4.4 Article

Development of a highly sensitive gold nanoparticle probe-based assay for bluetongue virus detection

Journal

JOURNAL OF VIROLOGICAL METHODS
Volume 183, Issue 1, Pages 45-48

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jviromet.2012.03.027

Keywords

Bluetongue virus; Gold nanoparticles; Real-time PCR; Magnetic microparticles

Funding

  1. China Postdoctoral Science Foundation [20090451505]

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A simple gold nanoparticle (GNP) probe based assay (GNPA) that was modified from a bio-barcode assay (BCA) technique, was developed for ultra-sensitive, rapid detection of the bluetongue virus (BTV) VP7 outer-core protein. This assay captures the VP7 target antigen using the GNP probe coated with anti-VP7 polyclonal antibodies and single-stranded signal DNA. Magnetic microparticle (MMP) probes coated with anti-VP7 monoclonal antibodies were then added to form a sandwich immuno-complex. The single-stranded signal DNA coated onto the GNP probe present in the immuno-complex could then be detected by PCR and real-time fluorescence PCR using a TagMan probe. The assay has a purified VP7 detection limit of 10(-2) fg/ml which is 8 orders of magnitude greater than that of conventional antigen capture ELISAs and 1 order of magnitude more sensitive than that of a conventional BCA. These results indicate that the GNPA is a highly sensitive method for easy detection of BTV proteins and that it can be modified as needed to measure the presence of other proteins. (C) 2012 Elsevier B.V. All rights reserved.

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