Preferência alimentar de Dione juno juno (CRAMER, 1779) (Lepidoptera: Nymphalidae) por genótipos de maracujazeiro

O presente trabalho teve por objetivo determinar o efeito de genótipos de maracujazeiro quanto à atratividade e à não-preferência para alimentação de lagartas de Dione juno juno, em diferentes idades, através de testes com e sem chance de escolha. Os experimentos foram conduzidos no Departamento de Fitossanidade da FCAV/UNESP de Jaboticabal-SP, sob condições ambientais controladas (T=26=±=1°C=U.=R.= 60 ± 10% e fotofase = 14 horas), utilizando-se dos genótipos Passiflora edulis, P. gibertii, P. alata, Sul Brasil, IAC-275, Flora FB 300, P. serrato-digitata, P. edulis f. flavicarpa, Maguary FB-100 e P. foetida. Para o teste com chance de escolha, foram utilizadas placas de Petri, onde foram distribuídos, de forma eqüidistante, um disco foliar (3,2 cm) de cada genótipo estudado e liberando-se em seguida, no centro da placa, 5 lagartas recém-eclodidas ou uma lagarta com 10 dias de idade por material. No teste sem chance de escolha, foi colocado apenas um disco de cada genótipo por placa de Petri (9 cm de diâmetro), mantendo-se o mesmo padrão de infestação utilizado no teste com chance. As avaliações foram realizadas em duas etapas, sendo que, na primeira, avaliou-se a atratividade, contando o número de lagartas em cada material a 1; 3; 5; 10; 15; 30; 60; 120; 240 minutos e 24 horas após a liberação das mesmas. Na segunda etapa, observou-se o consumo foliar 24 horas após o início do teste. O genótipo menos atrativo às lagartas recém-eclodidas e de 10 dias de idade foi P. alata em testes com e sem chance de escolha. O genótipo P. alata foi o menos consumido em teste com chance de escolha, sendo que, no teste sem chance, P. alata e P. foetida destacaram-se como os menos consumidos para as duas fases larvais.

Atratividade e preferência alimentar de Epicauta atomaria (Ger.) em algumas espécies de maracujá

Avaliou-se, em laboratório, a não-preferência para alimentação de Epicauta atomaria em diferentes espécies de maracuja, em teste com e sem chance de escolha. Verificou-se a melhor densidade de insetos que proporcionam a discriminação quanto aos graus de resistência. Para avaliação, utilizaram P. setacea, P. alata, P. edulis, P. cincinnata e P. laurifolia. Para os testes com e sem chance de escolha, a não-preferência para alimentação foi avaliada através da atratividade, onde foi contado o número de insetos atraídos por espécie, em placa de Petri. As espécies P. laurifolia e P. alata foram resistentes a E. atomaria, expressando o tipo de resistência à não-preferência para alimentação. As densidades de E. atomaria que melhor discriminaram as espécies de maracujazeiro, são três e cinco (teste com chance de escolha) e dois (teste sem chance de escolha). P. edulis, P. setacea e P. cincinnata são suscetíveis a E. atomaria.

Eficiência de argila silicatada no controle de Xanthomonas axonopodis pv. passiflorae, in vitro e em mudas de maracujazeiro-amarelo

A mancha bacteriana do maracujá, causada pela bactéria Xanthomonas axonopodis pv. passiflorae, ocorre em todas as regiões produtoras do País, sendo responsável por grandes perdas econômicas na cultura do maracujazeiro-amarelo. O presente trabalho teve como objetivos testar a eficiência de argila silicatada na inibição da bactéria X. axonopodis pv. passiflorae in vitro e no controle preventivo e curativo da mancha bacteriana em mudas de maracujazeiro-amarelo. A argila silicatada foi adicionada ao meio de cultura batata-dextrose-ágar fundente, nas concentrações de 0,0; 0,5; 1,0; 1,5 e 2,0%; vertido em placas de Petri. Após resfriamento do meio, repicou-se a suspensão bacteriana (10(7) UFC.mL-1) com uma alça, incubando-se as placas a 28 °C por três dias, quando se avaliou o crescimento bacteriano. Posteriormente, o produto, nas mesmas concentrações citadas, foi pulverizado em mudas de maracujá 'Afruvec' de forma preventiva ou curativa. A inoculação da bactéria foi realizada através de pulverização foliar da suspensão bacteriana (10(7) UFC.mL-1), 24 h antes ou após os tratamentos curativo e preventivo, respectivamente. A severidade da doença foi avaliada com auxílio de uma escala diagramática nas quatro primeiras folhas verdadeiras contadas de baixo para cima. Nas concentrações avaliadas, a argila silicatada inibiu a bactéria in vitro e os sintomas da mancha bacteriana no tratamento curativo, enquanto no tratamento preventivo, controle significativo foi obtido a partir de 1,0% de argila silicatada. Com base nestes resultados, a argila silicada pode ser recomendada, na concentração de 1,0-2,0%, para o controle da mancha bacteriana do maracujazeiro em pulverizações foliares.

The UlaG protein familly defines novel structural and functional motifs grafted on an ancient RNase fold

Background: Bacterial populations are highly successful at colonizing new habitats and adapting to changing environmental conditions, partly due to their capacity to evolve novel virulence and metabolic pathways in response to stress conditions and to shuffle them by horizontal gene transfer (HGT). A common theme in the evolution of new functions consists of gene duplication followed by functional divergence. UlaG, a unique manganese-dependent metallo-b-lactamase (MBL) enzyme involved in L-ascorbate metabolism by commensal and symbiotic enterobacteria, provides a model for the study of the emergence of new catalytic activities from the modification of an ancient fold. Furthermore, UlaG is the founding member of the so-called UlaG-like (UlaGL) protein family, a recently established and poorly characterized family comprising divalent (and perhaps trivalent)metal-binding MBLs that catalyze transformations on phosphorylated sugars and nucleotides. Results: Here we combined protein structure-guided and sequence-only molecular phylogenetic analyses to dissect the molecular evolution of UlaG and to study its phylogenomic distribution, its relatedness with present-day UlaGL protein sequences and functional conservation. Phylogenetic analyses indicate that UlaGL sequences are present in Bacteria and Archaea, with bona fide orthologs found mainly in mammalian and plant-associated Gramnegative and Gram-positive bacteria. The incongruence between the UlaGL tree and known species trees indicates exchange by HGT and suggests that the UlaGL-encoding genes provided a growth advantage under changing conditions. Our search for more distantly related protein sequences aided by structural homology has uncovered that UlaGL sequences have a common evolutionary origin with present-day RNA processing and metabolizing MBL enzymes widespread in Bacteria, Archaea, and Eukarya. This observation suggests an ancient origin for the UlaGL family within the broader trunk of the MBL superfamily by duplication, neofunctionalization and fixation. Conclusions: Our results suggest that the forerunner of UlaG was present as an RNA metabolizing enzyme in the last common ancestor, and that the modern descendants of that ancestral gene have a wide phylogenetic distribution and functional roles. We propose that the UlaGL family evolved new metabolic roles among bacterial and possibly archeal phyla in the setting of a close association with metazoans, such as in the mammalian gastrointestinal tract or in animal and plant pathogens, as well as in environmental settings. Accordingly, the major evolutionary forces shaping the UlaGL family include vertical inheritance and lineage-specific duplication and acquisition of novel metabolic functions, followed by HGT and numerous lineage-specific gene loss events.

Similar and Divergent Effects of ppGpp and DksA Deficiencies on Transcription in Escherichia coli.

The concerted action of ppGpp and DksA in transcription has been widely documented. In disparity with this model, phenotypic studies showed that ppGpp and DksA might also have independent and opposing roles in gene expression in Escherichia coli. In this study we used a transcriptomic approach to compare the global transcriptional patterns of gene expression in strains deficient in ppGpp (ppGpp0) and/or DksA ( dksA). Approximately 6 and 7% of all genes were significantly affected by more than twofold in ppGpp- and DksAdeficient strains, respectively, increasing to 13% of all genes in the ppGpp0 dksA strain. Although the data indicate that most of the affected genes were copositively or conegatively regulated by ppGpp and DksA, some genes that were independently and/or differentially regulated by the two factors were found. The large functional group of chemotaxis and flagellum synthesis genes were notably differentially affected, with all genes being upregulated in the DksA-deficient strain but 60% of them being downregulated in the ppGpp-deficient strain. Revealingly, mutations in the antipausing Gre factors suppress the upregulation observed in the DksA-deficient strain, emphasizing the importance of the secondary channel of the RNA polymerase for regulation and fine-tuning of gene expression in E. coli.

Similar and Divergent Effects of ppGpp and DksA Deficiencies on Transcription in Escherichia coli.

The concerted action of ppGpp and DksA in transcription has been widely documented. In disparity with this model, phenotypic studies showed that ppGpp and DksA might also have independent and opposing roles in gene expression in Escherichia coli. In this study we used a transcriptomic approach to compare the global transcriptional patterns of gene expression in strains deficient in ppGpp (ppGpp0) and/or DksA ( dksA). Approximately 6 and 7% of all genes were significantly affected by more than twofold in ppGpp- and DksAdeficient strains, respectively, increasing to 13% of all genes in the ppGpp0 dksA strain. Although the data indicate that most of the affected genes were copositively or conegatively regulated by ppGpp and DksA, some genes that were independently and/or differentially regulated by the two factors were found. The large functional group of chemotaxis and flagellum synthesis genes were notably differentially affected, with all genes being upregulated in the DksA-deficient strain but 60% of them being downregulated in the ppGpp-deficient strain. Revealingly, mutations in the antipausing Gre factors suppress the upregulation observed in the DksA-deficient strain, emphasizing the importance of the secondary channel of the RNA polymerase for regulation and fine-tuning of gene expression in E. coli.

Magnetoestratigrafía de las sucesiones cenozoicas de la cuenca de As Pontes(La Coruña, Noroeste de España).

La cuenca terciaria de As Pontes (Noroeste de España), asociada a un corredor de fallas transcurrentes de dirección NW-SE, ha sido datada mediante magnetoestratigrafia, para lo cual se han estudiado un total de cuatro sucesiones magnetoestratigráficas. Las litologías estudiadas han sido sobre todo arcillas aluviales y palustres-lacustres, con un contenido variable de materia orgánica. En total se han desmagnetizado unos 900 especímenes, mediante desmagnetización térmica y por campos alternantes. Los minerales responsables de la magnetización en las rocas estudiadas son la magnetita y los sulfuros de hierro. A partir de los datos paleomagnéticos, se puede establecer que la sedimentación en la cuenca comenzó en el cron 10r (parte alta del Starnpiense) y se prolongó, como mínimo, hasta el subcron 6AAr.2n (Aquitaniense superior). Así, la duración de la sedimentación en la cuenca fue de unos 6,2 Ma, abarcando desde la última parte del Oligoceno temprano hasta el Mioceno temprano. La correlación magnetoestratigráfica de las diferentes sucesiones de la cuenca ha permitido establecer una correlación cronológica muy precisa a escala de cuenca, determinando la casi total isocronía de la mayor parte de los diferentes niveles de lignito y de las unidades litoestratigráficas de la cuenca. Por otro lado, las declinaciones medias muestran una rotación de 9'+4' para el relleno sedimentario de la cuenca de As Pontes, en sentido horario con respecto a la declinación del Oligoceno-Mioceno, coherente con el movimiento dextrógiro del corredor de fallas transcurrentes de dirección NW-SE. La datación del registro sedimentario de la cuenca de As Pontes permite establecer que los sistemas de fallas transcurrentes de orientación NW-SE del noroeste de la Península Ibérica fueron fuertemente activos desde la última parte del Oligoceno temprano hasta el Mioceno temprano. La finalización del movimiento principal de estos sistemas de fallas coincidió con el fin de actividad del margen entre la microplaca Ibérica y la placa Europea. Esto implicaría que el final de la actividad tectónica principal coincide en el ofshore y en el onshore del NW peninsular.

Allelic diversity and population structure in Vibrio cholerae O139 Bengal based on nucleotide sequence analysis

Comparative analysis of gene fragments of six housekeeping loci, distributed around the two chromosomes of Vibrio cholerae, has been carried out for a collection of 29 V. cholerae O139 Bengal strains isolated from India during the first epidemic period (1992 to 1993). A toxigenic O1 ElTor strain from the seventh pandemic and an environmental non-O1/non-O139 strain were also included in this study. All loci studied were polymorphic, with a small number of polymorphic sites in the sequenced fragments. The genetic diversity determined for our O139 population is concordant with a previous multilocus enzyme electrophoresis study in which we analyzed the same V. cholerae O139 strains. In both studies we have found a higher genetic diversity than reported previously in other molecular studies. The results of the present work showed that O139 strains clustered in several lineages of the dendrogram generated from the matrix of allelic mismatches between the different genotypes, a finding which does not support the hypothesis previously reported that the O139 serogroup is a unique clone. The statistical analysis performed in the V. cholerae O139 isolates suggested a clonal population structure. Moreover, the application of the Sawyer's test and split decomposition to detect intragenic recombination in the sequenced gene fragments did not indicate the existence of recombination in our O139 population.

Draft genome sequence of Aeromonas molluscorum strain 848TT, isolated from bivalve molluscs

We report here the draft genome sequence of Aeromonas molluscorum 848T, the type strain of this Aeromonas species, which was isolated from wedge shells (Donax trunculus) obtained from a retail market in Barcelona, Spain, in 1997.

Controle pós-colheita da antracnose do maracujazeiro: amarelo com aplicação de óleo de copaíba

O objetivo deste trabalho foi avaliar a aplicação de óleo essencial de copaíba no controle da antracnose, nos frutos do maracujazeiro-amarelo, e comparar sua ação fungicida/fungistática in vitro com o óleo resina de copaíba. No experimento in vivo, os frutos foram inoculados com uma suspensão de esporos da ordem de 10(6) conídios mL-1 e 1% de Tween 80, acondicionados em bandejas de polipropileno e colocados em câmara incubadora com temperatura de 25ºC e 90% de umidade relativa do ar. Passadas 24 horas da inoculação, pulverizou-se óleo essencial nas seguintes concentrações: T1= 0 mL L-1; T2= 0,25 mL L-1; T3= 0,5 mL L-1; T4= 0,75 mL L-1; T5= 1,0 mL L-1, sendo avaliados a perda de massa do fruto, a severidade da antracnose e o número de lesões, ambas aos seis dias. Para o experimento in vitro, utilizou-se do meio de cultura batata-dextrose-ágar (BDA) que, após ser esterilizado em autoclave (120 ºC), recebeu óleo essencial e óleo resina de copaíba (0; 0,5; 1,0; 1,5 e 2,0 mL L-1). Após o resfriamento do meio de cultura, foi repicado para o centro da placa um disco de micélio de 12,5 mm de diâmetro de Colletotrichum gloeosporioides; e as placas, incubadas a 25ºC e 90% de umidade. A aferição do crescimento micelial foi verificada com o auxílio de paquímetro analógico, após sete dias de crescimento micelial. O óleo essencial de copaíba, nas concentrações de 0,25 mL L-1 a 1.0 mL L-1, não foi eficaz no controle pós-colheita do fungo da antracnose in vivo e na perda de massa dos frutos de maracujá. O óleo resina de copaíba inibiu o crescimento de C. gloeosporioides in vitro de forma mais eficiente que o óleo essencial de copaíba.

Genome sequence of Plesiomonas shigelloides strain 302-73 (serotype O1)

Plesiomonas shigelloides, the only species of the genus, is an emergent pathogenic bacterium associated with human diarrheal and extraintestinal disease. We present the whole-genome sequence analysis of the representative strain for the O1 serotype (strain 302-73), providing a tool for studying bacterial outbreaks, virulence factors, and accurate diagnostic methods.

MASSA SECA E ACÚMULO DE NUTRIENTES EM MUDAS ENXERTADAS DE PEREIRA EM SISTEMA HIDROPÔNICO

RESUMOO trabalho objetivou determinar a produção de massa da matéria seca das partes da planta e o acúmulo total de macro e micronutrientes pelas mudas enxertadas de cultivares de pereira em condições hidropônicas. Utilizou-se do delineamento experimental inteiramente casualizado, em esquema fatorial 3x 3, com quatro repetições. Os fatores emestudo foram: três cultivares (Triunfo, Tenra e Cascatense) e três tipos de enxertia (borbulhia em placa - BP; borbulhia em ‘T’ invertido – BT, e garfagem de fenda cheia –GF). Avaliaram-se a massa seca da parte área, do sistema radicular e total, e o acúmulo total de nutrientes. O método de enxertia de garfagem de fenda cheia e as cultivares Tenra e Triunfo são indicados para a produção de mudas de pereira em sistema hidropônico. No acúmulo de nutrientes nas mudas de pereira, independentemente da cultivar, estabeleceu-se a seguinte ordem para macronutrientes: N>Mg>K>Ca>P>S; e para os micronutrientes: Fe>Mn>B>Zn>Cu.

Bacterial adhesion efficiency on implant abutments: a comparative study

The attachment of Escherichia coli ATCC 25922 and Staphylococcus aureus ATCC 28213 onto six different materials used to manufacture dental implant abutments was quantitatively determined after 2 and 24 h of contact between the materials and the bacterial cultures. The materials were topographically characterized and their wettability determined, with both parameters subsequently related to bacterial adhesion. Atomic force microscopy, interferometry, and contact angle measurement were used to characterize the materials" surfaces. The results showed that neither roughness nor nano-roughness greatly influenced bacterial attachment whereas wettability strongly correlated with adhesion. After 2 h the degree of E. coli attachment markedly differed depending on the material whereas similar differences were not observed for S. aureus, which yielded consistently higher counts of adhered cells. Nevertheless, after 24 h the adhesion of the two species to the different test materials no longer significantly differed, although on all surfaces the numbers of finally adhered E. coli were higher than those of S. aureus

Melanization and pathogenicity in Tenebrio molitor and Pacifastacus leniusculus by Aeromonas hydrophila.

Aeromonas hydrophila is the most common Aeromonas species causing infections in human and other animals such as amphibians, reptiles, fish and crustaceans. Pathogenesis of Aeromonas species have been reported to be associated with virulence factors such as lipopolysaccharides (LPS), bacterial toxins, bacterial secretion systems, flagella, and other surface molecules. Several mutant strains of A. hydrophila AH-3 were initially used to study their virulence in two animal species, Pacifastacus leniusculus (crayfish) and Tenebrio molitor larvae (mealworm). The AH-3 strains used in this study have mutations in genes involving the synthesis of flagella, LPS structures, secretion systems, and some other factors, which have been reported to be involved in A. hydrophila pathogenicity. Our study shows that the LPS (O-antigen and external core) is the most determinant A. hydrophila AH-3 virulence factor in both animals. Furthermore, we studied the immune responses of these hosts to infection of virulent or non-virulent strains of A. hydrophila AH-3. The AH-3 wild type (WT) containing the complete LPS core is highly virulent and this bacterium strongly stimulated the prophenoloxidase activating system resulting in melanization in both crayfish and mealworm. In contrast, the ΔwaaE mutant which has LPS without O-antigen and external core was non-virulent and lost ability to stimulate this system and melanization in these two animals. The high phenoloxidase activity found in WT infected crayfish appears to result from a low expression of pacifastin, a prophenoloxidase activating enzyme inhibitor, and this gene expression was not changed in the ΔwaaE mutant infected animal and consequently phenoloxidase activity was not altered as compared to non-infected animals. Therefore we show that the virulence factors of A. hydrophila are the same regardless whether an insect or a crustacean is infected and the O-antigen and external core is essential for activation of the proPO system and as virulence factors for this bacterium.

Dual role of LldR in regulation of the lldPRD operon, involved in l-Lactate metabolism in Escherichia coli.

The lldPRD operon of Escherichia coli, involved in L-lactate metabolism, is induced by growth in this compound. We experimentally identified that this system is transcribed from a single promoter with an initiation site located 110 nucleotides upstream of the ATG start codon. On the basis of computational data, it had been proposed that LldR and its homologue PdhR act as regulators of the lldPRD operon. Nevertheless, no experimental data on the function of these regulators have been reported so far. Here we show that induction of an lldP-lacZ fusion by L-lactate is lost in an lldR mutant, indicating the role of LldR in this induction. Expression analysis of this construct in a pdhR mutant ruled out the participation of PdhR in the control of lldPRD. Gel shift experiments showed that LldR binds to two operator sites, O1 (positions 105 to 89) and O2 (positions 22 to 38), with O1 being filled at a lower concentration of LldR. L-Lactate induced a conformational change in LldR that did not modify its DNA binding activity. Mutations in O1 and O2 enhanced the basal transcriptional level. However, only mutations in O1 abolished induction by L-lactate. Mutants with a change in helical phasing between O1 and O2 behaved like O2 mutants. These results were consistent with the hypothesis that LldR has a dual role, acting as a repressor or an activator of lldPRD. We propose that in the absence of L-lactate, LldR binds to both O1 and O2, probably leading to DNA looping and the repression of transcription. Binding of L-lactate to LldR promotes a conformational change that may disrupt the DNA loop, allowing the formation of the transcription open complex.