[Detection of bovine papillomavirus DNA in equine sarcoids using the polymerase chain reaction (PCR)].
Abstract: Unfixed and formalin-fixed frozen sections and paraffin-sections of histopathologically confirmed sarcoids of 20 horses were studied in the PCR. The used set of primers was located in the E5 open reading frame fitting both to bovine papillomavirus 1 (BPV-1) and BPV-2. Independent of the quality of the used tissues BPV-DNA was detected in all 20 sarcoids. By cleaving with restriction endonuclease Bst XI it was shown that the DNA-sequences amplified by PCR were identical with that of BPV-1. The results support the general view that BPV play an important role in equine sarcoids.
Publication Date: 1991-06-01 PubMed ID: 1652932
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- English Abstract
- Journal Article
Summary
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The research article is about the study on detection of bovine papillomavirus DNA in horse sarcoids (tumours) using polymerase chain reaction (PCR).
Overview of the Research
- This research focuses on the use of Polymerase Chain Reaction (PCR), a technique used in molecular genetics to amplify particular DNA or RNA sequences, to detect Bovine Papillomavirus (BPV) DNA in horse sarcoids (tumors).
- The sarcoids, confirmed through histopathology, were taken from 20 different horses. Three different types of tissue samples were used: unfixed, formalin-fixed frozen sections, and paraffin-sections.
Process and Techniques Used
- A specific set of primers (short DNA sequences) designed to match BPV-1 and BPV-2 were used in the PCR. These were positioned in the E5 open reading frame—a portion of the virus genome where the transcription process begins.
- Through PCR, the researchers were able to identify the presence of BPV DNA in all of the sarcoid samples, regardless of the tissue types.
Findings of the Research
- The DNA sequences amplified through PCR were then subjected to the enzyme restriction endonuclease Bst XI. This enzyme is used to cut DNA at specific sequences, allowing the researchers to analyze the patterns of the DNA fragments.
- The results showed that the amplified DNA sequences were identical to BPV-1, thus indicating the presence of BPV-1 in horse sarcoids.
Implications of the Study
- This study supports the existing theory that Bovine Papillomavirus plays a significant role in the development of sarcoids in horses.
- The findings of the study can help in understanding the etiology of equine sarcoids, creating a foundation for development of preventive measures or possible treatments for this common equine skin disease.
Cite This Article
APA
Teifke JP, Weiss E.
(1991).
[Detection of bovine papillomavirus DNA in equine sarcoids using the polymerase chain reaction (PCR)].
Berl Munch Tierarztl Wochenschr, 104(6), 185-187.
Publication
Researcher Affiliations
- Institut für Veterinärpathologie, Justus-Liebig-Universität Giessen.
MeSH Terms
- Animals
- Base Sequence
- DNA, Viral / analysis
- DNA, Viral / chemistry
- Horse Diseases / microbiology
- Horses
- Molecular Sequence Data
- Papillomaviridae / genetics
- Papillomaviridae / isolation & purification
- Polymerase Chain Reaction
- Skin Neoplasms / microbiology
- Skin Neoplasms / veterinary
- Tumor Virus Infections / microbiology
- Tumor Virus Infections / veterinary
Citations
This article has been cited 5 times.- Lunardi M, de Alcântara BK, Otonel RA, Rodrigues WB, Alfieri AF, Alfieri AA. Bovine papillomavirus type 13 DNA in equine sarcoids.. J Clin Microbiol 2013 Jul;51(7):2167-71.
- Wobeser BK, Davies JL, Hill JE, Jackson ML, Kidney BA, Mayer MN, Townsend HG, Allen AL. Epidemiology of equine sarcoids in horses in western Canada.. Can Vet J 2010 Oct;51(10):1103-8.
- Belák S, Ballagi-Pordány A. Application of the polymerase chain reaction (PCR) in veterinary diagnostic virology.. Vet Res Commun 1993;17(1):55-72.
- Otten N, von Tscharner C, Lazary S, Antczak DF, Gerber H. DNA of bovine papillomavirus type 1 and 2 in equine sarcoids: PCR detection and direct sequencing.. Arch Virol 1993;132(1-2):121-31.
- Bloch N, Sutton RH, Spradbrow PB. Bovine cutaneous papillomas associated with bovine papillomavirus type 5.. Arch Virol 1994;138(3-4):373-7.
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