Aims: To investigate the effects of the endophyte Bacillus subtilis ALB629 on the growth of cacao seedlings at early developmental stage and to evaluate its antimicrobial properties. Methods and Results: Germinating cacao seeds were inoculated with ALB629, and seedlings growth was evaluated 30 days later. Significant increase (P < 0Á05) was observed in the root system (up to 30%), leaf area (14%) and stem height (7Á6%). ALB629 colonized the entire plant, prevailing over indigenous micro-organisms. In addition, it was tested in vitro, by pairing assays, and showed antagonistic effect against the phytopathogenic fungi Moniliophthora perniciosa, Colletotrichum sp. and C. gossypii. When tested in cacao-grafting procedure in the field, ALB629 increased the grafting success rate (24%), indicating its protective effect. In addition, this Bacillus secretes an antagonist compound, as shown by the antifungal activity of the cell-free culture. Conclusions: Bacillus subtilis ALB629 promotes cacao root growth, besides promoting growth of the aerial part of cacao seedlings. It has antimicrobial properties and produces an antifungal compound. Significance and Impact of the Study: ALB629 presented beneficial characteristics for cacao cultivation, being a good biological control agent candidate. Furthermore, it is a potential source of antifungal compound with potential for commercial exploitation.

The osmotin proteins of several plants display antifungal activity, which can play an important role in plant defense against diseases. Thus, this protein can be useful as a source for biotechnological strategies aiming to combat fungal diseases. In this work, we analyzed the antifungal activity of a cacao osmotin-like protein (TcOsm1) and of two osmotin-derived synthetic peptides with antimicrobial features, differing by five amino acids residues at the N-terminus. Antimicrobial tests showed that TcOsm1 expressed in Escherichia coli inhibits the growth of Moniliophthora perniciosa mycelium and Pichia pastoris X-33 in vitro. The TcOsm1-derived peptides, named Osm-pepA (H-RRLDRGGVWNLNVNPGTTGARVWARTK-NH2), located at R23-K49, and Osm-pepB (H-GGVWNLNVNPGTTGARVWARTK-NH2), located at G28-K49, inhibited growth of yeasts (Saccharomyces cerevisiae S288C and Pichia pastoris X-33) and spore germination of the phytopathogenic fungi Fusarium f. sp. glycines and Colletotrichum gossypi. Osm-pepA was more efficient than Osm-pepB for S. cerevisiae (MIC=40μM and MIC=127μM, respectively), as well as for P. pastoris (MIC=20μM and MIC=127μM, respectively). Furthermore, the peptides presented a biphasic performance, promoting S. cerevisiae growth in doses around 5μM and inhibiting it at higher doses. The structural model for these peptides showed that the five amino acids residues, RRLDR at Osm-pepA N-terminus, significantly affect the tertiary structure, indicating that this structure is important for the peptide antimicrobial potency. This is the first report of development of antimicrobial peptides from T. cacao. Taken together, the results indicate that the cacao osmotin and its derived peptides, herein studied, are good candidates for developing biotechnological tools aiming to control phytopathogenic fungi.

The cupuassu tree (Theobroma grandiflorum) (Willd. ex Spreng.) Schum. is a fruitful species from the Amazon with great economical potential, due to the multiple uses of its fruit´s pulp and seeds in the food and cosmetic industries, including the production of cupulate, an alternative to chocolate. In order to support the cupuassu breeding program and to select plants presenting both pulp/seed quality and fungal disease resistance, SSRs from Next Generation Sequencing ESTs were obtained and used in diversity analysis. From 8,330 ESTs, 1,517 contained one or more SSRs (1,899 SSRs identified). The most abundant motifs identified in the EST-SSRs were hepta- and trinucleotides, and they were found with a minimum and maximum of 2 and 19 repeats, respectively. From the 1,517 ESTs containing SSRs, 70 ESTs were selected based on their functional annotation, focusing on pulp and seed quality, as well as resistance to pathogens. The 70 ESTs selected contained 77 SSRs, and among which, 11 were polymorphic in cupuassu genotypes. These EST-SSRs were able to discriminate the cupuassu genotype in relation to resistance/susceptibility to witches’ broom disease, as well as to pulp quality (SST/ATT values). Finally, we showed that these markers were transferable to cacao genotypes, and that genome availability might be used as a predictive tool for polymorphism detection and primer design useful for both Theobroma species. To our knowledge, this is the first report involving EST-SSRs from cupuassu and is also a pioneer in the analysis of marker transferability from cupuassu to cacao. Moreover, these markers might contribute to develop or saturate the cupuassu and cacao genetic maps, respectively.

Cupuassu (Theobroma grandiflorum [Willd. ex Spreng.] Schum) is a species of high economic importance in Brazil with great potential at international level due to the multiple uses of both its seeds and pulp in the industry of sweets and cosmetics. For this reason, the cupuassu breeding program focused on the selection of genotypes with high pulp and seed quality—selection associated with the understanding of the mechanisms involved in fruit formation. Gene expression is one of the most used approaches related to such understanding. In this sense, quantitative real-time PCR (qPCR) is a powerful tool, since it rapidly and reliably quantifies gene expression levels across different experimental conditions. The analysis by qPCR and the correct interpretation of data depend on signal normalization using reference genes, i.e. genes presenting a uniform pattern of expression in the analyzed samples. Here, we selected and analyzed the expression of five genes from cupuassu (ACP, ACT, GAPDH, MDH, TUB) to be used as candidates for reference genes on pulp and seed of young, maturing and mature cupuassu fruits. The evaluation of the gene expression stability was obtained using the NormFinder, geNorm and BestKeeper programs. In general, our results indicated that the GAPDH and MDH genes constituted the best combination as reference genes to analyze the expression of cupuassu samples. To our knowledge, this is the first report of reference gene definition in cupuassu, and these results will support subsequent analysis related to gene expression studies in cupuassu plants subjected to different biotic or abiotic conditions as well as serve as a tool for diversity analysis based on pulp and seed quality.

No abstract

Witches' broom and pod rot are the two most devastating diseases of cocoa in South America and Africa, respectively. Their control by means of phytosanitation and chemical fungicides is labor-intensive, costly and, in many cases, environmentally undesirable. Therefore efforts are made in order to identify alternative, environmentally safe and cost-efficient methods for the control of these pathogens. Promising candidates are components of the neem tree (Azadirachta indica), that have been used for centuries in Asia as insecticides, fungicides, anticonceptionals in popular medicine. Here we report about tests on the effect of various concentrations of extracts from neem leaves on growth of mycelia of Crinipellis and Phytophthora and on germination of spores of Crinipellis. We show a 35% growth reduction of mycelia of Phytophthora on neem leaf extract media, whereas growth of mycelia of Crinipellis was not affected, even at the highest concentration of neem leaf extracts used (35%). However, the most dramatic effect of neem leaf extracts is observed on Crinipellis spore germination, here the extracts (20-35%) reduced germination almost completely. Based on these results, we believe that the neem tree might be a source for the production, on small and medium scale, of an effective and cheap formulation for the control of Crinipellis and Phytophthora.

Cupuassu (Theobroma grandiflorum [Willd. ex Sprengel] Schumann) seeds constitute the raw material for oil extraction and fabrication of cupulate (product similar to chocolate). However, fungal diseases such as witches’ broom caused by Moniliophthora perniciosa have interfered with the large-scale development of cupuassu plantations. Cupuassu genetic breeding programmes focus on a variety of biotechnological tools or approaches to select genes related to quality or resistance mechanisms. In this study, we used expression and interactomics analyses of preselected genes involved in fruit quality and/or resistance to better understand the molecular and physiological mechanisms associated with these plant processes. It was found that i) resistant and susceptible cupuassu genotypes showed different pulp characteristics as well as gene expression patterns; ii) monosaccharide and carbohydrate transport pathways were enhanced during fruit maturation; iii) sugar accumulation participated in signal transduction associated with fruit development and stress response in maturing fruits; and iv) maturing pulp and seeds showed increased phospholipid metabolism and translocation, as well as immune system activation. The TgSTP1, TgWRKY33, TgCZF1, and TgUBA1 genes in cupuassu and the orthologues of DIN10, CNI1, and TET8 identified by the interactomics approach may be good candidates for marker-assisted selection in breeding programmes focusing on both fruit quality and resistance/tolerance to biotic/abiotic stress.

O tratamento sanitário de substratos é uma operação importante no processo de produção de mudas e no cultivo de plantas em vasos ou outros recipientes. O processo visa eliminar organismos causadores de doenças que podem provocar a morte das mudas e/ou servir como fonte de inóculo para disseminação de patógenos durante o transplante. Tradicionalmente no Brasil, temse utilizado o gás brometo de metila para o tratamento de substrato. Todavia, este gás é também um dos agentes destruidores da camada de ozônio e por isso, o seu uso deverá ser reduzido em 50% até o ano 2005 e suspenso até 2010. Assim, há necessidade de se buscar opções para o tratamento de solo e substratos (Müller, 1998). SILVA, J.B.C.; OLIVEIRA-NAPOLEÃO, I.T.; FALCÃO, L.L. Desinfestação de substratos para produção de mudas, utilizando vapor de água. Horticultura Brasileira, Brasília, v. 19, n. 2, RESUMOO tratamento sanitário de substratos é uma operação importante no processo de produção de mudas e no cultivo de plantas em vasos ou outros contentores. Tradicionalmente tem-se utilizado o gás brometo de metila como agente desinfetante. Entretanto, a produção deste gás deverá ser abolida até o ano 2010, forçando-se a busca de novas opções. Desenvolveu-se na Embrapa Hortaliças um equipamento que utiliza o vapor de água à baixa pressão, produzido por uma caldeira industrial, com capacidade para evaporar 30 L/h de água, para aquecer o substrato contido em uma caixa metálica cilín-drica com capacidade de 2000 L. O vapor é aplicado no fundo da caixa que contém uma camada de brita coberta com uma tela metá-lica de malha de 2 mm, que favorece a distribuição uniforme do vapor por toda a massa de substrato. O tempo de aquecimento é de aproximadamente 3 horas e o calor armazenado durante este perío-do mantém a massa de substrato aquecida a temperaturas pasteurizantes, por até 4 horas após a aplicação do vapor. Para testar a eficácia do sistema avaliou-se a sobrevivência dos patógenos Ralstonia solanacearum, Fusarium oxysporum, Sclerotinia sclerotiorum e Rhizoctonia solani. Aplicou-se vapor por uma hora, não considerando o período de aquecimento, e coletaram-se as amostras após uma, duas, três ou quatro horas o início da aplicação de vapor. O tratamento por uma hora, em adição ao período de aquecimento, resultou na eliminação dos patógenos. Palavras-chave: termoterapia, esterilização. ABSTRACTDisinfesting substrate for transplants production employing hot water steam.The disinfestation of substrate is an important process for transplanting production and for plant cultivation in pots or boxes. Traditionally, metyl bromide gas has been employed to eliminate microorganisms. However the production of bromide gas in Brazil will be interrupted by the year 2010 and it is necessary to search for new options. We have devised an equipment that utilizes hot steam water at low pressure produced into a boiler machine with the capacity of evaporating 30L/h of water, and heating 2,000 L of substrate contained into a cylindrical metallic box. The steam is applied under the box...