ABSTRACT
Bovine papillomavirus (BPV) DNA sequences were detected in different tissues, in addition to epithelium. Cytogenetic abnormalities were observed in blood lymphocytes. The presence of more than one virus in a single tissue is a difficult aspect to evaluate, especially when the DNA sequences are detected in tissues that are not specifically targeted by the virus. BPV and bovine leukemia virus (BLV) are clastogenic, causing chromosome aberrations in peripheral blood lymphocytes. In the present study, we investigated the simultaneous presence of DNA sequences of both viruses and the possibility of vertical transmission and compared the types of chromosome aberrations related to viral action. BPV 1, 2, and 4 DNA sequences were found in three females of the herd and in their offspring. BLV DNA sequences were not detected in their progeny. A newborn calf that was negative for BLV infection showed specific chromosome rearrangements possibly related to the effect of infection with BPV.
Subject(s)
Animals , Female , Cytogenetic Analysis/methods , In Situ Hybridization/methods , Bovine papillomavirus 1/genetics , Leukemia Virus, Bovine/genetics , Animals, Newborn , Cattle , Chromosome Aberrations , Chromosome Banding , Papillomavirus Infections/diagnosis , Papillomavirus Infections/veterinary , Papillomavirus Infections/virology , Karyotyping , Enzootic Bovine Leukosis/diagnosis , Enzootic Bovine Leukosis/virology , Polymerase Chain Reaction , Bovine papillomavirus 1/isolation & purification , Leukemia Virus, Bovine/isolation & purificationABSTRACT
Bovine papillomatosis is a common viral infection in Brazil that is caused by a bovine papillomavirus(BPV). Dissemination is by direct contact between infected animals, although the investigation of othermodes of transmission is a very important aspect in the management of this condition. BPV DNA sequenceshave been detected in many tissues by using the polymerase chain reaction. In this work, we used in situhybridization to detect BPV DNA sequences in bovine reproductive tissues and cells. The detection ofBPV in these tissues strongly suggests that these sequences could be an important alternative of viraltransmission that could contribute to the widespread incidence of bovine papillomatosis and its complexpathology. Alternatively, the viral sequences could result from cell apoptosis and may therefore not bedirectly involved in the infection.
Subject(s)
Animals , Male , Female , Cattle , Apoptosis , Bovine papillomavirus 1 , In Situ Hybridization/veterinary , In Situ Hybridization , Papillomavirus Infections , Bovine papillomavirus 1/genetics , Papilloma/pathology , Papilloma/diagnosis , Papilloma/genetics , Papilloma/veterinaryABSTRACT
The bovine papillomavirus type 2 (BPV-2) involvement in the aetiology of chronic enzootic haematuria associated to bracken fern ingestion has been suggested for a long time. However, a few reports have shown the presence of the BPV-2 in urinary bladder tumors of cattle. The aim of this study was to investigate the presence of the BPV-2 infection in the urinary bladder of cattle with chronic enzootic haematuria in Brazilian cattle herds. Sixty-two urinary bladders were collected from adult cattle in beef herds from the north region of the state of Paraná, Brazil. According to clinical and pathological finds the specimens were distributed in three groups: the group A was constituted by 22 urinary bladders with macroscopic lesions collected at necropsy of cattle with clinical signs of chronic enzootic haematuria; the group B by 30 urinary bladders with macroscopic lesions collected in a slaughterhouse of cows coming from bracken fern-endemic geographical region; and the group C (control) by 10 urinary bladders without macroscopic lesions collected from asymptomatic cattle in a bracken fern-free geographical region. By a semi-nested polymerase chain reaction (PCR) assay, with an internal control, a fragment of the BPV-2 L1 gene with 386 bp length was amplified in 36 (58 percent) urinary bladder. The rate of BPV-2 positive urinary bladders was 50 percent (11/22) for group A, 80 percent (24/30) for group B, and 10 percent (1/10) for group C (control). The rate of the positive results found in groups A and B that included urinary bladder samples with macroscopic lesions was 67 percent (35/52) and the detection of the BPV-2 in both groups was significantly higher (P < 0.05) than in the control group. RFLP with Rsa I and Hae III enzymes evaluated the specificity of the BPV-2 amplicons. The PCR internal control that amplified a 626 bp fragment of the ND5 gene of the bovine mitochondrial genome was amplified in all analyzed samples and excluded false-negatives or invalid results in the semi-nested PCR...