RESUMEN
We describe here the isolation and identification of a Shiga toxin 1 (Stx1)-producing Enterobacter cloacae strain, M12X01451, from a human clinical specimen. The bacterial isolate was identified as E. cloacae using a polyphasic approach that included phenotypic, genetic, and proteomic analyses. The M12X01451 stx1 was sequenced, and the holotoxin was found to share only 87% amino acid sequence identity with the nearest Stx1 subtype reference sequence. Sequence analysis of the regions immediately flanking stx1 displayed similarities with bacteriophage-related sequences, suggesting a prophage origin. The stx1 gene was a stable element within the M12X01451 genome, as demonstrated by real-time PCR detection following successive subculturing of the bacterial isolate. Culture supernatant from M12X01451 was cytotoxic to Vero cells but was not neutralized by an anti-Stx1 monoclonal antibody. In addition, Stx1 from M12X01451 demonstrated limited antigenicity with two commercially available lateral flow immunoassays. The M12X01451 Stx represents a new Stx1 subtype based on the degree of sequence dissimilarity with Stx1 subtype reference sequences and its limited reactivity with anti-Stx1 antibodies.
Asunto(s)
Enterobacter cloacae/genética , Enterobacter cloacae/aislamiento & purificación , Toxina Shiga/genética , Toxina Shiga/metabolismo , Secuencia de Aminoácidos , Animales , Técnicas de Tipificación Bacteriana , Supervivencia Celular/efectos de los fármacos , Chlorocebus aethiops , ADN Bacteriano/química , ADN Bacteriano/genética , Infecciones por Enterobacteriaceae/microbiología , Humanos , Datos de Secuencia Molecular , Profagos/genética , Proteoma/análisis , Análisis de Secuencia de ADN , Homología de Secuencia de Aminoácido , Células VeroRESUMEN
The aim of this study is to document the isolation of a hypermucoviscosity (HMV) phenotype of Klebsiella pneumoniae from 25 cases of suppurative pneumonia and pleuritis and two cases of abscesses in California sea lions (Zalophus californianus) from the central California coast, representing the first report of this zoonotic pathogen from the marine environment and only the second report in non-humans. Animals died 2h to 4 days after first being observed sick on beaches. Clinical signs varied from dyspnoea to coma. Gross post-mortem examination of 25 cases revealed fibrinous pleuritis, copious pus in the pleural cavity and suppurative bronchopneumonia. K. pneumoniae isolates obtained from lung and pleural swabs and the hepatic and subcuticular abscesses were highly mucoid on blood agar culture media and were positive to the "string test". Twenty-one of the 27 isolates were examined by PCR and all were positive for rmpA and K2wyz and negative for K1magA genes. Although pneumonia and pleuritis have previously commonly been observed in marine mammals, their association with pure cultures of a zoonotic bacteria, K. pneumoniae HMV phenotype, has not. This report provides further evidence of the role marine mammals play as sentinels of health risks to humans from coastal waters.
Asunto(s)
Infecciones por Klebsiella/veterinaria , Klebsiella pneumoniae/fisiología , Fenotipo , Pleuresia/veterinaria , Neumonía/veterinaria , Leones Marinos/microbiología , Animales , Infecciones por Klebsiella/microbiología , Infecciones por Klebsiella/patología , Klebsiella pneumoniae/clasificación , Klebsiella pneumoniae/genética , Klebsiella pneumoniae/patogenicidad , Pleuresia/microbiología , Pleuresia/patología , Neumonía/microbiología , Neumonía/patología , Reacción en Cadena de la PolimerasaRESUMEN
A comparative analysis of the Bordetella pertussis, B. bronchiseptica, and B. parapertussis genome assemblies permitted the identification of regions with significant sequence divergence and the design of two new real-time PCR assays, BP283 and BP485, for the specific detection of B. pertussis. The performance characteristics of these two assays were evaluated and compared to those of culture and an existing real-time PCR assay targeting the repetitive element IS481. The testing of 324 nasopharyngeal specimens indicated that, compared to culture, the BP283 assay had a sensitivity and specificity of 100 and 96.8% and the BP485 assay had a sensitivity and specificity of 92.3 and 97.1%. Notably, B. holmesii was isolated from two specimens that were positive by the IS481 assay but negative by the BP283 and BP485 assays. These two assays represent an improvement in specificity over those of PCR assays targeting only IS481 and may be duplexed or used in conjunction with existing PCR assays to improve the molecular detection of B. pertussis.
Asunto(s)
Técnicas Bacteriológicas/métodos , Bordetella pertussis/genética , Bordetella pertussis/aislamiento & purificación , Cartilla de ADN/genética , ADN Bacteriano/genética , Reacción en Cadena de la Polimerasa/métodos , Tos Ferina/diagnóstico , Elementos Transponibles de ADN , Humanos , Nasofaringe/microbiología , Sensibilidad y EspecificidadRESUMEN
We compared a set of commercial Salmonella somatic and flagellar serotyping antisera to in-house-prepared antisera from the Microbial Diseases Laboratory, California Department of Public Health, using 327 Salmonella enterica strains belonging to subgroups I, II, IIIa, IIIb, and IV. The sensitivities of Denka Seiken (Tokyo, Japan) somatic and flagellar antisera (using a tube agglutination assay) were 94.0% and 99.2%, respectively, and the specificity was 100% for both sets of sera. Polyvalent O and O1 antiserum sensitivity and specificity were >90%, with the exception of polyvalent O1 antiserum, for which sensitivity was 88.9%. When Denka Seiken flagellar antisera were used in a slide agglutination assay, the sensitivity and accuracy dropped to 88.9% and the specificity fell to 91%. Overall, Denka Seiken commercial antisera performed very well and, together with the comprehensive range of factors available, offer laboratories quality reagents suitable for serotyping strains of salmonellae.
Asunto(s)
Pruebas de Aglutinación/métodos , Sueros Inmunes , Salmonella enterica/clasificación , Serotipificación/métodos , Anticuerpos Antibacterianos , Antígenos Bacterianos/inmunología , California , Antígenos O/inmunología , Juego de Reactivos para Diagnóstico , Sensibilidad y EspecificidadRESUMEN
The identification of Brucella can be a time-consuming and labor-intensive process that places personnel at risk for laboratory-acquired infection. Here, we describe a real-time PCR assay for confirmation of presumptive Brucella isolates. The assay was designed in a multiplex format that will allow the rapid identification of Brucella spp., B. abortus, and B. melitensis in a single test.
Asunto(s)
Brucella abortus/aislamiento & purificación , Brucella melitensis/aislamiento & purificación , Brucella/aislamiento & purificación , Reacción en Cadena de la Polimerasa/métodos , Secuencia de Bases , Brucella/clasificación , Brucella/genética , Brucella abortus/clasificación , Brucella abortus/genética , Brucella melitensis/clasificación , Brucella melitensis/genética , Sistemas de Computación , Cartilla de ADN , ARN Bacteriano/genética , ARN Ribosómico 16S/genéticaRESUMEN
The incidence of serogroup Y meningococcal disease has increased recently in the United States. Here, we describe the development of a 5' exonuclease assay for the detection of serogroup Y Neisseria meningitidis and demonstrate the usefulness of this assay for resolving serogroup identification of strains that are resistant to conventional serogrouping and for the nonculture identification of serogroup Y meningococcal disease.