Fitopatologia - Artigos
URI permanente para esta coleçãohttps://locus.ufv.br/handle/123456789/11741
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Item Caracterização de isolados de Phytophthora infestans do Distrito Federal e de Goiás(Fitopatologia Brasileira, 2006-05) Ribeiro, Fabiana H. S.; Mizubuti, Eduardo S. G.; Reis, AiltonForam caracterizados 123 isolados de Phytophthora infestans obtidos de 21 lavouras de tomateiro e oito de batateira, em municípios do Estado de Goiás e Cidades Satélites de Brasília, no período de abril de 2001 a setembro de 2003. Os isolados foram caracterizados para os marcadores grupo de compatibilidade (123 isolados); isoenzima glucose 6-fosfato-isomerase (Gpi) (34 isolados) e resistência aos fungicidas mefenoxam (77 isolados) e metalaxyl (32 isolados de batateira), usando o método de disco de folhas. Todos os 78 isolados de tomateiro foram classificados no grupo de compatibilidade A1, enquanto os 45 de batateira foram do grupo A2. Os fenótipos para Gpi dos isolados de tomateiro (19) e de batateira (15) foram 86/100, típico da linhagem clonal US-1, e 100/100, típico da linhagen clonal BR-1, respectivamente. Quanto à resistência a mefenoxam, constataram-se isolados de tomateiro resistentes (36%), intermediários (48%) e sensíveis (16%). A maioria dos isolados de batateira foi classificada como sensível (82%) e apenas 9% de intermediários e resistentes. Dos isolados de batateira avaliados para resistência ao metalaxyl, 25% foram resistentes, 62% intermediários e 13% sensíveis. A população de P. infestans no Distrito Federal e no Estado de Goiás é constituída de duas linhagens clonais, com especificidade por hospedeiro.Item Bactérias endofíticas como agentes promotores do crescimento de plantas de tomateiro e de inibição in vitro de Ralstonia solanacearum(Ciência e Agrotecnologia, 2008-05) Barretti, Patrícia Baston; Souza, Ricardo Magela de; Pozza, Edson AmpélioA partir de 150 isolados de bactérias endofíticas obtidos de folhas, caules e raízes de tomateiros sadios, 53 destacaram-se quanto à habilidade em promover o crescimento de plantas de tomateiro (Solanum lycopersicum L.). Submetidos a uma nova seleção, os isolados UFV-E17, UFV-E22, UFV-E25, UFV-E26, UFV-E27, Bacillus cereus (UFV-E29), UFV-E49, UFLA 06-LS, UFLA 08-LS e UFLA 11-LS apresentaram maior promoção do crescimento. Avaliações semanais de altura e número de folhas e folíolos das plantas aconteceram durante 45 dias. Após a sexta avaliação, mensurou-se a área foliar e o peso da matéria fresca e seca da parte aérea e da raiz das plantas. O isolado UFV-E49 apresentou melhor resultado para altura, área foliar, número de folhas e peso da matéria fresca e seca, tanto da parte aérea quanto da raiz. Dos isolados selecionados, somente dois apresentaram efeito inibitório direto in vitro a Ralstonia solanacearum.Item Genetic structure of the population of Alternaria solani in Brazil(Journal of Phytopathology, 2011-04) Lourenço Jr, Valdir; Rodrigues, Tatiana T. M. S.; Campos, Antonio M. D.; Bragança, Carlos A. D.; Scheuermann, Klaus K.; Reis, Ailton; Brommonschenkel, Sérgio H.; Maffia, Luiz A.; Mizubuti, Eduardo S. G.Understanding the genetic structure of the population of Alternaria solani (AS) is an important component of epidemiological studies of early blight, a severe disease that affects potato (Po) and tomato (To) worldwide. Up to 150 isolates obtained from both hosts were analysed with RAPD and AFLP markers to estimate the amount and distribution of genetic variability of AS in Brazil. Using RAPD, gene diversity (h=0.20) and scaled indices of diversity of Shannon (H′=0.66) and Stoddart and Taylor’s (G=0.31) for the Po population were higher than those of the To (h=0.07, H′=0.34, G=0.17). For AFLP, the statistics for the Po (h=0.17, H′=0.86, G=0.49) and To (h= 0.17, H′=0.85, G=0.36) populations were similar. For each RAPD and AFLP locus, the allele frequency for the overall population ranged from 0.006 to 0.988, and 0.007 to 0.993, respectively. Genetic differentiation was high (GST=0.41 and θ=0.59) and moderately high (GST=0.23 and θ=0.37) when estimated with RAPD and AFLP, respectively. Based on cluster analyses, there was strong evidence of association of pathogen haplotypes with host species. The null hypothesis of random association of alleles was rejected in the analysis of both RAPD (IA=13.1, P<0.001) and AFLP (IA=2.2, P<0.001) markers. The average number of migrants was estimated to be around one and two individuals per generation, using RAPD and AFLP, respectively. There was no correlation between genetic distance and geographical origin of AS haplotypes for RAPD (r=−0.07, P=0.84) and AFLP (r=−0.03, P=0.70). The AS population is clonal with high genetic variability, and there is genetic differentiation between the populations that affect To and Po.Item Biological control of eucalyptus bacterial wilt with rhizobacteria(Biological Control, 2015-01) Santiago, Thais R.; Rossato, Mauricio; Romeiro, Reginaldo S.; Mizubuti, Eduardo S. G.; Grabowski, CristhianThe antagonistic potential of 298 rhizobacteria obtained from the rhizosphere and rhizoplane of tomato and eucalyptus plants was assessed for the control of bacterial wilt of eucalyptus caused by Ralstonia solanacearum. Several tests were performed using tomato plants as a screening system to select efficient rhizobacteria. Different methods for antagonist delivery and pathogen inoculation were evaluated: (1) seeds were microbiolized (soaked for 12 h in a suspension of the antagonist propagules) and germinated seedlings had their roots immersed in the pathogen inoculum suspension; (2) seedlings originated from microbiolized seeds were transplanted to soil infested with R. solanacearum and (3) roots of seedlings were immersed in a suspension of propagules of the antagonist and subsequently in a suspension of R. solanacearum. Nine isolates (UFV-11, 32, 40, 56, 62, 101, 170, 229, and 270) were selected as potential antagonists to R. solanacearum as they suppressed bacterial wilt in at least one of the methods assessed. The selected antagonists were evaluated against two isolates of R. solanacearum using in vitro and in vivo (inoculated eucalyptus) tests. Isolates UFV-56 (Bacillus thuringiensis), UFV-62 (Bacillus cereus) and a commercial formulation of several rhizobacteria (Rizolyptus®) suppressed bacterial wilt in eucalyptus protecting the plants during the early stages of development.Item Synergism and negative interference during co-infection of tomato and Nicotiana benthamiana with two bipartite begomoviruses(Virology, 2009-03-12) Alves-Júnior, Miguel; Alfenas-Zerbini, Poliane; Andrade, Eduardo C.; Esposito, Débora A.; Silva, Fábio N.; Cruz, Ana Cláudia F. da; Ventrella, Marília C.; Otoni, Wagner C.; Zerbini, F. MuriloIn Brazil, at least eight begomoviruses including Tomato rugose mosaic virus (ToRMV) and Tomato yellow spot virus (ToYSV) infect tomatoes. ToYSV symptoms in tomato and Nicotiana benthamiana appear earlier and are more severe compared to those of ToRMV. We investigated the role of several factors in this differential adaptation. To analyze infection kinetics, a single leaf was inoculated and subsequently detached after different periods of time. Viral DNA accumulation was quantified in plants, viral replication was analyzed in protoplasts, and tissue tropism was determined by in situ hybridization. Results indicate that ToYSV establishes a systemic infection and reaches a higher concentration earlier than ToRMV in both hosts. ToRMV negatively interferes with ToYSV during the initial stages of infection, but once systemic infection is established this interference ceases. In N. benthamiana, ToYSV invades the mesophyll, while ToRMV is phloem-restricted. During dual infection in this host, ToYSV releases ToRMV from the phloem.Item Recombination and pseudorecombination driving the evolution of the begomoviruses Tomato severe rugose virus (ToSRV) and Tomato rugose mosaic virus (ToRMV): two recombinant DNA-A components sharing the same DNA-B(Virology Journal, 2014-04-05) Silva, Fábio N; Lima, Alison TM; Rocha, Carolina S; Castillo-Urquiza, Gloria P; Alves-Júnior, Miguel; Zerbini, F MuriloBegomoviruses are dicot-infecting, whitefly-transmitted viruses with a genome comprised of one or two molecules of circular, single-stranded DNA. In Brazil, tomato-infecting begomoviruses have emerged as serious pathogens since the introduction of a new biotype of the insect vector in the mid-1990’s. Tomato rugose mosaic virus (ToRMV) and Tomato severe rugose virus (ToSRV) are often found in tomato fields. The complete sequence of the DNA-B components of ToSRV and ToRMV show an identity of 98.2%. Additionally, the high nucleotide identity (96.2%) between their common regions indicates that these two viruses may share the same DNA-B. Tomato seedlings were biolistically inoculated with ToSRV (DNA-A and DNA-B) and ToRMV (DNA-A and DNA-B) infectious clones in every possible combination of single or mixed infection. Symptom expression was evaluated for up to 35 days post-inoculation (dpi). DNA was extracted at 28 dpi and the presence of each viral genomic component was examined by rolling circle amplification (RCA) followed by digestion, as well as by quantitative, real-time PCR. Sequence comparisons, recombination and phylogenetic analyzes were performed using EMBOSS needle, RDP program and maximum likelihood inference, respectively. Symptoms in tomato plants inoculated with the different combinations of ToRMV and ToSRV DNA-A and DNA-B components consisted of a typical mosaic in all combinations. Pseudorecombinants were formed in all possible combinations. When two DNA-A or two DNA-B components were inoculated simultaneously, the ToRMV components were detected preferentially in relation to the ToSRV components. The combination of minor changes in both the Rep protein and the CR may be involved in the preferential replication of ToRMV components. Recombination and phylogenetic analyzes support the exchange of genetic material between ToRMV and ToSRV. ToRMV and ToSRV form viable pseudorecombinants in their natural host (Solanum lycopersicum) and share the same DNA-B. ToRMV DNA components are preferentially replicated over ToSRV components. These results indicate that the emergence of ToRMV involved both recombination and pseudorecombination, further highlighting the importance of these mechanisms in the emergence and adaptation of begomoviruses.