Cort-PCR Assay for the discrimination of endogenous reverse transcriptase activity in eukaryotic cell lines from infectious retrovirus contamination

Abstract

The present invention relates to the detection of the presence of reverse transcriptase enzymatic activity in eukaryotic cell lines. Specifically, the present invention comprises a method for discriminating between endogenous reverse transcriptase activity in a substrate cell line (e.g., avian) used as substrates for the manufacture of biological products (including viral vaccines) from exogenous infectious retrovirus by using a combination of transmissibility assay (viral replication) and PBRT assay (RT-PCR). Appropriate levels of viral amplification and number of PCR cycles are determined and employed that permit detection of exogenous infectious RT activity but not endogenous RT activity.

We claim:  
     
         1 . A method for detecting the presence of greater than or equal to a pre-selected level of infectious retrovirus in a biological sample, the method comprising: 
 a) conducting a PBRT assay on a cellular substrate permissive to retrovirus infection to determine the minimum number of PCR cycles in the PBRT assay necessary to detect endogenous reverse transcriptase activity in the cellular substrate;    b) conducting an initial transmissibility assay to determine the transmissibility parameters that result in an amount of amplification necessary for the pre-selected level of retrovirus infection to yield a reverse transcriptase activity detectable in a PBRT assay using less than the minimum number of PCR cycles necessary to detect endogenous reverse transcriptase activity in the cellular substrate;    c) subjecting the biological sample to a transmissibility assay employing the parameters determined in b) to yield an amplified biological sample;    d) subjecting the amplified biological sample from c) to a PBRT assay employing less than the minimum number of PCR cycles necessary to detect endogenous reverse transcriptase activity in the cellular substrate;    e) detecting the presence of PCR product, which is indicative of a level of infectious retrovirus in the biological sample greater than or equal to the pre-selected level.    
     
     
         2 . The method according to  claim 1  wherein the cellular substrate is from an avian species.  
     
     
         3 . The method according to  claim 1  wherein the cellular substrate is chicken embryo fibroblasts.  
     
     
         4 . The method according to  claim 2  wherein the number of PCR cycles in the PBRT assay is from 24-26.  
     
     
         5 . A method for detecting the presence of greater than or equal to a pre-selected level of an infectious retrovirus in a biological sample, the method comprising: 
 a) co-culturing the biological sample with a cellular substrate permissive of retroviral infection under conditions that permit retrovirus amplification, wherein infectious retrovirus present in the biological sample is amplified to yield a level of infectious retrovirus RT activity greater than the endogenous, non-infectious retrovirus RT activity of the cellular substrate;    b) subjecting the co-culture to a PBRT assay, wherein a number of PCR cycles is employed that is equal to or greater than the number required for detection of the exogenous, infectious RT activity in the co-culture but less than the number required for detection of the endogenous, non-infectious RT activity;    c) observing whether PCR-amplified nucleic acid is present in the co-culture subjected to the PBRT assay.    
     
     
         6 . The method according to  claim 5  wherein the cellular substrate is from an avian species.  
     
     
         7 . The method according to  claim 5  wherein the cellular substrate is chicken embryo fibroblasts.  
     
     
         8 . The method according to  claim 6  wherein the number of PCR cycles in the PBRT assay is from 24-26.  
     
     
         9 . In a method for the detection of reverse transcriptase activity in a biological sample using a PBRT assay, the improvement comprising: 
 a) before conducting the PBRT assay, amplifying infectious retroviruses in the biological sample such that the RT activity level is above the endogenous RT activity level;    b) conducting the PBRT assay on the amplified product of (a) using a number of PCR cycles less than necessary to detect endogenous reverse transcriptase activity and greater than required to detect amplified exogenous, infectious reverse transcriptase activity.    
     
     
         10 . The method according to  claim 9  wherein the cellular substrate is from an avian species.  
     
     
         11 . The method according to  claim 9  wherein the cellular substrate is chicken embryo fibroblasts.  
     
     
         12 . The method according to  claim 11  wherein the number of PCR cycles in the PBRT assay is from 24-26.