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.
Canine leishmaniosis
Dog
Leishmania infantum
Point-of-care immunoassay
Serology
Journal
Veterinary parasitology, regional studies and reports
ISSN: 2405-9390
Titre abrégé: Vet Parasitol Reg Stud Reports
Pays: Netherlands
ID NLM: 101680410
Informations de publication
Date de publication:
Aug 2024
Aug 2024
Historique:
received:
11
03
2024
revised:
22
05
2024
accepted:
04
06
2024
medline:
19
7
2024
pubmed:
19
7
2024
entrez:
18
7
2024
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 39025539
pii: S2405-9390(24)00081-9
doi: 10.1016/j.vprsr.2024.101061
pii:
doi:
Substances chimiques
Antibodies, Protozoan
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
101061Informations de copyright
Copyright © 2024 IDEXX Laboratories, Inc. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest “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.” Kristen A. Davenport, Joe Liu, Juliana Sarquis, Melissa Beall, Ana Montoya, Jan Drexel, Tori Denis, Ryan Toste, Donato Traversa, Guadalupe Miró The following authors are employees of IDEXX Laboratories, Inc.: Kristen A. Davenport, Joe Liu, Melissa Beall, Jan Drexel, Tori Denis, Ryan Toste The following authors have received research grant support and/or provided consulting services for IDEXX Laboratories, Inc.: Donato Traversa, Guadalupe Miró