A. Kappeler et al., DETECTION OF BOVINE POLYOMAVIRUS CONTAMINATION IN FETAL BOVINE SERA AND MODIFIED-LIVE VIRAL VACCINES USING POLYMERASE CHAIN-REACTION, Biologicals, 24(2), 1996, pp. 131-135
A nested polymerase chain reaction (PCR) assay has been developed for
the detection of bovine polyomavirus (BPyV) DNA. The assay has been us
ed to screen commercial lots of fetal bovine serum and modified live v
eterinary vaccines for the presence of the agent. A PCR product of the
expected size was detected after the first round of PCR for eight out
of 20 serum lots, but in none of the 14 vaccines tested. The subseque
nt nested assay revealed that four more serum lots were positive for B
PyV DNA, as well as two vaccine lots. When hybridized with a labelled
probe, blots of the PCR products from vaccines revealed that in one of
the two positive samples a specific product was present after the fir
st PCR at a level not detectable in gel electrophoresis. Nested PCR ap
pears to be a useful tool for the detection of low level contamination
with BPyV DNA of products used in, and derived from cell culture. (C)
1996 The International Association of Biological Standardization