Oral DNA vaccination of rainbow trout, Oncorhynchus mykiss (Walbaum), against infectious haematopoietic necrosis virus using PLGA [Poly(D,L-Lactic-Co-Glycolic Acid)] nanoparticles

• Published in: Journal of fish diseases 2012-03, Vol.35 (3), p.203-214
• Main Authors: Adomako, M, St-Hilaire, S, Zheng, Y, Eley, J, Marcum, R D, Sealey, W, Donahower, B C, LaPatra, S, Sheridan, P P
• Format: Article
• Language: English
• Subjects: Animals; Antibodies, Neutralizing - blood; Antibodies, Viral - blood; DNA vaccine; Fish Diseases - mortality; Fish Diseases - prevention & control; Freshwater; Gene Expression Regulation, Viral; Infectious haematopoietic necrosis virus; Infectious hematopoietic necrosis virus; Lactic Acid - immunology; Nanoparticles; Oncorhynchus mykiss; Oncorhynchus mykiss - immunology; Oncorhynchus mykiss - physiology; Oncorhynchus mykiss - virology; PLGA; Polyglycolic Acid; rainbow trout; Rhabdoviridae Infections - mortality; Rhabdoviridae Infections - prevention & control; Rhabdoviridae Infections - veterinary; Survival Analysis; Vaccines, DNA - immunology; Viral Proteins - metabolism; Viral Vaccines - administration & dosage; Viral Vaccines - immunology
• ISSN: 0140-7775; 1365-2761
• DOI: 10.1111/j.1365-2761.2011.01338.x

A DNA vaccine against infectious haematopoietic necrosis virus (IHNV) is effective at protecting rainbow trout, Oncorhynchus mykiss, against disease, but intramuscular injection is required and makes the vaccine impractical for use in the freshwater rainbow trout farming industry. Poly (D,L‐lactic‐co‐glycolic acid) (PLGA) is a U.S. Food and Drug Administration (FDA) approved polymer that can be used to deliver DNA vaccines. We evaluated the in vivo absorption of PLGA nanoparticles containing coumarin‐6 when added to a fish food pellet. We demonstrated that rainbow trout will eat PLGA nanoparticle coated feed and that these nanoparticles can be detected in the epithelial cells of the lower intestine within 96 h after feeding. We also detected low levels of gene expression and anti‐IHNV neutralizing antibodies when fish were fed or intubated with PLGA nanoparticles containing IHNV G gene plasmid. A virus challenge evaluation suggested a slight increase in survival at 6 weeks post‐vaccination in fish that received a high dose of the oral vaccine, but there was no difference when additional fish were challenged at 10 weeks post‐vaccination. The results of this study suggest that it is possible to induce an immune response using an orally delivered DNA vaccine, but the current system needs improvement.