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全基因组分析鉴定卢旺达疫苗接种后出现多种重组轮状病毒株。

Whole-Genome Analyses Identifies Multiple Reassortant Rotavirus Strains in Rwanda Post-Vaccine Introduction.

机构信息

Next Generation Sequencing Unit and Division of Virology, Faculty of Health Sciences, University of the Free State, Bloemfontein 9300, South Africa.

Department of Laboratory, Clinical Biology, Kigali University Teaching Hospital, P.O. Box 4285, Kigali, Rwanda.

出版信息

Viruses. 2021 Jan 12;13(1):95. doi: 10.3390/v13010095.

Abstract

Children in low-and middle-income countries, including Rwanda, experience a greater burden of rotavirus disease relative to developed countries. Evolutionary mechanisms leading to multiple reassortant rotavirus strains have been documented over time which influence the diversity and evolutionary dynamics of novel rotaviruses. Comprehensive rotavirus whole-genome analysis was conducted on 158 rotavirus group A (RVA) samples collected pre- and post-vaccine introduction in children less than five years in Rwanda. Of these RVA positive samples, five strains with the genotype constellations G4P[4]-I1-R2-C2-M2-A2-N2-T1-E1-H2 (n = 1), G9P[4]-I1-R2-C2-M2-A1-N1-T1-E1-H1 (n = 1), G12P[8]-I1-R2-C2-M1-A1-N2-T1-E2-H3 (n = 2) and G12P[8]-I1-R1-C1-M1-A2-N2-T2-E1-H1 (n = 1), with double and triple gene reassortant rotavirus strains were identified. Phylogenetic analysis revealed a close relationship between the Rwandan strains and cognate human RVA strains as well as the RotaTeq vaccine strains in the VP1, VP2, NSP2, NSP4 and NSP5 gene segments. Pairwise analyses revealed multiple differences in amino acid residues of the VP7 and VP4 antigenic regions of the RotaTeq vaccine strain and representative Rwandan study strains. Although the impact of such amino acid changes on the effectiveness of rotavirus vaccines has not been fully explored, this analysis underlines the potential of rotavirus whole-genome analysis by enhancing knowledge and understanding of intergenogroup reassortant strains circulating in Rwanda post vaccine introduction.

摘要

在包括卢旺达在内的中低收入国家,儿童患轮状病毒病的负担比发达国家更大。随着时间的推移,已经记录了导致多种重组轮状病毒株的进化机制,这些机制影响了新型轮状病毒的多样性和进化动态。对卢旺达 5 岁以下儿童在疫苗引入前后收集的 158 份轮状病毒 A 组(RVA)样本进行了全面的轮状病毒全基因组分析。在这些 RVA 阳性样本中,有 5 株具有基因型组合 G4P[4]-I1-R2-C2-M2-A2-N2-T1-E1-H2(n = 1)、G9P[4]-I1-R2-C2-M2-A1-N1-T1-E1-H1(n = 1)、G12P[8]-I1-R2-C2-M1-A1-N2-T1-E2-H3(n = 2)和 G12P[8]-I1-R1-C1-M1-A2-N2-T2-E1-H1(n = 1),鉴定出具有双重和三重基因重配的轮状病毒株。系统进化分析显示,卢旺达毒株与相应的人类 RVA 株以及 RotaTeq 疫苗株在 VP1、VP2、NSP2、NSP4 和 NSP5 基因片段中具有密切关系。成对分析显示,RotaTeq 疫苗株和代表性卢旺达研究株在 VP7 和 VP4 抗原区的氨基酸残基存在多个差异。尽管这些氨基酸变化对轮状病毒疫苗有效性的影响尚未得到充分探讨,但这种全基因组分析突出了轮状病毒全基因组分析的潜力,增强了对卢旺达疫苗引入后循环的种间重配株的了解和认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d832/7828107/d429cb5d2e2a/viruses-13-00095-g001.jpg

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