Following the first official report of a clinically severe outbreak of bovi
ne viral diarrhoea disease occurring in a farm in northern Italy, which had
originated from the use of a live vaccine contaminated with a strain of BV
D genotype II virus, a retrospective study on the prevalence of BVDV genoty
pes in Italy became highly relevant. For this purpose, the genotype of 78 B
VDV-positive specimens, obtained in 1998-1999 from dairy cattle in an area
near to where the outbreak occurred, was characterized by PCR technology. T
wo sets of primers, spanning the 5' UTR of BVDV genome, were used sequentia
lly in a first round of RT-PCR, performed on viral RNA extracted directly f
rom 15 clinical samples and 63 BVDV-infected cell-culture fluids; a second
PCR assay followed to selectively amplify only BVDV genotype II. All the vi
ruses under study were characterized as BVDV genotype I. As well as contrib
uting to a better understanding of the prevalence of BVDV genotypes in the
field, the results of the present study illustrate the possibility that nov
el BVDV strains can emerge in susceptible animals through the use of contam
inated immunobiological products for bovine use.