Diagnostic accuracy of Dengue NS1 lateral flow immunoassay in comparison to reverse transcriptase polymerase chain reaction and enzyme linked Immunosorbent Assay

IF 2.2 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS
Ajaikumar Sukumaran , R. Arun Krishnan, Dhanesh Mandam Kulathil, P.R. Haritha, T.N. Varun, Biby T. Edwin, K.V. Sarath, Jofy K. Paul, C.S. Satheesh Kumar, D.M. Vasudevan
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Abstract

The most widely used invitro diagnostic qualitative screening method for dengue virus infection is the lateral flow immunoassay technique. Testing of dengue non-structural antigen NS1 offers specificity in determining the active infection while testing of IgM and IgG helps in differentiating the primary and secondary dengue infections. The ELISA functions as the golden standard for dengue testing and PCR credits for the most accurate determination tool at the genetic level. The RT-PCR endorsed NS1 gene and in ELISA or LFIA NS1 antigen is used as the marker owing to the specificity and lesser chances of mutation effects. This study evaluated the performance of AG-Q Dengue NS1 LFIA kit in comparison with RT-PCR quantification cycle (Cq) Values and ELISA NS1 quantitation. The study also focused on differentiating the samples among dengue serotypes using the RealStar Dengue Type RT-PCR Kit 1.0. Dengue serotype 2 is the prominent viral strain in Kerala region succeeded by serotype 3 and 1 with a prevalence rate of 64 %, 20 % and 6 % respectively. Dengue serotype 4 was not reported during this study period. 10 % co-infection with DENV 1 & DENV 2 was also reported. The AG-Q Dengue NS1 kit stood as efficient in screening by providing positive results with samples having RT-PCR Cq values up to 43 and ELISA NS1 quantification minimum of 14 Panbio units.

登革热 NS1 侧流免疫测定与逆转录酶聚合酶链反应和酶联免疫吸附测定的诊断准确性比较
最广泛使用的登革热病毒感染体外诊断定性筛查方法是侧流免疫测定技术。登革热非结构抗原 NS1 的检测具有确定活动性感染的特异性,而 IgM 和 IgG 的检测则有助于区分原发性和继发性登革热感染。ELISA 是登革热检测的黄金标准,而 PCR 则是基因水平上最准确的检测工具。RT-PCR认可NS1基因,而在ELISA或LFIA中,NS1抗原因其特异性和较少的突变效应而被用作标记。本研究评估了 AG-Q 登革热 NS1 LFIA 试剂盒与 RT-PCR 定量周期 (Cq) 值和 ELISA NS1 定量值的性能比较。研究还重点使用 RealStar 登革热型 RT-PCR 试剂盒 1.0 对登革热血清型样本进行了区分。登革热血清型 2 是喀拉拉邦地区的主要病毒株,其次是血清型 3 和 1,流行率分别为 64%、20% 和 6%。本研究期间没有登革热血清 4 型的报告。此外,还报告了10%的登革热病毒1型和登革热病毒2型合并感染病例。AG-Q 登革热 NS1 检测试剂盒的筛查效率很高,RT-PCR Cq 值高达 43,ELISA NS1 定量最低为 14 Panbio 单位。
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来源期刊
CiteScore
5.80
自引率
0.00%
发文量
209
审稿时长
41 days
期刊介绍: The Journal of Virological Methods focuses on original, high quality research papers that describe novel and comprehensively tested methods which enhance human, animal, plant, bacterial or environmental virology and prions research and discovery. The methods may include, but not limited to, the study of: Viral components and morphology- Virus isolation, propagation and development of viral vectors- Viral pathogenesis, oncogenesis, vaccines and antivirals- Virus replication, host-pathogen interactions and responses- Virus transmission, prevention, control and treatment- Viral metagenomics and virome- Virus ecology, adaption and evolution- Applied virology such as nanotechnology- Viral diagnosis with novelty and comprehensive evaluation. We seek articles, systematic reviews, meta-analyses and laboratory protocols that include comprehensive technical details with statistical confirmations that provide validations against current best practice, international standards or quality assurance programs and which advance knowledge in virology leading to improved medical, veterinary or agricultural practices and management.
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