Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/10599
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dc.contributor.authorGrabsch, Elizabeth A-
dc.contributor.authorChua, Kyra Y L-
dc.contributor.authorXie, S-
dc.contributor.authorByrne, J-
dc.contributor.authorBallard, Susan A-
dc.contributor.authorWard, P B-
dc.contributor.authorGrayson, M Lindsay-
dc.date.accessioned2015-05-16T00:06:32Z
dc.date.available2015-05-16T00:06:32Z
dc.date.issued2008-04-23-
dc.identifier.citationJournal of Clinical Microbiology 2008; 46(6): 1961-4en_US
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/10599en
dc.description.abstractWe have isolated a number of vanB-containing Enterococcus faecium isolates on bile esculin screening agar containing 6 mg/liter vancomycin, which on subsequent susceptibility testing using Etest have repeatedly demonstrated vancomycin MICs of <or=4 mg/liter. To investigate this genotype-phenotype incongruence of "low-MIC vancomycin-resistant enterococci" (LM-VRE), we examined the molecular characteristics of these isolates, including the presence of the vanB operon, using PCR amplification and DNA sequencing. All LM-VRE isolates contained vanB associated with the transposon Tn1549 and were polyclonal. Sequencing of the vanB ligase gene showed no differences from the prototype vanB2. In addition, we examined supplemented media to improve phenotypic detection of these isolates. Etest detection of LM-VRE improved when Mueller-Hinton agar (MHA) and brain heart infusion agar (BHIA) were supplemented with 10 g/liter oxgall (MHA-Oxg and BHIA-Oxg, respectively). We assessed the sensitivity and specificity of these media to detect vancomycin resistance using vancomycin-resistant vanB-containing E. faecium (n = 11), vancomycin-susceptible (van negative) E. faecium (n = 11), vancomycin-susceptible (van negative) E. faecalis (n = 11), and our LM-VRE (n = 23) isolates. After 48 h of incubation, both MHA-Oxg and BHIA-Oxg were 100% (34/34) sensitive and 100% (22/22) specific in the identification of vancomycin resistance. These findings suggest that supplementation of MHA or BHIA with 10 g/liter oxgall should be considered in laboratories where VRE detection protocols rely primarily on strain phenotype rather than early vanB gene detection by PCR.en_US
dc.language.isoenen
dc.subject.otherAnimalsen
dc.subject.otherAnti-Bacterial Agents.pharmacologyen
dc.subject.otherBacterial Proteins.genetics.metabolismen
dc.subject.otherBacteriological Techniquesen
dc.subject.otherBile.metabolismen
dc.subject.otherCulture Media.chemistryen
dc.subject.otherEnterococcus faecium.classification.drug effects.genetics.isolation & purificationen
dc.subject.otherHumansen
dc.subject.otherMicrobial Sensitivity Tests.methodsen
dc.subject.otherMolecular Sequence Dataen
dc.subject.otherSensitivity and Specificityen
dc.subject.otherVancomycin.pharmacologyen
dc.titleImproved detection of vanB2-containing enterococcus faecium with vancomycin susceptibility by Etest using oxgall supplementation.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Clinical Microbiologyen_US
dc.identifier.affiliationMicrobiologyen_US
dc.identifier.doi10.1128/JCM.01778-07en_US
dc.description.pages1961-4en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/18434564en
dc.type.contentTexten_US
dc.type.austinJournal Articleen
local.name.researcherChua, Kyra Y L
item.languageiso639-1en-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptMicrobiology-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptInfectious Diseases-
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