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利用专用DNA微阵列轻松快速检测高危型人乳头瘤病毒并进行基因分型。

Easy and fast detection and genotyping of high-risk human papillomavirus by dedicated DNA microarrays.

作者信息

Albrecht Valérie, Chevallier Anne, Magnone Virginie, Barbry Pascal, Vandenbos Fanny, Bongain André, Lefebvre Jean-Claude, Giordanengo Valérie

机构信息

Laboratoire de Virologie, Hôpital de l'Archet, BP 3079, 151 route de Saint-Antoine de Ginestière, 06200 Nice Cedex 3, France.

出版信息

J Virol Methods. 2006 Nov;137(2):236-44. doi: 10.1016/j.jviromet.2006.06.023. Epub 2006 Aug 1.

Abstract

Persistent cervical high-risk human papillomavirus (HPV) infection is correlated with an increased risk of developing a high-grade cervical intraepithelial lesion. A two-step method was developed for detection and genotyping of high-risk HPV. DNA was firstly amplified by asymmetrical PCR in the presence of Cy3-labelled primers and dUTP. Labelled DNA was then genotyped using DNA microarray hybridization. The current study evaluated the technical efficacy of laboratory-designed HPV DNA microarrays for high-risk HPV genotyping on 57 malignant and non-malignant cervical smears. The approach was evaluated for a broad range of cytological samples: high-grade squamous intraepithelial lesions (HSIL), low-grade squamous intraepithelial lesions (LSIL) and atypical squamous cells of high-grade (ASC-H). High-risk HPV was also detected in six atypical squamous cells of undetermined significance (ASC-US) samples; among them only one cervical specimen was found uninfected, associated with no histological lesion. The HPV oligonucleotide DNA microarray genotyping detected 36 infections with a single high-risk HPV type and 5 multiple infections with several high-risk types. Taken together, these results demonstrate the sensitivity and specificity of the HPV DNA microarray approach. This approach could improve clinical management of patients with cervical cytological abnormalities.

摘要

持续性宫颈高危型人乳头瘤病毒(HPV)感染与高级别宫颈上皮内瘤变风险增加相关。开发了一种用于检测高危型HPV并进行基因分型的两步法。首先在存在Cy3标记引物和dUTP的情况下通过不对称PCR扩增DNA。然后使用DNA微阵列杂交对标记的DNA进行基因分型。本研究评估了实验室设计的HPV DNA微阵列对57份恶性和非恶性宫颈涂片进行高危型HPV基因分型的技术效果。该方法针对广泛的细胞学样本进行了评估:高级别鳞状上皮内病变(HSIL)、低级别鳞状上皮内病变(LSIL)和高级别非典型鳞状细胞(ASC-H)。在6份意义不明确的非典型鳞状细胞(ASC-US)样本中也检测到了高危型HPV;其中仅发现1份宫颈标本未感染,且无组织学病变。HPV寡核苷酸DNA微阵列基因分型检测到36例单一高危型HPV感染和5例多种高危型HPV混合感染。综上所述,这些结果证明了HPV DNA微阵列方法的敏感性和特异性。该方法可改善宫颈细胞学异常患者的临床管理。

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