Publication | Open Access
A multiplex liquid-chip assay based on Luminex xMAP technology for simultaneous detection of six common respiratory viruses
20
Citations
34
References
2017
Year
Multiplex TechnologyViral DiagnosticsReal-time Rt-pcr AssayVirus TransmissionCovid-19Influenza VaccinesReal-time Rt-pcrMolecular DiagnosticsDiagnostic VirologyLuminex Xmap TechnologyCommon Respiratory VirusesAllergyRespiratory DiseasesVirologyMolecular Diagnostic TechniquesMultiplex Liquid-chip AssayEmerging Infectious DiseasesType BInfectious Respiratory DiseaseMicrobiologyMedicine
We utilized one-step multiplex reverse transcription-PCR (RT-PCR) and Luminex xMAP technology to develop a respiratory multiplex liquid-chip assay (rMLA) for simultaneous detection of 6 common respiratory viruses, including influenza virus type A (FluA) and type B (FluB), para-influenza virus type 3 (PIV-3), respiratory syncytial virus (RSV), human metapneumovirus (MPV) and a threatening virus to China, Middle East Respiratory Syndrome coronavirus (MERS-CoV). Performance of rMLA was evaluated by comparing with real-time RT-PCR. Detection data from clinical specimens showed that the rMLA had diagnostic sensitivities of 97.10% for FluA, 94.59% for FluB, 98.68% for PIV-3, 94.87% for RSV and 95.92% for MPV (No Data for MERS-CoV due to the lack of positive specimens). Data of analytical sensitivities showed that the detection limits of the rMLA assay were 5-25 viral RNA copies per μl for FluA, FluB, PIV-3 and MERS-CoV, approximate to the real-time RT-PCR assay; while the values were 8 and 22copies/μl for MPV and RSV, lower than the real-time RT-PCR(78 and 114 copies/μl respectively). The results indicated that the rMLA is a sensitive, specific detection tool and comparable to real-time RT-PCR, especially suitable for high-throughput detection of respiratory specimens.
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