scholarly journals Case Study of Bovine Papilloma Virus in Aceh Cattle in Lhoknga Aceh Besar

Author(s):  
Budianto Panjaitan ◽  
Syafruddin ◽  
Roslizawaty ◽  
Muhammad Hasan ◽  
Herrialfian Herrialfian ◽  
...  
2021 ◽  
Vol 71 (1) ◽  
pp. 131-136
Author(s):  
Eroksuz Yesari ◽  
Abayli Hasan ◽  
Canpolat Ibrahim ◽  
Akdeniz Incili Canan ◽  
Karabulut Burak ◽  
...  

Abstract Sarcoid tumors were described by means of histopathological and molecular procedures in a 5-year-old donkey. Histopathological examination showed epithelial changes including hyperkeratosis, epithelial hyperplasia, koilocytosis, and rete peg formation. Neoplastic fibroblastic cells were plumb, large spindle to stellate and embedded in dense collagenous tissue. Results of Polymerase Chain Reaction and DNA sequence analysis showed that the etiological agent belonged to Bovine Papilloma Virus-II species in the delta papilloma virus genus. This case study represents the first report demonstrating the presence of Bovine Papilloma Virus-II in donkey sarcoid.


1986 ◽  
Vol 187 (4) ◽  
pp. 557-568 ◽  
Author(s):  
Patrick Matthias ◽  
Uta Boeger ◽  
Ulrich Danesch ◽  
Günther Schütz ◽  
Hans-Ulrich Bernard

Nature ◽  
1963 ◽  
Vol 199 (4897) ◽  
pp. 1016-1018 ◽  
Author(s):  
PAUL H. BLACK ◽  
JANET W. HARTLEY ◽  
WALLACE P. ROWE ◽  
ROBERT J. HUEBNER

1983 ◽  
Vol 3 (2) ◽  
pp. 233-240
Author(s):  
S Mitrani-Rosenbaum ◽  
L Maroteaux ◽  
Y Mory ◽  
M Revel ◽  
P M Howley

A 1.6-kilobase DNA segment of the genomic human interferon beta 1 (IF-beta 1) gene was inserted into each of two possible orientations at the single HindIII site of a recombinant plasmid pBPV69T, consisting of the 69% transforming region of the bovine papilloma virus type 1 (BPV-1) and a modified SalI-SalI fragment of plasmid pBR322. After cleavage of the pBR322 sequences from this recombinant, BPV69T-IF-beta 1 hybrid DNAs were transfected onto C127 mouse cells by the standard calcium precipitation technique. Mouse cells transformed by this hybrid DNA produced low levels of human IF-beta 1 constitutively and responded to induction with either inactivated Newcastle disease virus or polyriboinosinic acid-polyribocytidylic acid. The BPV69T-IF-beta 1 hybrid DNA was nonintegrated in the transformed mouse cells but had acquired DNA sequences as a result of the transfection. Accurate transcripts of the IF-beta 1 mRNA were detected in cells only after induction. When the IF-beta 1 gene was oriented in the plasmid in the same direction of transcription as the BPV-1 genome, transcription was promoted from within the BPV-1 sequences. These results indicate that the regulatory sequences responsible for the inducible expression of the human IF-beta 1 gene are present in the 1.6-kilobase genomic segment and that these sequences can function in a free extrachromosomal state linked to BPV-1 sequences.


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