19 research outputs found

    Effect of alternative seed treatments on seed-borne fungal diseases in tomato

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    The fungus Didymella lycopersici infects tomato seed and results in great losses before and after germination. To control the disease, seed companies use thiram preventively, although human allergy problems have been reported. For this reason as well as to address needs in organic agriculture, this study has focused on the effects of alternative methods of control. Nitrite solutions and resistance inducers were tested in a growth chamber. Results showed that soaking the seed in a nitrite solution with a concentration of 300mΜ (in citric acid buffer, pH 2) for 10 minutes reduced losses due to low seed germination and disease incidence in the germinated seedlings completely. When applied for longer intervals sodium nitrite proved phytotoxic whereas in shorter intervals it was not as effective. The resistance inducer Tillecur (mustard seed extract) at the rate of 0.05g/ml was as much effective as sodium nitrite inhibiting disease incidence in germinated seedlings. None of the above treatments was significantly different to thiram and they could replace the fungicide in the control of seedborne D. lycopersici in tomato

    Pseudomonas viridiflava, a Multi Host Plant Pathogen with Significant Genetic Variation at the Molecular Level

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    The pectinolytic species Pseudomonas viridiflava has a wide host range among plants, causing foliar and stem necrotic lesions and basal stem and root rots. However, little is known about the molecular evolution of this species. In this study we investigated the intraspecies genetic variation of P. viridiflava amongst local (Cretan), as well as international isolates of the pathogen. The genetic and phenotypic variability were investigated by molecular fingerprinting (rep-PCR) and partial sequencing of three housekeeping genes (gyrB, rpoD and rpoB), and by biochemical and pathogenicity profiling. The biochemical tests and pathogenicity profiling did not reveal any variability among the isolates studied. However, the molecular fingerprinting patterns and housekeeping gene sequences clearly differentiated them. In a broader phylogenetic comparison of housekeeping gene sequences deposited in GenBank, significant genetic variability at the molecular level was found between isolates of P. viridiflava originated from different host species as well as among isolates from the same host. Our results provide a basis for more comprehensive understanding of the biology, sources and shifts in genetic diversity and evolution of P. viridiflava populations and should support the development of molecular identification tools and epidemiological studies in diseases caused by this species

    Biological control of cucumber and sugar beet damping-off caused by Pythium ultimum with bacterial and fungal antagonists

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    Aims: Five bacterial strains belonging to Bacillus subtilis , Pseudomonas fluorescens and Ps . corrugata and two fungal strains belonging to Trichoderma viride and Gliocladium virens were evaluated for their efficacy in controlling sugar beet and cucumber damping-off caused by Pythium ultimum . Methods and Results: The in vitro antagonistic activity of bacteria against various Pythium spp. was evaluated with dual cultures in various media. Pseudomonas strains inhibited the pathogen better than Bacillus strains. To identify potentially useful antagonist combinations, dual compatibility of antagonists was also evaluated, based on growth in two liquid media containing substrate previously used by other antagonists. Four pairs of bacteria were selected. Sugar beet damping-off biocontrol was attempted with bacterial seed treatments (individually and in pairs). Cucumber damping-off biocontrol was attempted with bacterial seed treatments and bacterial and fungal compost treatments. In sugar beet, satisfactory biocontrol was only achieved with Pseudomonas antagonists. Antagonist combinations did not show any superior biocontrol ability to individual antagonists and compatibility of bacteria in vitro did not correlate with compatibility in vivo . Bacterial seed treatments and fungal compost treatments failed to control cucumber damping-off. Better biocontrol in cucumber was achieved when bacterial antagonists were applied by drenching or by coating seed with bacteria in a peat carrier. Conclusions: Pseudomonas antagonists were superior to Bacillus antagonists in controlling damping-off in cucumber and sugar beet. Pseudomonas peat inocula maintained a good shelf-life 2 years after preparation. Significance and Impact of the Study : Pseudomonas peat formulations have the potential for development into commercial biopesticides

    Screening of melon populations for resistance to Didymella bryoniae in greenhouse and plastic tunnel conditions

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    Studies were carried out to evaluate melon populations for resistance to Gummy Stem Blight, caused by Didymella bryoniae for use in breeding programs under greenhouse and plastic tunnel conditions. Were evaluated reactions of half-sib populations of PI 140471 and AnĂŽ nÂș 2 had as with susceptible check Eldorado 300. Plants were inoculated 45 days for needle prickling followed by application of 0.05 ml of 5.0 x 10(5) spores/ml suspension in axis of third and fourth true leaves.Resistance evaluation was made after 90 days of age using a scale varying one to five. PI 140471 and AnĂŽ nÂș 2 progenies were found superior and differed significantly with the checker Eldorado 300 for the F Test. AnĂŽ nÂș 2 possessing multiple resistance to diseases and desirable commercial characteristics, constituted the best resistance source to be used in breeding programs.<br>O presente trabalho objetiva avaliar populaçÔes de melĂŁo para resistĂȘncia ao Crestamento Gomoso do Caule, causado por Didymella bryoniae, para uso em programas de melhoramento em condiçÔes de casa de vegetação e tĂșnel plĂĄstico. Foram avaliadas populaçÔes de meio irmĂŁos das introduçÔes PI 140471 e AnĂŽ nÂș 2 e a testemunha suscetĂ­vel Eldorado 300. As plantas foram inoculadas aos 45 dias por picada de agulha na axila da terceira e da quarta folhas verdadeiras seguida da aplicação de 0,05 ml de suspensĂŁo de esporos a uma concentração de 5,0 x 10(5) esporos/ml, e sob condiçÔes de tĂșnel plĂĄstico. A avaliação da resistĂȘncia foi efetuada atravĂ©s de uma escala de notas variando de zero a cinco atĂ© as plantas atingirem 90 dias de idade. As progĂȘnies de meio irmĂŁos de PI 140471 e de AnĂŽ nÂș 2 mostraram-se superiores e diferiram significativamente da testemunha Eldorado 300 pelo Teste de Tukey a nĂ­vel de 5%. A cultivar AnĂŽ nÂș 2, por possuir resistĂȘncia mĂșltipla a doenças e caracterĂ­sticas comerciais desejĂĄveis, constitui-se na melhor fonte de resistĂȘncia a ser utilizada em programas de melhoramento de melĂŁo

    Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization

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    Small supernumerary marker chromosomes (sSMCs) cannot be identified or characterized unambiguously by conventional cytogenetic banding techniques. Until recently, the large variety of marker chromosomes, as well as the limitations in their identification, have presented a diagnostic problem. In order to determine the origin of sSMCs, we used a variety of fluorescence in situ hybridization (FISH) methods, including centromere-specific multicolor FISH, acrocentric specific multicolor FISH, subcentromere-specific multicolor FISH and multicolor FISH with whole chromosome paint probes. Moreover, uniparental disomy testing was in all cases attempted. From a total of 28,000 pre-natal samples from four diagnostic genetics laboratories in Greece, 23 (0.082%) supernumerary marker chromosomes were detected. The mean maternal age was 36.2 years (range 27-43) and the mean gestational age at which amniocentesis was performed was 18.5 weeks (range 16-23). Eighteen markers were de novo and 5 markers were inherited. Molecular cytogenetic methods were applied to determine the chromosomal origin and composition of the sSMC. In total, 17 markers were derived from acrocentric chromosomes (14, 15, 21 and 22) and 6 markers were non-acrocentric, derived from chromosomes 9, 16, 18, 20 and Y. Uniparental disomy was not detected in any of the cases studied. With regard to pregnancy outcome, 13 pregnancies resulted in normal healthy neonates, while 10 pregnancies were terminated due to ultrasound abnormalities. A total of 23 marker chromosomes from 28,000 pre-natal samples (0.082%) were identified. Molecular cytogenetic techniques provided valuable information on the chromosomal origin and composition of all the sSMCs. Especially in cases with normal ultrasound, the FISH results rendered genetic counseling possible in a category of cases previously considered a diagnostic problem. Abnormal outcome was observed in 10 cases (43,5%), 7 of which showed abnormal ultrasound findings. New technologies, such as array-comparative genomic hybridization, should be used in future genotype-phenotype correlation studies, although the high mosaicism rate poses a problem

    Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization

    No full text
    Small supernumerary marker chromosomes (sSMCs) cannot be identified or characterized unambiguously by conventional cytogenetic banding techniques. Until recently, the large variety of marker chromosomes, as well as the limitations in their identification, have presented a diagnostic problem. In order to determine the origin of sSMCs, we used a variety of fluorescence in situ hybridization (FISH) methods, including centromere-specific multicolor FISH, acrocentric specific multicolor FISH, subcentromere-specific multicolor FISH and multicolor FISH with whole chromosome paint probes. Moreover, uniparental disomy testing was in all cases attempted. From a total of 28,000 pre-natal samples from four diagnostic genetics laboratories in Greece, 23 (0.082%) supernumerary marker chromosomes were detected. The mean maternal age was 36.2 years (range 27-43) and the mean gestational age at which amniocentesis was performed was 18.5 weeks (range 16-23). Eighteen markers were de novo and 5 markers were inherited. Molecular cytogenetic methods were applied to determine the chromosomal origin and composition of the sSMC. In total, 17 markers were derived from acrocentric chromosomes (14, 15, 21 and 22) and 6 markers were non-acrocentric, derived from chromosomes 9, 16, 18, 20 and Y. Uniparental disomy was not detected in any of the cases studied. With regard to pregnancy outcome, 13 pregnancies resulted in normal healthy neonates, while 10 pregnancies were terminated due to ultrasound abnormalities. A total of 23 marker chromosomes from 28,000 pre-natal samples (0.082%) were identified. Molecular cytogenetic techniques provided valuable information on the chromosomal origin and composition of all the sSMCs. Especially in cases with normal ultrasound, the FISH results rendered genetic counseling possible in a category of cases previously considered a diagnostic problem. Abnormal outcome was observed in 10 cases (43,5%), 7 of which showed abnormal ultrasound findings. New technologies, such as array-comparative genomic hybridiza-tion, should be used in future genotype-phenotype correlation studies, although the high mosaicism rate poses a problem
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