Taubenberger J K
Department of Molecular Pathology, Armed Forces Institute of Pathology, Rockville, Maryland 20850-3125, USA.
Arch Virol Suppl. 2005(19):101-15. doi: 10.1007/3-211-29981-5_9.
The 1918 influenza pandemic caused acute illness in 25-30% of the world's population and resulted in the death of up to 40 million people. Using lung tissue of 1918 influenza victims, the complete genomic sequence of the 1918 influenza virus is being deduced. Neither the 1918 hemagglutinin nor neuraminidase genes possess mutations known to increase tissue tropicity that account for virulence of other influenza virus strains, such as A/WSN/33 or the highly pathogenic avian influenza H5 or H7 viruses. Using reverse genetics approaches, influenza virus constructs containing the 1918 hemagglutinin and neuraminidase on an A/WSN/33 virus background were lethal in mice. The genotypic basis of this virulence has not yet been elucidated. The complete sequence of the non-structural (NS) gene segment of the 1918 virus was deduced and also tested to determine the validity of the hypothesis that enhanced virulence in 1918 could have been due to type I interferon inhibition by the NS1 protein. Results from these experiments suggest that in human cells the 1918 NS1 is a very effective interferon antagonist. Sequence analysis of the 1918 influenza virus is allowing us to test hypotheses as to the origin and virulence of this strain. This information should help elucidate how pandemic influenza virus strains emerge and what genetic features contribute to virulence in humans.
1918年的流感大流行致使全球25%至30%的人口罹患急性疾病,造成多达4000万人死亡。利用1918年流感受害者的肺组织,正在推导1918年流感病毒的完整基因组序列。1918年的血凝素基因和神经氨酸酶基因均未发生已知的可增加组织嗜性的突变,而这种突变可解释其他流感病毒株(如A/WSN/33或高致病性禽流感H5或H7病毒)的毒力。采用反向遗传学方法,在A/WSN/33病毒背景上构建的含有1918年血凝素和神经氨酸酶的流感病毒构建体对小鼠具有致死性。这种毒力的基因型基础尚未阐明。推导了1918年病毒非结构(NS)基因片段的完整序列,并进行了测试,以确定1918年毒力增强可能是由于NS1蛋白抑制I型干扰素这一假说的有效性。这些实验结果表明,在人类细胞中,1918年的NS1是一种非常有效的干扰素拮抗剂。对1918年流感病毒的序列分析使我们能够检验关于该毒株起源和毒力的假说。这些信息应有助于阐明大流行性流感病毒株是如何出现的,以及哪些基因特征导致其对人类具有毒力。