Evaluation of an accelerated workflow for surveillance of ESBL (CTX-M)-producing Escherichia coli using amplicon-based Next-Generation Sequencing and automated analysisPeker, N., Rossen, J. W. A., Deurenberg, R. H., Langereis, P. C., Raangs, E. G. C., Kluytmans, J. A., Friedrich, A. W., Veenemans, J. & Sinha, B., 11-Jan-2018, In : Microorganisms. 6, 1, 8 p.
Research output: Contribution to journal › Article › Academic › peer-review
Outbreak management of extended spectrum β-lactamase (ESBL)-producing pathogens requires rapid and accurate diagnosis. However, conventional screening is slow and labor-intensive. The vast majority of the screened samples are negative and detection of non-outbreak-related resistant micro-organisms often complicates outbreak management. In a CTX-M-15-producing Escherichia coli outbreak, 149 fecal samples and rectal eSwabs were collected by a cross-sectional survey in a Dutch nursing home. Samples were processed by routine diagnostic methods. Retrospectively, ESBL-producing bacteria and resistance genes were detected directly from eSwab medium by an accelerated workflow without prior enrichment cultures by an amplicon-based next-generation sequencing (NGS) method, and culture. A total of 27 (18.1%) samples were positive in either test. Sensitivity for CTX-M detection was 96.3% for the phenotypic method and 85.2% for the NGS method, and the specificity was 100% for both methods, as confirmed by micro-array. This resulted in a positive predictive value (PPV) of 100% for both methods, and a negative predictive value (NPV) of 99.2% and 96.8% for the phenotypic method and the NGS method, respectively. Time to result was four days and 14 h for the phenotypic method and the NGS method, respectively. In conclusion, the sensitivity without enrichment shows promising results for further use of amplicon-based NGS for screening during outbreaks.
|Number of pages||8|
|Publication status||Published - 11-Jan-2018|
- Journal Article