Publication:
Simultaneous discrimination and detection of influenza A(H1N1)pdm09 and seasonal influenza A viruses using a rapid immunogold biosensor

dc.contributor.authorChayachon Apiwaten_US
dc.contributor.authorNatpapas Wiriyachaipornen_US
dc.contributor.authorWeerakanya Maneeprakornen_US
dc.contributor.authorTararaj Dharakulen_US
dc.contributor.authorCharin Thepthaien_US
dc.contributor.authorPilaipan Puthavathanaen_US
dc.contributor.authorSontana Siritantikornen_US
dc.contributor.authorNavin Horthongkhamen_US
dc.contributor.otherThailand National Science and Technology Development Agencyen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-09T02:23:39Z
dc.date.available2018-11-09T02:23:39Z
dc.date.issued2014-01-01en_US
dc.description.abstractA rapid immunogold biosensor for the simultaneous discrimination of influenza A(H1N1)pdm09 and seasonal influenza A viruses was developed successfully. Monoclonal antibodies (mAbs) that were specific for the hemagglutinin protein of the A(H1N1)pdm09 virus were produced, and the best mAb pairs were selected. Using an mAb that was specific for the influenza A nucleoprotein, a rapid immunogold biosensor for the discrimination and detection of A(H1N1)pdm09/seasonal influenza viruses was developed. When tested with 72 virus isolates, the system achieved 100% detection of the A(H1N1)pdm09 virus without cross-reactivity against seasonal influenza A (H1, H3 subtypes) and B viruses, parainfluenza viruses, respiratory syncytial viruses, and adenoviruses. The detection limits for A(H1N1)pdm09 and seasonal strains were 5 × 102-7.5 × 103 and 1 × 103-7.5 × 105 TCID50/mL, respectively. When tested with 49 clinical specimens, the specificity was high (100%). The sensitivity for the detection of A(H1N1)pdm09 and seasonal strains was 90% and 100%, respectively, which correlated with the results of real-time reverse transcription polymerase chain reaction as a reference method. The ability of the system to detect and discriminate the A(H1N1)pdm09 strain from the seasonal strains suggests that this method may be beneficial for investigation of outbreaks and diagnostic applications. Furthermore, this method might be a useful platform for developing a rapid diagnostic system for the simultaneous discrimination of other influenza virus subtypes during future outbreaks. © 2014 Springer-Verlag Wien.en_US
dc.identifier.citationArchives of Virology. Vol.159, No.7 (2014), 1603-1611en_US
dc.identifier.doi10.1007/s00705-013-1974-2en_US
dc.identifier.issn03048608en_US
dc.identifier.other2-s2.0-84903639043en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/34024
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84903639043&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.titleSimultaneous discrimination and detection of influenza A(H1N1)pdm09 and seasonal influenza A viruses using a rapid immunogold biosensoren_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84903639043&origin=inwarden_US

Files

Collections