Occurrence, diagnosis and follow-up of canine strongyloidiosis in naturally infected shelter dogs.
Animals
Antibodies, Helminth
/ blood
Cohort Studies
DNA, Helminth
/ analysis
Dog Diseases
/ diagnosis
Dogs
Enzyme-Linked Immunosorbent Assay
/ veterinary
Feces
/ parasitology
Female
Fluorescent Antibody Technique
/ veterinary
Male
ROC Curve
Real-Time Polymerase Chain Reaction
Sensitivity and Specificity
Strongyloides stercoralis
/ genetics
Strongyloidiasis
/ diagnosis
Coprology
Strongyloides stercoralis
diagnosis
dogs
molecular biology
serology
Journal
Parasitology
ISSN: 1469-8161
Titre abrégé: Parasitology
Pays: England
ID NLM: 0401121
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
pubmed:
31
7
2018
medline:
8
1
2020
entrez:
31
7
2018
Statut:
ppublish
Résumé
Strongyloidiosis by Strongyloides stercoralis is a disease of increasing interest in human and animal medicine. The scientific knowledge on canine strongyloidiosis is hindered by the poor diagnostics available. To assess the most sensitive and specific diagnostic method, feces and blood from 100 shelter dogs were screened for S. stercoralis by coprological, molecular and serological tests. Thirty-six dogs (36%) scored positive to S. stercoralis by coprology (22.3% to Baermann) and/or 30% to real time-polymerase chain reaction (rt-PCR). According to two composite reference standards (CRS) based on all coprological methods and rt-PCR (first CRS) or in combination with serology (second CRS), the most sensitive test was IFAT (93.8%; CI 82.8-98.7), followed by rt-PCR (80.6%; 95% CI 64-91.8) and Baermann (60.6%; 95% CI 42.1-77.1). The inconsistent shedding of L1 during the 4-week follow-up in infected dogs suggests the importance of multiple faecal collections for a reliable diagnosis. A combination of serological and coprological tests is recommended for the surveillance and diagnosis of S. stercoralis infection in dogs.
Identifiants
pubmed: 30058514
pii: S0031182018001312
doi: 10.1017/S0031182018001312
doi:
Substances chimiques
Antibodies, Helminth
0
DNA, Helminth
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM