Detection of pandemic (H1N1) 2009 influenza virus by allele discrimination

被引:4
|
作者
Chiou, Chiuan-Chian
Chen, Tai-Long [2 ]
Tsao, Kuo-Chien [3 ]
Shih, Shin-Ru [3 ]
Huang, Chung-Guei [3 ]
Huang, Ya-Ling [3 ]
Chang, Chung-Ming [1 ]
机构
[1] Chang Gung Univ, Res Ctr Emerging Viral Infect, Dept Med Biotechnol & Lab Sci, Tao Yuan 333, Taiwan
[2] Chang Gung Univ, Div Biotechnol, Grad Inst Biomed Sci, Tao Yuan 333, Taiwan
[3] Chang Gung Mem Hosp, Lin Kou Med Ctr, Dept Lab Med, Tao Yuan, Taiwan
关键词
Influenza virus; Pandemic; Allele discrimination; Real-time RT-PCR; PCR;
D O I
10.1016/j.cca.2010.04.002
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: The pandemic (H1N1) 2009 has become a threat of public health. To manage rapidly increased infections and disease control, a simple and reliable first-line screening test for viral infection is on urgent demand. Methods: Through comprehensive bioinformatics analysis, a single nucleotide polymorphism in nucleoprotein gene which differentiates swine lineage virus and human seasonal H1N1 virus was selected as target. A TaqMan probe-based allele discrimination analysis was designed to analyze clinical samples. In total. 93 clinical specimens and 39 viral isolates were used to test the assay efficacy. Traditional viral culture and molecular analysis were used as gold standard. Results: The testing results showed that the established assay has high sensitivity and specificity (92% and 100%) for pandemic (H1N1) 2009. The assay could detect as low as 5 copies of NP gene of pandemic (H1N1) 2009 or 2 viral particles of human seasonal H1N1. Conclusion: This assay can be used as a first-line screening and confirmation test for pandemic (H1N1) 2009 virus and human seasonal flu in one-tube reaction. The assay can serve as a convenient method to reduce the burden of PCR manipulation for diagnostic laboratories when large amount of samples need to be analyzed in a short time. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1080 / 1083
页数:4
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