Development of a multiplex real-time PCR assay for the rapid diagnosis of neonatal late onset sepsis

M. van den Brand, R.P.H. Peters, A. Catsburg, A. Rubenjan, F.J. Broeke, F.A.M. van den Dungen, M.M. van Weissenbruch, A.M. van Furth, T. Koressaar, M. Remm, P.H.M. Savelkoul, M.P. Bos

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The diagnosis of late onset sepsis (LOS), a severe condition with high prevalence in preterm infants, is hampered by the suboptimal sensitivity and long turnaround time of blood culture. Detection of the infecting pathogen directly in blood by PCR would provide a much more timely result. Unfortunately, PCR-based assays reported so far are labor intensive and often lack direct species identification. Therefore we developed a real-time multiplex PCR assay tailored to LOS diagnosis which is easy-to-use, is applicable on small blood volumes and provides species-specific results within 4 h. Species-specific PCR assays were selected from literature or developed using bioinformatic tools for the detection of the most prevalent etiologic pathogens: Enterococcus faecalis, Staphylococcus aureus, Staphylococcus spp., Streptococcus agalactiae, Escherichia coli, Pseudomonas aeruginosa, Klebsiella spp. and Serratia marcescens. The PCR assays showed 100% specificity, full coverage of the target pathogens and a limit of detection (LOD) of <= 10 CFU eq./reaction. These LOD values were maintained in the multiplex format or when bacterial DNA was isolated from blood. Clinical evaluation showed high concordance between the multiplex PCR and blood culture. In conclusion, we developed a multiplex PCR that allows the direct detection of the most important bacterial pathogens causing LOS in preterm infants. (C) 2014 Elsevier B.V. All rights reserved.
Original languageEnglish
Pages (from-to)8-15
JournalJournal of Microbiological Methods
Volume106
DOIs
Publication statusPublished - 1 Jan 2014

Cite this