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Ecological and immunological determinants of influenza evolution

机译:流感演变的生态和免疫学决定因素

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In pandemic and epidemic forms, influenza causes substantial, sometimes catastrophic, morbidity and mortality. Intense selection from the host immune system drives antigenic change in influenza A and B, resulting in continuous replacement of circulating strains with new variants able to re-infect hosts immune to earlier types. This 'antigenic drift'(1) often requires a new vaccine to be formulated before each annual epidemic. However, given the high transmissibility and mutation rate of influenza, the constancy of genetic diversity within lineages over time is paradoxical. Another enigma is the replacement of existing strains during a global pandemic caused by 'antigenic shift'-the introduction of a new avian influenza A subtype into the human population(1). Here we explore ecological and immunological factors underlying these patterns using a mathematical model capturing both realistic epidemiological dynamics and viral evolution at the sequence level. By matching model output to phylogenetic patterns seen in sequence data collected through global surveillance(2), we find that short-lived strain-transcending immunity is essential to restrict viral diversity in the host population and thus to explain key aspects of drift and shift dynamics. [References: 29]
机译:流感以大流行和流行的形式造成大量的,有时是灾难性的,发病率和死亡率。从宿主免疫系统的强烈选择驱动了甲型和乙型流感的抗原变化,从而导致循环菌株不断被新的变种替代,这些新变种能够重新感染对早期类型免疫的宿主。这种“抗原性漂移”(1)通常需要在每年的流行病发生之前配制一种新疫苗。然而,鉴于流感的高传播性和突变率,世系内遗传多样性随时间的恒定是自相矛盾的。另一个谜是在由“抗原转移”引起的全球大流行期间替换了现有的菌株-将新的A型禽流感亚型引入人类(1)。在这里,我们使用数学模型在序列水平上捕获现实的流行病学动态和病毒进化,探索了这些模式背后的生态和免疫因素。通过将模型输出与通过全球监测收集的序列数据中看到的系统发育模式进行匹配(2),我们发现短暂的超越应变的免疫对于限制宿主种群中的病毒多样性至关重要,从而解释了漂移和转移动力学的关键方面。 [参考:29]

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