Detection of murine leukemia virus or mouse DNA in commercial RT-PCR reagents and human DNAs.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 22205995.
- Also identified by DOI 10.1371/journal.pone.0029050 and PMC identifier 3243700.
- Licence recorded as CC0.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
The xenotropic murine leukemia virus (MLV)-related viruses (XMRV) have been reported in persons with prostate cancer, chronic fatigue syndrome, and less frequently in blood donors. Polytropic MLVs have also been described in persons with CFS and blood donors. However, many studies have failed to confirm these findings, raising the possibility of contamination as a source of the positive results. One PCR reagent, Platinum Taq polymerase (pol) has been reported to contain mouse DNA that produces false-positive MLV PCR results. We report here the finding of a large number of PCR reagents that have low levels of MLV sequences. We found that recombinant reverse-transcriptase (RT) enzymes from six companies derived from either MLV or avian myeloblastosis virus contained MLV pol DNA sequences but not gag or mouse DNA sequences. Sequence and phylogenetic analysis showed high relatedness to Moloney MLV, suggesting residual contamination with an RT-containing plasmid. In addition, we identified contamination with mouse DNA and a variety of MLV sequences in commercially available human DNAs from leukocytes, brain tissues, and cell lines. These results identify new sources of MLV contamination and highlight the importance of careful pre-screening of commercial specimens and diagnostic reagents to avoid false-positive MLV PCR results.
Medical subject headings
- Animals
- Cell Line, Tumor
- DNA Contamination
- DNA, Viral
- DNA, Viral/analysis
- False Positive Reactions
- Humans
- Indicators and Reagents
- Leukemia Virus, Murine
- Leukemia Virus, Murine/enzymology
- Leukemia Virus, Murine/genetics
- Mice
- Plasmids
- Plasmids/genetics
- RNA-Directed DNA Polymerase
- Reverse Transcriptase Polymerase Chain Reaction
- Reverse Transcriptase Polymerase Chain Reaction/methods