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卡波西肉瘤疱疹病毒扩展的ORF26基因座上的全局聚类模式和毒株变异评估。

Evaluation of global clustering patterns and strain variation over an extended ORF26 gene locus from Kaposi's sarcoma herpesvirus.

作者信息

Zong Jian-Chao, Kajumbula Henry, Boto William, Hayward Gary S

机构信息

Viral Oncology Program, Department of Oncology, Blunting Blaustein Cancer Research Building, Sydney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, MD 21231-1000, United States.

出版信息

J Clin Virol. 2007 Sep;40(1):19-25. doi: 10.1016/j.jcv.2007.06.013. Epub 2007 Aug 8.

Abstract

BACKGROUND

Small 233-bp or 330-bp DNA fragments of the ORF26 gene of human Kaposi's sarcoma herpesvirus (KSHV) have been used extensively to identify KSHV by PCR in clinical samples; to associate KSHV with novel diseases and to correlate KSHV strain differences with pathogenicity.

OBJECTIVES

We evaluated the nature, extent and source of nucleotide sequence variability among a large and diverse set of known KSHV-positive DNA samples.

STUDY DESIGN

Direct DNA PCR sequencing was carried out on 136 distinct Kaposi's sarcoma and primary effusion lymphoma-related samples from different geographic locations.

RESULTS

The presence of 26 diagnostic nucleotide polymorphisms across an expanded 965-bp PCR locus define eight distinct ORF26E genotypes, three being of Eurasian origin, one from the Pacific Rim, and five from Sub-Saharan Africa. Previous ambiguities between some genotype patterns in the 330-bp locus data are fully resolved.

CONCLUSIONS

This analysis provides an expanded database for understanding and evaluating ORF26 polymorphisms. In particular, the eight genotype clusters correlated with specific ethnic and geographic origins of the patients. Furthermore, the very low level of additional sporadic nucleotide variation found permits detection of spurious sequence errors or contamination present in some published data.

摘要

背景

人类卡波西肉瘤疱疹病毒(KSHV)的ORF26基因的233 bp或330 bp小DNA片段已被广泛用于通过聚合酶链反应(PCR)在临床样本中鉴定KSHV;将KSHV与新疾病相关联,并将KSHV毒株差异与致病性相关联。

目的

我们评估了大量不同的已知KSHV阳性DNA样本中核苷酸序列变异的性质、程度和来源。

研究设计

对来自不同地理位置的136个不同的卡波西肉瘤和原发性渗出性淋巴瘤相关样本进行直接DNA PCR测序。

结果

在一个扩展的965 bp PCR位点上存在26个诊断性核苷酸多态性,定义了8种不同的ORF26E基因型,其中3种来自欧亚大陆,1种来自环太平洋地区,5种来自撒哈拉以南非洲。330 bp位点数据中一些基因型模式之间以前的模糊性已完全解决。

结论

该分析为理解和评估ORF26多态性提供了一个扩展的数据库。特别是这8个基因型簇与患者的特定种族和地理来源相关。此外,发现的极低水平的额外散发性核苷酸变异允许检测一些已发表数据中存在的虚假序列错误或污染。

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