Department of Microbiology and Immunology, University of Leuven, Leuven, Belgium.
Virology. 2010 Aug 1;403(2):111-27. doi: 10.1016/j.virol.2010.04.004. Epub 2010 May 6.
RotaTeq is a pentavalent rotavirus vaccine that contains five human-bovine reassortant strains (designated G1, G2, G3, G4, and P1) on the backbone of the naturally attenuated tissue culture-adapted parental bovine rotavirus (BRV) strain WC3. The viral genomes of each of the reassortant strains were completely sequenced and compared pairwise and phylogenetically among each other and to human rotavirus (HRV) and BRV reference strains. Reassortants G1, G2, G3, and G4 contained the VP7 gene from their corresponding HRV parent strains, while reassortants G1 and G2 also contained the VP3 gene (genotype M1) from the HRV parent strain. The P1 reassortant contained the VP4 gene from the HRV parent strain and all the other gene segments from the BRV WC3 strain. The human VP7s had a high level of overall amino acid identity (G1: 95-99%, G2: 94-99% G3: 96-100%, G4: 93-99%) when compared to those of representative rotavirus strains of their corresponding G serotypes. The VP4 of the P1 reassortant had a high identity (92-97%) with those of serotype P1A[8] HRV reference strains, while the BRV VP7 showed identities ranging from 91% to 94% to those of serotype G6 HRV strains. Sequence analyses of the BRV or HRV genes confirmed that the fundamental structure of the proteins in the vaccine was similar to those of the HRV and BRV references strains. Sequences analyses showed that RotaTeq exhibited a high degree of genetic stability as no mutations were identified in the material of each reassortant, which undergoes two rounds of replication cycles in cell culture during the manufacturing process, when compared to the final material used to fill the dosing tubes. The infectivity of each of the reassortant strains of RotaTeq, like HRV strains, did not require the presence of sialic acid residues on the cell surface. The molecular and biologic characterization of RotaTeq adds to the significant body of clinical data supporting the consistent efficacy, immunogenicity, and safety of RotaTeq.
罗特律是一种五价轮状病毒疫苗,它以天然减毒的组织培养适应牛轮状病毒(BRV)亲本株 WC3 为骨架,包含五种人-牛重组株(分别指定为 G1、G2、G3、G4 和 P1)。每个重组株的病毒基因组都进行了完全测序,并在彼此之间以及与人类轮状病毒(HRV)和 BRV 参考株进行了成对比较和系统进化分析。重组株 G1、G2、G3 和 G4 含有与其相应 HRV 亲本株的 VP7 基因,而重组株 G1 和 G2 还含有 HRV 亲本株的 VP3 基因(基因型 M1)。P1 重组株含有 HRV 亲本株的 VP4 基因和 BRV WC3 株的所有其他基因片段。与相应 G 血清型的代表性轮状病毒株相比,人类 VP7 具有很高的整体氨基酸同一性(G1:95-99%,G2:94-99%,G3:96-100%,G4:93-99%)。P1 重组株的 VP4 与 P1A[8]HRV 参考株具有很高的同一性(92-97%),而 BRV VP7 与 G6 HRV 株的同一性在 91%至 94%之间。BRV 或 HRV 基因的序列分析证实,疫苗中蛋白质的基本结构与 HRV 和 BRV 参考株相似。序列分析表明,与用于填充剂量管的最终材料相比,在制造过程中每个重组株在细胞培养中经历两轮复制循环时,RotaTeq 表现出高度的遗传稳定性,没有发现任何突变。像 HRV 株一样,RotaTeq 的每个重组株的感染性都不需要细胞表面上存在唾液酸残基。RotaTeq 的分子和生物学特性增加了大量支持 RotaTeq 一致疗效、免疫原性和安全性的临床数据。