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Peer-reviewed veterinary case report

Summer eczema in horses linked to Culicoides sonorensis midge saliva

By Langner, Kathrin F A et al.·Published in International journal for parasitology·2009·University of Veterinary Medicine, Germany·View original on PubMed

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Original publication title: Identification, expression and characterisation of a major salivary allergen (Cul s 1) of the biting midge Culicoides sonorensis relevant for summer eczema in horses.

Species:
horse

Plain-English summary

A group of horses with summer eczema (a seasonal skin allergy) were tested for a specific allergen found in the saliva of biting midges called Culicoides sonorensis. Researchers identified a protein called Cul s 1 that triggered allergic reactions in most of the affected horses but not in healthy ones. When exposed to this allergen, the horses with summer eczema showed skin reactions and signs of an allergic response, while the control horses did not. This discovery could help improve diagnosis and treatment options for horses suffering from this condition.

People also search for: horse summer eczema treatment · biting midge allergy in horses · Culicoides sonorensis skin reaction

Abstract

Salivary proteins of Culicoides biting midges are thought to play a key role in summer eczema (SE), a seasonal recurrent allergic dermatitis in horses. The present study describes the identification, expression and clinical relevance of a candidate allergen of the North American midge Culicoides sonorensis. Immunoblot analysis of midge saliva revealed a 66 kDa protein (Cul s 1) that was bound by IgE from several SE-affected (SE+) horses. Further characterisation by fragmentation, mass spectrometry and bioinformatics identified Cul s 1 as maltase, an enzyme involved in sugar meal digestion. A cDNA encoding Cul s 1 was isolated and expressed as a polyhistidine-tagged fusion protein in a baculovirus/insect cell expression system. The clinical relevance of the affinity-purified recombinant Cul s 1 (rCul s 1) was investigated by immunoblotting, histamine release testing (HRT) and intradermal testing (IDT) in eight SE+ and eight control horses. Seven SE+ horses had rCul s 1-specific IgE, whereas only one control animal had IgE directed against this allergen. Furthermore, the HRT showed rCul s 1 induced basophil degranulation in samples from seven of eight SE+ horses but in none of the control animals. rCul s 1 also induced immediate (7/8), late-phase (8/8) and delayed (1/8) skin reactivity in IDT on all SE+ horses that had a positive test with the whole body extract (WBE) of C. sonorensis. None of the control horses showed immediate or delayed skin reactivity with rCul s 1, and only one control horse had a positive late-phase response, while several non-specific late-phase reactions were observed with the insect WBE. Thus, we believe rCul s 1 is the first specific salivary allergen of C. sonorensis to be described that promises to advance both in vitro and in vivo diagnosis and may contribute to the development of immunotherapy for SE in horses.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/18708061/