Abstract
Due to the functional inactivation of the gene encoding for the enzyme that is involved in the oligosaccharide galactose-α-1,3-galactose (α-Gal) synthesis, humans and Old-World primates are able to produce a large amount of antibodies against the glycan epitope. Apart from being involved in the hyperacute organ rejection in humans, anti-α-Gal antibodies have shown a protective effect against some pathogenic agents and an implication in the recently recognized tick-induced mammalian meat allergy. Conversely, non-primate mammals, including dogs, have the ability to synthetize α-Gal and, thus, their immune system is not expected to naturally generate the antibodies toward this self-antigen molecule. However, in the current study, we detected specific IgG, IgM, and IgE antibodies to α-Gal in sera of clinically healthy dogs by an indirect enzyme-linked immunosorbent assay (ELISA) for the first time. Furthermore, in a tick infestation experiment, we showed that bites of Ixodes ricinus induce the immune response to α-Gal in dogs and that the resulting antibodies (IgM) might be protective against Anaplasma phagocytophilum. These findings may help lead to a better understanding of the underlying mechanisms involved in mammalian meat allergy and tick-host-pathogen interactions, but they also open up the question about the possibility that dogs could develop an allergy to mammalian meat after tick bites, similar to that in humans.
Highlights
Galactose-α-1,3-galactose (α-Gal) is an oligosaccharide abundantly expressed on glycoproteins and glycolipids of non-primate mammals, prosimians, and New World monkeys
These findings suggest the specificity of the canine immune response to α-Gal and further confirm the presence of α-Gal moieties in the saliva of both
Preliminary due to the limited sample size, the results of this study demonstrate the the occurrence of canine Abs against α-Gal and indicate that tick bites can sensitize dogs to α-Gal
Summary
Galactose-α-1,3-galactose (α-Gal) is an oligosaccharide abundantly expressed on glycoproteins and glycolipids of non-primate mammals, prosimians, and New World monkeys. IgG and IgM), which were found to be protective against vector-borne and non-vector-borne pathogens carrying α-Gal on their surface [6,7] These antibodies are involved in the hyperacute rejection of xeno-transplants in humans [8]. The epitopes in mammalian meat are exposed but unable to induce an anti-α-Gal IgE response until the individual is bitten by a tick, which suggests that certain tick salivary antigen(s) may break the peripheral food tolerance and trigger the immune complex reaction [4]. The results of this preliminary study demonstrated the specific immune response to α-Gal in dogs and suggested its possible relation to tick bites, and protection against tick-borne pathogens
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