Format

Send to

Choose Destination
Sheng Wu Gong Cheng Xue Bao. 2018 Oct 25;34(10):1579-1586. doi: 10.13345/j.cjb.180034.

[Development and verification of reference nucleic acid materials of H9N2 influenza viruses by real-time RT-PCR].

[Article in Chinese; Abstract available in Chinese from the publisher]
Song J#1,2, Li C#3, Li J1,2, Zhang S1, Fan W1, Liu L1, Jia H4, Yu A4, Hao K4, Niu C5, Wang J5, Zhao Q3, Liu W1,2.

Author information

1
Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
2
University of Chinese Academy of Sciences, Beijing 100049, China.
3
China Institute of Veterinary Drug Control, Beijing 100081, China.
4
Beijing Haidian Foreign Language Experiment School, Beijing 100195, China.
5
National Institute of Metrology, Beijing 100013, China.
#
Contributed equally

Abstract

in English, Chinese

The HA gene of H9N2 influenza virus (A/chicken/Hunan/04.14 (H9N2)) was amplified and sequenced. The RNA was synthesized by in vitro transcription. The RNA transcription solutions were diluted to 10⁹ copies/μL using the RNA storage solution. The aliquoted RNA solutions were used to evaluate the homogeneity and stability. The results were determined by the average value obtained from four independent laboratories. Furthermore, the fluorescence quantitative RT-PCR method was also developed to verify the detection accuracy of clinical samples. The detection limit of this method is approximately 10 copies. Taken together, the RNA transcription solution established in our study can used as positive standard reference for rapid detection of H9N2 influenza virus.

KEYWORDS:

H9N2 subtype influenza virus; HA gene; real-time RT-PCR; reference materials

PMID:
30394025
DOI:
10.13345/j.cjb.180034
Free full text

Supplemental Content

Full text links

Icon for Editorial Office of Sheng Wu Gong Cheng Xue Bao
Loading ...
Support Center