Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2012 Nov;185(2):259-66.
doi: 10.1016/j.jviromet.2012.07.010. Epub 2012 Jul 11.

Comparison of fast-track diagnostics respiratory pathogens multiplex real-time RT-PCR assay with in-house singleplex assays for comprehensive detection of human respiratory viruses

Affiliations
Comparative Study

Comparison of fast-track diagnostics respiratory pathogens multiplex real-time RT-PCR assay with in-house singleplex assays for comprehensive detection of human respiratory viruses

Senthilkumar K Sakthivel et al. J Virol Methods. 2012 Nov.

Abstract

Fast-track Diagnostics respiratory pathogens (FTDRP) multiplex real-time RT-PCR assay was compared with in-house singleplex real-time RT-PCR assays for detection of 16 common respiratory viruses. The FTDRP assay correctly identified 26 diverse respiratory virus strains, 35 of 41 (85%) external quality assessment samples spiked with cultured virus and 232 of 263 (88%) archived respiratory specimens that tested positive for respiratory viruses by in-house assays. Of 308 prospectively tested respiratory specimens selected from children hospitalized with acute respiratory illness, 270 (87.7%) and 265 (86%) were positive by FTDRP and in-house assays for one or more viruses, respectively, with combined test results showing good concordance (K=0.812, 95% CI=0.786-0.838). Individual FTDRP assays for adenovirus, respiratory syncytial virus and rhinovirus showed the lowest comparative sensitivities with in-house assays, with most discrepancies occurring with specimens containing low virus loads and failed to detect some rhinovirus strains, even when abundant. The FTDRP enterovirus and human bocavirus assays appeared to be more sensitive than the in-house assays with some specimens. With the exceptions noted above, most FTDRP assays performed comparably with in-house assays for most viruses while offering enhanced throughput and easy integration by laboratories using conventional real-time PCR instrumentation.

PubMed Disclaimer

References

    1. Arens M.Q., Buller R.S., Rankin A., Mason S., Whetsell A., Agapov E., Lee W.M., Storch G.A. Comparison of the eragen multi-code respiratory virus panel with conventional viral testing and real-time multiplex PCR assays for detection of respiratory viruses. Journal of Clinical Microbiology. 2010;48:2387–2395. - PMC - PubMed
    1. Beck E.T., Henrickson K.J. Molecular diagnosis of respiratory viruses. Future Microbiology. 2010;5:901–916. - PubMed
    1. Bibby D.F., McElarney I., Breuer J., Clark D.A. Comparative evaluation of the Seegene Seeplex RV15 and real-time PCR for respiratory virus detection. Journal of Medical Virology. 2011;83:1469–1475. - PMC - PubMed
    1. Brittain-Long R., Westin J., Olofsson S., Lindh M., Andersson L.M. Prospective evaluation of a novel multiplex real-time PCR assay for detection of fifteen respiratory pathogens-duration of symptoms significantly affects detection rate. Journal of Clinical Virology. 2010;47:263–267. - PMC - PubMed
    1. Caliendo A.M. Multiplex PCR and emerging technologies for the detection of respiratory pathogens. Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America. 2011;52(Suppl. 4):S326–S330. - PMC - PubMed

Publication types

MeSH terms

Substances