Peer-reviewed veterinary case report
How well a quick test detects leishmaniosis in dogs from endemic areas
By Davenport, Kristen et al.·Published in Veterinary parasitology, regional studies and reports·2024·IDEXX Laboratories, United States·View original on PubMed →
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Original publication title: Performance of a point-of-care test for the detection of anti-Leishmania infantum antibodies is associated with immunofluorescent antibody titer and clinical stage of leishmaniosis in dogs from endemic regions.
- Species:
- dog
Plain-English summary
A group of dogs in Greece and Italy showing signs of illness were tested for leishmaniosis, a disease caused by a parasite transmitted by sand flies. Researchers evaluated a new point-of-care test that detects antibodies against the parasite and found it to be highly accurate, especially in dogs with advanced stages of the disease. The test showed nearly perfect agreement with a more traditional testing method, making it a useful tool for veterinarians to diagnose leishmaniosis in sick dogs or assess healthy dogs before vaccination. This could help ensure better management of the disease in areas where it is common.
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Abstract
Canine leishmaniosis (CanL) is caused by the protozoal parasite Leishmania infantum, which is transmitted by sand flies in warm climates across the world. Because dogs are considered a primary domestic reservoir for the parasite that causes leishmaniosis in humans, it is important from a One Health perspective that CanL be properly managed. In endemic regions, CanL is a common differential diagnosis in sick dogs because the clinical signs and clinicopathological disorders of the disease are non-specific, variable, and may overlap those of other common conditions. Diagnosis is based on the presence of compatible clinical signs, laboratory abnormalities, and confirmation by serological and parasitological evidence of infection. Here, we describe the performance of a point-of-care (POC) immunoassay that uses recombinant antigens to detect canine anti- L. infantum antibodies in a convenience sample set from a diagnostic laboratory, a group of canine patients with clinical staging, and in apparently healthy dogs from endemic areas. An immunofluorescence antibody test (IFAT) was used as the semiquantitative reference method. In the convenience sample set with high IFAT titers (≥ 1:800), the POC immunoassay demonstrated perfect agreement with IFAT (100%; 90/90). Using samples from dogs staged as either LeishVet Stage 2 or 3 or LeishVet Stage 1, positive agreement of the POC immunoassay with the IFAT was 98.8% (82/83) and 83.8% (31/37), respectively. The negative agreement with IFAT was 98.9% (272/275) in apparently healthy dogs from endemic areas of Greece and Italy. Since the performance of the POC immunoassay was associated with IFAT titer and clinical stage of CanL, the test may help veterinarians when determining if CanL is likely responsible for a patient's clinical picture or when evaluating an apparently healthy patient prior to vaccination.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/39025539/