“…The genetic characterization by PCR using the degenerated primer pairs originally designed for HPV detection (FAP59/FAP64 or MY09/MY11), which amplifies a highly conserved region of PV L1 gene (Forslund, Antonsson, Nordin, Stenquist, & Hansson, ; Snijders et al., ), has enabled the identification and characterization of several PV types in almost all affected PV species (Antonsson & Hansson, ; Gottschling, Wibbelt, Wittstatt, Stockfleth, & Nindl, ; Munday, Dunowska, Hills, & Laurie, ; Rector et al., ), as well as in new BPV types in both dairy and beef cattle from distinct geographical regions worldwide (Lunardi, De Alcântara, et al., ; Ogawa et al., ). Also, putative and new BPV types, partially or totally sequenced by Sanger or NGS, have been published recently (Da Silva et al., ; Daudt, da Silva, Streck, et al., ; Lunardi et al., ). However, the development of NGS has enabled the discovery of new BPV types that were not amplified using FAP or MY primer pairs (Da Silva et al., ; Daudt, da Silva, Streck, et al., ).…”