Padayachee A, Sanders C M, Maitland N J
Oral and Dental Research Institute, Faculty of Dentistry, University of Stellenbosch, Tygerberg, South Africa.
J Oral Pathol Med. 1995 Aug;24(7):329-34. doi: 10.1111/j.1600-0714.1995.tb01194.x.
The polymerase chain reaction (PCR) and direct DNA sequencing have been used to identify strain variants of HPV types 2a/57 in formalin-fixed sections of human oral verrucae, where the virus had previously been detected by both immunofluorescence and in situ hybridization. By employing type-specific and type-common PCR primers we show that these lesions contain a mixture of viral DNAs which vary by up to 27% in DNA sequence, in a region where the variation between HPV types 2a and 57 is only 4%. The extra discriminatory power of fluorescent sequencing indicates that the lesions may also contain wild-type HPV2a/57 DNA which could provide a helper function for defective viral DNA molecules or indicate a mosaic origin for the lesions.
聚合酶链反应(PCR)和直接DNA测序已被用于在人类口腔疣的福尔马林固定切片中鉴定2a/57型人乳头瘤病毒(HPV)的菌株变体,此前通过免疫荧光和原位杂交均已在这些切片中检测到该病毒。通过使用型特异性和型通用PCR引物,我们发现这些病变包含多种病毒DNA的混合物,其DNA序列差异高达27%,而在该区域中,2a型和57型HPV之间的差异仅为4%。荧光测序的额外鉴别能力表明,这些病变可能还含有野生型HPV2a/57 DNA,其可为有缺陷的病毒DNA分子提供辅助功能,或表明这些病变具有镶嵌起源。