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A human papillomavirus related to human papillomavirus MM7/LVX82 produces distinct histological abnormalities in human foreskin implants grown as athymic mouse xenografts.

机译:与人乳头瘤病毒MM7 / LVX82相关的人乳头瘤病毒在作为无胸腺小鼠异种移植物生长的人包皮植入物中产生明显的组织学异常。

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Studies of human papillomaviruses (HPVs) are hampered by the lack of a conventional culture system because HPV completes its life cycle only in fully differentiated human tissue. To overcome this obstacle, the athymic mouse xenograft system has been used to study the pathogenesis of HPV 11 and to develop neutralizing assays for vaccine development. Recently, HPV 40 has been produced in this system, and HPV 16 has been produced using mice with severe combined immune deficiency. To identify and characterize additional genital HPV types for similar studies, condylomata acuminata lesions containing a high copy number of HPV and detectable L1 major capsid protein were used to prepare infectious virus stocks. Human foreskin fragments were infected with the virus preparations and implanted under the renal capsules of athymic mice. After 5 months of growth, implant tissue was removed and processed for studies to detect HPV infection. Evidence of HPV infection was noted in some of the implants, but in contrast to HPV 11-infected epithelium, the implants derived from the new virus preparations contained a lesser degree of acanthosis, less developed koilocytosis, and a reduced number of preserved nuclei in the hyperkeratotic material within the cyst lining. The L1 consensus region was amplified by polymerase chain reaction from implant DNA and sequenced. Alignment of the amplified sequences with those in the HPV sequence database showed that the 452-bp amplimer was closely related but not identical to HPV LVX82 and HPV MM7 (also called Pap 291). The entire 7.9-kb genome was amplified by polymerase chain reaction and cloned. The presence of virions of the new isolate (named HPV IU) in the implants was verified by immunohistochemical detection of L1 major capsid protein and by demonstration of virion particles by electron microscopy. A second extract was made from one of the new implants and used to successfully propagate HPV IU. These experiments demonstrate that experimental infection of human epithelium with the new isolate, HPV IU, is associated with histological abnormalities that differ in potentially important ways from the changes observed in experimental HPV 11 infection. Copyright 1998 Academic Press.
机译:缺乏常规培养系统阻碍了人类乳头瘤病毒(HPV)的研究,因为HPV仅在完全分化的人类组织中完成了其生命周期。为克服这一障碍,无胸腺小鼠异种移植系统已用于研究HPV 11的发病机理并开发用于疫苗开发的中和测定法。最近,已经在该系统中产生了HPV 40,并且已经使用具有严重的联合免疫缺陷的小鼠产生了HPV 16。为了鉴定和表征其他生殖器HPV类型以进行类似研究,使用含有高拷贝数HPV和可检测的L1主要衣壳蛋白的尖锐湿疣病变来制备传染性病毒原种。用病毒制剂感染人包皮片段,并将其植入无胸腺小鼠的肾囊下。生长5个月后,取出植入物组织并进行处理以进行研究以检测HPV感染。在某些植入物中发现了HPV感染的证据,但与HPV 11感染的上皮相比,源自新病毒制剂的植入物含有较少的棘皮症,较不发达的白细胞增多症,并且保留的核数目减少。囊壁内的角化过度物质。通过聚合酶链反应从植入物DNA扩增L1共有区并测序。扩增的序列与HPV序列数据库中的序列的比对表明452bp的扩增子紧密相关,但与HPV LVX82和HPV MM7(也称为Pap 291)不相同。通过聚合酶链反应扩增并克隆了整个7.9kb的基因组。通过对L1主要衣壳蛋白的免疫组织化学检测以及通过电子显微镜证实的病毒粒子颗粒,验证了植入物中新分离株(称为HPV IU)的病毒粒子的存在。从其中一种新植入物中提取了第二种提取物,并用于成功繁殖HPV IU。这些实验表明,新分离株HPV IU对人上皮的实验性感染与组织学异常有关,这种异常在潜在的重要方面与在实验性HPV 11感染中观察到的变化有所不同。版权所有1998学术出版社。

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