82 research outputs found

    Vibrio parahaemolyticus, enterotoxigenic Escherichia coli, enterohemorrhagic Escherichia coli and Vibrio cholerae

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    This review highlighted the following: (i) pathogenic mechanism of the thermostable direct hemolysin produced by Vibrio parahaemolyticus, especially on its cardiotoxicity, (ii) heat-labile and heat-stable enterotoxins produced by enterotoxigenic Escherichia coli, especially structure–activity relationship of heat-stable enterotoxin, (iii) RNA N-glycosidase activity of Vero toxins (VT1 and VT2) produced by enterohemorrhagic Escherichia coli O157:H7, (iv) discovery of Vibrio cholerae O139, (v) isolation of new variant of Vibrio cholerae O1 El Tor that carries classical ctxB, and production of high concentration of cholera toxin by these strains, and (vi) conversion of viable but nonculturable (VBNC) Vibrio cholerae to culturable state by co-culture with eukaryotic cells

    Pyrosequencing-Based Comparative Genome Analysis of Vibrio vulnificus Environmental Isolates

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    Between 1996 and 2006, the US Centers for Disease Control reported that the only category of food-borne infections increasing in frequency were those caused by members of the genus Vibrio. The Gram-negative bacterium Vibrio vulnificus is a ubiquitous inhabitant of estuarine waters, and is the number one cause of seafood-related deaths in the US. Many V. vulnificus isolates have been studied, and it has been shown that two genetically distinct subtypes, distinguished by 16S rDNA and other gene polymorphisms, are associated predominantly with either environmental or clinical isolation. While local genetic differences between the subtypes have been probed, only the genomes of clinical isolates have so far been completely sequenced. In order to better understand V. vulnificus as an agent of disease and to identify the molecular components of its virulence mechanisms, we have completed whole genome shotgun sequencing of three diverse environmental genotypes using a pyrosequencing approach. V. vulnificus strain JY1305 was sequenced to a depth of 33×, and strains E64MW and JY1701 were sequenced to lesser depth, covering approximately 99.9% of each genome. We have performed a comparative analysis of these sequences against the previously published sequences of three V. vulnificus clinical isolates. We find that the genome of V. vulnificus is dynamic, with 1.27% of genes in the C-genotype genomes not found in the E- genotype genomes. We identified key genes that differentiate between the genomes of the clinical and environmental genotypes. 167 genes were found to be specifically associated with environmental genotypes and 278 genes with clinical genotypes. Genes specific to the clinical strains include components of sialic acid catabolism, mannitol fermentation, and a component of a Type IV secretory pathway VirB4, as well as several other genes with potential significance for human virulence. Genes specific to environmental strains included several that may have implications for the balance between self-preservation under stress and nutritional competence

    Relationship Between Equilibrium Hydrogen Pressure and Exchange Current for the Hydrogen Electrode-Reaction at Mmni(3.9-X)Mn(0.4)A1(X)Co(0.7) Alloy Electrodes

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    We present a theoretical relationship between equilibrium hydrogen pressure and exchange current for the hydrogen electrode reaction which considers the degree of hydrogen coverage at the electrode surface. Electrochemical measurements at MmNi3.9–xMn0.4AlxCo0.7 (0 x 0.8) electrodes were performed to prove the theoretical model. The equilibrium hydrogen pressures were analyzed from electrochemical pressure-composition isotherms, and the exchange currents were determined by linear polarization measurements. Fitting the experimental data to the theoretical model indicated that the rate constants for the chargetransfer reaction as well as the charge-transfer coefficient were influenced by the partial substitution of nickel by aluminum. Also, the exchange current passed through a maximum with decreasing equilibrium hydrogen pressure, i.e., with increasing aluminum content, indicating that it is possible to design new materials which combine high electrocatalytic activity with an appropriate equilibrium hydrogen pressure. Because of its high energy density and high power density, MmNi3.6Mn0.4Al0.3Co0.7 was found to be the most appropriate composition

    Relationship Between Equilibrium Hydrogen Pressure and Exchange Current for the Hydrogen Electrode-Reaction at Mmni(3.9-X)Mn(0.4)A1(X)Co(0.7) Alloy Electrodes

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    We present a theoretical relationship between equilibrium hydrogen pressure and exchange current for the hydrogen electrode reaction which considers the degree of hydrogen coverage at the electrode surface. Electrochemical measurements at MmNi3.9–xMn0.4AlxCo0.7 (0 x 0.8) electrodes were performed to prove the theoretical model. The equilibrium hydrogen pressures were analyzed from electrochemical pressure-composition isotherms, and the exchange currents were determined by linear polarization measurements. Fitting the experimental data to the theoretical model indicated that the rate constants for the chargetransfer reaction as well as the charge-transfer coefficient were influenced by the partial substitution of nickel by aluminum. Also, the exchange current passed through a maximum with decreasing equilibrium hydrogen pressure, i.e., with increasing aluminum content, indicating that it is possible to design new materials which combine high electrocatalytic activity with an appropriate equilibrium hydrogen pressure. Because of its high energy density and high power density, MmNi3.6Mn0.4Al0.3Co0.7 was found to be the most appropriate composition
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