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Validation of a Rapid Rabies Diagnostic Tool for Field Surveillance in Developing Countries

BACKGROUND: One root cause of the neglect of rabies is the lack of adequate diagnostic tests in the context of low income countries. A rapid, performance friendly and low cost method to detect rabies virus (RABV) in brain samples will contribute positively to surveillance and consequently to accurat...

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Autores principales: Léchenne, Monique, Naïssengar, Kemdongarti, Lepelletier, Anthony, Alfaroukh, Idriss Oumar, Bourhy, Hervé, Zinsstag, Jakob, Dacheux, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5051951/
https://www.ncbi.nlm.nih.gov/pubmed/27706156
http://dx.doi.org/10.1371/journal.pntd.0005010
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author Léchenne, Monique
Naïssengar, Kemdongarti
Lepelletier, Anthony
Alfaroukh, Idriss Oumar
Bourhy, Hervé
Zinsstag, Jakob
Dacheux, Laurent
author_facet Léchenne, Monique
Naïssengar, Kemdongarti
Lepelletier, Anthony
Alfaroukh, Idriss Oumar
Bourhy, Hervé
Zinsstag, Jakob
Dacheux, Laurent
author_sort Léchenne, Monique
collection PubMed
description BACKGROUND: One root cause of the neglect of rabies is the lack of adequate diagnostic tests in the context of low income countries. A rapid, performance friendly and low cost method to detect rabies virus (RABV) in brain samples will contribute positively to surveillance and consequently to accurate data reporting, which is presently missing in the majority of rabies endemic countries. METHODOLOGY/PRINCIPAL FINDINGS: We evaluated a rapid immunodiagnostic test (RIDT) in comparison with the standard fluorescent antibody test (FAT) and confirmed the detection of the viral RNA by real time reverse transcription polymerase chain reaction (RT-qPCR). Our analysis is a multicentre approach to validate the performance of the RIDT in both a field laboratory (N’Djamena, Chad) and an international reference laboratory (Institut Pasteur, Paris, France). In the field laboratory, 48 samples from dogs were tested and in the reference laboratory setting, a total of 73 samples was tested, representing a wide diversity of RABV in terms of animal species tested (13 different species), geographical origin of isolates with special emphasis on Africa, and different phylogenetic clades. Under reference laboratory conditions, specificity was 93.3% and sensitivity was 95.3% compared to the gold standard FAT test. Under field laboratory conditions, the RIDT yielded a higher reliability than the FAT test particularly on fresh and decomposed samples. Viral RNA was later extracted directly from the test filter paper and further used successfully for sequencing and genotyping. CONCLUSION/SIGNIFICANCE: The RIDT shows excellent performance qualities both in regard to user friendliness and reliability of the result. In addition, the test cassettes can be used as a vehicle to ship viral RNA to reference laboratories for further laboratory confirmation of the diagnosis and for epidemiological investigations using nucleotide sequencing. The potential for satisfactory use in remote locations is therefore very high to improve the global knowledge of rabies epidemiology. However, we suggest some changes to the protocol, as well as careful further validation, before promotion and wider use.
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spelling pubmed-50519512016-10-27 Validation of a Rapid Rabies Diagnostic Tool for Field Surveillance in Developing Countries Léchenne, Monique Naïssengar, Kemdongarti Lepelletier, Anthony Alfaroukh, Idriss Oumar Bourhy, Hervé Zinsstag, Jakob Dacheux, Laurent PLoS Negl Trop Dis Research Article BACKGROUND: One root cause of the neglect of rabies is the lack of adequate diagnostic tests in the context of low income countries. A rapid, performance friendly and low cost method to detect rabies virus (RABV) in brain samples will contribute positively to surveillance and consequently to accurate data reporting, which is presently missing in the majority of rabies endemic countries. METHODOLOGY/PRINCIPAL FINDINGS: We evaluated a rapid immunodiagnostic test (RIDT) in comparison with the standard fluorescent antibody test (FAT) and confirmed the detection of the viral RNA by real time reverse transcription polymerase chain reaction (RT-qPCR). Our analysis is a multicentre approach to validate the performance of the RIDT in both a field laboratory (N’Djamena, Chad) and an international reference laboratory (Institut Pasteur, Paris, France). In the field laboratory, 48 samples from dogs were tested and in the reference laboratory setting, a total of 73 samples was tested, representing a wide diversity of RABV in terms of animal species tested (13 different species), geographical origin of isolates with special emphasis on Africa, and different phylogenetic clades. Under reference laboratory conditions, specificity was 93.3% and sensitivity was 95.3% compared to the gold standard FAT test. Under field laboratory conditions, the RIDT yielded a higher reliability than the FAT test particularly on fresh and decomposed samples. Viral RNA was later extracted directly from the test filter paper and further used successfully for sequencing and genotyping. CONCLUSION/SIGNIFICANCE: The RIDT shows excellent performance qualities both in regard to user friendliness and reliability of the result. In addition, the test cassettes can be used as a vehicle to ship viral RNA to reference laboratories for further laboratory confirmation of the diagnosis and for epidemiological investigations using nucleotide sequencing. The potential for satisfactory use in remote locations is therefore very high to improve the global knowledge of rabies epidemiology. However, we suggest some changes to the protocol, as well as careful further validation, before promotion and wider use. Public Library of Science 2016-10-05 /pmc/articles/PMC5051951/ /pubmed/27706156 http://dx.doi.org/10.1371/journal.pntd.0005010 Text en © 2016 Léchenne 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
Léchenne, Monique
Naïssengar, Kemdongarti
Lepelletier, Anthony
Alfaroukh, Idriss Oumar
Bourhy, Hervé
Zinsstag, Jakob
Dacheux, Laurent
Validation of a Rapid Rabies Diagnostic Tool for Field Surveillance in Developing Countries
title Validation of a Rapid Rabies Diagnostic Tool for Field Surveillance in Developing Countries
title_full Validation of a Rapid Rabies Diagnostic Tool for Field Surveillance in Developing Countries
title_fullStr Validation of a Rapid Rabies Diagnostic Tool for Field Surveillance in Developing Countries
title_full_unstemmed Validation of a Rapid Rabies Diagnostic Tool for Field Surveillance in Developing Countries
title_short Validation of a Rapid Rabies Diagnostic Tool for Field Surveillance in Developing Countries
title_sort validation of a rapid rabies diagnostic tool for field surveillance in developing countries
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5051951/
https://www.ncbi.nlm.nih.gov/pubmed/27706156
http://dx.doi.org/10.1371/journal.pntd.0005010
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