Single step multiplex real-time RT-PCR for H5N1 influenza A virus detection

被引:158
作者
Payungporn, S
Chutinimitkul, S
Chaisingh, A
Damrongwantanapokin, S
Buranathai, C
Amonsin, A
Theamboonlers, A
Poovorawan, Y [1 ]
机构
[1] Chulalongkorn Univ, Fac Med, Ctr Excellence Viral Hepatitis Res, Bangkok 10330, Thailand
[2] Natl Inst Anim Hlth, Dept Livestock Dev, Bangkok 10900, Thailand
[3] Chulalongkorn Univ, Fac Vet Sci, Bangkok 10330, Thailand
关键词
lnfluenza A virus; H5N1; real-time RT-PCR;
D O I
10.1016/j.jviromet.2005.08.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
H5N1 influenza A virus causes a rapidly fatal systemic disease in domestic Poultry and spreads directly from poultry to mammalian species such as leopards, tigers and humans. The aim of this study was to develop a multiplex real-time RT-PCR for rapid detection of H5N1 influenza A virus. The selected primers and various labeled TaqMan MGB reporter probes corresponding to M, H5 and N1 were used in a single step multiplex real-time RT-PCR to simultaneously detect triple fluorescent signals. In order to validate the method. 75 clinical specimens infected with H5N1 isolated from both poultry and mammals, as well as various specimens of other subtypes and RNA from other viral pathogens of poultry and human were tested. The results showed that the multiplex real-time RT-PCR assays can be applied to detect virus Suspensions of H5N1 influenza A virus from a wide host range and demonstrated the sensitivity of the assay amounted to approximately 10(2)-10(3) copies/mu l. In conclusion, the highlights of this particular method fie in its rapidity, specificity and sensitivity thus rendering it feasible and effective for large-scale screening at times of H5N1 influenza A virus outbreaks. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 147
页数:5
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