Validation of a loop-mediated isothermal amplification assay for rapid diagnosis of pertussis infection in nasopharyngeal samples

Expert Rev Mol Diagn. 2016;16(1):125-30. doi: 10.1586/14737159.2016.1112741. Epub 2015 Nov 13.

Abstract

Objective: To develop and validate a novel loop-mediated amplification (LAMP) assay for rapid diagnosis (<1 hour) of whooping cough in nasopharyngeal samples versus the gold standard: real-time PCR.

Methods: The study included all nasopharyngeal samples (n = 213) collected from children with clinical suspicion of pertussis admitted to Children's University Hospital Sant Joan de Déu (Barcelona, Spain) during July-December 2014. Fresh samples were routinely analyzed by real-time PCR and stored for retrospective LAMP analysis, following an easy 30 minute DNA extraction step by Chelex-100.

Results: Performance results of the LAMP assay were: linearity, 10(5)-10(1) CFU/ml; Limit of Detection, 2 CFU/ml; precision (mean CV), 7.38%; diagnostic sensitivity, 96.55%; diagnostic specificity, 99.46%; time to detection, 12-30 minutes.

Conclusion: The new test was shown to be 2.5-fold faster than real-time PCR while maintaining similar levels of analytical and clinical performance. Therefore it could become a useful diagnostic tool for molecular point-of-care testing.

Keywords: Bordetella pertussis; children; loop-mediated isothermal amplification; point of care; rapid diagnosis; validation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Bordetella pertussis / isolation & purification*
  • Bordetella pertussis / pathogenicity
  • Child
  • Child, Preschool
  • DNA, Bacterial / genetics
  • DNA, Bacterial / isolation & purification*
  • Female
  • Humans
  • Male
  • Nucleic Acid Amplification Techniques / methods
  • Pathology, Molecular*
  • Real-Time Polymerase Chain Reaction / methods
  • Whooping Cough / diagnosis*
  • Whooping Cough / genetics
  • Whooping Cough / microbiology
  • Whooping Cough / pathology

Substances

  • DNA, Bacterial