No abstract

A tristeza causada pelo vírus da tristeza dos citros (Citrus tristeza virus, CTV) é uma das principais viroses dos citros (Citrus spp.) no Brasil. Alguns autores têm utilizado a intensidade de caneluras produzidas nos ramos para selecionar plantas com resistência ao vírus. Neste trabalho foi avaliada a reação de porta-enxertos híbridos, provenientes do programa de melhoramento genético de citros da Embrapa Mandioca e Fruticultura ao CTV e elaboradas duas escalas, uma fotográfica e outra diagramática, para quantificação de resistência ao CTV. Entre os porta-enxertos avaliados, a maioria apresentou poucas caneluras, sendo portanto considerados resistentes à tristeza. Verificou-se a manutenção da resistência ao vírus nos híbridos produzidos a partir de progenitores que possuíam algum nível de resistência.

ABSTRACT. This study aimed to develop a methodology for eliminating cassava frogskin disease (CFSD) from in vitro shoot tip culture by associating thermotherapy and tetracycline. Cuttings from different accessions (BGM0232, BGM0315, BGM0464, BGM584, BGM0841, and BGM1342), infected with CFSD according to visual inspection of the disease symptoms, were used for cleaning. To verify the absence of other diseases, the plants were indexed for Cassava common mosaic virus -CsCMV (by ELISA) and Cassava vein mosaic virus -CsVMV (by polymerase chain reaction, PCR), proving that the accessions were free of these viruses, except for BGM0315 and BGM0464, which were infected with CsVMV. Subsequently, the cuttings were submitted to different tetracycline concentrations for 3 min, and then subjected to thermotherapy under different temperatures (35°, 38°, 40°, 45°, and 55°C). Shoots of 2 cm were harvested, and their surfaces were sterilized in a laminar flow chamber. Subsequently, the shoot tips of different sizes were removed (0.2, 0.4, 0.5, and 1.0 2 M.J.S. Carvalho et al.Genetics and Molecular Research 16 (2): gmr16029556 mm) for inoculation in a culture medium with tetracycline at the same concentrations in which the cuttings were dipped. After 60 days of cultivation, the explants were transferred to a multiplication medium without antibiotics. Thirty days after the transfer, the viability of the regenerated plants was evaluated, which were then acclimatized for 70 days in a greenhouse and transferred to the field. After 7 months, a visual analysis of the symptomatic roots and a PCR analysis were held to prove the elimination of CFSD and CsVMV from the accessions infected with these viruses (BGM0315 and BGM0464), respectively. Most of the treatments resulted in 100% cleaning of CFSD-infected plants. From accessions that were also infected with CsVMV, only 2% of the plants remained infected, also demonstrating the cleaning efficiency of this protocol for this disease.

Situado no município de Cruz das Almas, Recôncavo Baiano, o Programa de Melhoramento Genético de Citros da Embrapa Mandioca e Fruticultura possui ações dirigidas ao desenvolvimento de novos porta-enxertos, adaptados a condições de cultivo tropicais, compreendendo: hibridações controladas, visando à exploração da ampla variabilidade genética existente em Citrus e gêneros afins; introdução de novas variedades a partir de várias regiões do País e do exterior; seleção de clones nucelares, relacionados a porta-enxertos tradicionais, porém possuidores de características de interesse agronômico que os distinguem de seus padrões varietais. O presente trabalho refere-se a estudos pertinentes a esta última linha de pesquisa, baseados em avaliações dirigidas a 20 seleções de tangerina 'Sunki', tendo como objetivo principal a identificação de indivíduos que se destacam pela produção de frutos com um número médio de sementes superior ao comumente verificado nesse porta-enxerto. As análises realizadas compreenderam os seguintes caracteres: número médio de sementes por fruto, número médio de embriões por semente, intervalo de variação do número de embriões por semente, porcentagem de poliembrionia e tamanho de embrião. Os resultados obtidos permitem indicar a seleção 'Sunki Tropical' como alternativa de uso em programas de diversificação de porta-enxertos nas condições em que esta tangerina apresenta boa adaptação, principalmente em função de seu elevado número médio de sementes por fruto (18,7) e previsível uniformidade de seedlings, esta decorrente de sua elevada porcentagem de poliembrionia, próxima a 100%.

No abstract

O objetivo deste trabalho foi identificar cultivares geneticamente divergentes de mamoneira (Ricinus communis) com uso de marcadores RAPD. Um total de 58 iniciadores RAPD foi usado na genotipagem de 15 cultivares. A dissimilaridade genética entre as cultivares foi calculada a partir do índice de Jaccard, tendo-se utilizado o método da média aritmética não ponderada (UPGMA). Foram identificados 552 fragmentos, sendo 311 polimórficos (56,3%). As cultivares foram agrupadas em cinco grupos, evidência de que há divergência genética entre elas. Os marcadores moleculares do tipo RAPD são eficientes no estudo da dissimilaridade em mamoneira.

Several molecular techniques have been used to differentiate species or genetic lineages of microorganisms prior to sequencing. Among them, BOX-and ERIC-PCRs may provide specific banding patterns for different species, allowing its differentiation.Therefore, the objective of this study was to evaluate these techniques as a tool for differentiation of phylogenetic lineages belonging to the Colletotrichum gloeosporioides species complex associated with cassava anthracnose disease. Sets of BOX-and ERIC-PCR primers were used to assess the differentiation of lineages belonging to the complex with 81 C. gloeosporioides sensu lato (s.l.) isolates from different cassava producing regions. Some were identified by sequencing, such as Colletotrichum fructicola, Colletotrichum tropicale, C. gloeosporioides s.s, Colletotrichum theobromicola, Colletotrichum siamense, Colletotrichum brevisporum and Colletotrichum sichuanensis.The primers were able to amplify DNA fragments from all isolates. The ERIC-PCR presented a wider range of banding patterns in comparison to BOX-PCR, providing better differentiation of the individuals, as well as a higher correlation with the phylogenetic data was obtained by ERIC-PCR and the combined data set for "BOX-/ ERIC-PCRs," inferred by Mantel test. However, the use of concatenated data (BOX-/ ERIC-PCRs) reduced the discriminatory capacity presented by ERIC-PCR alone, probably due to the lowest resolution of BOX-PCR. Therefore, ERIC-PCR technique enabled efficient differentiation of isolates belonging to the C. gloeosporioides complex and can be used to analyse multiple isolates in a collection and also being an important tool as a guide in the decision-making process prior to sequencing. Based on this methodology, it was possible to identify two new species associated with cassava anthracnose disease, C. brevisporum and C. sichuanensis, being the first report of these two species associated with cassava anthracnose disease in Brazil. K E Y W O R D SColletotrichum spp., DNA fingerprint, Rep-PCR, species complex | 219 LOPES SILVA Et AL.

A survey to investigate the occurrence of cassava anthracnose disease (CAD) and distribution of Colletotrichum spp. in cassava plantations in different eco-zones of the Reconcavo Region in Bahia, Brazil, investigated during the rainy season of 2014. A total of 50 cassava fields distributed among 18 municipalities were visited and intensity of anthracnose evaluated. The highest disease incidence (DI) (83.3%) was in samples collected in São Félix, and the lowest (34.4%), in Varzedo. Municipalities that presented the highest values for DI were located within the 'Af' Köppen-Geiger eco-zone, also presenting the highest values for the estimated McKinney disease index. Based on previous studies of multilocus phylogeny, seven different species of Colletotrichum were identified (Colletotrichum fructicola, Colletotrichum tropicale, Colletotrichum gloeosporioides s.s, Colletotrichum theobromicola, Colletotrichum siamense, Colletotrichum brevisporum and Colletotrichum plurivorum) and a new approach based on ERIC-PCR was used aiming to group the 82 isolates according to these findings. The highest percentage of genetic variance (> 78%) was among isolates within fields. Based on the survey and genetic analysis, C. fructicola is probably the main causal agent of cassava anthracnose in the Recôncavo Region, since this species was present with highest incidence in all eco-zones, 47.61, 42.86 and 57.14% for Af (tropical rainforest climate), As (tropical dry savanna climate) and Aw (tropical wet savanna climate), respectively. This study is the first report of C. fructicola lineages as the most likely pathogen causing anthracnose disease of cassava in Brazil, and these findings may be used to guide the selection of resistant varieties.