Laboratory Medicine ›› 2019, Vol. 34 ›› Issue (3): 259-262.DOI: 10.3969/j.issn.1673-8640.2019.03.016

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Establishment of fluorescence quantitation PCR to amplify human adenovirus-B55

DONG Lei1, LIU Juan2, AI Xianyin3, MA Hongyu1, QUAN Shouzhen1, JIANG Tao4   

  1. 1. Clinical Laboratory Center,the General Hospital of Peoples' Liberation Army Air Force,Beijing 100142,China
    2. Department of Blood Transfusion,the General Hospital of Peoples' Liberation Army Air Force,Beijing 100142,China
    3. Army Health Company 32143 of Chinese People's Liberation Army, Xinyang 464000, Henan,China
    4. Beijing Institute of Microbiology and Epidemiology,State Key Laboratory of Pathogen and Biosecurity,Beijing 100071,China
  • Received:2018-01-10 Online:2019-03-30 Published:2019-03-27

Abstract:

Objective To establish real-time fluorescence quantitation polymerase chain reaction (PCR)to amplify human adenovirus(HAdV)-B55,and to verify its performance. Methods The specific primers for the Hexon sequence of HAdV-B55 were designed with Beacon Designer 7 software,and the real-time fluorescence quantitation PCR was established. The sensitivity and specificity were evaluated. Results The specific primers for HAdV-B55 were obtained,and the real-time fluorescence quantitation PCR for HAdV-B55 had been established. The sensitivity was 0.08 PFU/reaction,and the specificity was good. There was no cross reaction with HAdVB Conclusions The real-time fluorescence quantitation PCR to detect HAdV-B55 has been established,which lays the foundation for the rapid detection and prevention of HAdV-B55.

Key words: Human adenovirus, Real-time fluorescence quantitation polymerase chain reaction, Rapid detection

CLC Number: