Hamzah, Hairul Aini and Omar, Abdul Rahman and Bejo, Mohd Hair and Ideris, Aini (2008) Comparison of Sybr Green I, ELISA and conventional agarose gel-based PCR in the detection of infectious bursal disease virus. Microbiological Research, 163 (5). pp. 556-563. ISSN 0944-5013
Full text not available from this repository.
Official URL: http://dx.doi.org/10.1016/j.micres.2006.08.003
The current available molecular method to detect infectious bursal disease virus (IBDV) is by reverse transcriptase-polymerase chain reaction (RT-PCR). However, the conventional PCR is time consuming, prone to error and less sensitive. In this study, the performances of Sybr Green I real-time PCR, enzyme-linked immunosorbent assay (ELISA) and conventional agarose detection methods in detecting specific IBDV PCR products were compared. We found the real-time PCR was at least 10 times more sensitive than ELISA detection method with a detection limit of 0.25 pg. The latter was also at least 10 times more sensitive than agarose gel electrophoresis detection method. The developed assay detects both very virulent and vaccine strains of IBDV but not other RNA viruses such as Newcastle disease virus and infectious bronchitis virus. Hence, Sybr Green I-based real-time PCR is a highly sensitive assay for the detection of IBDV.
|Keyword:||Infectious bursal, disease virus, Real-time PCR, ELISA PCR|
|Faculty or Institute:||Faculty of Veterinary Medicine|
|Deposited By:||Azizan Arshad|
|Deposited On:||13 May 2010 03:55|
|Last Modified:||19 Aug 2010 05:06|
Repository Staff Only: Edit item detail
Document Download Statistics
This item has been downloaded for since 13 May 2010 03:55.