Development and Characterization of Monoclonal Antibodies against Nucleoprotein for Diagnosis of Influenza A Virus

被引:9
作者
Nguyen Hong Phuong [1 ,2 ]
Kwak, Chaewon [1 ,2 ]
Heo, Chang-Kyu [3 ]
Cho, Eun Wie [3 ]
Yang, Jihyun [1 ]
Poo, Haryoung [1 ,2 ]
机构
[1] Korea Res Inst Biosci & Biotechnol, Infect Dis Res Ctr, Daejeon 34141, South Korea
[2] Univ Sci & Technol, KRIBB Sch Biotechnol, Dept Biosyst & Bioengn, Daejeon 34113, South Korea
[3] Korea Res Inst Biosci & Biotechnol, Rare Dis Res Ctr, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
Influenza A virus; nucleoprotein; monoclonal antibody; diagnosis; sensitivity; EVOLUTION; PURIFICATION; ORIGIN; IMPACT;
D O I
10.4014/jmb.1801.01002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:809 / 815
页数:7
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