Wang Zeng, Yang Huanliang, Chen Yan, Tao Shiyu, Liu Liling, Kong Huihui, Ma Shujie, Meng Fei, Suzuki Yasuo, Qiao Chuanling, Chen Hualan
State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences (CAAS), Harbin, People's Republic of China.
College of Life and Health Sciences, Chubu University, Aichi, Japan.
J Virol. 2017 Oct 13;91(21). doi: 10.1128/JVI.00800-17. Print 2017 Nov 1.
Efficient transmission from human to human is the prerequisite for an influenza virus to cause a pandemic; however, the molecular determinants of influenza virus transmission are still largely unknown. In this study, we explored the molecular basis for transmission of Eurasian avian-like H1N1 (EAH1N1) swine influenza viruses by comparing two viruses that are genetically similar but differ in their transmissibility in guinea pigs: the A/swine/Guangxi/18/2011 virus (GX/18) is highly transmissible by respiratory droplet in guinea pigs, whereas the A/swine/Heilongjiang/27/2012 virus (HLJ/27) does not transmit in this animal model. We used reverse genetics to generate a series of reassortants and mutants in the GX/18 background and tested their transmissibility in guinea pigs. We found that a single-amino-acid substitution of glycine (G) for glutamic acid (E) at position 225 (E225G) in the HA1 protein completely abolished the respiratory droplet transmission of GX/18, whereas the substitution of E for G at the same position (G225E) in HA1 enabled HLJ/27 to transmit in guinea pigs. We investigated the underlying mechanism and found that viruses bearing 225E in HA1 replicated more rapidly than viruses bearing 225G due to differences in assembly and budding efficiencies. Our study indicates that the amino acid 225E in HA1 plays a key role in EAH1N1 swine influenza virus transmission and provides important information for evaluating the pandemic potential of field influenza virus strains. Efficient transmission among humans is a prerequisite for a novel influenza virus to cause a human pandemic. Transmissibility of influenza viruses is a polygenic trait, and understanding the genetic determinants for transmissibility will provide useful insights for evaluating the pandemic potential of influenza viruses in the field. Several amino acids in the hemagglutinin (HA) protein of influenza viruses have been shown to be important for transmissibility, usually by increasing virus affinity for human-type receptors. In this study, we explored the genetic basis of the transmissibility difference between two Eurasian avian-like H1N1 (EAH1N1) swine influenza viruses in guinea pigs and found that the amino acid glutamic acid at position 225 in the HA1 protein plays a critical role in the transmission of EAH1N1 virus by increasing the efficiency of viral assembly and budding.
人传人高效传播是流感病毒引发大流行的前提条件;然而,流感病毒传播的分子决定因素仍大多未知。在本研究中,我们通过比较两种基因相似但在豚鼠中传播能力不同的病毒,探究了欧亚禽源样H1N1(EAH1N1)猪流感病毒传播的分子基础:A/猪/广西/18/2011病毒(GX/18)在豚鼠中可通过呼吸道飞沫高效传播,而A/猪/黑龙江/27/2012病毒(HLJ/27)在该动物模型中不传播。我们利用反向遗传学在GX/18背景下产生了一系列重配体和突变体,并测试了它们在豚鼠中的传播能力。我们发现,HA1蛋白第225位的谷氨酸(E)被甘氨酸(G)单氨基酸取代(E225G)完全消除了GX/18的呼吸道飞沫传播,而HA1中同一位置的G被E取代(G225E)则使HLJ/27能够在豚鼠中传播。我们研究了其潜在机制,发现由于组装和出芽效率的差异,HA1中携带225E的病毒比携带225G的病毒复制更快。我们的研究表明,HA1中的225E氨基酸在EAH1N1猪流感病毒传播中起关键作用,并为评估野外流感病毒株的大流行潜力提供了重要信息。人传人高效传播是新型流感病毒引发人类大流行的前提条件。流感病毒的传播能力是一个多基因性状,了解传播能力的遗传决定因素将为评估野外流感病毒的大流行潜力提供有用的见解。流感病毒血凝素(HA)蛋白中的几个氨基酸已被证明对传播能力很重要,通常是通过增加病毒对人源型受体的亲和力。在本研究中,我们探究了两种欧亚禽源样H1N1(EAH1N1)猪流感病毒在豚鼠中传播能力差异 的遗传基础,发现HA1蛋白第225位的谷氨酸氨基酸通过提高病毒组装和出芽效率在EAH1N1病毒传播中起关键作用。