- Meeting abstract
- Open Access
Development of a real time PCR assay using SYBR Green chemistry for bovine leukemia virus detection
© Rama et al; licensee BioMed Central Ltd. 2011
- Published: 6 June 2011
- Bovine Leukemia Virus
- Positive Animal
- Gp51 Gene
- Bovine Leukemia Virus Infection
- SYBR Green Chemistry
In Uruguay, more than 50% of dairy cattle individuals are infected by Bovine Leukemia Virus (BLV). A main goal of our country is to decrease this extremely high prevalence by developing efficient eradication programs for this disease.
The aim of this study was to develop a rapid and sensitive real time PCR assay using SYBR green chemistry to detect and quantify BLV proviral DNA by amplifying gp51 gene from bovine peripheral blood.
By using plasmid containing gp51 gene diluted in non-infected bovine genomic DNA we could determine the assay sensitivity. A comparative analysis with validated diagnostic tests (AGID, ELISA and direct nested PCR) was performed in 45 dairy cattle samples. All AGID positive animals (n=14) were positive by ELISA, while three negative AGID samples were also positive by ELISA. All ELISA positive animals (n=17) were positive by nested PCR. Real-time PCR technique shown that 15 out of 17 positive ELISA samples were positive whereas 10 out of 28 negative ELISA samples were also positive. These results reveal high agreement with nested PCR, and confirm an increased sensitivity of the PCR (real-time and nested) over the ELISA and AGID tests respectively.
Overall, our results show that this SYBR Green -based PCR assay may be a useful, simple, and rapid tool to detect BLV infection in dairy cattle samples that could be adapted to high-troughput diagnostic procedures.
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.