Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/77853
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dc.contributorDepartment of Health Technology and Informatics-
dc.creatorLee, AWT-
dc.creatorLam, JKS-
dc.creatorLam, RKW-
dc.creatorNg, WH-
dc.creatorLee, ENL-
dc.creatorLee, VTY-
dc.creatorSze, PP-
dc.creatorRajwani, R-
dc.creatorFung, KSC-
dc.creatorTo, WK-
dc.creatorLee, RA-
dc.creatorTsang, DNC-
dc.creatorSiu, GKH-
dc.date.accessioned2018-08-28T01:35:13Z-
dc.date.available2018-08-28T01:35:13Z-
dc.identifier.issn1664-302Xen_US
dc.identifier.urihttp://hdl.handle.net/10397/77853-
dc.language.isoenen_US
dc.publisherFrontiers Research Foundationen_US
dc.rightsCopyright © 2018 Lee, Lam, Lam, Ng, Lee, Lee, Sze, Rajwani, Fung, To, Lee, Tsang and Siu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.en_US
dc.rightsThe following publication Lee AWT, Lam JKS, Lam RKW, Ng WH, Lee ENL, Lee VTY, Sze PP, Rajwani R, Fung KSC, To WK, Lee RA, Tsang DNC and Siu GKH (2018) Comprehensive Evaluation of the MBT STAR-BL Module for Simultaneous Bacterial Identification and β-Lactamase-Mediated Resistance Detection in Gram-Negative Rods from Cultured Isolates and Positive Blood Cultures. Front. Microbiol. 9:334,1-13 is available at https://dx.doi.org/10.3389/fmicb.2018.00334en_US
dc.subjectBacterialen_US
dc.subjectBeta-lactamasesen_US
dc.subjectBlood cultureen_US
dc.subjectDrug hydrolysis testen_US
dc.subjectDrug resistanceen_US
dc.subjectMALDI-TOF MSen_US
dc.subjectMBT STAR-BLen_US
dc.titleComprehensive evaluation of the MBT STAR-BL module for simultaneous bacterial identification and β-lactamase-mediated resistance detection in Gram-negative rods from cultured isolates and positive blood culturesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1en_US
dc.identifier.epage13en_US
dc.identifier.volume9en_US
dc.identifier.doi10.3389/fmicb.2018.00334en_US
dcterms.abstractObjective: This study evaluated the capability of a MALDI Biotyper system equipped with the newly introduced MBT STAR-BL module to simultaneously perform species identification and β-lactamase-mediated resistance detection in bacteremia -causing bacteria isolated from cultured isolates and patient-derived blood cultures (BCs). Methods: Two hundred retrospective cultured isolates and 153 prospective BCs containing Gram-negative rods (GNR) were collected and subjected to direct bacterial identification, followed by the measurement of β-lactamase activities against ampicillin, piperacillin, cefotaxime, ceftazidime, and meropenem using the MBT STAR-BL module. The results and turnaround times were compared with those of routine microbiological processing. All strains were also characterized by beta-lactamase PCR and sequencing. Results: Using the saponin-based extraction method, MALDI-TOF MS correctly identified bacteria in 116/134 (86.6%) monomicrobial BCs. The detection sensitivities for β-lactamase activities against ampicillin, piperacillin, third-generation cephalosporin and meropenem were 91.3, 100, 97.9, and 100% for cultured isolates, and 80.4, 100, 68.8, and 40% for monomicrobial BCs (n = 134) respectively. The overall specificities ranged from 91.5 to 100%. Furthermore, the MBT STAR-BL and conventional drug susceptibility test results were concordant in 14/19 (73.7%) polymicrobial cultures. Reducing the logRQ cut-offvalue from 0.4 to 0.2 increased the direct detection sensitivities for β-lactamase activities against ampicillin, cefotaxime and meropenem in BCs to 85.7, 87.5, and 100% respectively. The MBT STAR-BL test enabled the reporting of β-lactamase-producing GNR at 14.16 and 47.64 h before the interim and final reports of routine BCs processing, respectively, were available. Conclusion: The MALDI Biotyper system equipped with the MBT STAR-BL module enables the simultaneous rapid identification of bacterial species and β-lactamase-mediated resistance from BCs and cultured isolates. Adjustment of the logRQ cut-offvalue to 0.2 significantly increased the detection sensitivities for clinically important drug-resistant pathogens.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationFrontiers in microbiology, 23 Feb. 2018, v. 9, 334, p. 1-13-
dcterms.isPartOfFrontiers in microbiology-
dcterms.issued2018-02-23-
dc.identifier.isiWOS:000425950400001-
dc.identifier.scopus2-s2.0-85042429902-
dc.identifier.artn334en_US
dc.identifier.rosgroupid2017004196-
dc.description.ros2017-2018 > Academic research: refereed > Publication in refereed journalen_US
dc.description.validate201808 bcrcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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