Generation of mouse monoclonal antibodies specific to tilapia immunoglobulin using fish immunoglobulin/BSA complex for monitoring of the immune response in Nile tilapia Oreochromis niloticus

• Published in: Aquaculture research Vol. 50; no. 1; pp. 277 - 283
• Main Authors: Soonthonsrima, Tanapon, Wangman, Pradit, Chaivisuthangkura, Parin, Pengsuk, Chalinan, Sithigorngul, Paisarn, Longyant, Siwaporn
• Format: Journal Article
• Language: English
• Published: Oxford Hindawi Limited 01.01.2019
• Subjects: Antibodies; Antigens; Bovine serum albumin; Chains; Clones; Commercialization; Defence mechanisms; dot blot; ELISA; Enzyme-linked immunosorbent assay; Fish; Freshwater fishes; Immune response; Immune system; Immunity; Immunization; Immunoglobulin M; Immunoglobulins; Immunoprecipitation; Monoclonal antibodies; monoclonal antibody; Nile tilapia; Oreochromis niloticus; Peritoneum; Ponds; Serum; Serum albumin; Tilapia; Western blot
• ISSN: 1355-557X; 1365-2109
• DOI: 10.1111/are.13894

The simple immunoprecipitation method was used to isolate tilapia immunoglobulin (Ig) for immunization in order to produce monoclonal antibodies (MAbs) specific to tilapia Ig. First, the tilapia antiserum against bovine serum albumin (BSA) was prepared by peritoneal injection of BSA into tilapia, and the tilapia anti‐BSA antiserum was used to precipitate BSA to form the Ig/BSA immune complex. The Ig/BSA immune complex was then injected into Swiss mice for hybridoma production. After fusion, three hybridoma clones producing MAbs specific to the tilapia antibody were selected by dot blot and Western blot. All MAbs (101A, 59G, and 11A) were bound specifically to the heavy chain of immunoglobulin M (IgM). The MAbs 101A and 59G demonstrated twofold higher affinity than MAb 11A and the commercialized antibody. However, MAbs 11A could also bind to the heavy chain of IgM in Asian seabass, Lates calcarifer, as well. These MAbs can be used to monitor the immune responses of individual fish by indirect ELISA upon exposure to various antigens.