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Comparison of Recombinant A2-Elisa With Rke16 Dipstick and Direct Agglutination Tests for Diagnosis of Visceral Leishmaniasis in Dogs in Northwestern Iran Publisher Pubmed



Farahmand M1 ; Khalaj V2 ; Mohebali M3 ; Khalili G4 ; Naderi S5 ; Ghaffarinejad P6 ; Nahrevanian H1
Authors
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Authors Affiliations
  1. 1. Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran
  2. 2. Department of Biotechnology, Pasteur Institute of Iran, Tehran, Iran
  3. 3. Department of Parasitology, Institute of Public Health Research, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Immunology, Pasteur Institute of Iran, Tehran, Iran
  5. 5. Islamic Azad University, Science and Research Branch of Kurdestan, Sanandaj, Iran
  6. 6. Islamic Azad University of Oloum Tahghighat, Amol, Iran

Source: Revista da Sociedade Brasileira de Medicina Tropical Published:2015


Abstract

Introduction: Various methods are used for the diagnosis of visceral leishmaniasis (VL), such as microscopic examination, culture and inoculation of laboratory animals; however, serological assays are commonly used for the detection of antibodies in serum samples with a wide range of specifi city and sensitivity. Methods: The purpose of this study was to compare three serological methods, including rA2-ELISA, the recombinant KE16 (rKE16) dipstick test and the direct agglutination test (DAT), for the detection of antibodies against VL antigens. The assays utilized 350 statistically based random serum samples from domestic dogs with clinical symptoms as well as samples from asymptomatic and healthy dogs from rural and urban areas of the Meshkinshahr district, northwestern Iran. Results: Samples were assessed, and the following positive rates were obtained: 11.5% by rKE16, 26.9% by DAT and 49.8% by ELISA. The sensitivity among symptomatic dogs was 32.4% with rKE16, 100% with DAT and 52.9% with ELISA. Conversely, rA2-ELISA was less specifi c for asymptomatic dogs, at 46.5%, compared with DAT, at 88.9%. Conclusions: This study recommends rA2-ELISA as a parallel assay combined with DAT to detect VL infection among dogs. Further evaluations should be performed to develop an inexpensive and reliable serologic test for the detection of Leishmania infantum among infected dogs. © 2015, Sociedade Brasileira de Medicina Tropical. All rights reserved.
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