Characterization of the Blastocystis‐specific faecal IgA immune response in pigs

• Published in: Parasite immunology 2014-10, Vol.36 (10), p.503-508
• Main Authors: Wang, W., Cuttell, L., Traub, R. J., Owen, H., Bielefeldt‐Ohmann, H.
• Format: Article
• Language: English
• Subjects: animal model; Animals; antibody; Blastocystis; Blastocystis - isolation & purification; Blastocystis Infections - immunology; Blastocystis Infections - parasitology; Blastocystis Infections - veterinary; Feces - parasitology; Female; immune response; Immunoglobulin A - immunology; immunosuppression; Male; pig; Swine; Swine Diseases - immunology; Swine Diseases - parasitology
• ISSN: 0141-9838; 1365-3024
• DOI: 10.1111/pim.12123

Summary Blastocystis is an intestinal protist found in many species including humans and pigs. It has a controversial pathogenesis and has been implicated as a potential cause of irritable bowel syndrome. Our previous studies identified pigs as potential animal models for blastocystosis by demonstrating that they were likely natural hosts of Blastocystis and can harbour subtypes (ST) in common with humans. Furthermore, our finding of a lack of intestinal histopathology associated with Blastocystis infection in pigs is also a consistent finding in examined infected humans. In this study, we aimed to identify and characterize the Blastocystis‐specific mucosal IgA response in pigs by immunoblotting, using pig faecal antibodies and Blastocystis antigen. Faeces from 233 pigs representing three age groups (sows/boars, growers/weaners and piglets) and including five dexamethasone‐immunosuppressed research pigs were tested. The majority (81·5%) of the pigs had faecal IgA reactivity against Blastocystis proteins of molecular weights of 17·5–120 kDa. Reactivity to a >250 kDa protein was found in 18·5% of pigs. Notably, immunosuppressed pigs and piglets were statistically more likely to have reactivity to this protein compared to growers/weaners and sows/boars, respectively. These results corroborate other findings suggesting that compromised immunity may predispose to blastocystosis and support our contention that pigs are potentially good models for pathogenesis studies.