Vancomycin-resistant <it>vanB</it>-type <it>Enterococcus faecium</it> isolates expressing varying levels of vancomycin resistance and being highly prevalent among neonatal patients in a single ICU
<p>Abstract</p> <p>Background</p> <p>Vancomycin-resistant isolates of <it>E. faecalis</it> and <it>E. faecium</it> are of special concern and patients at risk of acquiring a VRE colonization/infection include also intensively-cared neonates. We d...
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doaj-8901a30b368b4d65bde99398c47bddc82020-11-24T21:50:59ZengBMCAntimicrobial Resistance and Infection Control2047-29942012-05-01112110.1186/2047-2994-1-21Vancomycin-resistant <it>vanB</it>-type <it>Enterococcus faecium</it> isolates expressing varying levels of vancomycin resistance and being highly prevalent among neonatal patients in a single ICUWerner GuidoKlare IngoFleige CarolaGeringer UtaWitte WolfgangJust Heinz-MichaelZiegler Renate<p>Abstract</p> <p>Background</p> <p>Vancomycin-resistant isolates of <it>E. faecalis</it> and <it>E. faecium</it> are of special concern and patients at risk of acquiring a VRE colonization/infection include also intensively-cared neonates. We describe here an ongoing high prevalence of VanB type <it>E. faecium</it> in a neonatal ICU hardly to identify by routine diagnostics.</p> <p>Methods</p> <p>During a 10 months’ key period 71 <it>E. faecium</it> isolates including 67 <it>vanB</it>-type isolates from 61 patients were collected non-selectively. Vancomycin resistance was determined by different MIC methods (broth microdilution, Vitek® 2) including two Etest® protocols (McFarland 0.5/2.0. on Mueller-Hinton/Brain Heart Infusion agars). Performance of three chromogenic VRE agars to identify the <it>vanB</it> type outbreak VRE was evaluated (Brilliance<sup>TM</sup> VRE agar, chromID<sup>TM</sup> VRE agar, CHROMagar<sup>TM</sup> VRE). Isolates were genotyped by <it>Sma</it>I- and <it>Ceu</it>I-macrorestriction analysis in PFGE, plasmid profiling, <it>vanB</it> Southern hybridisations as well as MLST typing.</p> <p>Results</p> <p>Majority of <it>vanB</it> isolates (n = 56, 79%) belonged to a single ST192 outbreak strain type showing an identical PFGE pattern and analyzed representative isolates revealed a chromosomal localization of a <it>vanB2</it>-Tn<it>5382</it> cluster type. Vancomycin MICs in cation-adjusted MH broth revealed a susceptible value of ≤4 mg/L for 31 (55%) of the 56 outbreak VRE isolates. Etest® vancomycin on MH and BHI agars revealed only two <it>vanB</it> VRE isolates with a susceptible result; in general Etest® MIC results were about 1 to 2 doubling dilutions higher than MICs assessed in broth and values after the 48 h readout were 0.5 to 1 doubling dilutions higher for <it>vanB</it> VRE. Of all <it>vanB</it> type VRE only three, three and two isolates did not grow on Brilliance<sup>TM</sup> VRE agar, chromID<sup>TM</sup> VRE agar and CHROMagar<sup>TM</sup> VRE, respectively. Permanent cross contamination via the patients’ surrounding appeared as a possible risk factor for permanent VRE colonization/infection.</p> <p>Conclusions</p> <p>Low level expression of <it>vanB</it> resistance may complicate a proper routine diagnostics of <it>vanB</it> VRE and mask an ongoing high VRE prevalence. A high inoculum and growth on rich solid media showed the highest sensitivity in identifying <it>vanB</it> type resistance.</p> http://www.aricjournal.com/content/1/1/21 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Werner Guido Klare Ingo Fleige Carola Geringer Uta Witte Wolfgang Just Heinz-Michael Ziegler Renate |
spellingShingle |
Werner Guido Klare Ingo Fleige Carola Geringer Uta Witte Wolfgang Just Heinz-Michael Ziegler Renate Vancomycin-resistant <it>vanB</it>-type <it>Enterococcus faecium</it> isolates expressing varying levels of vancomycin resistance and being highly prevalent among neonatal patients in a single ICU Antimicrobial Resistance and Infection Control |
author_facet |
Werner Guido Klare Ingo Fleige Carola Geringer Uta Witte Wolfgang Just Heinz-Michael Ziegler Renate |
author_sort |
Werner Guido |
title |
Vancomycin-resistant <it>vanB</it>-type <it>Enterococcus faecium</it> isolates expressing varying levels of vancomycin resistance and being highly prevalent among neonatal patients in a single ICU |
title_short |
Vancomycin-resistant <it>vanB</it>-type <it>Enterococcus faecium</it> isolates expressing varying levels of vancomycin resistance and being highly prevalent among neonatal patients in a single ICU |
title_full |
Vancomycin-resistant <it>vanB</it>-type <it>Enterococcus faecium</it> isolates expressing varying levels of vancomycin resistance and being highly prevalent among neonatal patients in a single ICU |
title_fullStr |
Vancomycin-resistant <it>vanB</it>-type <it>Enterococcus faecium</it> isolates expressing varying levels of vancomycin resistance and being highly prevalent among neonatal patients in a single ICU |
title_full_unstemmed |
Vancomycin-resistant <it>vanB</it>-type <it>Enterococcus faecium</it> isolates expressing varying levels of vancomycin resistance and being highly prevalent among neonatal patients in a single ICU |
title_sort |
vancomycin-resistant <it>vanb</it>-type <it>enterococcus faecium</it> isolates expressing varying levels of vancomycin resistance and being highly prevalent among neonatal patients in a single icu |
publisher |
BMC |
series |
Antimicrobial Resistance and Infection Control |
issn |
2047-2994 |
publishDate |
2012-05-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Vancomycin-resistant isolates of <it>E. faecalis</it> and <it>E. faecium</it> are of special concern and patients at risk of acquiring a VRE colonization/infection include also intensively-cared neonates. We describe here an ongoing high prevalence of VanB type <it>E. faecium</it> in a neonatal ICU hardly to identify by routine diagnostics.</p> <p>Methods</p> <p>During a 10 months’ key period 71 <it>E. faecium</it> isolates including 67 <it>vanB</it>-type isolates from 61 patients were collected non-selectively. Vancomycin resistance was determined by different MIC methods (broth microdilution, Vitek® 2) including two Etest® protocols (McFarland 0.5/2.0. on Mueller-Hinton/Brain Heart Infusion agars). Performance of three chromogenic VRE agars to identify the <it>vanB</it> type outbreak VRE was evaluated (Brilliance<sup>TM</sup> VRE agar, chromID<sup>TM</sup> VRE agar, CHROMagar<sup>TM</sup> VRE). Isolates were genotyped by <it>Sma</it>I- and <it>Ceu</it>I-macrorestriction analysis in PFGE, plasmid profiling, <it>vanB</it> Southern hybridisations as well as MLST typing.</p> <p>Results</p> <p>Majority of <it>vanB</it> isolates (n = 56, 79%) belonged to a single ST192 outbreak strain type showing an identical PFGE pattern and analyzed representative isolates revealed a chromosomal localization of a <it>vanB2</it>-Tn<it>5382</it> cluster type. Vancomycin MICs in cation-adjusted MH broth revealed a susceptible value of ≤4 mg/L for 31 (55%) of the 56 outbreak VRE isolates. Etest® vancomycin on MH and BHI agars revealed only two <it>vanB</it> VRE isolates with a susceptible result; in general Etest® MIC results were about 1 to 2 doubling dilutions higher than MICs assessed in broth and values after the 48 h readout were 0.5 to 1 doubling dilutions higher for <it>vanB</it> VRE. Of all <it>vanB</it> type VRE only three, three and two isolates did not grow on Brilliance<sup>TM</sup> VRE agar, chromID<sup>TM</sup> VRE agar and CHROMagar<sup>TM</sup> VRE, respectively. Permanent cross contamination via the patients’ surrounding appeared as a possible risk factor for permanent VRE colonization/infection.</p> <p>Conclusions</p> <p>Low level expression of <it>vanB</it> resistance may complicate a proper routine diagnostics of <it>vanB</it> VRE and mask an ongoing high VRE prevalence. A high inoculum and growth on rich solid media showed the highest sensitivity in identifying <it>vanB</it> type resistance.</p> |
url |
http://www.aricjournal.com/content/1/1/21 |
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