Biomedical Research Center, Qatar University, 2713, Doha, Qatar.
Department of Experimental Pathology, Immunology, and Microbiology, American University of Beirut, Beirut, Lebanon.
Pediatr Res. 2023 Aug;94(2):477-485. doi: 10.1038/s41390-023-02468-7. Epub 2023 Jan 19.
We characterized and identified the genetic and antigenic variations of circulating rotavirus strains in comparison to used rotavirus vaccines.
Rotavirus-positive samples (n = 231) were collected and analyzed. The VP7 and VP4 genes were sequenced and analyzed against the rotavirus vaccine strains. Antigenic variations were illustrated on the three-dimensional models of surface proteins.
In all, 59.7% of the hospitalized children were vaccinated, of which only 57.2% received two doses. There were no significant differences between the vaccinated and non-vaccinated groups in terms of clinical outcome. The G3 was the dominant genotype (40%) regardless of vaccination status. Several amino acid changes were identified in the VP7 and VP4 antigenic epitopes compared to the licensed vaccines. The highest variability was seen in the G3 (6 substitutions) and P[4] (11 substitutions) genotypes in comparison to RotaTeq®. In comparison to Rotarix®, G1 strains possessed three amino acid changes in 7-1a and 7-2 epitopes while P[8] strains possessed five amino acid changes in 8-1 and 8-3 epitopes.
The current use of Rotarix® vaccine might not be effective in preventing the infection due to the higher numbers of G3-associated cases. The wide range of mutations in the antigenic epitopes compared to vaccine strains may compromise the vaccine's effectiveness.
The reduced rotavirus vaccine effectiveness necessitate regular evaluation of the vaccine content to ensure optimal protection. We characterized and identified the genetic and antigenic variations of circulating rotavirus strains in comparison to the Rotarix vaccine strain that is used in Qatar. The study highlight the importance for regular monitoring of emerging rotavirus variants and their impact on vaccine effectiveness in young children.
我们对循环轮状病毒株的遗传和抗原变异进行了特征描述和鉴定,并与已使用的轮状病毒疫苗进行了比较。
收集并分析了轮状病毒阳性样本(n=231)。对 VP7 和 VP4 基因进行测序,并与轮状病毒疫苗株进行比较分析。在表面蛋白的三维模型上展示了抗原变异。
所有住院患儿中,59.7%接受了疫苗接种,其中只有 57.2%接种了两剂。在临床结局方面,接种组和未接种组之间没有显著差异。无论接种状态如何,G3 都是主要基因型(40%)。与许可疫苗相比,VP7 和 VP4 抗原表位中发现了几个氨基酸变化。与 RotaTeq®相比,G3(6 个取代)和 P[4](11 个取代)基因型的变异性最高。与 Rotarix®相比,G1 株在 7-1a 和 7-2 表位中具有三个氨基酸变化,而 P[8]株在 8-1 和 8-3 表位中具有五个氨基酸变化。
由于 G3 相关病例数量较多,目前使用 Rotarix®疫苗可能无法有效预防感染。与疫苗株相比,抗原表位中的突变范围广泛可能会降低疫苗的有效性。
轮状病毒疫苗效力降低,需要定期评估疫苗内容,以确保最佳保护效果。我们对循环轮状病毒株的遗传和抗原变异进行了特征描述和鉴定,并与在卡塔尔使用的 Rotarix 疫苗株进行了比较。该研究强调了定期监测新出现的轮状病毒变异及其对幼儿疫苗效力的影响的重要性。