Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2334-6-40
Title: Specific detection of H5NI avian influenza A virus in field specimens by a one-step RT-PCR assay
Authors: Ng, L.F.P. 
Barr, I.
Nguyen, T.
Noor, S.M.
Tan, R.S.-P.
Agathe, L.V.
Gupta, S.
Khalil, H.
To, T.L.
Hassan, S.S.
Ren, E.-C. 
Issue Date: 2-Mar-2006
Source: Ng, L.F.P., Barr, I., Nguyen, T., Noor, S.M., Tan, R.S.-P., Agathe, L.V., Gupta, S., Khalil, H., To, T.L., Hassan, S.S., Ren, E.-C. (2006-03-02). Specific detection of H5NI avian influenza A virus in field specimens by a one-step RT-PCR assay. BMC Infectious Diseases 6 : -. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2334-6-40
Abstract: Background: Continuous outbreaks of the highly pathogenic H5N1 avian influenza A in Asia has resulted in an urgent effort to improve current diagnostics to aid containment of the virus and lower the threat of a influenza pandemic. We report here the development of a PCR-based assay that is highly specific for the H5N1 avian influenza A virus. Methods: A one-step reverse-transcription PCR assay was developed to detect the H5N1 avian influenza A virus. The specificity of the assay was shown by testing sub-types of influenza A virus and other viral and bacterial pathogens; and on field samples. Results: Validation on 145 field specimens from Vietnam and Malaysia showed that the assay was specific without cross reactivity to a number of other infuenza strains as well as human respiratory related pathogens. Detection was 100% from allantoic fluid in H5N1 positive samples, suggesting it to be a reliable sampling source for accurate detection. Conclusion: The assay developed from this study indicates that the primers are specific for the H5N1 influenza virus. As shown by the field tested results, this assay would be highly useful as a diagnostic tool to help identify and control influenza epidemics. © 2006 Ng et al; licensee BioMed Central Ltd.
Source Title: BMC Infectious Diseases
URI: http://scholarbank.nus.edu.sg/handle/10635/130580
ISSN: 14712334
DOI: 10.1186/1471-2334-6-40
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