학술논문

Development of a highly sensitive magneto-enzyme lateral flow immunoassay for dengue NS1 detection
Document Type
Report
Source
PeerJ. September 25, 2019, Vol. 7 e7779
Subject
Israel
California
France
Japan
Language
English
ISSN
2167-8359
Abstract
Background Dengue infection represents a global health issue of growing importance. Dengue non-structural protein 1 (NS1) plays a central role in the early detection of the disease. The most common method for NS1 detection is testing by lateral flow immunoassays (LFIAs) with varying sensitivity. In this study, we present a highly sensitive magneto-enzyme LFIA for prompt diagnosis of dengue. Methods We have demonstrated the development of a magneto-enzyme LFIA combining super-paramagnetic nanoparticles as labels and Biotin-Streptavidin signal amplification strategy to detect dengue NS1. Factors affecting the test performance including antibody pair, super-paramagnetic nanoparticle size, nitrocellulose membrane type, amounts of detection and capture antibodies, and amounts of Streptavidin-polyHRP were optimized. Analytical sensitivity and cross-reactivity were determined. Clinical performance of the novel assay was evaluated using a panel of 120 clinical sera. Results This newly developed assay could detect NS1 of all four serotypes of dengue virus (DENV). The limit of detection (LOD) was found to be as low as 0.25 ng ml.sup.-1 for DENV-1 and DENV-3, 0.1 ng ml.sup.-1 for DENV-2, and 1.0 ng ml.sup.-1 for DENV-4. The LOD for DENV-2 was a 50-fold improvement over the best values previously reported. There was an absence of cross-reactivity with Zika NS1, Hepatitis B virus, Hepatitis C virus, and Japanese encephalitis virus. The sensitivity and specificity of the novel assay were 100% when tested on clinical samples. Conclusions We have successfully developed a magneto-enzyme LFIA, allowing rapid and highly sensitive detection of dengue NS1, which is essential for proper management of patients infected with DENV.
Author(s): Tien V. Tran (1,*), Ba V. Nguyen (1,*), Thao T.P. Nguyen (2), Tung T. Tran (2), Khanh G. Pham (1), Quang B. Le (1), Binh N. Do (1), Hung [...]