• Title of article

    Rapid label-free visual assay for the detection and quantification of viral RNA using peptide nucleic acid (PNA) and gold nanoparticles (AuNPs) Original Research Article

  • Author/Authors

    Vinay G. Joshi، نويسنده , , Kantaraja Chindera، نويسنده , , Arvind Kumar Singh، نويسنده , , Aditya P. Sahoo، نويسنده , , Vikas D. Dighe، نويسنده , , Dimpal Thakuria، نويسنده , , Ashok K. Tiwari، نويسنده , , Satish Kumar، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2013
  • Pages
    7
  • From page
    1
  • To page
    7
  • Abstract
    A rapid label-free visual assay for the detection of viral RNA using peptide nucleic acid (PNA) probes and gold nanoparticles (AuNPs) is presented in this study. Diagnosis is a crucial step for the molecular surveillance of diseases, and a rapid visual test with high specificity could play a vital role in the management of viral diseases. In this assay, the specific agglomerative behavior of PNA with gold nanoparticles was manipulated by its complementation with viral RNA. The assay was able to detect 5–10 ng of viral RNA from various biological samples, such as allantoic fluids, cell culture fluids and vaccines, in 100 μl of test solution. The developed assay was more sensitive than a hemagglutination (HA) test, a routine platform test for the detection of Newcastle disease virus (NDV), and the developed assay was able to visually detect NDV with as little as 0.25 HA units of virus. In terms of the specificity, the test could discriminate single nucleotide differences in the target RNA and hence could provide visual viral genotyping/pathotyping. This observation was confirmed by pathotyping different known isolates of NDV. Further, the PNA-induced colorimetric changes in the presence of the target RNA at different RNA to PNA ratios yielded a standard curve with a linear coefficient of R2 = 0.990, which was comparable to the value of R2 = 0.995 from real-time PCR experiments with the same viral RNA. Therefore, the viral RNA in a given samples could be quantified using a simple visual spectrophotometer available in any clinical laboratory. This assay may find application in diagnostic assays for other RNA viruses, which are well known to undergo mutations, thus presenting challenges for their molecular surveillance, genotyping and quantification.
  • Keywords
    Label-free assay , Viral RNA quantification , Gold nanoparticles (AuNPs) , Peptide nucleic acid (PNA) , Visual RNA detection
  • Journal title
    Analytica Chimica Acta
  • Serial Year
    2013
  • Journal title
    Analytica Chimica Acta
  • Record number

    1029650