4.5 Article

Development of an Immunoassay Detection System for Koi Herpesvirus Using Recombinant Single-Chain Variable Fragments

Journal

FISHES
Volume 7, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/fishes7060370

Keywords

Koi herpesvirus; scFv; biopanning; human phage display; immunoassay

Funding

  1. Bio & Medical Technology Development Program of the National Research Foundation (NRF) - Ministry of Science and ICT
  2. Korea Institute of Marine Science & Technology Promotion in the Ministry of Oceans and Fisheries (MOF) of the Republic of Korea
  3. [NRF-2017M3A9E4072753]
  4. [202104662]

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Koi herpesvirus (KHV) is a highly contagious virus that causes high mortality in koi and common carp. Current diagnostic methods cannot detect KHV virus particles, so researchers have proposed a method using specific antibodies to detect the virus. The study found that F6 and C5 scFvs have sufficient binding affinity for KHV particles and can be used in immunoassays.
Koi herpesvirus (KHV) is a highly contagious virus that causes high mortality in koi and common carp, leading to a reduction in production worldwide. Recent diagnostic tests based on molecular methods alone (nucleic acid amplification) and indirect immunoassay methods (antibody detection) can be confirmed over KHV infections or prior exposure and latent infections. Unfortunately, there is no established method to detect KHV virus particles, especially when virus titers are low. Therefore, we propose an alternative, direct immunoassay method for viral detection using a single-chain variable fragment (scFv), a specific region of IgG antibodies that binds specifically to KHV particles. The results of functional analyses indicated that four putative scFv candidates, C5, F8, F6, and E4, were specific to KHV, but only F6 and C5 had a high binding affinity. The binding characteristics were confirmed by indirect competitive and sandwich enzyme-linked immunosorbent assays, which indicated that F6 and C5 have a broad penetration area to the binding region and share a similar epitope with commercial KHV monoclonal antibodies. These characteristics were further confirmed by their interactions with purified KHV coat protein by indirect ELISA and Western blot analyses. In conclusion, the F6 and C5 scFvs have adequate binding affinity to KHV particles to permit their use in immunoassays.

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