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Published in: Archives of Virology 6/2018

01-06-2018 | Original Article

A teat papillomatosis case in a Damascus goat (Shami goat) in Hatay province, Turkey: a new putative papillomavirus?

Authors: Fırat Dogan, Selvi Deniz Dorttas, Seval Bilge Dagalp, Veysel Soydal Ataseven, Feray Alkan

Published in: Archives of Virology | Issue 6/2018

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Abstract

Papillomaviruses (PVs) are epitheliotropic viruses that cause benign proliferative lesions in the skin (warts or papillomas) and mucous membranes of their natural hosts. Recently, new PVs have been found in many animal species. The most common current approach for identifying novel PV types is based on PCR, using various consensus or degenerated primer (broad-range primers), designed on the basis of the multiple alignment of nucleotide or amino acid sequences of a large number of different human papillomaviruses (HPV). PVs have been classified according to the sequence similarity of one of their capsid proteins, L1, without taking into account other regions of the genome and without considering the phenotypic characteristics of the viral infection. In this study, we performed molecular detection and typing of a PV in a goat with teat papillomatosis. Firstly, PCR was performed using the FAP59/FAP64 and MY09/MY11 primer pairs for the L1 gene region. The PV DNA was found to be positive only with the FAP59/FAP64 primer pair. PV DNA was then tested with three primer sets in four different combinations (L2Bf/FAP64, L2Bf/L1Br, FAP59/FAP64, L1Bf/LCRBr) for the gene region encoding the L1, L2 and LCR proteins. The goat teat papilloma sample was amplified using FAP59/FAP64 primers and two primer pairs (L2Bf/FAP64 and L2Bf/L1Br). We obtained products matching approximately 604 bp of the L1 region of the virus. PV DNA was used for typing using sequence analysis/PCR with some type-specific primers for bovids, caprids and cervids. The results of the sequence analysis suggested one new putative PV type with sequence identity ranging from 46.45 to 80.09% to other known papillomaviruses, including Capra hircus papillomavirus (ChPV-2), bovine papillomavirus (BPV) 6, 7, 10, 11 and 12, Rangifer tarandus papillomavirus 3 (RtPV-3) and BPV-7Z (Alpine wild ruminant papillomavirus; Cervus elaphus papillomavirus). We therefore propose that this is the first identification of a new putative type, MG523274 (HTY-goat-TR2016), in a goat with teat papillomatosis. It is essential to identify PV types in different animal species and investigate their prevalence/distribution and clinical consequences in order to develop appropriate prophylactic and/or therapeutic procedures and to determine the interspecies transmission potential and evolution of PVs.
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Literature
1.
go back to reference Altschul SF, Madden TL, Schäffer AA (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 17:3389–3402CrossRef Altschul SF, Madden TL, Schäffer AA (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 17:3389–3402CrossRef
2.
go back to reference Antonsson A, Hansson BG (2002) Healthy skin of many animal species harbors papillomaviruses which are closely related to their human counterparts. J Virol 76:12537–12542CrossRefPubMedPubMedCentral Antonsson A, Hansson BG (2002) Healthy skin of many animal species harbors papillomaviruses which are closely related to their human counterparts. J Virol 76:12537–12542CrossRefPubMedPubMedCentral
3.
go back to reference Ataseven VS, Kanat Ö, Ergün Y (2016) Molecular identification of bovine papillomaviruses in dairy and beef cattle: first description of Xi- and Epsilonpapillomaviruses in Turkey. Turk J Vet Anim Sci 40(6):757–763CrossRef Ataseven VS, Kanat Ö, Ergün Y (2016) Molecular identification of bovine papillomaviruses in dairy and beef cattle: first description of Xi- and Epsilonpapillomaviruses in Turkey. Turk J Vet Anim Sci 40(6):757–763CrossRef
4.
go back to reference Bernard HU, Burk RD, Chen Z, van Doorslaer K, Hause H, de Villiers EM (2010) Classification of papillomaviruses (PVs) based on 189 PV types and proposal of taxonomic amendments. Virology 401:70–79CrossRefPubMedPubMedCentral Bernard HU, Burk RD, Chen Z, van Doorslaer K, Hause H, de Villiers EM (2010) Classification of papillomaviruses (PVs) based on 189 PV types and proposal of taxonomic amendments. Virology 401:70–79CrossRefPubMedPubMedCentral
5.
go back to reference Bilge Dagalp S, Dogan F, Farzanı TA, Salar S, Bastan A (2017) The genetic diversity of bovine papillomaviruses (BPV) from different papillomatosis cases in dairy cows in Turkey. Arch Virol 162:1507–1518CrossRef Bilge Dagalp S, Dogan F, Farzanı TA, Salar S, Bastan A (2017) The genetic diversity of bovine papillomaviruses (BPV) from different papillomatosis cases in dairy cows in Turkey. Arch Virol 162:1507–1518CrossRef
6.
go back to reference Bogaert L, Martens A, Kast W, Van Marck E, De Cock H (2010) Bovine papillomavirus DNA can be detected in keratinocytes of equine sarcoid tumors. Vet Microbiol 146:269–275CrossRefPubMed Bogaert L, Martens A, Kast W, Van Marck E, De Cock H (2010) Bovine papillomavirus DNA can be detected in keratinocytes of equine sarcoid tumors. Vet Microbiol 146:269–275CrossRefPubMed
7.
go back to reference Campo MS (2006) Bovine papillomavirus: old system, new lessons? In: Campo MS (ed) Papillomavirus research: from natural history to vaccine and beyond. Caister Academic Press, Poole, United Kingdom, pp 373–387 Campo MS (2006) Bovine papillomavirus: old system, new lessons? In: Campo MS (ed) Papillomavirus research: from natural history to vaccine and beyond. Caister Academic Press, Poole, United Kingdom, pp 373–387
8.
go back to reference Carvalho CCR, Batista MVA, Silva MAR, Balbino VQ, Freitas AC (2012) Detection of bovine papillomavirus types, co-infection and new BPV11 subtype in cattle. Transbound Emerg Dis 59:441–447CrossRefPubMed Carvalho CCR, Batista MVA, Silva MAR, Balbino VQ, Freitas AC (2012) Detection of bovine papillomavirus types, co-infection and new BPV11 subtype in cattle. Transbound Emerg Dis 59:441–447CrossRefPubMed
9.
go back to reference Claus MP, Lunardi M, Alfieri AF (2009) Identification of the recently described new type of bovine papillomavirus (BPV-8) in a Brazilian beef cattle herd. Pesqui Vet Bras 29:25–28CrossRef Claus MP, Lunardi M, Alfieri AF (2009) Identification of the recently described new type of bovine papillomavirus (BPV-8) in a Brazilian beef cattle herd. Pesqui Vet Bras 29:25–28CrossRef
10.
go back to reference Daszak P, Cunningham AA, Hyatt AD (2000) Emerging infectious diseases of wildlife—threats to biodiversity and human health. Science 287(5452):443CrossRefPubMed Daszak P, Cunningham AA, Hyatt AD (2000) Emerging infectious diseases of wildlife—threats to biodiversity and human health. Science 287(5452):443CrossRefPubMed
11.
go back to reference de Villiers EM, Fauquet C, Broker TR, Bernard HU, Hausen H (2004) Classification of papillomaviruses. Virology 1:17–27CrossRef de Villiers EM, Fauquet C, Broker TR, Bernard HU, Hausen H (2004) Classification of papillomaviruses. Virology 1:17–27CrossRef
12.
13.
go back to reference Erdélyi K, Bálint Á, Dencső L, Dán Á, Ursu K (2008) Characterisation of the first complete genome sequence of the roe deer (Capreolus capreolus) papillomavirus. Virus Res 135(2):307–311CrossRefPubMed Erdélyi K, Bálint Á, Dencső L, Dán Á, Ursu K (2008) Characterisation of the first complete genome sequence of the roe deer (Capreolus capreolus) papillomavirus. Virus Res 135(2):307–311CrossRefPubMed
14.
go back to reference Forslund O, Antonsson A, Nordin P (1999) A broad range of human papillomavirus types detected with a general PCR method suitable for analysis of cutaneous tumours and normal skin. J Gen Virol 80:2437–2443CrossRefPubMed Forslund O, Antonsson A, Nordin P (1999) A broad range of human papillomavirus types detected with a general PCR method suitable for analysis of cutaneous tumours and normal skin. J Gen Virol 80:2437–2443CrossRefPubMed
15.
go back to reference Freitas AC, Silva MAR, Jesus ALS, Mariz FC, Cordeiro MN, Albuquerque BMF, Batista MVA (2011) Recent insights into bovine papillomavirus. Afr J Microbiol Res 5(33):6004–6012 (31) CrossRef Freitas AC, Silva MAR, Jesus ALS, Mariz FC, Cordeiro MN, Albuquerque BMF, Batista MVA (2011) Recent insights into bovine papillomavirus. Afr J Microbiol Res 5(33):6004–6012 (31) CrossRef
17.
go back to reference Groff DE, Sundberg JP, Lancaster WD (1983) Extrachromosomal deer fibromavirus DNA in deer fibromas and virus-transformed mouse cells. Virology 131:545–550CrossRef Groff DE, Sundberg JP, Lancaster WD (1983) Extrachromosomal deer fibromavirus DNA in deer fibromas and virus-transformed mouse cells. Virology 131:545–550CrossRef
18.
go back to reference Hall TA (1999) BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser 41:95–98 Hall TA (1999) BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser 41:95–98
19.
go back to reference Jackson ME, Pennie WD, McCaffery RE, Smith KT, Grindlay GJ, Campo MS (1991) The B subgroup bovine papillomaviruses lack an identifiable E6 open reading frame. Mol Carcinog 4:382–387CrossRefPubMed Jackson ME, Pennie WD, McCaffery RE, Smith KT, Grindlay GJ, Campo MS (1991) The B subgroup bovine papillomaviruses lack an identifiable E6 open reading frame. Mol Carcinog 4:382–387CrossRefPubMed
20.
go back to reference Kumar P, Nagarajan N, Saikumar G, Arya RS, Somvanshi R (2013) Detection of bovine papilloma viruses in wart-like lesions of upper gastrointestinal tract of cattle and buffaloes. Transbound Emerg Dis 63:56–67 Kumar P, Nagarajan N, Saikumar G, Arya RS, Somvanshi R (2013) Detection of bovine papilloma viruses in wart-like lesions of upper gastrointestinal tract of cattle and buffaloes. Transbound Emerg Dis 63:56–67
21.
go back to reference Lambert PF, Baker CC, Howley PM (1988) The genetics of bovine papillomavirus type 1. Annu Rev Genet 22:235–258CrossRefPubMed Lambert PF, Baker CC, Howley PM (1988) The genetics of bovine papillomavirus type 1. Annu Rev Genet 22:235–258CrossRefPubMed
22.
go back to reference Lindsey CL, Almeida ME, Vicari CF, Carvalho C, Yaguiu A, Freitas AC, Becak W, Stocco RC (2009) Bovine papillomavirus DNA in milk, blood, urine, semen, and spermatozoa of bovine papillomavirus-infected animals. Genet Mol Res 8:310–318CrossRefPubMed Lindsey CL, Almeida ME, Vicari CF, Carvalho C, Yaguiu A, Freitas AC, Becak W, Stocco RC (2009) Bovine papillomavirus DNA in milk, blood, urine, semen, and spermatozoa of bovine papillomavirus-infected animals. Genet Mol Res 8:310–318CrossRefPubMed
23.
go back to reference Literak I, Tomita Y, Ogawa T, Shirasawa H, Smid B, Novotny L, Adamec M (2006) Papilomatosis in a European bison. J Wildl Dis 42:149–153CrossRefPubMed Literak I, Tomita Y, Ogawa T, Shirasawa H, Smid B, Novotny L, Adamec M (2006) Papilomatosis in a European bison. J Wildl Dis 42:149–153CrossRefPubMed
24.
go back to reference Löhr CV, Juan-Sallés C, Rosas-Rosas A, Parás García A, Garner MM, Teifk JP (2005) Sarcoids in captive zebras (Equus burchellii): association with bovine papillomavirus type 1 infection. J Zoo Wildl Med 36:74–81CrossRefPubMed Löhr CV, Juan-Sallés C, Rosas-Rosas A, Parás García A, Garner MM, Teifk JP (2005) Sarcoids in captive zebras (Equus burchellii): association with bovine papillomavirus type 1 infection. J Zoo Wildl Med 36:74–81CrossRefPubMed
25.
go back to reference Lunardi M, Claus MP, Alfieri AA, Fungaro MHP, Alfieri AF (2010) Phylogenetic position of an uncharacterized Brazilian strain of bovine papillomavirus in the genus Xipapillomavirus based on sequencing of the L1 open reading frame. Genet Mol Biol 33(4):745–749CrossRefPubMedPubMedCentral Lunardi M, Claus MP, Alfieri AA, Fungaro MHP, Alfieri AF (2010) Phylogenetic position of an uncharacterized Brazilian strain of bovine papillomavirus in the genus Xipapillomavirus based on sequencing of the L1 open reading frame. Genet Mol Biol 33(4):745–749CrossRefPubMedPubMedCentral
26.
go back to reference Lunardi M, de Alcantara BK, Otonel RA, Rodrigues WB, Alfieri AF, Alfieri AA (2013) Bovine papillomavirus type 13 DNA in equine sarcoids. J Clin Microbiol 51:2167–2171CrossRefPubMedPubMedCentral Lunardi M, de Alcantara BK, Otonel RA, Rodrigues WB, Alfieri AF, Alfieri AA (2013) Bovine papillomavirus type 13 DNA in equine sarcoids. J Clin Microbiol 51:2167–2171CrossRefPubMedPubMedCentral
27.
go back to reference Maiolino PA, Ozkul A, Sepici-Dincel A, Roperto F, Yucel G, RussoV Urraro C, Luca R, Riccardi MG, Martano M, Borzacchiello G, Esposito I, Roperto S (2013) Bovine papillomavirus type 2 infection and microscopic patterns of urothelial tumors of the urinary bladder in water buffaloes. Biomed Res Int 146:269–275 Maiolino PA, Ozkul A, Sepici-Dincel A, Roperto F, Yucel G, RussoV Urraro C, Luca R, Riccardi MG, Martano M, Borzacchiello G, Esposito I, Roperto S (2013) Bovine papillomavirus type 2 infection and microscopic patterns of urothelial tumors of the urinary bladder in water buffaloes. Biomed Res Int 146:269–275
28.
go back to reference Manni V, Ropertob F, Di Guardoc G, Galatid D, Condoleoc RU, Venutia A (1998) Presence of papillomavirus-like DNA sequences in cutaneous fibropapillomas of the goat udder. Vet Microbiol 61(1–2):1–6CrossRefPubMed Manni V, Ropertob F, Di Guardoc G, Galatid D, Condoleoc RU, Venutia A (1998) Presence of papillomavirus-like DNA sequences in cutaneous fibropapillomas of the goat udder. Vet Microbiol 61(1–2):1–6CrossRefPubMed
29.
go back to reference Manos MM, Ting Y, Wright DK, Lewis AJ, Broker TR, Wolinsky SM (1989) The use of polymerase chain reaction amplification for the detection of genital human papillomaviruses. Cancer Cell 7:209–214 Manos MM, Ting Y, Wright DK, Lewis AJ, Broker TR, Wolinsky SM (1989) The use of polymerase chain reaction amplification for the detection of genital human papillomaviruses. Cancer Cell 7:209–214
30.
go back to reference Mengual-Chulia B, Garcia-Perez R, Gottschling M, Nindl I, Bravo IG (2012) Novel animal papillomavirus sequences and accurate phylogenetic placement. Mol Phylogenet Evol 65:883–891CrossRefPubMed Mengual-Chulia B, Garcia-Perez R, Gottschling M, Nindl I, Bravo IG (2012) Novel animal papillomavirus sequences and accurate phylogenetic placement. Mol Phylogenet Evol 65:883–891CrossRefPubMed
31.
go back to reference Moreno-Lopez J, Pettersson U, Dinter Z, Philipson L (1981) Characterization of a papilloma virus from the European elk (EEPV). Virology 112:589–595CrossRefPubMed Moreno-Lopez J, Pettersson U, Dinter Z, Philipson L (1981) Characterization of a papilloma virus from the European elk (EEPV). Virology 112:589–595CrossRefPubMed
32.
go back to reference Moreno-Lopez J, Ahola H, Eriksson A, Bergman P, Pettersson U (1987) Reindeer papillomavirus transforming properties correlate with a highly conserved E5 region. J Virol 61:3394–3400PubMedPubMedCentral Moreno-Lopez J, Ahola H, Eriksson A, Bergman P, Pettersson U (1987) Reindeer papillomavirus transforming properties correlate with a highly conserved E5 region. J Virol 61:3394–3400PubMedPubMedCentral
33.
go back to reference Moar MH, Jarrett WFH (1985) A cutaneous fibropapilloma from a red deer (Cervus elaphus) associated with a papillomavirus. Intervirology 24:108–118CrossRefPubMed Moar MH, Jarrett WFH (1985) A cutaneous fibropapilloma from a red deer (Cervus elaphus) associated with a papillomavirus. Intervirology 24:108–118CrossRefPubMed
34.
go back to reference Munger K, Howley PM (2002) Human papillomavirus immortalization and transformation functions. Virus Res 89:213–228CrossRefPubMed Munger K, Howley PM (2002) Human papillomavirus immortalization and transformation functions. Virus Res 89:213–228CrossRefPubMed
35.
go back to reference Munday JS, Knight CG (2010) Amplification of feline sarcoidassociated papillomavirus DNA sequences from bovine skin. Vet Dermatol 21:341–344CrossRefPubMed Munday JS, Knight CG (2010) Amplification of feline sarcoidassociated papillomavirus DNA sequences from bovine skin. Vet Dermatol 21:341–344CrossRefPubMed
36.
go back to reference Nasir L, Campo MS (2008) Bovine papillomaviruses: their role in the aetiology of cutaneous tumours of bovids and equids. Vet Dermatol 19:243–254CrossRefPubMed Nasir L, Campo MS (2008) Bovine papillomaviruses: their role in the aetiology of cutaneous tumours of bovids and equids. Vet Dermatol 19:243–254CrossRefPubMed
37.
go back to reference Ogawa T, Tomita Y, Okada M, Schinozaki K, Kubonoya H, Kaiho I, Shirisawa H (2004) Broad-spectrum detection of papillomaviruses in bovine teat papillomas and healthy teat skin. J Gen Virol 85:2191–2197CrossRefPubMed Ogawa T, Tomita Y, Okada M, Schinozaki K, Kubonoya H, Kaiho I, Shirisawa H (2004) Broad-spectrum detection of papillomaviruses in bovine teat papillomas and healthy teat skin. J Gen Virol 85:2191–2197CrossRefPubMed
38.
go back to reference Pangty K, Singh S, Goswami R, Saikumar G, Somvanshi R (2010) Detection of BPV-1 and -2 and quantification of BPV-1 by real-time PCR in cutaneous warts in cattle and buffaloes. Transbound Emerg Dis 57:185–196CrossRefPubMed Pangty K, Singh S, Goswami R, Saikumar G, Somvanshi R (2010) Detection of BPV-1 and -2 and quantification of BPV-1 by real-time PCR in cutaneous warts in cattle and buffaloes. Transbound Emerg Dis 57:185–196CrossRefPubMed
40.
go back to reference Roperto S, Russo V, Ozkul A, Corteggio A, Sepici-Dincel A, Catoi C, Esposito I, Riccardi MG, Urraro C, Luca R, Ceccarelli DM, Longo M, Roperto F (2013) Productive infection of bovine papillomavirus type 2 in the urothelial cells of naturally occurring urinary bladder tumors in cattle and water buffaloes. PLoS One 8:e62227CrossRefPubMedPubMedCentral Roperto S, Russo V, Ozkul A, Corteggio A, Sepici-Dincel A, Catoi C, Esposito I, Riccardi MG, Urraro C, Luca R, Ceccarelli DM, Longo M, Roperto F (2013) Productive infection of bovine papillomavirus type 2 in the urothelial cells of naturally occurring urinary bladder tumors in cattle and water buffaloes. PLoS One 8:e62227CrossRefPubMedPubMedCentral
41.
go back to reference Ruiz de Ybáñez MR, Martínez-Carrasco C, Alonso FD, León L (2009) Lungworm infection of wild ruminants in the Sierras de Cazorla, Segura and Villas Natural Park (Jaén, España). Acta Parasitol Port 16:184–185 Ruiz de Ybáñez MR, Martínez-Carrasco C, Alonso FD, León L (2009) Lungworm infection of wild ruminants in the Sierras de Cazorla, Segura and Villas Natural Park (Jaén, España). Acta Parasitol Port 16:184–185
42.
go back to reference Sambrook J, Russell DW (2001) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, New York Sambrook J, Russell DW (2001) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, New York
43.
go back to reference Santos EUD, Silva MAR, Pontes NE, Coutinho LCA, Paiva SSL, Castro RS, Freitas AC (2016) Detection of different bovine papillomavirus types and co-infection in bloodstream of cattle. Transbound Emerg Dis 63:103–108CrossRef Santos EUD, Silva MAR, Pontes NE, Coutinho LCA, Paiva SSL, Castro RS, Freitas AC (2016) Detection of different bovine papillomavirus types and co-infection in bloodstream of cattle. Transbound Emerg Dis 63:103–108CrossRef
44.
go back to reference Savini F, Gallina L, Alberti A, Müller M, Scagliarini A (2016) Bovine papillomavirus type 7 in Italy: complete genomes and sequence variants. Virus Genes 52(2):253–260CrossRefPubMed Savini F, Gallina L, Alberti A, Müller M, Scagliarini A (2016) Bovine papillomavirus type 7 in Italy: complete genomes and sequence variants. Virus Genes 52(2):253–260CrossRefPubMed
45.
go back to reference Scagliarini A, Gallina L, Battilani M, Turrini F, Savini F, Lavazza A, Alberti A (2013) Cervus elaphus papillomavirus (CePV1): new insights on viral evolution in deer. Vet Microbiol 165(3):252–259CrossRefPubMed Scagliarini A, Gallina L, Battilani M, Turrini F, Savini F, Lavazza A, Alberti A (2013) Cervus elaphus papillomavirus (CePV1): new insights on viral evolution in deer. Vet Microbiol 165(3):252–259CrossRefPubMed
46.
go back to reference Silva MS, Weiss M, Brum MCS, Anjos BL, Torres FD, Weiblen R, Flores EF (2010) Molecular identification of bovine papillomaviruses associated with cutaneous warts in southern Brazil. J Vet Diagn Investig 22:603–606CrossRef Silva MS, Weiss M, Brum MCS, Anjos BL, Torres FD, Weiblen R, Flores EF (2010) Molecular identification of bovine papillomaviruses associated with cutaneous warts in southern Brazil. J Vet Diagn Investig 22:603–606CrossRef
47.
go back to reference Silvestre O, Borzacchiello G, Nava D, Iovane D, Russo V, Vecchio D, D’Ausilio F, Gault EA, Campo MS, Paciello O (2009) Bovine papillomavirus type 1 DNA and E5 oncoprotein expression in water buffalo fibropapillomas. Vet Pathol 46:636–641CrossRefPubMed Silvestre O, Borzacchiello G, Nava D, Iovane D, Russo V, Vecchio D, D’Ausilio F, Gault EA, Campo MS, Paciello O (2009) Bovine papillomavirus type 1 DNA and E5 oncoprotein expression in water buffalo fibropapillomas. Vet Pathol 46:636–641CrossRefPubMed
48.
go back to reference Simeonea P, Romanuccib M, Rizzoa C, Brandia R, Malatestab D, Di Guardob G, Bongiovannib L, Salda LD, Venuti A (2008) Papillomaviruses in multiple tumours of twin goats. Open Vet Sci J 2:33–36CrossRef Simeonea P, Romanuccib M, Rizzoa C, Brandia R, Malatestab D, Di Guardob G, Bongiovannib L, Salda LD, Venuti A (2008) Papillomaviruses in multiple tumours of twin goats. Open Vet Sci J 2:33–36CrossRef
49.
go back to reference Singh V, Somvanshi R, Tiwari AK (2009) Papillomatosis in Indian cattle: occurance and etiopathology. Indian J Vet Pathol 33:52–57 Singh V, Somvanshi R, Tiwari AK (2009) Papillomatosis in Indian cattle: occurance and etiopathology. Indian J Vet Pathol 33:52–57
50.
go back to reference Smits SL, Schapendonk CM, van Leeuwen M, Kuiken T, Bodewes R, Raj VS, Haegmans BL, das Neves CG, Tryland M, Osterhaus AD (2013) Identification and characterization of two novel viruses in ocular infections in reindeer. PloS One 8(7):e69711CrossRefPubMedPubMedCentral Smits SL, Schapendonk CM, van Leeuwen M, Kuiken T, Bodewes R, Raj VS, Haegmans BL, das Neves CG, Tryland M, Osterhaus AD (2013) Identification and characterization of two novel viruses in ocular infections in reindeer. PloS One 8(7):e69711CrossRefPubMedPubMedCentral
51.
go back to reference Tamura K, Dudley J, Nei M, Kumar S (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28:2731–2739CrossRefPubMedPubMedCentral Tamura K, Dudley J, Nei M, Kumar S (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28:2731–2739CrossRefPubMedPubMedCentral
52.
go back to reference Tan MT, Yildirim Y, Sozmen M, Bilge Dagalp S, Yilmaz V, Kirmizigul AH, Gokce E (2012) A histopathological, ımmunohistochemical and molecular study of cutaneous bovine papillomatosis. Kafkas Univ Vet Fak Derg 18:739–744 Tan MT, Yildirim Y, Sozmen M, Bilge Dagalp S, Yilmaz V, Kirmizigul AH, Gokce E (2012) A histopathological, ımmunohistochemical and molecular study of cutaneous bovine papillomatosis. Kafkas Univ Vet Fak Derg 18:739–744
53.
go back to reference Terai M, DeSalle R, Burk RD (2002) Lack of canonical E6 and E7 open reading frames in bird papillomaviruses: Fringilla coelebs papillomavirus and Psittacus erithacus timneh papillomavirus. J Virol 76:10020–10023CrossRefPubMedPubMedCentral Terai M, DeSalle R, Burk RD (2002) Lack of canonical E6 and E7 open reading frames in bird papillomaviruses: Fringilla coelebs papillomavirus and Psittacus erithacus timneh papillomavirus. J Virol 76:10020–10023CrossRefPubMedPubMedCentral
54.
go back to reference Van Dyk E, Bosman AM, van Wilpe E, Williams JH, Bengis RG, vanHeerden J, Venter EH (2011) Detection and characterisation of papillomavirus in skin lesions of giraffe and sable antelope in South Africa. J S Afr Vet Assoc 82(2):80–85PubMed Van Dyk E, Bosman AM, van Wilpe E, Williams JH, Bengis RG, vanHeerden J, Venter EH (2011) Detection and characterisation of papillomavirus in skin lesions of giraffe and sable antelope in South Africa. J S Afr Vet Assoc 82(2):80–85PubMed
55.
go back to reference Van Doorslaer Rector A, Vos P, van Ranst M (2006) Genetic characterization of the Capra hircus papillomavirus: A novel close-to-root artiodactyl papillomavirus. Virus Res 118:164–169CrossRefPubMed Van Doorslaer Rector A, Vos P, van Ranst M (2006) Genetic characterization of the Capra hircus papillomavirus: A novel close-to-root artiodactyl papillomavirus. Virus Res 118:164–169CrossRefPubMed
Metadata
Title
A teat papillomatosis case in a Damascus goat (Shami goat) in Hatay province, Turkey: a new putative papillomavirus?
Authors
Fırat Dogan
Selvi Deniz Dorttas
Seval Bilge Dagalp
Veysel Soydal Ataseven
Feray Alkan
Publication date
01-06-2018
Publisher
Springer Vienna
Published in
Archives of Virology / Issue 6/2018
Print ISSN: 0304-8608
Electronic ISSN: 1432-8798
DOI
https://doi.org/10.1007/s00705-018-3781-2

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