Wosiacki Sheila R, Claus Marlise P, Alfieri Alice F, Alfieri Amauri A
Laboratório de Virologia Animal, Departamento de Medicina Veterinária Preventiva, Universidade Estadual de Londrina, Londrina, PR, 86051-990, Brasil.
Mem Inst Oswaldo Cruz. 2006 Sep;101(6):635-8. doi: 10.1590/s0074-02762006000600009.
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%) urinary bladder. The rate of BPV-2 positive urinary bladders was 50% (11/22) for group A, 80% (24/30) for group B, and 10% (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% (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. These results suggest the BPV-2 involvement in the chronic enzootic haematuria aetiology and open the perspective of the development of new strategies for the control of this disease that is the major cause of economical losses in beef herds from many Brazilian geographical regions.
长期以来,人们一直认为牛乳头瘤病毒2型(BPV - 2)与因摄入蕨菜而引发的慢性地方流行性血尿的病因有关。然而,少数报告显示在牛的膀胱肿瘤中存在BPV - 2。本研究的目的是调查巴西牛群中患有慢性地方流行性血尿的牛膀胱中BPV - 2感染的情况。从巴西巴拉那州北部地区肉牛群的成年牛中收集了62个膀胱。根据临床和病理检查结果,将标本分为三组:A组由22个在患有慢性地方流行性血尿临床症状的牛尸检时收集的有宏观病变的膀胱组成;B组由30个在来自蕨菜流行地理区域的奶牛屠宰场收集的有宏观病变的膀胱组成;C组(对照组)由10个在无蕨菜地理区域从无症状牛收集的无宏观病变的膀胱组成。通过半巢式聚合酶链反应(PCR)检测,并设有内部对照,在36个(58%)膀胱中扩增出了长度为386 bp的BPV - 2 L1基因片段。A组BPV - 2阳性膀胱的比例为50%(11/22),B组为80%(24/30),C组(对照组)为10%(1/10)。在包括有宏观病变的膀胱样本的A组和B组中,阳性结果的比例为67%(35/52),两组中BPV - 2的检测率显著高于(P < 0.05)对照组。用Rsa I和Hae III酶进行的限制性片段长度多态性分析(RFLP)评估了BPV - 2扩增子的特异性。扩增牛线粒体基因组ND5基因626 bp片段的PCR内部对照在所有分析样本中均被扩增出来,排除了半巢式PCR中的假阴性或无效结果。这些结果表明BPV - 2与慢性地方流行性血尿的病因有关,并为开发控制这种疾病的新策略开辟了前景,这种疾病是巴西许多地理区域肉牛群经济损失的主要原因。