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Investigation of canine visceral leishmaniasis in a non-endemic area in Brazil and the comparison of serological and molecular diagnostic tests

INTRODUCTION: Visceral leishmaniasis (VL) is an important zoonosis in Brazil. Previous identification of parasitized dogs can also help prevent the disease in humans, even in non-endemic areas of the country. The Brazilian Ministry of Health recommends diagnosis in dogs using a DPP(®) (rapid test) a...

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Detalles Bibliográficos
Autores principales: Sevá, Anaiá da Paixão, Brandão, Ana Pérola Drulla, Godoy, Silvia Neri, Soares, Rodrigo Martins, Langoni, Helio, Rodrigues, Bruna Cristine, Gava, Mariana Zanchetta e, Zanotto, Paula Ferraz de Camargo, Jimenez-Villegas, Tatiana, Hiramoto, Roberto, Ferreira, Fernando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Medicina Tropical - SBMT 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8437447/
https://www.ncbi.nlm.nih.gov/pubmed/34495256
http://dx.doi.org/10.1590/0037-8682-0182-2021
Descripción
Sumario:INTRODUCTION: Visceral leishmaniasis (VL) is an important zoonosis in Brazil. Previous identification of parasitized dogs can also help prevent the disease in humans, even in non-endemic areas of the country. The Brazilian Ministry of Health recommends diagnosis in dogs using a DPP(®) (rapid test) as a screening test and an immunoenzymatic assay (ELISA) as a confirmatory test (DPP(®)+ELISA), and culling infected dogs as a legal control measure. However, the accuracy of these serological tests has been questioned. METHODS: VL in dogs was investigated in a non-endemic area of the São Paulo state for three consecutive years, and the performances of different diagnostic tests were compared. RESULTS: A total of 331 dog samples were collected in 2015, 373 in 2016, and 347 in 2017. The seroprevalence by DPP(®)+ELISA was 3.3, 3.2, and 0.3%, respectively, and by indirect immunofluorescence assay (IFA), it was 3.0, 5.6, and 5.5%, respectively. ELISA confirmed 18.4% of DPP(®) positive samples. The concordance between the IFA and DPP(®) was 83.9%. The concordance between IFA and DPP(®)+ELISA was 92.9%. A molecular diagnostic test (PCR) was performed in 63.2% of the seropositive samples, all of which were negative. CONCLUSIONS: In non-endemic areas, diagnostic tests in dogs should be carefully evaluated to avoid false results.