Vaccine Translational Research Center, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea.
Department of Integrated OMICS for Biomedical Science, College of World Class University, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea.
Viruses. 2018 Apr 7;10(4):183. doi: 10.3390/v10040183.
Glycosylation of the hemagglutinin (HA) and neuraminidase (NA) of the influenza provides crucial means for immune evasion and viral fitness in a host population. However, the time-dependent dynamics of each glycosylation sites have not been addressed. We monitored the potential N-linked glycosylation (NLG) sites of over 10,000 HA and NA of H1N1 subtype isolated from human, avian, and swine species over the past century. The results show a shift in glycosylation sites as a hallmark of 1918 and 2009 pandemics, and also for the 1976 "abortive pandemic". Co-segregation of particular glycosylation sites was identified as a characteristic of zoonotic transmission from animal reservoirs, and interestingly, of "reverse zoonosis" of human viruses into swine populations as well. After the 2009 pandemic, recent isolates accrued glycosylation at canonical sites in HA, reflecting gradual seasonal adaptation, and a novel glycosylation in NA as an independent signature for adaptation among humans. Structural predictions indicated a remarkably pleiotropic influence of glycans on multiple HA epitopes for immune evasion, without sacrificing the receptor binding of HA or the activity of NA. The results provided the rationale for establishing the ecological niche of influenza viruses among the reservoir and could be implemented for influenza surveillance and improving pandemic preparedness.
流感血凝素 (HA) 和神经氨酸酶 (NA) 的糖基化提供了宿主人群中免疫逃逸和病毒适应性的重要手段。然而,每个糖基化位点的时间依赖性动态尚未得到解决。我们监测了过去一个世纪中从人类、禽类和猪种中分离的 H1N1 亚型超过 10000 个 HA 和 NA 的潜在 N 连接糖基化 (NLG) 位点。结果表明,糖基化位点的转移是 1918 年和 2009 年大流行以及 1976 年“流产大流行”的标志,也是动物宿主中动物源性传播的特征,有趣的是,也是人类病毒向猪群中“反向动物源传播”的特征。2009 年大流行后,最近的分离株在 HA 的典型位点上获得了糖基化,反映了逐渐的季节性适应,而 NA 中的新型糖基化则是人类适应性的独立标志。结构预测表明,聚糖对多个 HA 表位的免疫逃逸具有显著的多效性影响,而不会牺牲 HA 的受体结合或 NA 的活性。这些结果为确定流感病毒在宿主中的生态位提供了依据,并可用于流感监测和改善大流行准备。