The recombinant protein rSP03B is a valid antigen for screening dog exposure to Phlebotomus perniciosus across foci of canine leishmaniasis
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
27718267
DOI
10.1111/mve.12192
Knihovny.cz E-resources
- Keywords
- Leishmania infantum, Mediterranean region, Phlebotomus spp., antibody response, dog, markers of exposure, salivary proteins, sandflies,
- MeSH
- Antigens analysis MeSH
- Insect Vectors parasitology physiology MeSH
- Insect Proteins analysis MeSH
- Insect Bites and Stings epidemiology etiology MeSH
- Leishmania infantum physiology MeSH
- Leishmaniasis parasitology veterinary MeSH
- Dog Diseases epidemiology etiology MeSH
- Phlebotomus parasitology physiology MeSH
- Dogs MeSH
- Recombinant Proteins analysis MeSH
- Salivary Proteins and Peptides analysis MeSH
- Animals MeSH
- Check Tag
- Dogs MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Italy epidemiology MeSH
- Portugal epidemiology MeSH
- Names of Substances
- Antigens MeSH
- Insect Proteins MeSH
- Recombinant Proteins MeSH
- Salivary Proteins and Peptides MeSH
The frequency of sandfly-host contacts can be measured by host antibody levels against sandfly salivary proteins. Recombinant salivary proteins are suggested to represent a valid replacement for salivary gland homogenate (SGH); however, it is necessary to prove that such antigens are recognized by antibodies against various populations of the same species. Phlebotomus perniciosus (Diptera: Psychodidae) is the main vector of Leishmania infantum (Trypanosomatida: Trypanosomatidae) in southwest Europe and is widespread from Portugal to Italy. In this study, sera were sampled from naturally exposed dogs from distant regions, including Campania (southern Italy), Umbria (central Italy) and the metropolitan Lisbon region (Portugal), where P. perniciosus is the unique or principal vector species. Sera were screened for anti-P. perniciosus antibodies using SGH and 43-kDa yellow-related recombinant protein (rSP03B). A robust correlation between antibodies recognizing SGH and rSP03B was detected in all regions, suggesting substantial antigenic cross-reactivity among different P. perniciosus populations. No significant differences in this relationship were detected between regions. Moreover, rSP03B and the native yellow-related protein were shown to share similar antigenic epitopes, as canine immunoglobulin G (IgG) binding to the native protein was inhibited by pre-incubation with the recombinant form. These findings suggest that rSP03B should be regarded as a universal marker of sandfly exposure throughout the geographical distribution of P. perniciosus.
Department of Biomedical and Medical Sciences University of Algarve Faro Portugal
Department of Parasitology Faculty of Science Charles University Prague Prague Czech Republic
Department of Veterinary Medicine and Animal Production University Federico 2 Naples Italy
Department of Veterinary Medicine University of Perugia Perugia Italy
Faculty of Veterinary Medicine Lusophone University of Humanities and Technologies Lisbon Portugal
Unit of Vector Borne Diseases and International Health Istituto Superiore di Sanità Rome Italy
References provided by Crossref.org
Field study of the improved rapid sand fly exposure test in areas endemic for canine leishmaniasis
Synthetic peptides as a novel approach for detecting antibodies against sand fly saliva