Phuong Nguyen Hong, Kwak Chaewon, Heo Chang-Kyu, Cho Eun Wie, Yang Jihyun, Poo Haryoung
Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 34141, Republic of Korea.
Department of Biosystems and Bioengineering, KRIBB School of Biotechnology, University of Science and Technology, Daejeon 34113, Republic of Korea.
J Microbiol Biotechnol. 2018 May 28;28(5):809-815. doi: 10.4014/jmb.1801.01002.
Influenza, which is a highly contagious disease caused by the influenza A virus, continues to be a major health concern worldwide. Although the accurate and early diagnosis of influenza virus infection is important for controlling the spread of this disease and rapidly initiating antiviral therapy, the current influenza diagnostic kits are limited by their low sensitivity. In this study, we developed several new influenza nucleoprotein (NP)-specific monoclonal antibodies (mAbs) and compared their sensitivity and specificity of those with commercially available anti-NP mAbs. Three mAbs, designated M24.11, M34.3, and M34.33, exhibited higher reactivities to recombinant NPs and A/Puerto Rico/8/1934 (H1N1) viral lysates compared with the commercial mAbs, as assessed using enzyme-linked immunosorbent assays. M34.3 and M34.33 showed higher reactivities with A/California/04/09 (pandemic H1N1) and A/Philippines/2/82 (H3N2) viral lysates than the commercial mAbs. In contrast, M24.11 had marked reactivity with H3N2 but not with pandemic H1N1. Immunofluorescent confocal microscopy showed that the three mAbs effectively detected the presence of influenza virus in lung tissues of mice infected with A/Puerto Rico/8/1934. These results indicate that the newly developed M34.3 and M34.33 mAbs could be useful for the development of influenza diagnostics.
流感是一种由甲型流感病毒引起的高度传染性疾病,在全球范围内仍然是一个主要的健康问题。尽管准确早期诊断流感病毒感染对于控制该疾病的传播以及迅速启动抗病毒治疗很重要,但目前的流感诊断试剂盒受到其低灵敏度的限制。在本研究中,我们开发了几种新的流感核蛋白(NP)特异性单克隆抗体(mAb),并将它们的灵敏度和特异性与市售抗NP mAb进行了比较。使用酶联免疫吸附测定法评估,三种命名为M24.11、M34.3和M34.33的mAb与重组NP以及A/波多黎各/8/1934(H1N1)病毒裂解物相比,对市售mAb表现出更高的反应性。M34.3和M34.33与A/加利福尼亚/04/09(大流行H1N1)和A/菲律宾/2/82(H3N2)病毒裂解物的反应性高于市售mAb。相反,M24.11对H3N2有明显反应性,但对大流行H1N1没有反应性。免疫荧光共聚焦显微镜显示,这三种mAb有效地检测到感染A/波多黎各/8/1934的小鼠肺组织中流感病毒的存在。这些结果表明,新开发的M34.3和M34.33 mAb可用于流感诊断的开发。