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塞尔维亚患者的 EBV 相关单核细胞增多症和肿瘤中 LMP1 基因羧基末端序列的变异。

Carboxy-terminal sequence variation of LMP1 gene in Epstein-Barr-virus-associated mononucleosis and tumors from Serbian patients.

机构信息

Institute of Microbiology and Immunology, University of Belgrade, Serbia.

出版信息

J Med Virol. 2012 Apr;84(4):632-42. doi: 10.1002/jmv.23217.

DOI:10.1002/jmv.23217
PMID:22337303
Abstract

Seven strains of Epstein-Barr virus (EBV) are defined based on C-terminal sequence variations of the latent membrane protein 1 (LMP1). Some strains, especially those with a 30-bp deletion, are thought to be related to tumorigenic activity and geographical localization. The aims of the study were to determine the prevalence of different LMP1 strains and to investigate sequence variation in the C-terminal region of LMP1 in Serbian isolates. This study included 53 EBV-DNA-positive plasma and tissue block samples from patients with mononucleosis syndrome, renal transplantation, and tumors, mostly nasopharyngeal carcinoma. The sequence of the 506-bp fragment of LMP1 C terminus was used for phylogenetic analyses and identification of LMP1 strains, deletions, and mutations. The majority of isolates were non-deleted (66%), and the rest had 30-bp, rare 69-bp, or yet unknown 27-bp deletions, which were not related to malignant or non-malignant isolate origin. However, the majority of 69-bp deletion isolates were derived from patients with nasopharyngeal carcinoma. Less than five 33-bp repeats were found in the majority of non-deleted isolates (68.6%), whereas most 69-bp deletion isolates (75%) had five or six repeats. Serbian isolates were assigned to four LMP1 strains: B95-8 (32.1%), China 1 (24.5%), North Carolina (NC; 18.9%), and Mediterranean (Med; 24.5%). In NC isolates, three new mutations unique for this strain were identified. EBV EBNA2 genotypes 1 and 2 were both found, with dominance of genotype 1 (90.7%). This study demonstrated noticeable geographical-associated characteristics in the LMP1 C terminus of investigated isolates.

摘要

七种 Epstein-Barr 病毒 (EBV) 株系是基于潜伏膜蛋白 1 (LMP1) 的 C 末端序列变化来定义的。一些株系,特别是具有 30 个碱基对缺失的株系,被认为与肿瘤发生活性和地理定位有关。本研究的目的是确定不同 LMP1 株系的流行情况,并研究塞尔维亚分离株 LMP1 C 末端区的序列变异。本研究包括 53 份 EBV-DNA 阳性的血浆和组织块样本,来自单核细胞增多症综合征、肾移植和肿瘤患者,主要是鼻咽癌。使用 LMP1 C 末端的 506 个碱基对片段的序列进行系统发育分析和 LMP1 株系、缺失和突变的鉴定。大多数分离株为非缺失型(66%),其余的有 30 个碱基对、罕见的 69 个碱基对或尚未知的 27 个碱基对缺失,但与恶性或非恶性分离株的起源无关。然而,大多数 69 个碱基对缺失分离株来自鼻咽癌患者。在大多数非缺失型分离株中发现不到五个 33 个碱基对重复(68.6%),而大多数 69 个碱基对缺失分离株(75%)有五个或六个重复。塞尔维亚分离株被分配到四个 LMP1 株系:B95-8(32.1%)、中国 1(24.5%)、北卡罗来纳州(NC;18.9%)和地中海(Med;24.5%)。在 NC 分离株中,鉴定出了三个该株系特有的新突变。发现了 EBV EBNA2 基因型 1 和 2,其中基因型 1 占主导地位(90.7%)。本研究表明,在所研究的分离株中,LMP1 C 末端存在明显的与地理位置相关的特征。

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