One-Stage Polymerase Chain Reaction for the Comprehensive Detection of Type D Retrovirus Provial DNA.
- Author:
Yong Seok JEONG
- Publication Type:Original Article
- MeSH:
Animals;
Betaretrovirus*;
Clone Cells;
DNA*;
Enzyme-Linked Immunosorbent Assay;
Ethidium;
Genome;
Haplorhini;
Humans;
Mason-Pfizer monkey virus;
Mass Screening;
Molecular Weight;
Plasmids;
Polymerase Chain Reaction*;
Retroviruses, Simian;
Sensitivity and Specificity;
Siblings;
Simian Immunodeficiency Virus
- From:Journal of the Korean Society of Virology
1997;27(1):19-27
- CountryRepublic of Korea
- Language:English
-
Abstract:
To develop the polymerase chain reaction (PCR) for the detection of type D simian retrovirus (SRV) infection, an oligonucleotide primer pair was designed to hybridize to the sequences within euv gene of SRV subtype 1 (SRV-1). The 3'proximal env sequences annealing to the primers had been rather conserved among three different subtypes of SRV, SRV-1, SRV-2, and SRV-3 (Mason-Pfizer Monkey Virus: MPMV). The PCR using the primer pair targetingan an env region the successfully detected and amplified all three subtypes of SRV with excellent specificity after single round of reaction. The tests with peripheral blood mononuclear cells infected either with simian immunodeficiency virus or simian T-lymphotropic virus type 1, maior immunosuppressive viral agents together with SRV in simian, verified the specificity of the PCR by excluding any cross reactivity. Semiquantitative titration PCR, amplifying serially diluted plasmid DNA of each subtype, was performed to evaluate sensitivity limits of the reaction. Based on molecular weight of each cloned SRV genome, the PCR should be able to detect one SRV-infected cell per more than 5-7x104 uninfected cells after simple ethidium bromide staining of resulting products. The PCR must be very efficient screening sisters with its quickness, certainty, and sensitivity for SRV-infected animals used in human AIDS research model. Second round amplification of the reaction products from the first PCR, or Southern hybridization by radiolabeled probes shall render to compete its efficacy to ELISA which has been the most sensitive technique to screen SRV infection but with frequent ambiguity problem.
