Diagnostics & Vaccines Section, ICAR-National Institute of High Security Animal Diseases, Bhopal, 462022, India.
Diagnostics & Vaccines Section, ICAR-National Institute of High Security Animal Diseases, Bhopal, 462022, India.
Anal Chim Acta. 2020 Jan 6;1093:123-130. doi: 10.1016/j.aca.2019.09.060. Epub 2019 Sep 25.
Accurate and rapid diagnosis of Influenza A viruses (IAVs) is challenging because of multiple strains circulating in humans and animal populations, and the emergence of new strains. In this study, we demonstrate a simple and rapid strategy for visual detection of multiple strains of IAVs (H1 to H16 subtypes) using peptide nucleic acid (PNA) as a biosensor and unmodified gold nanoparticles (AuNPs) as a reporter. The design principle of the assay is based on the color change on account of free PNA-induced aggregation of AuNPs in the presence of non-complementary viral RNA sequence and vice-versa. The assay could detect IAV RNA with a visual limit of detection of 2.3 ng. The quantification of RNA with a considerable accuracy on a simple spectrophotometer was achieved on plotting the PNA-induced colorimetric changes (absorption ratio of A/A) in the presence of a varying concentration of complementary RNA. As a proof-of-concept, the visual assay was validated on 419 avian clinical samples and receiver operating characteristic (ROC) curve analysis showed a high diagnostic specificity (96.46%, 95% CI = 93.8 to 98.2) and sensitivity (82.41%, 95% CI = 73.9 to 89.1) when RT-qPCR was used as reference test. Hence, the simplicity, rapidity, and universality of this strategy make it a potential candidate visual assay for clinical diagnosis and surveillance of IAVs, especially in the resource-limited settings. The proposed strategy establishes new avenues for developing a simple and rapid diagnostic system for viral infections and biomolecules.
准确快速地诊断甲型流感病毒 (IAV) 具有挑战性,因为其在人类和动物种群中存在多种毒株,并且新的毒株不断出现。在本研究中,我们展示了一种使用肽核酸 (PNA) 作为生物传感器和未经修饰的金纳米粒子 (AuNPs) 作为报告器来可视化检测多种 IAV (H1 至 H16 亚型)的简单快速策略。该测定的设计原理基于在存在非互补病毒 RNA 序列的情况下,游离 PNA 诱导 AuNP 聚集而导致的颜色变化,反之亦然。该测定法可以检测到 2.3ng 的 IAV RNA,具有视觉检测限。通过在存在不同浓度互补 RNA 的情况下绘制 PNA 诱导的比色变化(A/A 的吸光度比),可以在简单的分光光度计上相当准确地定量 RNA。作为概念验证,该可视化测定法在 419 份禽临床样本上进行了验证,当以 RT-qPCR 作为参考测试时,ROC 曲线分析显示出高诊断特异性(96.46%,95%CI=93.8 至 98.2)和敏感性(82.41%,95%CI=73.9 至 89.1)。因此,该策略的简单性、快速性和通用性使其成为一种有潜力的临床诊断和监测 IAV 的可视化测定法,特别是在资源有限的环境中。该策略为开发用于病毒感染和生物分子的简单快速诊断系统开辟了新途径。