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人类疱疹病毒7可能的染色体及种系整合。

Possible chromosomal and germline integration of human herpesvirus 7.

作者信息

Prusty Bhupesh K, Gulve Nitish, Rasa Santa, Murovska Modra, Hernandez Pilar Collado, Ablashi Dharam V

机构信息

Department of Microbiology, Biocenter, University of Würzburg, 97074 Würzburg, Germany.

August Kirchenstein Institute of Microbiology and Virology, Riga Stradins University, 1069 Riga, Latvia.

出版信息

J Gen Virol. 2017 Feb;98(2):266-274. doi: 10.1099/jgv.0.000692.

Abstract

Human herpesvirus 7 (HHV-7) is a betaherpesvirus, and is phylogenetically related to both HHV-6A and HHV-6B. The presence of telomeric repeat sequences at both ends of its genome should make it equally likely to integrate into the human telomere as HHV-6. However, numerous studies have failed to detect germline integration of HHV-7, suggesting an important difference between the HHV-6A/-6B and HHV-7 genomes. In search of possible germline integrated HHV-7, we developed a sensitive and quantitative real-time PCR assay and discovered that primers designed against some parts of the HHV-7 genome can frequently miss HHV-7 positive clinical samples even though they work efficiently in cell-culture-derived HHV-7 positive materials. Using a primer pair against the U90 ORF of HHV-7, we identified a possible case of germline integration of HHV-7 with one copy of viral genome per cell in both peripheral blood cells and hair follicles. Chromosomal integration of HHV-7 in these individuals was confirmed by fluorescence in situ hybridization analysis. Germline integration of HHV-7 was further confirmed by detection of ~2.6 copies of HHV-7 in the hair follicles of one of the parents. Our results shed light on the complex nature of the HHV-7 genome in human-derived materials in comparison to cell-culture-derived materials and show the need for stringent criteria in the selection of primers for epidemiological HHV-7 studies.

摘要

人类疱疹病毒7型(HHV - 7)是一种β疱疹病毒,在系统发育上与HHV - 6A和HHV - 6B均相关。其基因组两端存在端粒重复序列,这使其与HHV - 6一样,有同等可能性整合到人类端粒中。然而,众多研究未能检测到HHV - 7的种系整合,这表明HHV - 6A/ - 6B与HHV - 7基因组之间存在重要差异。为寻找可能的种系整合HHV - 7,我们开发了一种灵敏且定量的实时PCR检测方法,并发现针对HHV - 7基因组某些部分设计的引物,即便在细胞培养来源的HHV - 7阳性材料中能有效发挥作用,但在检测HHV - 7阳性临床样本时却常常出现漏检情况。使用一对针对HHV - 7 U90开放阅读框的引物,我们在一名个体的外周血细胞和毛囊中均鉴定出一个可能的HHV - 7种系整合案例,每个细胞含有一个病毒基因组拷贝。通过荧光原位杂交分析证实了这些个体中HHV - 7的染色体整合。通过检测其中一位家长毛囊中约2.6个HHV - 7拷贝,进一步证实了HHV - 7的种系整合。我们的研究结果揭示了与细胞培养来源材料相比,人类来源材料中HHV - 7基因组的复杂性质,并表明在进行HHV - 7流行病学研究时,引物选择需要严格的标准。

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