2009年至2022年美国猪甲型流感病毒基因组多样性的来源和汇

IF 3.8 2区 医学 Q2 VIROLOGY
Journal of Virology Pub Date : 2025-09-23 Epub Date: 2025-08-26 DOI:10.1128/jvi.00541-25
Garrett M Janzen, Blake T Inderski, Jennifer Chang, Zebulun W Arendsee, Alicia Janas-Martindale, Mia Kim Torchetti, Amy L Baker, Tavis K Anderson
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引用次数: 0

摘要

美国对猪的甲型流感病毒(IAV)进行了监测,以监测基因进化,为干预工作提供信息,并帮助预防大流行。我们描述了2009年至2022年美国农业部国家猪流感病毒监测计划的数据。临床呼吸道病例分型,血凝素(HA)和神经氨酸酶(NA)测序,病毒亚群全基因组测序。系统发育分析确定了IAV重配的地理和时间热点。对作为IAV基因组多样性源或汇的区域进行了量化,并对传播进行了定性和建模。主要亚型为H1N2 (1B.2.1)、H3N2(1990.4)。H1N1 (H1-1A.3.3.3-c3)。内部基因被分类为三重重组(T)或2009年大流行(P),三个基因组星座在过去2年中占检测的73.5%。在某些年份,IAV多样性的分布非常狭窄,以至于呈现出与局部适应相关的统计信号。我们还证明,大多数IAV基因组多样性的来源在中西部各州(伊利诺伊州,密苏里州,伊利诺伊州),虽然这与猪库存相关,但多样性的出现和持续存在与美国猪运输有关。持续的独特HA, NA和基因组星座的区域检测为有针对性的干预提供了支持,以改善动物健康和加强大流行防范。甲型流感病毒(IAV)在猪体内的遗传多样性随时间和地区的变化影响着控制工作。本研究量化了2009年至2022年在区域和国家层面收集的猪流感病毒的基因组多样性,并对该多样性的来源和汇进行了建模。观察到IAV传播的季节性模式,一些地点对基因组多样性的出现做出了不成比例的贡献。少数病毒有可能通过动物运动在美国传播。这些模式的识别表明了一个强有力的监测系统为反映遗传多样性区域模式的疫苗更新提供信息的重要性。我们展示了在猪IAV多样性中心进行先发制人的干预如何减少重组和新基因组多样性的出现,以及这些努力如何可能减少IAV在猪体内和猪与人之间的传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sources and sinks of influenza A virus genomic diversity in swine from 2009 to 2022 in the United States.

Sources and sinks of influenza A virus genomic diversity in swine from 2009 to 2022 in the United States.

Sources and sinks of influenza A virus genomic diversity in swine from 2009 to 2022 in the United States.

Sources and sinks of influenza A virus genomic diversity in swine from 2009 to 2022 in the United States.

Influenza A virus (IAV) in swine in the U.S. is surveilled to monitor genetic evolution to inform intervention efforts and aid pandemic preparedness. We describe data from the U.S. Department of Agriculture National Surveillance Plan for Influenza A Virus in Pigs from 2009 to 2022. Clinical respiratory cases were subtyped, followed by sequencing of hemagglutinin (HA) and neuraminidase (NA), and a subset of viruses was whole genome sequenced. Phylogenetic analysis identified geographic and temporal IAV reassortment hotspots. Regions acting as IAV genomic diversity sources or sinks were quantified, and dissemination was qualified and modeled. The dominant IAV clades were H1N2 (1B.2.1), H3N2 (1990.4.a), and H1N1 (H1-1A.3.3.3-c3). Internal genes were classified as triple-reassortant (T) or pandemic 2009 (P), and three genome constellations represented 73.5% of detections across the last 2 years. In some years, the distribution of IAV diversity was so narrow that it presented a statistical signal associated with local adaptation. We also demonstrated that the source of most IAV genomic diversity was in Midwest states (IL, MO, IA), and while this was correlated with swine inventory, the emergence and persistence of diversity were tied to swine transport across the U.S. The continued regional detection of unique HA, NA, and genome constellations provides support for targeted interventions to improve animal health and enhance pandemic preparedness.IMPORTANCEVariation in the genetic diversity of influenza A virus (IAV) in swine through time and between regions impacts control efforts. This study quantified the genomic diversity of swine IAV collected from 2009 to 2022 at regional and national levels and modeled sources and sinks of that diversity. Seasonal patterns of IAV transmission were observed, and some locations contributed disproportionately to the emergence of genomic diversity. Minor groups of viruses had the potential to disseminate across the U.S. with animal movement. The identification of these patterns demonstrates the importance of a robust surveillance system to inform vaccine updates that reflect regional patterns of genetic diversity. We show how preemptive interventions in swine IAV diversity hubs could reduce reassortment and the emergence of novel genomic diversity, and how these efforts are likely to reduce the transmission of IAV within swine and between swine and humans.

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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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