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The Rapid Test Based on Leishmania infantum Chimeric rK28 Protein Improves the Diagnosis of Canine Visceral Leishmaniasis by Reducing the Detection of False-Positive Dogs

Visceral Leishmaniasis (VL) has spread to many urban centers worldwide. Dogs are considered the main reservoir of VL, because canine cases often precede the occurrence of human cases. Detection and euthanasia of serologically positive dogs is one of the primary VL control measures utilized in some c...

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Autores principales: Fraga, Deborah Bittencourt Mothé, Pacheco, Luciano Vasconcellos, Borja, Lairton Souza, Tuy, Pétala Gardênia da Silva Estrela, Bastos, Leila Andrade, Solcà, Manuela da Silva, Amorim, Leila Denise Alves Ferreira, Veras, Patrícia Sampaio Tavares
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701173/
https://www.ncbi.nlm.nih.gov/pubmed/26731098
http://dx.doi.org/10.1371/journal.pntd.0004333
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author Fraga, Deborah Bittencourt Mothé
Pacheco, Luciano Vasconcellos
Borja, Lairton Souza
Tuy, Pétala Gardênia da Silva Estrela
Bastos, Leila Andrade
Solcà, Manuela da Silva
Amorim, Leila Denise Alves Ferreira
Veras, Patrícia Sampaio Tavares
author_facet Fraga, Deborah Bittencourt Mothé
Pacheco, Luciano Vasconcellos
Borja, Lairton Souza
Tuy, Pétala Gardênia da Silva Estrela
Bastos, Leila Andrade
Solcà, Manuela da Silva
Amorim, Leila Denise Alves Ferreira
Veras, Patrícia Sampaio Tavares
author_sort Fraga, Deborah Bittencourt Mothé
collection PubMed
description Visceral Leishmaniasis (VL) has spread to many urban centers worldwide. Dogs are considered the main reservoir of VL, because canine cases often precede the occurrence of human cases. Detection and euthanasia of serologically positive dogs is one of the primary VL control measures utilized in some countries, including Brazil. Using accurate diagnostic tests can minimize one undesirable consequence of this measure, culling false-positive dogs, and reduce the maintenance of false-negative dogs in endemic areas. In December 2011, the Brazilian Ministry of Health replaced the ELISA (EIE CVL) screening method and Indirect Immunofluorescence Test (IFI CVL) confirmatory method with a new protocol using the rapid DPP CVL screening test and EIE CVL confirmatory test. A study of diagnostic accuracy of these two protocols was done by comparing their performance using serum samples collected from a random sample of 780 dogs in an endemic area of VL. All samples were evaluated by culture and real time PCR; 766 out of the 780 dogs were tested using the previous protocol (IFI CVL + EIE CVL) and all 780 were tested using the current protocol (DPP CVL + EIE CVL). Performances of both diagnostic protocols were evaluated using a latent class variable as the gold standard. The current protocol had a higher specificity (0.98 vs. 0.95) and PPV (0.83 vs. 0.70) than the previous protocol, although sensitivity of these two protocols was similar (0.73). When tested using sera from asymptomatic animals, the current protocol had a much higher PPV (0.63 vs. 0.40) than the previous protocol (although the sensitivity of either protocol was the same, 0.71). Considering a range of theoretical CVL prevalences, the projected PPVs were higher for the current protocol than for the previous protocol for each theoretical prevalence value. The findings presented herein show that the current protocol performed better than previous protocol primarily by reducing false-positive results.
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spelling pubmed-47011732016-01-15 The Rapid Test Based on Leishmania infantum Chimeric rK28 Protein Improves the Diagnosis of Canine Visceral Leishmaniasis by Reducing the Detection of False-Positive Dogs Fraga, Deborah Bittencourt Mothé Pacheco, Luciano Vasconcellos Borja, Lairton Souza Tuy, Pétala Gardênia da Silva Estrela Bastos, Leila Andrade Solcà, Manuela da Silva Amorim, Leila Denise Alves Ferreira Veras, Patrícia Sampaio Tavares PLoS Negl Trop Dis Research Article Visceral Leishmaniasis (VL) has spread to many urban centers worldwide. Dogs are considered the main reservoir of VL, because canine cases often precede the occurrence of human cases. Detection and euthanasia of serologically positive dogs is one of the primary VL control measures utilized in some countries, including Brazil. Using accurate diagnostic tests can minimize one undesirable consequence of this measure, culling false-positive dogs, and reduce the maintenance of false-negative dogs in endemic areas. In December 2011, the Brazilian Ministry of Health replaced the ELISA (EIE CVL) screening method and Indirect Immunofluorescence Test (IFI CVL) confirmatory method with a new protocol using the rapid DPP CVL screening test and EIE CVL confirmatory test. A study of diagnostic accuracy of these two protocols was done by comparing their performance using serum samples collected from a random sample of 780 dogs in an endemic area of VL. All samples were evaluated by culture and real time PCR; 766 out of the 780 dogs were tested using the previous protocol (IFI CVL + EIE CVL) and all 780 were tested using the current protocol (DPP CVL + EIE CVL). Performances of both diagnostic protocols were evaluated using a latent class variable as the gold standard. The current protocol had a higher specificity (0.98 vs. 0.95) and PPV (0.83 vs. 0.70) than the previous protocol, although sensitivity of these two protocols was similar (0.73). When tested using sera from asymptomatic animals, the current protocol had a much higher PPV (0.63 vs. 0.40) than the previous protocol (although the sensitivity of either protocol was the same, 0.71). Considering a range of theoretical CVL prevalences, the projected PPVs were higher for the current protocol than for the previous protocol for each theoretical prevalence value. The findings presented herein show that the current protocol performed better than previous protocol primarily by reducing false-positive results. Public Library of Science 2016-01-05 /pmc/articles/PMC4701173/ /pubmed/26731098 http://dx.doi.org/10.1371/journal.pntd.0004333 Text en © 2016 Fraga et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Research Article
Fraga, Deborah Bittencourt Mothé
Pacheco, Luciano Vasconcellos
Borja, Lairton Souza
Tuy, Pétala Gardênia da Silva Estrela
Bastos, Leila Andrade
Solcà, Manuela da Silva
Amorim, Leila Denise Alves Ferreira
Veras, Patrícia Sampaio Tavares
The Rapid Test Based on Leishmania infantum Chimeric rK28 Protein Improves the Diagnosis of Canine Visceral Leishmaniasis by Reducing the Detection of False-Positive Dogs
title The Rapid Test Based on Leishmania infantum Chimeric rK28 Protein Improves the Diagnosis of Canine Visceral Leishmaniasis by Reducing the Detection of False-Positive Dogs
title_full The Rapid Test Based on Leishmania infantum Chimeric rK28 Protein Improves the Diagnosis of Canine Visceral Leishmaniasis by Reducing the Detection of False-Positive Dogs
title_fullStr The Rapid Test Based on Leishmania infantum Chimeric rK28 Protein Improves the Diagnosis of Canine Visceral Leishmaniasis by Reducing the Detection of False-Positive Dogs
title_full_unstemmed The Rapid Test Based on Leishmania infantum Chimeric rK28 Protein Improves the Diagnosis of Canine Visceral Leishmaniasis by Reducing the Detection of False-Positive Dogs
title_short The Rapid Test Based on Leishmania infantum Chimeric rK28 Protein Improves the Diagnosis of Canine Visceral Leishmaniasis by Reducing the Detection of False-Positive Dogs
title_sort rapid test based on leishmania infantum chimeric rk28 protein improves the diagnosis of canine visceral leishmaniasis by reducing the detection of false-positive dogs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701173/
https://www.ncbi.nlm.nih.gov/pubmed/26731098
http://dx.doi.org/10.1371/journal.pntd.0004333
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