Detection of novel swine origin influenza A virus (H1N1) by real-time nucleic acid sequence-based amplification

J Virol Methods. 2010 Feb;163(2):495-7. doi: 10.1016/j.jviromet.2009.10.025. Epub 2009 Oct 31.

Abstract

Rapid detection of novel swine origin influenza A virus (S-OIV) (H1N1) is crucial for timely implementation of infection control measures. In this study, a haemagglutinin (HA) gene-based real-time nucleic acid sequence-based amplification (NASBA) assay was developed for the specific detection of S-OIV (H1N1). The assay was evaluated and validated by comparing it with existing detection methods for S-OIV (H1N1). Results obtained in a 10-fold dilution series assay demonstrated the analytic sensitivity of the present assay was comparable to that of a commercial S-OIV (H1N1) real-time RT-PCR kit and higher than that of the Centers for Disease Control and Prevention (CDC) TaqMan assay. The actual detection limit of the real-time NASBA assay was approximately 50 copies per reaction. Compared with reference methods (viral culture, conventional RT-PCR, and real-time RT-PCR), the sensitivity, specificity, positive predictive value, and negative predictive value of the present assay were all 100%. Overall, the results showed that the real-time NASBA assay could be used for sensitive and specific detection of S-OIV (H1N1).

Publication types

  • Comparative Study
  • Evaluation Study
  • Validation Study

MeSH terms

  • Hemagglutinins, Viral / genetics
  • Humans
  • Influenza A Virus, H1N1 Subtype / genetics
  • Influenza A Virus, H1N1 Subtype / isolation & purification*
  • Influenza, Human / diagnosis*
  • Influenza, Human / virology
  • Predictive Value of Tests
  • Self-Sustained Sequence Replication / methods*
  • Sensitivity and Specificity

Substances

  • Hemagglutinins, Viral
  • hemagglutinin fusogenic peptide, influenza virus