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Title: Detection of Newcastle disease virus using a SYBR Green I real time polymerase chain reaction. Author: Tan SW, Omar AR, Aini I, Yusoff K, Tan WS. Journal: Acta Virol; 2004; 48(1):23-8. PubMed ID: 15230471. Abstract: A two-step SYBR Green I real time polymerase chain reaction (PCR, real time PCR) for the detection of Newcastle disease virus (NDV) was developed. A melting curve analysis was performed to distinguish specific from non-specific products and primer dimers. Regardless of different virus pathotypes the melting temperature (Tm) ranged from 86 degrees C to 87 degrees C. The sensitivity of the real time PCR was compared with the reverse transcription (RT)-nested PCR enzyme-linked immunosorbent assay (ELISA, RT-nested PCR ELISA). Whereas the detection limit of the real time PCR was 10 pg DNA, the RT-nested PCR ELISA and conventional PCR could only detect up to 1 ng and 10 ng DNA, respectively. Thus the real time PCR offers a sensitive, rapid and convenient method for screening large number of NDV specimens.[Abstract] [Full Text] [Related] [New Search]