Bovine adenoviruses (BAVs), causing both respiratory and/or enteral di
seases in cattle, have been isolated in many countries all over the wo
rld. In this study we report on the molecular cloning of the internal
EcoRI fragments spanning 20.6-90.5%, and the internal SalI fragments s
panning 3.1-65.2% of the BAV type 2 (BAV2; strain No. 19) genome into
the plasmid vector pUC19. Moreover, the subcloning of the BAV2 genome
facilitated the construction of a detailed physical restriction endonu
clease map for BamHI, ClaI, EcoRI, HindIII, KpnI, NotI, NspV, PstI, Pv
uI, SalI, XbaI and XhoI.