Detection of bovine Deltapapillomavirus DNA in peripheral blood of healthy sheep (Ovis aries)

Blood samples from 65 sheep were tested for the presence of bovine Deltapapillomavirus (δPVs) DNA. The sheep were divided into three groups. Sheep in groups 1 and 2 were from Sardinia and Campania, respectively, and were in contact with cattle and grazed on lands contaminated with bracken fern. Sheep in Group 3 lived in closed pens and had no contact with cattle. These sheep were fed hay that did not contain bracken fern. Bovine δPV E5 DNA was detected in blood from 24 of 27 (89%) sheep in Group 1. A single bovine δPV type was detected in the blood from nine (33%) sheep, including the detection of bovine δPV-1 DNA in four sheep, bovine δPV-2 in four and δPV-13 in one sheep. Two δPV types were detected in 33% of the sheep, and three bovine δPV types were detected in 22% of the sheep. Bovine δPVs were detected in 17 of 20 (85%) sheep from Group 2. The detection rate by a single δPV type was 40% with just δPV-1 DNA amplified from two, just δPV-2 DNA from four, and just δPV-13 DNA from two sheep. Two and three δPVs were detected in 30% and 15%, respectively. All sequenced amplicons showed a 100% identity with papillomaviral E5 DNA deposited in GenBank. Bovine δPV-14 DNA sequences were not detected from any sheep. No bovine δPV DNA was revealed in blood samples from sheep in Group 3. The detection of bovine δPV DNA in the blood of sheep means that sheep may be able to be infected by these PVs. This suggests that bovine δPVs could potentially be a previously unrecognized cause of disease in sheep. Furthermore, it is possible that sheep could act as a reservoir for these viruses.

[1]  G. Altamura,et al.  Felis catus papillomavirus type-2 but not type-1 is detectable and transcriptionally active in the blood of healthy cats. , 2018, Transboundary and emerging diseases.

[2]  J. Christopher-Hennings,et al.  A novel bovine papillomavirus type in the genus Dyokappapapillomavirus , 2017, Archives of Virology.

[3]  S. H. van der Burg,et al.  The presence of human papillomavirus (HPV) in placenta and/or cord blood might result in Th2 polarization , 2017, European Journal of Clinical Microbiology & Infectious Diseases.

[4]  E. Kirkness,et al.  The blood DNA virome in 8,000 humans , 2017, PLoS pathogens.

[5]  F. Berardi,et al.  Sigma 2 receptor expression levels in blood and bladder from healthy and bladder cancer cattle , 2017, Veterinary and comparative oncology.

[6]  M. Riccardi,et al.  Bovine Papillomavirus Type 13 Expression in the Urothelial Bladder Tumours of Cattle. , 2016, Transboundary and emerging diseases.

[7]  M. Goria,et al.  Detection of bovine papillomavirus type 14 DNA sequences in urinary bladder tumors in cattle. , 2016, Veterinary microbiology.

[8]  F. Savini,et al.  PAPILLOMAVIRUS IN HEALTHY SKIN AND MUCOSA OF WILD RUMINANTS IN THE ITALIAN ALPS , 2016, Journal of wildlife diseases.

[9]  C. Ligios,et al.  E5 oncoprotein of bovine Deltapapillomaviruses is expressed in congenital carcinosarcomatosis of lambs , 2016 .

[10]  W. Beçak,et al.  Bos taurus papillomavirus activity in peripheral blood mononuclear cells: demonstrating a productive infection. , 2015, Genetics and molecular research : GMR.

[11]  Chie-Pein Chen,et al.  Human Placenta-Derived Multipotent Mesenchymal Stromal Cells Involved in Placental Angiogenesis via the PDGF-BB and STAT3 Pathways1 , 2015, Biology of reproduction.

[12]  M. Dunowska,et al.  Genomic characterisation of the feline sarcoid-associated papillomavirus and proposed classification as Bos taurus papillomavirus type 14. , 2015, Veterinary microbiology.

[13]  O. Taglialatela‐Scafati,et al.  Ptaquiloside, the major carcinogen of bracken fern, in the pooled raw milk of healthy sheep and goats: an underestimated, global concern of food safety. , 2015, Journal of agricultural and food chemistry.

[14]  F. Mariz,et al.  Human papillomavirus vertical transmission: review of current data. , 2013, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[15]  M. Riccardi,et al.  Bovine papillomavirus type 2 infects the urinary bladder of water buffalo (Bubalus bubalis) and plays a crucial role in bubaline urothelial carcinogenesis. , 2013, The Journal of general virology.

[16]  A. Haug [Emerging diseases]. , 2013, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke.

[17]  O. Paciello,et al.  Productive Infection of Bovine Papillomavirus Type 2 in the Placenta of Pregnant Cows Affected with Urinary Bladder Tumors , 2012, PloS one.

[18]  J. Munday,et al.  Cutaneous Sarcoids in Captive African Lions Associated With Feline Sarcoid-Associated Papillomavirus Infection , 2011, Veterinary pathology.

[19]  S. Comazzi,et al.  PBMCs are additional sites of productive infection of bovine papillomavirus type 2. , 2011, The Journal of general virology.

[20]  E. Lane,et al.  Pathology and immunohistochemistry of papillomavirus-associated cutaneous lesions in Cape mountain zebra, giraffe, sable antelope and African buffalo in South Africa. , 2011, Journal of the South African Veterinary Association.

[21]  L. Nasir,et al.  Different contribution of bovine papillomavirus type 1 oncoproteins to the transformation of equine fibroblasts. , 2011, The Journal of general virology.

[22]  R. Somvanshi Papillomatosis in buffaloes: a less-known disease. , 2011, Transboundary and emerging diseases.

[23]  G. Saikumar,et al.  Detection of BPV-1 and -2 and quantification of BPV-1 by real-time PCR in cutaneous warts in cattle and buffaloes. , 2010, Transboundary and emerging diseases.

[24]  O. Paciello,et al.  A review of bovine urothelial tumours and tumour-like lesions of the urinary bladder. , 2010, Journal of comparative pathology.

[25]  A. Spurdle,et al.  Human papillomavirus DNA detected in peripheral blood samples from healthy Australian male blood donors , 2009, Journal of medical virology.

[26]  O. Paciello,et al.  Bovine Papillomavirus Type 1 DNA and E5 Oncoprotein Expression in Water Buffalo Fibropapillomas , 2009, Veterinary pathology.

[27]  E. Brambilla,et al.  Pathology and immunohistochemistry of lung cancer , 2009 .

[28]  A. Venuti,et al.  Detection of bovine papillomavirus type 2 in the peripheral blood of cattle with urinary bladder tumours: possible biological role. , 2008, The Journal of general virology.

[29]  E. P. Serafini,et al.  Transplacental transmission of Human Papillomavirus , 2008, Virology Journal.

[30]  C. Stanek,et al.  Peripheral blood mononuclear cells represent a reservoir of bovine papillomavirus DNA in sarcoid-affected equines. , 2008, The Journal of general virology.

[31]  Johanna Andrae,et al.  Role of platelet-derived growth factors in physiology and medicine. , 2008, Genes & development.

[32]  Claude Fauquet,et al.  Classification of papillomaviruses. , 2004, Virology.

[33]  Philippe Soriano,et al.  Roles of PDGF in animal development , 2003, Development.

[34]  M. Campo,et al.  Bovine papillomavirus type 4 in oesophageal papillomas of cattle from the south of Italy. , 2003, Journal of comparative pathology.

[35]  F. Arechavaleta-Velasco,et al.  Viral infection of the trophoblast: time to take a serious look at its role in abnormal implantation and placentation? , 2002, Journal of reproductive immunology.

[36]  S. Parry,et al.  The Mechanisms of Placental Viral Infection , 2001, Annals of the New York Academy of Sciences.

[37]  R. Schlegel,et al.  Expression of a transforming gene (E5) of bovine papillomavirus in sarcoids obtained from horses. , 2001, American journal of veterinary research.

[38]  G. Grindlay,et al.  Bovine papillomavirus type 4. , 1996, International journal of oncology.

[39]  M. Breen,et al.  Bovine papillomavirus type 4 in Australia. , 1995, Australian Veterinary Journal.

[40]  M. Campo,et al.  Association of bovine papillomavirus type 2 and bracken fern with bladder cancer in cattle. , 1992, Cancer research.

[41]  P. Spradbrow,et al.  Detection of papillomavirus DNA in precancerous lesions of the ears of sheep. , 1990, Veterinary microbiology.