Resistência de Xanthomonas campestris com relação à tilosina e vancomicina

Foi estudada a resistência da bactéria fitopatogênica Xanthomonas campestris (Pammel) Dowson com relação a dois antibióticos: Tilosina e Vancomicina. Para a vancomicina, colônias resistentes apareceram até na mais alta concentração usada (256 mcg/ml.). Para a tilosina, em concentrações maiores que 128 mcg/ml não foram encontradas bactérias, resistentes. Tais resultados indicam que a X. campestris seguiu o modelo de "um só passo" para adquirir resistência a vancomicina e, o modelo de "múltiplos passos" com relação a resistência a tilosina.

Contagem total de bactérias e enumeração de coliformes em cortes de varejo de carne bovina e em equipamentos de supermercados

No presente trabalho foi determinada a contagem total de bactérias (incubação a 32°C e a 5°C) existentes na superfície de alguns cortes de varejo de carne bovina comercializada por tres supermercados de Piracicaba, SP, bem como da superfície de diversos tipos de equipamento utilizado nas salas de desossa desses estabelecimentos. Foi determinado também o número mais provável (NMP) de coliformes totais e, para um grupo de amostras de carne, o NMP de Escherichia coli. Para um dos supermercados (o mais antigo e menos adequado sob o aspecto sanitário) foi possível constatar uma diferença significativa entre as contagens totais em cortes recebidos já desossados pelo estabelecimento, a favor destes, e as contagens em cortes preparados na sala de desossa. O equipamento, tanto no estado considerado limpo (após o dia de trabalho) e aquele em uso apresentaram contagens totais excessivas; não houve diferença significativa entre um e outro caso, e, em ambos, a temperatura de incubação 32°C resultou em valores estatisticamente superiores aos obtidos com a incubação a 5°C. As contagens provenientes de análises de superfícies de madeira foram significativamente mais elevadas que as verificadas em superfícies metálicas (serra elétrica, facas, afiadores). A ocorrência de coliformes totais foi geral, tanto na carne como no equipamento, muitas vezes em números elevados. Em amostras de carne, analisadas quanto à presença e ao número de coliformes totais e de Escherichia coli, verificou-se que 96% daquelas positivas para coliformes totais também o eram para esta bactéria. Atras de material em uso foram positivas quanto à ocorrência de coliformes totais. Tal como ocorreu a carne, o número mais possível (NMP) assumiu, em vários casos, elevados valores. Embora não comprovado estatisticamente, os resultados sugerem uma maior ocorrência desse grupo de microrganismos nas superfícies de madeira (mesa e ou cepo).

Contribuição ao estudo das Pasteurellas: pasteurella intermediária n. sp

Os autores decreveram uma nova bactéria - Pasteurella intermedia n. ap., obtida pela inoculação em cobaio de 2 cc. de sangue total de um indivíduo morto de bronco-pneumonia e suspeito de ter a forma grave de Tifo exantemático neotrópico. Têm a impressão que a Pasteurella marsupialis e a P. intermedia, constituem um grupo à parte, bem definido, dentro das Pasteurellas. Muito pequenas, de grande e persistente poder patogênico para os animais comuns de laboratório, mesmo quando as amostras das bactérias são conservadas pelos replantios em agar-comum, na temperatura e iluminação comum em laboratórios, durante anos. Estas duas Pasteurellas, ao contrário das demais, têm alto e inconfundível poder antígenico, para a formação de aglutininas e fixação do complemento e dão com constância uma "reação testicular" em cobaios machos, quando injetadas pela via intra-peritoneal, febre alta, esplenomegalia constante e às vezes notável, prestando-se à confusão para o diagnóstico diferencial e experimental com a raça VB do Tifo exantemático neotrófico no Brasil (Moléstia de Pisa, Gomes e Mayer).

Endocardite e septicemia pelo Corynebacterium haemolyticum n. sp

1 - Os A.A. referem, no presente trabalho, um caso de endocardite e septicemia com isolamento de uma bactéria difteróide do sangue, sangue, durante a vida e das lesões endocárdicas, sangue, baço e rins, post mortem. 2 - A referida bactéria apresenta caracteres especiais e é descrita com o nome de Corynebacterium haemolyticum n. sp. em vista da propriedade hemolítica que apresenta nos meios com sangue. 3 - No caso descrito não é possível atribui-se a outra causa, que não a êsse germe, a origem da doença, pois que nenhum outro foi isolado ou observado no seu decurso ou em material colhido do cadáver. 4 - Consultando a literatura médica, verificamos que os casos semelhantes, acompanhados de comprovação bacteriológica segura, são extremamente raros, podendo-se contar dois em que se isolou difteróide do sangue do doente e lesões cadavéricas do mesmo, figurando o nosso em 3.° lugar, desde 1893. Dois outros são referidos com isolamento das lesões do cadáver. Em maior número são os casos em que o difteróide aparece associado.

Ação bacteriolítica dos fosfatos (Fosfatólise bacteriana)

1) As bactérias são lisadas pelos fosfatos, cuja atividade lítica varia com o sal de fosfato, os trivalentes sendo mais ativos. 2) A fosfatólise independente da viabilidade da bactéria. 3) A fosfatólise póde interferir nas suspensões com tampões de fosfatos e na preservação de hemoculturas.

Ciclo "L" em Proteus vulgaris: I - massas nucleares em esferoplastos induzidos pela penicilina

Esferoplastos foram obtidos em Proteus vulgaris, cultivado em meio sintético simples, tendo como agente indutor a penicilina, em diferentes concentrações. Estabelecida a dosagem ótima, de sensibilidade da bactéria ao antibiótico, para obtenção de "grandes corpos" do Ciclo "L", definidos, morfologicamente, como esferoplastos, foi feita a coloração de massas nucleares, em diversas fases do crescimento bacteriano. A colheita do material foi feita por impessão em lamínula, usando-se ácido ósmico como fixador, seguindo-se hidrólise clorídrica, com aquecimento, e coloração pela fucsina. Dos resultados conseguidos ficou evidenciado: 1º - a posssibilidade de obtenção de "grandes corpos" em Proteus vulgaris em um meio sintético simples, a base de sais minerais e glicose; 2º - que houve uma concentração ótima de penicilina para surgir o efeito indutor de esferoplasto, na fase logarítmica de crescimento; 3º - a facilidade de coloração de massas nucleares nos esferoplastos em vários períodos de crescimento; 4º - a reversão ao tipo morfológico normal, depois de 24 horas de crescimento no meio com o antibiótico; 5º - modificação no crescimento do Proteus vulgaris em superfície de agar, com dose mínima de penicilina formando colônias localizadas.

Estudos sobre a esporulação de uma amostra de bacillus: IV - Outras evidências sobre a atividade do íon Mn[2+] na esporulação endotrófica

Foram feitas experimentações om o intuito de se buscar mais evidências sobre a participação do íon Mn[2+] no mecanismo esporogenético de uma amostra de Bacillus licheniformis. Quando as formas vegetativas desta bactéria eram depositadas em um meio mineral, carente de fonte de carbono utilizável, em conjunto com um agente seqüestrante de metais como EDTA, a esporulação endotrófica deixava de ocorrer. Entretanto, a esporulação pôde ser protegida quando as células eram previamente saturadas com um excesso de Mn[2+] exógeno. As formas esporuladas obtidas nas condições estudadas mostraram termorresistência a 85ºC durante 20 minutos.

Covariation between colony social structure and immune defences of workers in the ant Formica selysi

Several ant species vary in the number of queens per colony, yet the causes and consequences of this variation remain poorly understood. In previous experiments, we found that Formica selysi workers originating from multiple-queen (=polygyne) colonies had a lower resistance to a fungal pathogen than workers originating from single-queen (=monogyne) colonies. In contrast, group diversity improved disease resistance in experimental colonies. This discrepancy between field and experimental colonies suggested that variation in social structure in the field had antagonistic effects on worker resistance, possibly through a down-regulation of the immune system balancing the positive effect of genetic diversity. Here, we examined if workers originating from field colonies with alternative social structure differed in three major components of their immune system. We found that workers from polygyne colonies had a lower bacterial growth inhibitory activity than workers from monogyne colonies. In contrast, workers from the two types of colonies did not differ significantly in bacterial cell wall lytic activity and prophenoloxidase activity. Overall, the presence of multiple queens in a colony correlated with a slight reduction in one inducible component of the immune system of individual workers. This reduced level of immune defence might explain the lower resistance of workers originating from polygyne colonies despite the positive effect of genetic diversity. More generally, these results indicate that social changes at the group level can modulate individual immune defences.

Natural bradykinin antagonists

Bradykinin (BK) a nonapeptide generated in plasma during tissue injury, is involved in many physiological and pathological states. Kinin actions are mediated by specific membrane receptors and involve a complex signal transducer and also second messager mechanisms. Due to its inequivocal relevance, an intensive effort has been focused in recent years to develop selective and competitive BK antagonists. Thus, the development of a new series of peptide BK antagonists has made an important contribution to the understanding of the pharmacological, physiological and pathophysiological role of BK, and this is certain to provide a firm basis for developing new drugs to relieve pain and inflammation. However, BK antagonists derived from peptide origin reported to date have limited clinical use due to their poor oral absortion and short duration of effect. Thus, considerable effort has also been made in developing stable nonpeptide BK antagonists. Up to now, most nonpeptide compounds reported to exhibit BK antagonistic activity have been derived from plants, including many flavonoids, terpenes, and also synthetic substances with various molecular structures. Amongst them, the pregnane glycoside compounds isolated from the plant Mandevilla velutina are the most promising. These compounds are effective in antognizing BK responses in a variety of preparations, and they also exhibit potent and long-lasting analgesic and anti-inflammatory activities. The exact mechanism underlying their action however, is not yet completely understood.

Sex-dependent selection on an autosomal melanic female ornament promotes the evolution of sex ratio bias.

Sex-dependent selection often leads to spectacularly different phenotypes in males and females. In species in which sexual dimorphism is not complete, it is unclear which benefits females and males derive from displaying a trait that is typical of the other sex. In barn owls (Tyto alba), females exhibit on average larger black eumelanic spots than males but members of the two sexes display this trait in the same range of possible values. In a 12-year study, we show that selection exerted on spot size directly or on genetically correlated traits strongly favoured females with large spots and weakly favoured males with small spots. Intense directional selection on females caused an increase in spot diameter in the population over the study period. This increase is due to a change in the autosomal genes underlying the expression of eumelanic spots but not of sex-linked genes. Female-like males produced more daughters than sons, while male-like females produced more sons than daughters when mated to a small-spotted male. These sex ratio biases appear adaptive because sons of male-like females and daughters of female-like males had above-average survival. This demonstrates that selection exerted against individuals displaying a trait that is typical of the other sex promoted the evolution of specific life history strategies that enhance their fitness. This may explain why in many organisms sexual dimorphism is often not complete.

Role of the stress sigma factor RpoS in GacA/RsmA-controlled secondary metabolism and resistance to oxidative stress in Pseudomonas fluorescens CHA0.

In Pseudomonas fluorescens biocontrol strain CHA0, the two-component system GacS/GacA positively controls the synthesis of extracellular products such as hydrogen cyanide, protease, and 2,4-diacetylphloroglucinol, by upregulating the transcription of small regulatory RNAs which relieve RsmA-mediated translational repression of target genes. The expression of the stress sigma factor sigmaS (RpoS) was controlled positively by GacA and negatively by RsmA. By comparison with the wild-type CHA0, both a gacS and an rpoS null mutant were more sensitive to H2O2 in stationary phase. Overexpression of rpoS or of rsmZ, encoding a small RNA antagonistic to RsmA, restored peroxide resistance to a gacS mutant. By contrast, the rpoS mutant showed a slight increase in the expression of the hcnA (HCN synthase subunit) gene and of the aprA (major exoprotease) gene, whereas overexpression of sigmaS strongly reduced the expression of these genes. These results suggest that in strain CHA0, regulation of exoproduct synthesis does not involve sigmaS as an intermediate in the Gac/Rsm signal transduction pathway whereas sigmaS participates in Gac/Rsm-mediated resistance to oxidative stress.

Voriconazole-Induced Inhibition of the Fungicidal Activity of Amphotericin B in Candida Strains with Reduced Susceptibility to Voriconazole: an Effect Not Predicted by the MIC Value Alone.

An antagonistic effect of voriconazole on the fungicidal activity of sequential doses of amphotericin B has previously been demonstrated in Candida albicans strains susceptible to voriconazole. Because treatment failure and the need to switch to other antifungals are expected to occur more often in infections that are caused by resistant strains, it was of interest to study whether the antagonistic effect was still seen in Candida strains with reduced susceptibility to voriconazole. With the hypothesis that antagonism will not occur in voriconazole-resistant strains, C. albicans strains with characterized mechanisms of resistance against voriconazole, as well as Candida glabrata and Candida krusei strains with differences in their degrees of susceptibility to voriconazole were exposed to voriconazole or amphotericin B alone, to both drugs simultaneously, or to voriconazole followed by amphotericin B in an in vitro kinetic model. Amphotericin B administered alone or simultaneously with voriconazole resulted in fungicidal activity. When amphotericin B was administered after voriconazole, its activity was reduced (median reduction, 61%; range, 9 to 94%). Levels of voriconazole-dependent inhibition of amphotericin B activity differed significantly among the strains but were not correlated with the MIC values (correlation coefficient, -0.19; P = 0.65). Inhibition was found in C. albicans strains with increases in CDR1 and CDR2 expression but not in the strain with an increase in MDR1 expression. In summary, decreased susceptibility to voriconazole does not abolish voriconazole-dependent inhibition of the fungicidal activity of amphotericin B in voriconazole-resistant Candida strains. The degree of interaction could not be predicted by the MIC value alone.

A molecular framework for light and gibberellin control of cell elongation.

Cell elongation during seedling development is antagonistically regulated by light and gibberellins (GAs). Light induces photomorphogenesis, leading to inhibition of hypocotyl growth, whereas GAs promote etiolated growth, characterized by increased hypocotyl elongation. The mechanism underlying this antagonistic interaction remains unclear. Here we report on the central role of the Arabidopsis thaliana nuclear transcription factor PIF4 (encoded by PHYTOCHROME INTERACTING FACTOR 4) in the positive control of genes mediating cell elongation and show that this factor is negatively regulated by the light photoreceptor phyB (ref. 4) and by DELLA proteins that have a key repressor function in GA signalling. Our results demonstrate that PIF4 is destabilized by phyB in the light and that DELLAs block PIF4 transcriptional activity by binding the DNA-recognition domain of this factor. We show that GAs abrogate such repression by promoting DELLA destabilization, and therefore cause a concomitant accumulation of free PIF4 in the nucleus. Consistent with this model, intermediate hypocotyl lengths were observed in transgenic plants over-accumulating both DELLAs and PIF4. Destabilization of this factor by phyB, together with its inactivation by DELLAs, constitutes a protein interaction framework that explains how plants integrate both light and GA signals to optimize growth and development in response to changing environments.

Peroxisome proliferator-activated receptors mediate host cell proinflammatory responses to Pseudomonas aeruginosa autoinducer.

The pathogenic bacterium Pseudomonas aeruginosa utilizes the 3-oxododecanoyl homoserine lactone (3OC(12)-HSL) autoinducer as a signaling molecule to coordinate the expression of virulence genes through quorum sensing. 3OC(12)-HSL also affects responses in host cells, including the upregulation of genes encoding inflammatory cytokines. This proinflammatory response may exacerbate underlying disease during P. aeruginosa infections. The specific mechanism(s) through which 3OC(12)-HSL influences host responses is unclear, and no mammalian receptors for 3OC(12)-HSL have been identified to date. Here, we report that 3OC(12)-HSL increases mRNA levels for a common panel of proinflammatory genes in murine fibroblasts and human lung epithelial cells. To identify putative 3OC(12)-HSL receptors, we examined the expression patterns of a panel of nuclear hormone receptors in these two cell lines and determined that both peroxisome proliferator-activated receptor beta/delta (PPARbeta/delta) and PPARgamma were expressed. 3OC(12)-HSL functioned as an agonist of PPARbeta/delta transcriptional activity and an antagonist of PPARgamma transcriptional activity and inhibited the DNA binding ability of PPARgamma. The proinflammatory effect of 3OC(12)-HSL in lung epithelial cells was blocked by the PPARgamma agonist rosiglitazone, suggesting that 3OC(12)-HSL and rosiglitazone are mutually antagonistic negative and positive regulators of PPARgamma activity, respectively. These data identify PPARbeta/delta and PPARgamma as putative mammalian 3OC(12)-HSL receptors and suggest that PPARgamma agonists may be employed as anti-inflammatory therapeutics for P. aeruginosa infections.

RNA-based gene duplication sheds new light on mammalian sex chromosome evolution

ABSTRACT : Gene duplication is a fundamental source of raw material for the origin of genetic novelty. It has been assumed for a long time that DNA-based gene duplication was the only source of new genes. Recently however, RNA-based gene duplication (retroposition) was shown in multiple organisms to contribute significantly to their genetic diversity. This mechanism produces intronless gene copies (retrocopies) that are inserted in random genomic position, independent of the position of the parental source genes. In human, mouse and fruit fly, it was demonstrated that the X-linked genes spawned an excess of functional retroposed gene copies (retrogenes). In human and mouse, the X chromosome also recruited an excess of retrogenes. Here we further characterized these interesting biases related to the X chromosome in mammals. Firstly, we have confirmed presence of the aforementioned biases in dog and opossum genome. Then based on the expression profile of retrogenes during various spermatogenetic stages, we have provided solid evidence that meiotic sex chromosome inactivation (MSCI) is responsible for an excess of retrogenes stemming from the X chromosome. Moreover, we showed that the X-linked genes started to export an excess of retrogenes just after the split of eutherian and marsupial mammalian lineages. This suggests that MSCI has originated around this time as well. More fundamentally, as MSCI reflects the spread of recombination barrier between the X and Y chromosomes during their evolution, our observation allowed us to re-estimate the age of mammalian sex chromosomes. Previous estimates suggested that they emerged in the common ancestor of all mammals (before the split of monotreme lineage); whereas, here we showed that they originated around the split of marsupial and eutherian lineages, after the divergence of monotremes. Thus, the therian (marsupial and eutherian) sex chromosomes are younger than previously thought. Thereafter, we have characterized the bias related to the recruitment of genes to the X chromosome. Sexually antagonistic forces are most likely driving this pattern. Using our limited retrogenes expression data, it is difficult to determine the exact nature of these forces but some conclusions have been made. Lastly, we looked at the history of this biased recruitment: it commenced around the split of marsupial and eutherian lineages (akin to the biased export of genes out of the X). In fact, the sexually antagonistic forces are predicted to appear just around that time as well. Thereby, the history of the recruitment of genes to the X, provides an indirect evidence that these forces are responsible for this bias.