Salmonella enterica Serotype Uganda Infection in New York City and Chicago1

Outbreaks associated with distinct strains of Salmonella enterica serotype Uganda, a rare serotype, occurred in New York City and Chicago during the summer of 2001. Both outbreaks were linked to eating ready-to-eat pork products. This serotype may emerge as a more frequent cause of human infections

Evaluating genetic markers and neurobiochemical analytes for fluoxetine response using a panel of mouse inbred strains

RationaleIdentification of biomarkers that establish diagnosis or treatment response is critical to the advancement of research and management of patients with depression.ObjectiveOur goal was to identify biomarkers that can potentially assess fluoxetine response and risk to poor treatment outcome.MethodsWe measured behavior, gene expression, and the levels of 36 neurobiochemical analytes across a panel of genetically diverse mouse inbred lines after chronic treatment with water or fluoxetine.ResultsGlyoxylase 1 (GLO1) and guanine nucleotide-binding protein 1 (GNB1) mostly account for baseline anxiety-like and depressive-like behavior, indicating a common biological link between depression and anxiety. Fluoxetine-induced biochemical alterations discriminated positive responders, while baseline neurobiochemical differences differentiated negative responders (p < 0.006). Results show that glial fibrillary acidic protein, S100 beta protein, GLO1, and histone deacetylase 5 contributed most to fluoxetine response. These proteins are linked within a cellular growth/proliferation pathway, suggesting the involvement of cellular genesis in fluoxetine response. Furthermore, a candidate genetic locus that associates with baseline depressive-like behavior contains a gene that encodes for cellular proliferation/adhesion molecule (Cadm1), supporting a genetic basis for the role of neuro/gliogenesis in depression.ConclusionWe provided a comprehensive analysis of behavioral, neurobiochemical, and transcriptome data across 30 mouse inbred strains that has not been accomplished before. We identified biomarkers that influence fluoxetine response, which, altogether, implicate the importance of cellular genesis in fluoxetine treatment. More broadly, this approach can be used to assess a wide range of drug response phenotypes that are challenging to address in human samples.Electronic supplementary materialThe online version of this article (doi:10.1007/s00213-011-2574-z) contains supplementary material, which is available to authorized users

Comparative Phenotypic, Molecular, and Virulence Characterization of \u3cem\u3eVibrio parahaemolyticus\u3c/em\u3e O3:K6 Isolates

Historically, Vibrio parahaemolyticus infections have been characterizedby sporadic cases caused by multiple, diverse serotypes. However,since 1996, V. parahaemolyticus serotype O3:K6 strains havebeen associated with several large-scale outbreaks of illness,suggesting the emergence of a new group of organisms withenhanced virulence. We have applied three different molecularsubtyping techniques to identify an appropriate method for differentiatingO3:K6 isolates from other serotypes. Pulsed-field gel electrophoresis(PFGE) following NotI digestion differentiated seven closelyrelated subtypes among O3:K6 and related strains, which weredistinct from PFGE patterns for non-O3:K6 isolates. Ribotypingand tdh sequencing were less discriminatory than PFGE, but furtherconfirmed close genetic relationships among recent O3:K6 isolates.In vitro adherence and cytotoxicity studies with human epithelialcells showed that O3:K6 isolates exhibited statistically higherlevels of adherence and cytotoxicity to host cells than non-O3:K6isolates. Epithelial cell cytotoxicity patterns were determinedwith a lactate dehydrogenase release assay. At 3 h postinfection,high relative cytotoxicities (\u3e50% maximum lactate dehydrogenaseactivity) were found among a greater proportion of recentlyisolated O3:K6 and closely related strains (75%) than amongthe non-O3:K6 isolates (23%). A statistically significant relationshipbetween adherence and cytotoxicity suggests that the pathogenicpotential of some isolates may be associated with increasedadherence to epithelial cells. Our findings suggest that enhancedadherence and cytotoxicity may contribute to the apparent uniquepathogenic potential of V. parahaemolyticus O3:K6 strains

Comparative Phenotypic, Molecular, and Virulence Characterization of Vibrio parahaemolyticus O3:K6 Isolates

Historically, Vibrio parahaemolyticus infections have been characterized by sporadic cases caused by multiple, diverse serotypes. However, since 1996, V. parahaemolyticus serotype O3:K6 strains have been associated with several large-scale outbreaks of illness, suggesting the emergence of a “new” group of organisms with enhanced virulence. We have applied three different molecular subtyping techniques to identify an appropriate method for differentiating O3:K6 isolates from other serotypes. Pulsed-field gel electrophoresis (PFGE) following NotI digestion differentiated seven closely related subtypes among O3:K6 and related strains, which were distinct from PFGE patterns for non-O3:K6 isolates. Ribotyping and tdh sequencing were less discriminatory than PFGE, but further confirmed close genetic relationships among recent O3:K6 isolates. In vitro adherence and cytotoxicity studies with human epithelial cells showed that O3:K6 isolates exhibited statistically higher levels of adherence and cytotoxicity to host cells than non-O3:K6 isolates. Epithelial cell cytotoxicity patterns were determined with a lactate dehydrogenase release assay. At 3 h postinfection, high relative cytotoxicities (>50% maximum lactate dehydrogenase activity) were found among a greater proportion of recently isolated O3:K6 and closely related strains (75%) than among the non-O3:K6 isolates (23%). A statistically significant relationship between adherence and cytotoxicity suggests that the pathogenic potential of some isolates may be associated with increased adherence to epithelial cells. Our findings suggest that enhanced adherence and cytotoxicity may contribute to the apparent unique pathogenic potential of V. parahaemolyticus O3:K6 strains