AI Article Synopsis

  • The study aimed to create an easy-to-use gel microarray test for detecting influenza viruses, assessing their subtypes and resistance to neuraminidase inhibitors.
  • A single user could perform up to 24 tests in 8 hours with high sensitivity, especially for the A/H1 pdm09 HA gene that detected fewer than 100 gene copies.
  • The test results for influenza typing and subtyping matched with traditional RT-PCR results over 97% of the time, showcasing its potential as a reliable diagnostic tool.

Article Abstract

The objectives of this study were to develop a user-friendly, gel element microarray test for influenza virus detection, subtyping, and neuraminidase inhibitor resistance detection, assess the performance characteristics of the assay, and perform a clinical evaluation on retrospective nasopharyngeal swab specimens. A streamlined microarray workflow enabled a single user to run up to 24 tests in an 8h shift. The most sensitive components of the test were the primers and probes targeting the A/H1 pdm09 HA gene with an analytical limit of detection (LoD) <100 gene copies (gc) per reaction. LoDs for all targets in nasopharyngeal swab samples were ≤1000 gc, with the exception of one target in the seasonal A/H1N1 subtype. Seasonal H275Y variants were detectable in a mixed population when present at >5% with wild type virus, while the 2009 pandemic H1N1 H275Y variant was detectable at ≤1% in a mixture with pandemic wild type virus. Influenza typing and subtyping results concurred with those obtained with real-time RT-PCR assays on more than 97% of the samples tested. The results demonstrate that a large panel of single-plex, real-time RT-PCR tests can be translated to an easy-to-use, sensitive, and specific microarray test for potential diagnostic use.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4175443PMC
http://dx.doi.org/10.1016/j.jviromet.2014.07.019DOI Listing

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