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豚鼠巨细胞病毒糖蛋白H基因的鉴定与特性分析

Identification and characterization of the guinea-pig cytomegalovirus glycoprotein H gene.

作者信息

Brady R C, Schleiss M R

机构信息

Division of Infectious Diseases, Children's Hospital Research Foundation, Cincinnati, Ohio, USA.

出版信息

Arch Virol. 1996;141(12):2409-24. doi: 10.1007/BF01718640.

DOI:10.1007/BF01718640
PMID:9526546
Abstract

Subunit vaccines which target viral envelope glycoproteins offer promise for the prevention of congenital cytomegalovirus (CMV) infection. The guinea pig model of CMV infection is uniquely well suited to testing vaccines for prevention of congenital infection, since, in contrast to other animal cytomegaloviruses, the guinea pig CMV (GPCMV) crosses the placenta, producing intrauterine infection. Antibody to the CMV glycoproteins B (gB) and H (gH) appears to be important in conferring protective immunity. Unfortunately, little is known about specific GPCMV envelope glycoproteins. Sequencing of GPCMV genome fragments was therefore undertaken to test whether GPCMV encodes a gH homologue. Partial sequencing of the Hind III A fragment of the GPCMV genome revealed an open reading frame of 2,169 nucleotides capable of encoding a protein of 723 amino acids. Computer matrix analyses demonstrated identity between this ORF and the gH coding sequences of other herpesviruses. The GPCMV gH ORF encodes 12 highly conserved cysteine residues, contains 9 potential N-linked glycosylation sites, and has a predicted M(r) of 81.6 kDa. Northern blot hybridizations with gH-specific probes identified an abundant 5.1 kb mRNA with expression kinetics of an "early" gene. A polyclonal antiserum raised against a synthetic peptide derived from the deduced amino acid sequence of the gH ORF identified a virion-associated protein with an approximate M(r) of 85-kDa, the putative GPCMV gH, in immunoblot assays.

摘要

针对病毒包膜糖蛋白的亚单位疫苗有望预防先天性巨细胞病毒(CMV)感染。CMV感染的豚鼠模型非常适合测试预防先天性感染的疫苗,因为与其他动物巨细胞病毒不同,豚鼠巨细胞病毒(GPCMV)可穿过胎盘,导致子宫内感染。针对CMV糖蛋白B(gB)和H(gH)的抗体似乎在赋予保护性免疫方面很重要。不幸的是,对于特定的GPCMV包膜糖蛋白知之甚少。因此,对GPCMV基因组片段进行测序,以测试GPCMV是否编码gH同源物。GPCMV基因组Hind III A片段的部分测序揭示了一个2169个核苷酸的开放阅读框,能够编码一个723个氨基酸的蛋白质。计算机矩阵分析表明,该开放阅读框与其他疱疹病毒的gH编码序列相同。GPCMV gH开放阅读框编码12个高度保守的半胱氨酸残基,包含9个潜在的N-连接糖基化位点,预测分子量为81.6 kDa。用gH特异性探针进行的Northern印迹杂交鉴定出一种丰富的5.1 kb mRNA,其表达动力学为“早期”基因。在免疫印迹分析中,针对从gH开放阅读框推导的氨基酸序列衍生的合成肽产生的多克隆抗血清鉴定出一种与病毒体相关的蛋白质,其分子量约为85 kDa,即推定的GPCMV gH。

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本文引用的文献

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截短的人巨细胞病毒gH与UL115基因产物或截短的人成纤维细胞生长因子受体共表达会导致gH转运至细胞表面。
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