量化疫苗接种对猪体内甲型流感变种传播和多样性的影响。

IF 4 2区 医学 Q2 VIROLOGY
Chong Li, Marie R Culhane, Declan C Schroeder, Maxim C-J Cheeran, Lucina Galina Pantoja, Micah L Jansen, Montserrat Torremorell
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引用次数: 0

摘要

甲型流感病毒(IAV)的全球进化动态从根本上说是由病毒在宿主个体中产生、传播和形成的多样性程度所驱动的。疫苗接种如何影响可在猪体内传播和扩展的 IAV 遗传多样性程度尚不清楚。为了评估疫苗接种对基因不同的 IAV 变种的传播及其在猪体内传播后的多样性的影响,我们使用播种猪模型研究了同时感染 H1N1 和 H3N2 IAV 后接种不同流感免疫方案的猪从鼻腔中回收的 IAV 的全基因组。我们发现,与接触猪相比,播种猪体内的病毒群更加多样化。在接触猪中,从接种过一剂非匹配改良活疫苗的猪身上回收的 H3N2 和 H1N1 病毒通常比未接种过疫苗的猪积累了更多的基因突变。此外,单剂改良活疫苗引起的非灭菌免疫可能对 H1 抗原区产生了正选择,因为我们发现 H1 抗原区的非同义进化率明显高于非抗原区,但同义进化率却低于非抗原区。此外,我们还观察到,接种疫苗的猪与播种猪共享 H3N2 变体的比例明显低于未接种疫苗的猪。这些结果表明,接种疫苗可能会减少传播的流感变种对受种猪所蕴藏的 IAV 群体总体多样性的影响,而且接种了匹配不当的疫苗的猪更有可能发生 IAV 的宿主内遗传选择。重要意义 了解接种疫苗如何影响猪之间传播和繁殖的流感变种的多样性,对于设计有效的 IAV 监控计划至关重要。目前有关 IAV 变种传播的知识主要是在人类自然感染过程中探索的。然而,匹配不当的疫苗所引起的免疫力如何影响 IAV 基因多样性在猪体内全基因组水平上的传播和扩展程度尚不清楚。我们分析了每天从实验性感染猪只采集的样本中获得的 IAV 序列,这些猪只在现场代表的 IAV 共感染模型中接种了不同方案的疫苗。我们发现,疫苗诱导的非灭菌免疫可能会促进 IAV 基因组的遗传变异,并在感染过程中推动抗原位点的正选择。此外,播种猪和疫苗接种猪之间共享的 H3N2 病毒变体比例较小,这表明疫苗接种在传播过程中对受种猪病毒基因组多样性的形成产生了影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantifying the impact of vaccination on transmission and diversity of influenza A variants in pigs.

Global evolutionary dynamics of influenza A virus (IAV) are fundamentally driven by the extent of virus diversity generated, transmitted, and shaped in individual hosts. How vaccination affects the degree of IAV genetic diversity that can be transmitted and expanded in pigs is unknown. To evaluate the effect of vaccination on the transmission of genetically distinct IAV variants and their diversity after transmission in pigs, we examined the whole genome of IAV recovered from the nasal cavities of pigs vaccinated with different influenza immunization regimens after being infected simultaneously by H1N1 and H3N2 IAVs using a seeder pig model. We found that the seeder pigs harbored more diversified virus populations than the contact pigs. Among contact pigs, H3N2 and H1N1 viruses recovered from pigs vaccinated with a single dose of an unmatched modified live vaccine generally accumulated more extensive genetic mutations than non-vaccinated pigs. Furthermore, the non-sterilizing immunity elicited by the single-dose-modified live vaccine may have exerted positive selection on H1 antigenic regions as we detected significantly higher nonsynonymous but lower synonymous evolutionary rates in H1 antigenic regions than non-antigenic regions. In addition, we observed that the vaccinated pigs shared significantly less proportion of H3N2 variants with seeder pigs than unvaccinated pigs. These results indicated that vaccination might reduce the impact of transmitted influenza variants on the overall diversity of IAV populations harbored in recipient pigs and that within-host genetic selection of IAV is more likely to occur in pigs vaccinated with improperly matched vaccines.IMPORTANCEUnderstanding how vaccination shapes the diversity of influenza variants that transmit and propagate among pigs is essential for designing effective IAV surveillance and control programs. Current knowledge about the transmission of IAV variants has primarily been explored in humans during natural infection. However, how immunity elicited by improperly matched vaccines affects the degree of IAV genetic diversity that can be transmitted and expanded in pigs at the whole-genome level is unknown. We analyzed IAV sequences from samples collected daily from experimentally infected pigs vaccinated with various protocols in a field-represented IAV co-infection model. We found that vaccine-induced non-sterilizing immunity might promote genetic variation on the IAV genome and drive positive selection at antigenic sites during infection. In addition, a smaller proportion of H3N2 viral variants were shared between seeder pigs and vaccinated pigs, suggesting the influence of vaccination on shaping the virus genomic diversity in recipient pigs during the transmission events.

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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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