Abstract
Polymerase chain reaction-based bovine papillomavirus (BPV) detection methods using a combination of two primer sets, subAup/subAdw and subBup/subBdw, have enabled the broad-spectrum detection of most characterized BPV types. These methods were used to detect the partial L1 nucleotide sequence of BPV types from 167 cutaneous warts in cattle. Three potentially new viruses were detected using subBup/subBdw primer sets. The partial nucleotide sequences of these viruses were most similar to BPV-4, -6 and -9. Whole genome sequencing of one sample defines a new BPV type in the genus Xipapillomavirus, designated BPV-11.
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Acknowledgments
The authors would like to thank the staff of the livestock hygiene service centers in Hokkaido, Miyagi, Ibaraki and Yamanashi Prefectures for providing wart samples. This study was supported in part by a Grant-in-Aid for Specially Weighted Research, National Agriculture and Food Research Organization, and in part by a grant from Japan Society for the Promotion of Science (no. KAKENHI22780272).
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Nucleotide sequence data reported are available in the DDBJ/EMBL/GenBank databases under the accession numbers AB574430, AB574431, AB574432 and AB543507 for BPV-JPN/NIAH1, BPV-JPN/NIAH2, BPV-JPN/NIAH3 and BPV-11, respectively.
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Hatama, S., Ishihara, R., Ueda, Y. et al. Detection of a novel bovine papillomavirus type 11 (BPV-11) using xipapillomavirus consensus polymerase chain reaction primers. Arch Virol 156, 1281–1285 (2011). https://doi.org/10.1007/s00705-011-0970-7
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DOI: https://doi.org/10.1007/s00705-011-0970-7
Keywords
- Cattle Herd
- Nucleotide Sequence Alignment
- Partial Nucleotide Sequence
- Long Control Region
- Molecular Phylogenetic Tree