کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3346881 1215917 2015 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Multicenter evaluation of the Verigene Gram-negative blood culture nucleic acid test for rapid detection of bacteria and resistance determinants in positive blood cultures
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی میکروبیولوژی و بیوتکنولوژی کاربردی
پیش نمایش صفحه اول مقاله
Multicenter evaluation of the Verigene Gram-negative blood culture nucleic acid test for rapid detection of bacteria and resistance determinants in positive blood cultures
چکیده انگلیسی


• Verigene Gram-Negative Blood Culture Nucleic Acid Test was evaluated.
• Identification results agreed well with those of currently used automated systems.
• The performance in detecting antibiotic resistance determinants was highly specific.
• The assay is reliable in detecting the presence of ESBL-producing Enterobacteriaceae.
• Carbapenemase marker results were compatible with the phenotypes observed.

The Verigene Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) is a microarray-based assay that enables rapid detection of 9 common Gram-negative bacteria and 6 resistance determinants directly from positive blood cultures. We compared the performance of BC-GN with currently used automated systems, testing 141 clinical blood cultures and 205 spiked blood cultures. For identification of BC-GN target organisms in clinical and spiked blood cultures, the BC-GN assay showed 98.5% (130/132) and 98.9% (182/184) concordance, respectively. Of 140 resistance genes positively detected in clinical and spiked blood cultures with the BC-GN test, 139 (99.3%) were confirmed by PCR, and the detection results were consistent with the resistance phenotypes observed. The BC-GN assay, thus, can potentially improve care for sepsis patients by enabling timely detection and targeted antimicrobial therapy.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Diagnostic Microbiology and Infectious Disease - Volume 83, Issue 4, December 2015, Pages 344–348
نویسندگان
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