Injected phage-displayed-VP28 vaccine reduces shrimp Litopenaeus vannamei mortality by white spot syndrome virus infection

• Published in: Fish & shellfish immunology 2016-08, Vol.55, p.401-406
• Main Authors: Solís-Lucero, G., Manoutcharian, K., Hernández-López, J., Ascencio, F.
• Format: Article
• Language: English
• Subjects: Animals; Bacteriophage M13 - physiology; Brackish; Decapoda; Hemocytes - immunology; Hemocytes - virology; Litopenaeus vannamei; Marine; Nimaviridae; Penaeidae - immunology; Penaeidae - virology; Phage display; Shrimp vaccine; Vaccines, Synthetic - immunology; Viral Envelope Proteins - immunology; Viral Vaccines - immunology; VP28; White spot syndrome virus; White spot syndrome virus 1 - immunology; WSSV
• ISSN: 1050-4648; 1095-9947
• DOI: 10.1016/j.fsi.2016.05.027

White spot syndrome virus (WSSV) is the most important viral pathogen for the global shrimp industry causing mass mortalities with huge economic losses. Recombinant phages are capable of expressing foreign peptides on viral coat surface and act as antigenic peptide carriers bearing a phage-displayed vaccine. In this study, the full-length VP28 protein of WSSV, widely known as potential vaccine against infection in shrimp, was successfully cloned and expressed on M13 filamentous phage. The functionality and efficacy of this vaccine immunogen was demonstrated through immunoassay and in vivo challenge studies. In ELISA assay phage-displayed VP28 was bind to Litopenaeus vannamei immobilized hemocyte in contrast to wild-type M13 phage. Shrimps were injected with 2 × 1010 cfu animal−1 single dose of VP28-M13 and M13 once and 48 h later intramuscularly challenged with WSSV to test the efficacy of the vaccine against the infection. All dead challenged shrimps were PCR WSSV-positive. The accumulative mortality of the vaccinated and challenged shrimp groups was significantly lower (36.67%) than the unvaccinated group (66.67%). Individual phenoloxidase and superoxide dismutase activity was assayed on 8 and 48 h post-vaccination. No significant difference was found in those immunological parameters among groups at any sampled time evaluated. For the first time, phage display technology was used to express a recombinant vaccine for shrimp. The highest percentage of relative survival in vaccinated shrimp (RPS = 44.99%) suggest that the recombinant phage can be used successfully to display and deliver VP28 for farmed marine crustaceans. [Display omitted] •Phage protein pVIII was used to express multiple copies of VP28 on phage surface.•Displayed VP28 was functional as shown by binding to hemocyte membrane in ELISA.•Phage-displayed vaccine reduced shrimp mortality by WSSV infection.•This is the first report of phage-displayed vaccine for shrimp.