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International external quality control assessment for the serological diagnosis of dengue infections
BACKGROUND: Dengue is endemic to the tropics and subtropics, and the most frequent of arthropod-borne viral diseases. Reliable diagnosis of dengue infection is important not only in clinical care but also in disease surveillance, the control of outbreaks, and the development of new vaccines. The dia...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392463/ https://www.ncbi.nlm.nih.gov/pubmed/25886961 http://dx.doi.org/10.1186/s12879-015-0877-0 |
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author | Domingo, Cristina Alves, María Joao de Ory, Fernando Teichmann, Anette Schmitz, Herbert Müller, Rolf Niedrig, Matthias |
author_facet | Domingo, Cristina Alves, María Joao de Ory, Fernando Teichmann, Anette Schmitz, Herbert Müller, Rolf Niedrig, Matthias |
author_sort | Domingo, Cristina |
collection | PubMed |
description | BACKGROUND: Dengue is endemic to the tropics and subtropics, and the most frequent of arthropod-borne viral diseases. Reliable diagnosis of dengue infection is important not only in clinical care but also in disease surveillance, the control of outbreaks, and the development of new vaccines. The diagnosis of dengue infection is usually established by a variety of commercial or in-house serological protocols. The European Network for the Diagnostics of Imported Viral Diseases (ENIVD) recognized the need to survey the accuracy of dengue serological diagnostics in current use, and organized an external quality assurance (EQA) study of dengue serological practice in diagnostic laboratories. METHODS: A 15-sample panel, consisting of sera reactive against dengue plus specificity and negative controls, was sent to 48 laboratories for serological testing. The results returned by the participating laboratories were anonymized, scored, and subjected to comparison and statistical analysis. RESULTS: Ten laboratories rated all samples correctly with regard to IgM, and only three achieved the full score for IgG detection. The main handicaps in assay performance were suboptimal sensitivity of in-house IgM detection protocols by comparison with better-performing commercial ELISA tests, and the presence of IgG cross-reactivity with heterologous flaviviruses. Differences of detail in the methodology of dengue IgG antibody detection appear to underlie the disparities in accuracy observed between laboratories. CONCLUSION: This EQA study demonstrates that there is room for many laboratories to improve sensitivity in the detection of anti-dengue virus IgM antibodies, against the benchmark set by commercial antibody capture ELISA tests. The EQA shows also that cross-reactivity is a continuing issue, and IgG detection protocols must be optimized to increase their specificity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-015-0877-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4392463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43924632015-04-11 International external quality control assessment for the serological diagnosis of dengue infections Domingo, Cristina Alves, María Joao de Ory, Fernando Teichmann, Anette Schmitz, Herbert Müller, Rolf Niedrig, Matthias BMC Infect Dis Research Article BACKGROUND: Dengue is endemic to the tropics and subtropics, and the most frequent of arthropod-borne viral diseases. Reliable diagnosis of dengue infection is important not only in clinical care but also in disease surveillance, the control of outbreaks, and the development of new vaccines. The diagnosis of dengue infection is usually established by a variety of commercial or in-house serological protocols. The European Network for the Diagnostics of Imported Viral Diseases (ENIVD) recognized the need to survey the accuracy of dengue serological diagnostics in current use, and organized an external quality assurance (EQA) study of dengue serological practice in diagnostic laboratories. METHODS: A 15-sample panel, consisting of sera reactive against dengue plus specificity and negative controls, was sent to 48 laboratories for serological testing. The results returned by the participating laboratories were anonymized, scored, and subjected to comparison and statistical analysis. RESULTS: Ten laboratories rated all samples correctly with regard to IgM, and only three achieved the full score for IgG detection. The main handicaps in assay performance were suboptimal sensitivity of in-house IgM detection protocols by comparison with better-performing commercial ELISA tests, and the presence of IgG cross-reactivity with heterologous flaviviruses. Differences of detail in the methodology of dengue IgG antibody detection appear to underlie the disparities in accuracy observed between laboratories. CONCLUSION: This EQA study demonstrates that there is room for many laboratories to improve sensitivity in the detection of anti-dengue virus IgM antibodies, against the benchmark set by commercial antibody capture ELISA tests. The EQA shows also that cross-reactivity is a continuing issue, and IgG detection protocols must be optimized to increase their specificity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-015-0877-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-01 /pmc/articles/PMC4392463/ /pubmed/25886961 http://dx.doi.org/10.1186/s12879-015-0877-0 Text en © Domingo et al.; licensee BioMed Central. 2015 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Domingo, Cristina Alves, María Joao de Ory, Fernando Teichmann, Anette Schmitz, Herbert Müller, Rolf Niedrig, Matthias International external quality control assessment for the serological diagnosis of dengue infections |
title | International external quality control assessment for the serological diagnosis of dengue infections |
title_full | International external quality control assessment for the serological diagnosis of dengue infections |
title_fullStr | International external quality control assessment for the serological diagnosis of dengue infections |
title_full_unstemmed | International external quality control assessment for the serological diagnosis of dengue infections |
title_short | International external quality control assessment for the serological diagnosis of dengue infections |
title_sort | international external quality control assessment for the serological diagnosis of dengue infections |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392463/ https://www.ncbi.nlm.nih.gov/pubmed/25886961 http://dx.doi.org/10.1186/s12879-015-0877-0 |
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