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. 2010 Jun;17(6):949-53.
doi: 10.1128/CVI.00041-10. Epub 2010 Apr 21.

Utility of a commercial nonstructural protein 1 antigen capture kit as a dengue virus diagnostic tool

Kovi Bessoff  1 , Elena Phoutrides, Mark Delorey, Luz N Acosta, Elizabeth Hunsperger
Affiliations

Utility of a commercial nonstructural protein 1 antigen capture kit as a dengue virus diagnostic tool

Kovi Bessoff et al. Clin Vaccine Immunol. 2010 Jun.

Abstract

Annually, over 2.5 billion people are at risk for infection with dengue virus (DENV), while between 50 and 100 million people contract the infection. There is an urgent need for alternative diagnostic tools that can detect DENV during acute infection. Recent studies have shown that DENV nonstructural protein 1 (NS1) is detectable in the blood as early as the onset of symptoms and persists well into the convalescent phase of the infection. We evaluated the utility of the Bio-Rad Platelia DENV NS1 antigen capture kit in combination with real-time reverse transcriptase PCR (RT-PCR) and an IgM antibody capture enzyme-linked immunosorbent assay (MAC-ELISA) for refining a new algorithm for the diagnosis of acute- or convalescent-phase DENV infection with a single clinical sample. We tested the Bio-Rad kit with three panels of sera. These panels were designed to evaluate the sensitivities of the NS1 kit for (i) early-convalescent-phase samples, (ii) acute-phase samples with false-negative PCR results, and (iii) IgM-negative convalescent-phase samples from patients with confirmed secondary DENV infections. Results show that NS1 can be detected in 22% of serum samples collected more than 10 days after the onset of illness and in 22% of samples that did not elicit an IgM response. Additionally, NS1 was detected in 37% of the tested acute-phase samples with false-negative PCR results, suggesting that NS1 detection may be valuable in increasing the sensitivity of current acute-phase diagnostics. These results will improve diagnosis with a single acute-phase or early-convalescent-phase sample for disease surveillance and clinical diagnosis.

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Figures

FIG. 1.
FIG. 1.
(A) Proportion of all samples (acute and convalescent phase) that tested positive for NS1 at each DPO. (B) Levels of sensitivity as indicated by proportions of convalescent-phase samples for which the paired acute-phase sample was positive for NS1. Although the sensitivity appears to decrease with DPO, this trend was not statistically significant.
FIG. 2.
FIG. 2.
Proportion of NS1-positive panel B serum samples by DPO. Panel B includes acute-phase specimens with false-negative PCR results for which the corresponding convalescent-phase samples showed IgM seroconversion.
FIG. 3.
FIG. 3.
(A) Proportions of all samples from serum panel C that tested positive for NS1. (B) Sensitivities for NS1 detection versus DPO for only the convalescent-phase samples whose paired acute-phase sample tested positive for NS1.
See this image and copyright information in PMC

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