Broad bean wilt virus 1 (BBWV-1), BBWV-2 y Lamium mild mosaic virus (LMMV), aunque recientemente se ha propuesto una nueva especie, Gentian mosaic virus (GeMV). Estos virus afectan a un gran número de especies hortícolas y ornamentales y son transmitidos de manera no persistente por unas veinte especies de pulgones. El genoma está formado por dos cadenas de RNA monocatenario de polaridad positiva que se encapsidan separadamente con dos proteínas de cápsida formando viriones isométricos. BBWV-1 y BBWV-2 están distribuidos por todo el mundo. En España se ha encontrado BBWV-1 en cultivos de pimiento de Aragón, Cataluña, Castilla León, C. Valenciana, Murcia, Navarra, País Vasco y La Rioja. Los fabavirus son un grupo viral muy poco estudiado. Al comienzo de esta tesis, sólo se había determinado la secuencia nucleotídica del genoma completo de seis aislados de BBWV-2 procedentes de Extremo Oriente, mientras que no se disponía de ninguna secuencia completa de BBWV-1. Para desarrollar métodos rápidos, sensibles y específicos de detección, diferenciar aislados con secuencias divergentes y evaluar en su caso la efectividad de distintas estrategias de control se consideró necesario obtener la secuencia completa de al menos un aislado de BBWV-1 y secuencias parciales de aislados de distintos países. En esta tesis, se determinó la secuencia nucleotídica completa del genoma del aislado español 1S1 de BBWV-1 y se dedujo su organización genómica. El genoma está formado por dos moléculas de RNA monocatenario de polaridad positiva de 5814 y 3431 nt, respectivamente, con la organización genómica descrita para otros miembros de la familia Comoviridae. Al comparar esta secuencia con la única secuencia disponible de BBWV-1 correspondiente al aislado 1U2 de EEUU (publicado durante el desarrollo de esta tesis), se comprobó que los genomas de ambos aislados eran muy divergentes. / Ferrer Gual, RM. (2008). Caracterización molecular y desarrollo de métodos de diagnóstico del género Fabavirus Evaluación de BTH como método de control [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/8313

Doubled haploidy (DH) is a plant breeding technique that is often utilized by plant breeders to minimize the time required to reach homozygosity in breeding lines. The first objective of this study was to compare two methods of generating DH lines in tobacco (Nicotiana tabacum L.). Inbred burley tobacco varieties TN 90LC and GR 149LC were used to produce both androgenic derived doubled haploids (ADDH) and maternally derived doubled haploids (MDDH). The relative agronomic performance of TN 90LC and GR 149 LC ADDH and MDDH lines was compared when used either as pure-line cultivars or when used for the production of the KT 204LC and TN 97LC hybrid cultivars, respectively. The ADDH method was more efficient than the MDDH method in generating large numbers of haploid plants. On average the ADDH TN 90LC population was statistically inferior to the inbred TN 90LC for several agronomic traits; this inferiority of the ADDH method was not observed in the GR 149LC populations. For both genotypes, the MDDH populations were comparable to the inbred parental genotypes. The ADDH method was inferior for TN 90LC, but several individual TN 90LC ADDH lines were equal or superior to the inbred source. The agronomic variability observed in both ADDH and MDDH lines was decreased when they were used to produce hybrid cultivars. Less variation was observed in the DH-derived hybrids KT 204LC and TN 97LC compared to the ADDH and MDDH TN90LC and GR149LC parental lines, respectively. The significant inferiority of ADDH TN 90 lines in comparison to inbred TN 90LC was not observed in the ADDH derived KT 204 population compared to KT 204LC. The second objective of this study was to compare DH Lines derived from an F1 breeding population versus DH lines derived from a segregating F2 population where plants used for DH were pre-screened for quantitatively inherited resistance to soil-borne diseases black shank (Phytophthora nicotianae) and/or Fusarium wilt (Fusarium oxysporum f. nicotianae). There was a clear difference in susceptibility to black shank between the F1 and F2 derived DH populations, both in terms of average disease incidence, and more importantly, in the percentage of individual lines displaying high disease resistance. For two different burley crosses, DH lines derived from the F1 generation were considerably more susceptible to black shank than DH lines derived from the F2 generation. No differences in the incidence of Fusarium wilt were observed between DH lines of F1 and F2 generations; this was likely due to low overall disease incidence. Although delaying the DH process in tobacco from the F1 to the F2 generation could add time to the development of homozygous breeding lines, the delay may be offset by having to screen fewer finished DH lines to identify superior lines.

Receptor-like cytoplasmic kinases (RLCKs) form a large family of proteins in plants. RLCKs have been found in different plant species, regulating plant immunity to different bacterial and fungal pathogens. Previous studies implicated <i>Arabidopsis</i> <i>botrytis induced kinase1 (BIK1)</i> and <i>tomato protein kinase 1b (TPK1b)</i> in plant resistance to <i>Pseudomonas syringae</i> and <i>Botrytis cinerea</i>. In this study, we classified 195 putative maize RLCKs into ten subfamilies. Based on the amino acid sequence similarity to BIK1 and TPK1b, a novel maize RLCK,<i> zea mays bik1-like kinase 1 (ZmBLK1)</i> was identified. Enzyme assays with cloned <i>ZmBLK1</i> revealed a functional kinase when expressed in planta. The recombinant protein located to the plasma membrane. Expression of <i>ZmBLK1</i> is highest in maize leaves compared to other structures at silking stage. Expression of the recombinant <i>ZmBLK1</i> significantly reduced the rate of lesion spread in maize leaves inoculated with the Goss’s wilt pathogen. In maize kernels, expression of <i>ZmBLK1</i> increases during kernel maturation. Kernels from transgenic maize overexpressing <i>ZmBLK1</i> were not resistant to <i>Aspergillus flavus</i> or to aflatoxin contamination. In addition, mutations were made in <i>ZmBLK1</i> that were hypothesized to create a constitutively active kinase. However, resulting proteins had similar activity to the wild-type ZmBLK1 and transgenic plants showed similar responses to the Goss’s wilt and Aspergillus ear rot pathogens. Overall, this research established the first characterization of RLCKs in maize and described a potential contribution of ZmBLK1 to maize immune responses.

Made available in DSpace on 2017-07-25T19:31:03Z (GMT). No. of bitstreams: 1 Lucia Helena Wiecheteck.pdf: 1740264 bytes, checksum: af9a81f83324990acc7d9f7698e80267 (MD5) Previous issue date: 2017-03-28 / Determining the levels of water stored in the soil using indicator cultures allows gather information that can optimizing the natural use of resources in regions prone to drier periods. The objective of this work was to determine the permanent wilt point (PMP) for wheat and barley in sedimentar Latosols with different textural classes. The study was conducted in pots under greenhouse conditions. The design was in randomized blocks, in factorial arrangement (3x2x2). The treatments consisted in a combination of soils with three distinct texture classes (clayey, sandy loam, sandy loam), two cultures (wheat and barley) and four cultivars: wheat (NOBLE and MESTRE) and barley (BRS BRAU and ANAG 01). The soils were kept close to 90% of field capacity, up to 45 days, for the beginning water stress, when they didn’t receive water. At the first sign of wilt in cultures, the pots were transferred to a dark chamber, with relative air humidity close to 100%, to verify the definitive non-return of the turgidity. In PMP soil samples were collected without roots to determine the water content on gravimetric basis. By the laboratory method the determination of water content occurred in 1500 kPa tension. Volumetric rings were removed from plots and submitted to tension table at: -0,1, -10, -20, -40, -60, -80, -100, -300, -500, -700 kPa. Soil water content for PMP was obtained by physiological method and Richards chamber. The data were submitted to descriptive statistical analysis to observe the homogeneity. When, according to assumptions, F-test of significance was performed for 5%. The moisture variables obtained by two methods were correlated, presenting equivalence for the cultures. By regression, the potential in which the plants were wilted was estimated. Statistical analyzes were performed using software R (R CORE TEAM, 2013). The results showed that the structural soil variables present correlation with the higher water contents and the textural ones, assumed correlation with the water contents in higher values of tension. The physiological PMP could be used to indicate crops with greater tolerance to water deficit. / Determinar o conteúdo de água armazenada no solo utilizando culturas indicadoras, permite reunir informações que podem levar a uma otimização no uso de recursos naturais em regiões propensas a períodos mais secos. O objetivo deste trabalho foi determinar o ponto de murcha permanente (PMP) para trigo e cevada em Latossolos de origem sedimentar com diferentes classes texturais. O estudo foi conduzido em vasos em casa de vegetação. O delineamento foi em blocos casualizados, em arranjo fatorial (3x2x2). Os tratamentos constituíram-se da combinação de solos com três classes texturais distintas (argiloso, franco-argilo-arenoso e arenoso), duas culturas (trigo e cevada) e quatro cultivares: trigo (NOBLE e MESTRE) e cevada (BRS BRAU e ANAG 01). Os solos foram mantidos próximos a 90% da capacidade de campo, até 45 dias, para o início do estresse hídrico, momento em que passaram a não receber água. Ao primeiro sinal de murcha das culturas, os vasos foram transferidos para uma câmara escura, com umidade relativa do ar próxima de 100%, para constatação do não retorno definitivo da turgidez. Em PMP foram coletadas amostras de solo sem raízes, para determinar o teor de água em base gravimétrica. Pelo método laboratorial a determinação do teor de água ocorreu na tensão de 1500 kPa. Anéis volumétricos foram retirados dos vasos e submetidos a mesa de tensão, em tensões de -0,1, -10, -20, -40, -60, -80, -100, -300, -500, -700 kPa. O conteúdo de água dos solos para o PMP, foram obtidos pelo método fisiológico e pela câmara de Richards. Os dados foram submetidos a análise estatística descritiva para observação da homogeneidade. Quando em conformidade com as pressuposições, realizou-se o teste F de significância para 5%. As variáveis de umidade obtida pelos dois métodos, foram correlacionadas, apresentando equivalência para as culturas. Por regressão estimou-se o potencial em que as plantas murcharam. As análises estatísticas foram realizadas com o auxílio do software R (R CORE TEAM, 2013). Os resultados demostraram que as variáveis estruturais do solo apresentam correlação com os maiores teores de água e as texturais, assumiram correlação com os teores de água em maiores valores de tensão. O PMP fisiológico pôde ser utilizado para indicar cultura com maior tolerância ao déficit hídrico.

The reemergence of Goss’s wilt of corn in the western Corn Belt in 2006, along with subsequent identification of the disease in 16 states, has led to renewed interest in the disease and its epidemiology. Goss’s wilt, caused by the bacterium Clavibacter nebraskensis, is currently the third-leading cause of yield loss in corn from diseases in the United States. Its impact is exacerbated by the fact that cultural control methods are the only current means for its control. The objectives of our research were to (1) determine the role that alternative hosts of the bacterium play in the disease cycle and epidemiology of Goss’s wilt, and (2) determine if postemergence herbicide use affects disease severity. Through a greenhouse experiment, we discovered three new weedy alternative hosts of the disease. In a series of field and greenhouse experiments, we found that C. nebraskensis can overwinter on alternative host and corn debris in Indiana. We found that C. nebraskensis did not become seed-borne in alternative hosts. In contrast to corn, no systemic infections were observed on alternative hosts, with the bacterium being restricted to inoculated leaf tissue. Using herbicides to control C. nebraskensis-infected weeds did not reduce the pathogenicity of the bacterium recovered from treated plants. The use of nicosulfuron, dicamba plus diflufenzopyr, and a 2X rate of glyphosate postemergence increased disease severity in one experiment, but postemergence herbicides did not influence disease severity in a second experiment. Corn yield was not affected. This indicates that herbicide use may play a role in the epidemiology of Goss’s wilt in some years, but ultimately corn yield is not affected. Our results demonstrate that the host range of C. nebraskensis is wider than previously thought, and that postemergence control of alternative hosts may not be sufficient in reducing inoculum levels. Our results suggest that failure to control alternative hosts could negate some of the benefits of crop rotation to reduce inoculum levels in a field, thus playing an important role in the epidemiology of Goss’s wilt. <br>

Submitted by (lucia.rodrigues@ufrpe.br) on 2017-02-21T13:35:42Z No. of bitstreams: 1 Christtianno de Lima Rollemberg.pdf: 2445206 bytes, checksum: 4da0aaed00880d13a23b17cdb6cae239 (MD5) / Made available in DSpace on 2017-02-21T13:35:42Z (GMT). No. of bitstreams: 1 Christtianno de Lima Rollemberg.pdf: 2445206 bytes, checksum: 4da0aaed00880d13a23b17cdb6cae239 (MD5) Previous issue date: 2013-04-30 / This study evaluated the use of silicon (Si) in micropropagation of banana 'Silk' and 'Pacovan Ken' aiming to reduce the severity of fusarium wilt caused by Fusarium oxysporum f. sp. cubense and moko disease caused by Ralstonia solanacearum race 2. The banana plantlets were produced in vitro by adding calcium silicate and potassium silicate (0, 0.25, 0.5, 0.75 and 1 g L-1) to MS medium in the phases of multiplication and rooting. After in vitro culture, the plants were transferred to plastic tubes containing substrate plus the same sources of Si, and maintained in a greenhouse for 45 days, when they were inoculated with the pathogens. With respect to fusarium wilt in cultivars Silk and Pacovan Ken, the elevation of Si increased the incubation period (IP) and reduced the disease index (DI) and area under the disease progress curve (AUDPC). In cultivar Silk but not in Pacovan Ken calcium silicate was significantly more effective than potassium silicate. In shoots and roots of both cultivars in both sources, before and after acclimatization Si concentration was greater at a dose of 1.0 g L-1 compared to the control without Si. Before acclimatization, calcium silicate provided higher Si concentration in the shoots than potassium silicate. The opposite happened with the Si concentration in the roots. After acclimatization, there was no difference between the calcium silicate and potassium silicate, for both cultivars. In general, for both cultivars and sources of Si there were positive correlations with the concentration of Si and IP, and negative correlations with DI and AUDPC. Before and after acclimatization, the anatomical variable of roots: thickness of the root epidermis, cortex, endodermis and central cylinder of banana 'Silk' and 'Ken Pacovan' were influenced by Si sources. Calcium silicate was more efficient in increasing the thickness of the root epidermis, cortex and central cylinder, while potassium silicate was more efficient in thickening of the endodermis. In general, there were positive correlations among anatomical variable of roots with PI and negative correlations with DI and AUDPC, except for potassium silicate in cultivar Silk. The research conducted with moko disease showed that increase of Si in Silk and Pacovan Ken cultivars caused increase in IP and decreases the DI and AUDPC. At the dosage of 1.0 g L-1 AUCPD was reduced by 27.3%. In cultivar Silk, calcium silicate was more effective than potassium silicate (P≤0.05), while in „Pacovan Ken‟ there was no difference. In both cultivars, plants treated with Si showed, in general, concentrations of chlorophylls a, b and total higher than plants Si- up to six days after inoculation, which may have influenced the disease IP. In general, both the enzymes related to oxidative stress (CAT, SOD and APX), as the plant defense (POX, PPO, CHI and GLU), had increased its activities in plants treated with Si, especially those with calcium silicate, indicating a possible role in reducing the severity of the disease. The supply of Si in micropropagation of banana 'Silk' and 'Pacovan Ken' promoted reduction of Fusarium wilt and moko disease, and therefore can be used as a new technology in the management of these diseases. / Este estudo avaliou o uso do silício (Si) na micropropagação de bananeira „Maçã‟ e „Pacovan Ken‟ visando a redução da severidade da murcha-de-fusário, causada pelo Fusarium oxysporum f. sp. cubense e do moko da bananeira causado por Ralstonia solanacearum raça 2. As mudas de bananeira foram produzidas in vitro com adição de silicato de cálcio e silicato de potássio (0; 0,25; 0,5; 0,75 e 1 g L-1) ao meio de cultivo MS nas fases de multiplicação e enraizamento. Após o cultivo in vitro, as plantas foram transferidas para tubetes contendo substrato acrescido das mesmas fontes de Si, e mantidas em casa de vegetação por 45 dias, quando foram inoculadas com os patógenos. Com relação à murcha-de-fusário, nas cultivares Maçã e Pacovan Ken, a elevação das doses de Si aumentou o período de incubação (PI) e reduziu o índice de doença (IDO) e a área abaixo da curva de progresso da doença (AACPD). Em „Maçã‟ o silicato de cálcio foi significativamente mais eficiente que o silicato de potássio, o que não ocorreu na „Pacovan Ken‟. A concentração de Si na parte aérea e raízes das cultivares, em ambas as fontes, antes e após a aclimatização foi maior na dose de 1,0 g L-1 em relação à testemunha sem Si. Antes da aclimatização, o silicato de cálcio proporcionou maior concentração de Si na parte aérea que o silicato de potássio. O contrário aconteceu com a concentração de Si nas raízes. Após aclimatização, não houve diferença entre o silicato de cálcio e o silicato de potássio, para as duas cultivares. Em geral, para ambas as cultivares e fontes de Si foram observadas correlações positivas da concentração de Si com PI e correlações negativas com IDO e AACPD. Antes e após a aclimatização das plantas, as espessuras da epiderme radicular, córtex, endoderme e cilindro central das bananeiras „Maçã‟ e „Pacovan Ken‟ foram influenciadas pelas fontes de Si. O silicato de cálcio foi mais eficiente no aumento da espessura da epiderme radicular, córtex e cilindro central, enquanto o silicato de potássio foi mais eficiente no aumento da espessura da endoderme. Em geral, foram observadas correlações positivas das variáveis anatômicas das raízes com PI e correlações negativas com IDO e AACPD, exceto para silicato de potássio em bananeira „Maçã‟. Na pesquisa desenvolvida com o moko da bananeira, a elevação das doses de Si nas cultivares Maçã e Pacovan Ken causou aumento no PI e reduções do IDO e AACPD. Na dosagem de 1,0 g L-1, a AACPD foi reduzida em até 27,3%. Em bananeira „Maçã‟ o silicato de cálcio foi mais eficiente que o silicato de potássio (P≤0,05), enquanto na „Pacovan Ken‟ não houve diferença. Nas duas cultivares, plantas tratadas com Si apresentaram, de maneira geral, concentrações de clorofilas a, b e total maiores que as plantas Si- até os seis dias após inoculação, o que pode ter influenciado o PI da doença. Em geral, tanto as enzimas relacionadas ao estresse oxidativo (CAT, SOD e APX), quanto as de defesa da planta (POX, PFO, GLU e QUI), tiveram suas atividades aumentadas nos tratamentos com silício, especialmente naqueles com silicato de cálcio, indicando uma possível participação na redução da severidade da doença. O fornecimento de Si na micropropagação de bananeiras „Maçã‟ e „Pacovan Ken‟ promoveu redução da murcha-de-fusário e moko da bananeira, podendo ser utilizado como uma nova tecnologia no manejo dessas doenças.