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Early diagnosis of dengue in travelers: Comparison of a novel real-time RT-PCR,NS1 antigen detection and serology
Authors:Eili Huhtamo  Essi Hasu  Nathalie Y. Uzcátegui  Elina Erra  Simo Nikkari  Anu Kantele  Olli Vapalahti  Heli Piiparinen
Affiliation:1. Laboratorio Multidisciplinario en Ciencias Biomédicas, Instituto de Investigaciones Medico-Biológicas, Universidad Veracruzana. Avenida Iturbide S/N, Col. Centro, C.P, 91700 Veracruz, México;2. Hospital Regional de Alta Especialidad de Veracruz, Servicios de Salud de Veracruz. Av. 20 de Noviembre, Col. Centro. C.P. 91700 Veracruz, México;1. Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA;2. Focus Diagnostics, Cypress, CA 90630, USA;1. Department of Microbiology, The University of the West Indies, Mona, Kingston 7, Jamaica;2. Ministry of Health, Kingston, Jamaica
Abstract:BackgroundThe increased traveling to dengue endemic regions and the numerous epidemics have led to a rise in imported dengue. The laboratory diagnosis of acute dengue requires several types of tests and often paired samples are needed for obtaining reliable results. Although several diagnostic methods are available, proper comparative data on their performance are lacking.ObjectivesTo compare the performance of novel methods including a novel pan-DENV real-time RT-PCR and a commercially available NS1 capture-EIA in regard to IgM detection for optimizing the early diagnosis of DENV in travelers.Study designA panel of 99 selected early phase serum samples of dengue patients was studied by real-time RT-PCR, NS1 antigen ELISA, IgM-EIA, IgG-IFA and cell culture virus isolation.ResultsThe novel real-time RT-PCR was shown specific and sensitive for detection of DENV-1-4 RNA and suitable for diagnostic use. The diagnostic rate using combination of RNA and IgM detection was 99% and using NS1 and IgM detection 95.9%. The results of RNA and NS1 antigen detection disagreed in 15.5% of samples that had only RNA or NS1 antigen detected.ConclusionsThe diagnostic rates of early samples are higher when either RNA or NS1 antigen detection is combined with IgM detection. Besides the differences in the RNA and NS1 detection assays, the observed discrepancy of results could suggest individual variation or differences in timing of these markers in patient serum.
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