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采用通用且高度敏感的长片段 DNA PCR 策略鉴定新型人γ 乳头瘤病毒种 HPV156 的原型。

Identification of human papillomavirus type 156, the prototype of a new human gammapapillomavirus species, by a generic and highly sensitive PCR strategy for long DNA fragments.

机构信息

Instituto de Biología Molecular y Celular de Rosario (CONICET), Rosario, Argentina.

Area Virología, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Rosario, Argentina.

出版信息

J Gen Virol. 2013 Mar;94(Pt 3):524-533. doi: 10.1099/vir.0.048157-0. Epub 2012 Nov 7.

Abstract

This study developed a hanging-droplet long PCR, a generic and highly sensitive strategy to facilitate the identification of new human papillomavirus (HPV) genomes. This novel procedure used for the first time the hanging-droplet PCR technique for the amplification of long DNA fragments with generic primers targeting the L1 and E1 regions. It was first applied to the amplification of types belonging to the highly divergent genus Gammapapillovirus (γ-PV). The hanging-droplet long PCR was 100-fold more sensitive than a simple long PCR procedure, detecting as few as ten copies of HPV-4. Nineteen skin samples, potentially containing putative HPV types from the γ-PV genus, were also screened. The method identified four γ-PV genomic halves from new and previously described putative types, and made the full characterization of HPV-156 possible. This novel virus meets the criteria for a new species within the γ-PV genus, with nucleotide identities in the L1 ORF ranging from 58.3 to 67.3 % compared with representative types of the current γ-PV species. HPV-156 showed the highest identity to HPV-60 (67.3 %) from species γ-4, and was consistently closely related to it in both late- and early-gene-derived phylogenies. In conclusion, this report provides a versatile and highly sensitive approach that allowed identification of the prototype of a new species within the γ-PV genus. Its application with primers targeting the different genera in which both human and non-human PVs are distributed may facilitate characterization of the missing members of the family Papillomaviridae.

摘要

本研究开发了一种悬滴长 PCR 方法,这是一种通用且高度敏感的策略,可方便鉴定新的人乳头瘤病毒(HPV)基因组。该新方法首次将悬滴 PCR 技术用于通用引物靶向 L1 和 E1 区域的长 DNA 片段的扩增。该方法首先应用于高度分化的属γ-乳头瘤病毒(γ-PV)的型别扩增。与简单的长 PCR 程序相比,悬滴长 PCR 的灵敏度高 100 倍,可检测到低至 10 个 HPV-4 拷贝。还对 19 个皮肤样本进行了筛查,这些样本可能含有来自γ-PV 属的潜在 HPV 型。该方法从新的和以前描述的假定型别中鉴定出了四个γ-PV 基因组半部分,并使 HPV-156 的完整特征得以确定。这种新型病毒符合γ-PV 属内新种的标准,与 L1 ORF 中的核苷酸同一性与当前 γ-PV 种的代表型相比为 58.3-67.3%。HPV-156 与来自γ-4 种的 HPV-60 (67.3%)具有最高的同一性,并且在晚期和早期基因衍生的系统发育中始终与其密切相关。总之,本报告提供了一种通用且高度敏感的方法,可鉴定γ-PV 属内新种的原型。应用针对人类和非人类 PV 分布在不同属的引物,可能有助于描述缺失的乳头瘤病毒科成员。

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