Detection of the dengue virus NS1 antigen using an enzyme immunoassay

被引:14
|
作者
Anderson, Neil W. [1 ]
Jespersen, Deborah J. [1 ]
Rollins, Leonard [1 ]
Seaton, Brent [2 ]
Prince, Harry E. [2 ]
Theel, Elitza S. [1 ]
机构
[1] Mayo Clin, Dept Lab Med & Pathol, Div Clin Microbiol, Rochester, MN 55905 USA
[2] Focus Diagnost, Cypress, CA 90630 USA
关键词
Dengue virus; NS1; antigen; ELISA; Serum; EARLY-DIAGNOSIS; PROTEIN NS1; INFECTION; DISEASE; GLYCOPROTEIN; SERA;
D O I
10.1016/j.diagmicrobio.2014.02.001
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Current diagnostic methods for dengue virus (DV) rely primarily on detection of anti-DV antibodies and/or DV RNA by reverse transcriptase (RT) PCR. Several limitations exist however: seroconversion is delayed following infection, and DV RT-PCR assays are not yet readily available. The DV nonstructural protein 1 (NS1) antigen is an alternative acute phase DV biomarker, and here, we evaluated the new InBios (InBios International, Inc., Seattle, WA, USA) DENV Detect (TM) NS1 enzyme-linked immunoassay (ELISA) compared to DV RT-PCR and serology for detection of recent DV infection. We report a positive, negative, and overall percent agreement of 96% (24/25), 86.0% (43/50), and 89.3% (67/75) for the InBios NS1 ELISA compared to DV RT-PCR. Performance of the NS1 ELISA compared to serology for anti-DV IgM antibodies showed a positive, negative, and overall percent agreement of 78.0% (85/109), 90.7% (333/367), and 87.8% (418/476), respectively. Collectively, the InBios NS1 ELISA can be used as an alternative to DV RT-PCR for identification of acute DV infection. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:194 / 197
页数:4
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