Liu Liqi, Li Zi, Liu Jia, Li Xiyan, Zhou Jianfang, Xiao Ning, Yang Lei, Wang Dayan
National Institute for Viral Disease Control and Prevention, China CDC, Beijng, PR China.
Vaccine X. 2024 Jul 18;19:100531. doi: 10.1016/j.jvacx.2024.100531. eCollection 2024 Aug.
Since 2022, three human cases of a novel H3N8 avian influenza virus infection have been reported in three provinces in China. Specific vaccines are important means of preparing for the potential influenza pandemic. Thus, H3N8 viruses [A/Henan/cnic410/2022 (HN410) and A/Changsha/1000/2022(CS1000)] were isolated from the infected patients as prototype viruses to develop candidate vaccine viruses (CVVs) using the reverse genetics (RG) technology. Five reassortant viruses with different HA and NA combinations were constructed based on the two viruses to get a high-yield and safe CVV. The results showed that all viruses had similar antigenicity but different growth characteristics. Reassortant viruses carrying NA from CS1000 exhibited better growth ability and NA enzyme activity than the ones carrying HN410 NA. Furthermore, the NA gene of CS1000 had one more potential N-glycosylation site at position 46 compared with HN410. The substitution of position 46 showed that adding or removing N-glycosylation sites to different reassortant viruses had different effects on growth ability. A reassortant virus carrying HN410 HA and CS1000 NA with high growth ability was selected as a CVV, which met the requirements for a CVV. These data suggest that different surface gene combinations and the presence or absence of potential N-glycosylation sites on position 46 in the NA gene affect the growth characteristics of H3N8 CVVs.
自2022年以来,中国三个省份报告了三例新型H3N8禽流感病毒感染的人类病例。特定疫苗是应对潜在流感大流行的重要手段。因此,从感染患者中分离出H3N8病毒[A/河南/cnic410/2022(HN410)和A/长沙/1000/2022(CS1000)]作为原型病毒,利用反向遗传学(RG)技术开发候选疫苗病毒(CVV)。基于这两种病毒构建了五种具有不同HA和NA组合的重配病毒,以获得高产且安全的CVV。结果表明,所有病毒具有相似的抗原性,但生长特性不同。携带CS1000的NA的重配病毒比携带HN410 NA的重配病毒表现出更好的生长能力和NA酶活性。此外,与HN410相比,CS1000的NA基因在第46位多一个潜在的N-糖基化位点。第46位的替换表明,在不同重配病毒中添加或去除N-糖基化位点对生长能力有不同影响。选择一种携带HN410 HA和CS1000 NA且生长能力高的重配病毒作为CVV,其符合CVV的要求。这些数据表明,不同的表面基因组合以及NA基因中第46位潜在N-糖基化位点的存在与否会影响H3N8 CVV的生长特性。