Real time application of whole genome sequencing for outbreak investigation – What is an achievable turnaround time?

Patrick McGann*, Jessica L. Bunin, Erik Snesrud, Seema Singh, Rosslyn Maybank, Ana C. Ong, Yoon I. Kwak, Scott Seronello, Robert J. Clifford, Mary Hinkle, Stephen Yamada, Jason Barnhill, Emil Lesho

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

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.

Original languageEnglish
Pages (from-to)277-282
Number of pages6
JournalDiagnostic Microbiology and Infectious Disease
Volume85
Issue number3
DOIs
StatePublished - 1 Jul 2016
Externally publishedYes

Keywords

  • Enterococcus faecium
  • Turnaround time
  • Whole genome sequencing

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