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多中心Castleman 病和卡波西肉瘤相关疱疹病毒(KSHV)相关炎症细胞因子综合征患者中 Kaposi 肉瘤相关疱疹病毒(KSHV)microRNAs 的序列分析。

Sequence analysis of Kaposi sarcoma-associated herpesvirus (KSHV) microRNAs in patients with multicentric Castleman disease and KSHV-associated inflammatory cytokine syndrome.

机构信息

National Cancer Institute, Frederick, MD, USA.

出版信息

J Infect Dis. 2012 Jun;205(11):1665-76. doi: 10.1093/infdis/jis249. Epub 2012 Mar 23.

DOI:10.1093/infdis/jis249
PMID:22448005
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3415855/
Abstract

BACKGROUND

Kaposi sarcoma-associated herpesvirus (KSHV) encodes 12 pre-microRNAs that yield 25 mature microRNAs. We previously reported phylogenetic analysis of the microRNA-coding region of KSHV from Kaposi sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castleman disease (MCD) patients. We observed a high level of conservation for most sequences but also a divergent cluster of 5 KSHV sequences, including 2 from MCD patients.

METHODS

KSHV microRNA sequences from 23 MCD patients and 7 patients with a newly described KSHV-associated inflammatory cytokine syndrome (KICS) were examined by amplification, cloning, and sequencing of a 646-bp fragment of K12/T0.7 encoding microRNA-K12-10 and microRNA-K12-12 and a 2.8-kbp fragment containing the remaining 10 pre-microRNAs.

RESULTS

Phylogenetic analysis showed a distinct variant cluster consisting exclusively of MCD and KICS patients in all trees. Pearson χ(2) analysis revealed that 40 single-nucleotide polymorphisms (SNPs) at various loci were significantly associated with MCD and KICS risk. Cluster analysis of these SNPs generated several combinations of 3 SNPs as putative indicators of MCD and KICS risk.

CONCLUSIONS

These findings show that MCD and KICS patients frequently have unusual KSHV microRNA sequences and suggest an association between the observed sequence variation and risk of MCD and KICS.

摘要

背景

卡波西肉瘤相关疱疹病毒(KSHV)编码 12 个前 microRNA,可产生 25 个成熟的 microRNA。我们之前报道了卡波西肉瘤(KS)、原发性渗出性淋巴瘤(PEL)和多中心卡斯特曼病(MCD)患者的 KSHV 微 RNA 编码区的系统发育分析。我们观察到大多数序列高度保守,但也存在一个包含 5 个 KSHV 序列的分化簇,包括来自 MCD 患者的 2 个序列。

方法

通过扩增、克隆和测序 K12/T0.7 编码 microRNA-K12-10 和 microRNA-K12-12 的 646bp 片段以及包含其余 10 个前 microRNA 的 2.8kbp 片段,检查了 23 名 MCD 患者和 7 名新描述的 KSHV 相关炎症细胞因子综合征(KICS)患者的 KSHV 微 RNA 序列。

结果

系统发育分析显示,在所有树中,独特的变异簇仅由 MCD 和 KICS 患者组成。Pearson χ(2)分析显示,各种位置的 40 个单核苷酸多态性(SNP)与 MCD 和 KICS 风险显著相关。对这些 SNP 的聚类分析产生了几个 3SNP 的组合,作为 MCD 和 KICS 风险的潜在指标。

结论

这些发现表明,MCD 和 KICS 患者经常具有不寻常的 KSHV 微 RNA 序列,并提示观察到的序列变异与 MCD 和 KICS 风险之间存在关联。

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