MRC-University of Glasgow Centre for Virus Research, 464 Bearsden Road, Glasgow G61 1QH, UK.
Trends Microbiol. 2018 Sep;26(9):809-810. doi: 10.1016/j.tim.2018.05.013. Epub 2018 Jun 13.
This infographic briefly summarises the natural history, replication cycle, and pathogenesis of influenza viruses, the cause of seasonal influenza and of influenza pandemics. Influenza viruses infect many vertebrates, with Influenza A, B and C viruses (IAV, IBV, and ICV) infecting humans. High mutation rates allow the evasion of immunity. IAV from different host species can 'reassort' their segmented genomes, producing pandemic strains that are antigenically novel but otherwise well adapted to humans. The 'Great Influenza' pandemic of 1918 remains the worst outbreak of infectious disease in history. There is concern that highly pathogenic avian influenza viruses of the H5 and H7 subtypes may evolve to cause similar pandemics. In humans, influenza viruses infect the respiratory epithelium. The haemagglutinin (HA) proteins of IAV and IBV, or the haemagglutinin-esterase-fusion (HEF) proteins of ICV, bind sialic acid, causing endocytosis. Unusually among RNA viruses, the viral genome replicates in the nucleus. New viruses assemble at the cell surface and are released by the receptor-cleaving neuraminidase (NA) proteins of IAV and IBV or the ICV HEF protein.
本信息图简要总结了流感病毒的自然史、复制周期和发病机制,这些病毒是季节性流感和流感大流行的病原体。流感病毒感染许多脊椎动物,其中甲型、乙型和丙型流感病毒(IAV、IBV 和 ICV)感染人类。高突变率使免疫逃逸成为可能。来自不同宿主物种的 IAV 可以“重配”它们的分段基因组,产生具有新颖抗原性但对人类适应良好的大流行株。1918 年的“大流感”仍然是历史上最严重的传染病爆发。人们担心 H5 和 H7 亚型的高致病性禽流感病毒可能会进化为导致类似大流行的病毒。在人类中,流感病毒感染呼吸道上皮。IAV 和 IBV 的血凝素 (HA) 蛋白,或 ICV 的血凝素-酯酶-融合 (HEF) 蛋白,与唾液酸结合,导致内吞作用。与其他 RNA 病毒不同,病毒基因组在细胞核中复制。新病毒在细胞表面组装,然后被 IAV 和 IBV 的受体裂解神经氨酸酶 (NA) 蛋白或 ICV 的 HEF 蛋白释放。