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TEM-1 beta-lactamase as a source of resistance to sulbactam in clinical strains of Acinetobacter baumannii

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F13%3A10159322" target="_blank" >RIV/00216208:11310/13:10159322 - isvavai.cz</a>

  • Result on the web

    <a href="http://jac.oxfordjournals.org/content/68/12/2786" target="_blank" >http://jac.oxfordjournals.org/content/68/12/2786</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1093/jac/dkt275" target="_blank" >10.1093/jac/dkt275</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    TEM-1 beta-lactamase as a source of resistance to sulbactam in clinical strains of Acinetobacter baumannii

  • Original language description

    Objectives: Sulbactam is well known to have clinically relevant intrinsic activity against Acinetobacter baumannii. Although secondary resistance to this drug has long been reported in acinetobacters, virtually nothing is known about its molecular basis.The aim of this study was to test the hypothesis that beta-lactamase TEM-1 is responsible for sulbactam resistance in A. baumannii. Methods: Seventeen clinical strains of A. baumannii were selected to represent different combinations of quantitative susceptibilities to sulbactam and molecular typing characteristics. The strains were screened by PCR for the presence of the bla(TEM-1) gene and its variants. Amplicons encompassing the bla(TEM) genes, including their promoters, were sequenced. The expression and copy number of the bla(TEM) genes were assessed using semi-quantitative real-time PCR. Transfer of the bla(TEM-1) gene into a susceptible A. baumannii strain was achieved by electroporation. Results: Six strains were negative for t

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FN - Epidemiology, infection diseases and clinical immunology

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2013

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Antimicrobial Chemotherapy

  • ISSN

    0305-7453

  • e-ISSN

  • Volume of the periodical

    68

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    6

  • Pages from-to

    2786-2791

  • UT code for WoS article

    000326980000011

  • EID of the result in the Scopus database