Hukkanen V, Haarala M, Nurmi M, Klemi P, Kiilholma P
Department of Virology, University of Turku, Finland.
Urol Res. 1996;24(4):235-8. doi: 10.1007/BF00295898.
Microbes may be involved in the pathogenesis of interstitial cystitis (IC). Adenoviruses and BK virus (BKV) can infect epithelial cells in urinary bladder and they are causative agents for hemorrhagic cystitis. We therefore studied the presence of adenovirus and BKV genomes in urinary bladder tissue specimens of patients with IC using polymerase chain reaction (PCR) and in situ hybridization (ISH). Controls were specimens from cases with transitional cell carcinoma of the bladder. Nucleic acids were extracted from paraffin sections of the bladder tissue for PCR. Primers detecting all adenovirus types were used. In situ hybridization was carried out for the paraffin sections using digoxigenin-labeled DNA probes for adenovirus and BKV. The adenovirus DNA PCR was able to detect one to two infected cells/specimen. All the seven IC cases studied and six controls were negative for adenovirus DNA by PCR and ISH. The ISH test for BKV genomes was also considered negative in IC cases and controls. The specimens which were negative in PCR tests yielded a signal with beta-globin primers, thus being amplifiable. We conclude that adenovirus and BKV do not play a major pathogenetic role in interstitial cystitis.
微生物可能参与间质性膀胱炎(IC)的发病机制。腺病毒和BK病毒(BKV)可感染膀胱上皮细胞,它们是出血性膀胱炎的病原体。因此,我们使用聚合酶链反应(PCR)和原位杂交(ISH)研究了IC患者膀胱组织标本中腺病毒和BKV基因组的存在情况。对照为膀胱移行细胞癌病例的标本。从膀胱组织石蜡切片中提取核酸用于PCR。使用能检测所有腺病毒类型的引物。使用地高辛标记的腺病毒和BKV DNA探针,对石蜡切片进行原位杂交。腺病毒DNA PCR能够检测到每个标本中有1至2个感染细胞。通过PCR和ISH检测,所有7例研究的IC病例和6例对照的腺病毒DNA均为阴性。IC病例和对照中BKV基因组的ISH检测也被认为是阴性。PCR检测呈阴性的标本用β-珠蛋白引物产生信号,因此可被扩增。我们得出结论,腺病毒和BKV在间质性膀胱炎中不发挥主要致病作用。