| Literature DB >> 27185645 |
Patrick McGann1, Jessica L Bunin2, Erik Snesrud3, Seema Singh4, Rosslyn Maybank3, Ana C Ong3, Yoon I Kwak3, Scott Seronello4, Robert J Clifford3, Mary Hinkle3, Stephen Yamada5, Jason Barnhill4, Emil Lesho3.
Abstract
Whole genome sequencing (WGS) is increasingly employed in clinical settings, though few assessments of turnaround times (TAT) have been performed in real-time. In this study, WGS was used to investigate an unfolding outbreak of vancomycin resistant Enterococcus faecium (VRE) among 3 patients in the ICU of a tertiary care hospital. Including overnight culturing, a TAT of just 48.5 h for a comprehensive report was achievable using an Illumina Miseq benchtop sequencer. WGS revealed that isolates from patient 2 and 3 differed from that of patient 1 by a single nucleotide polymorphism (SNP), indicating nosocomial transmission. However, the unparalleled resolution provided by WGS suggested that nosocomial transmission involved two separate events from patient 1 to patient 2 and 3, and not a linear transmission suspected by the time line. Rapid TAT's are achievable using WGS in the clinical setting and can provide an unprecedented level of resolution for outbreak investigations. Published by Elsevier Inc.Entities:
Keywords: Enterococcus faecium; Turnaround time; Whole genome sequencing
Mesh:
Year: 2016 PMID: 27185645 DOI: 10.1016/j.diagmicrobio.2016.04.020
Source DB: PubMed Journal: Diagn Microbiol Infect Dis ISSN: 0732-8893 Impact factor: 2.803