Chou S W, Dennison K M
Medical Service, VA Medical Center, Portland, OR 97207.
J Infect Dis. 1991 Jun;163(6):1229-34. doi: 10.1093/infdis/163.6.1229.
Nucleotide sequences of a part of the envelope glycoprotein B (gB) gene of human cytomegalovirus (CMV), encoding epitopes recognized by virus-neutralizing monoclonal antibodies, were determined for 12 distinct clinical strains of CMV after amplification of suitable templates using the polymerase chain reaction. Sequence analysis of this region (codons 384-717) revealed that the clinical strains and previously sequenced laboratory strains Towne and AD169 belong to one of four variant groups, each with a characteristic nucleotide and peptide sequence. Peptide homology was greater than 99% for strains within a group, and varied from 91% to 98% for strains in different groups. Variation was most frequent between codons 448 and 480. The gB group of a CMV strain could be determined by restriction analysis of a small target sequence amplified from viral genomic DNA, and an additional 28 clinical strains were grouped in this manner. The existence of a limited number of variants of gB among clinical strains facilitates analysis of biologic function and cross-reactivity of immune responses.
利用聚合酶链反应扩增合适模板后,测定了12种不同的人巨细胞病毒(CMV)临床分离株包膜糖蛋白B(gB)基因部分的核苷酸序列,该序列编码病毒中和单克隆抗体识别的表位。对该区域(密码子384 - 717)的序列分析表明,临床分离株以及先前测序的实验室毒株汤氏株(Towne)和AD169属于四个变异组之一,每个变异组都有其独特的核苷酸和肽序列。同一组内毒株的肽同源性大于99%,不同组毒株的肽同源性在91%至98%之间。密码子448和480之间的变异最为频繁。通过对从病毒基因组DNA扩增的小目标序列进行限制性分析,可以确定CMV毒株的gB组,另外28种临床分离株也用这种方法进行了分组。临床分离株中gB变异体数量有限这一情况有助于分析免疫反应的生物学功能和交叉反应性。