Liqi Liu, Zi Li, Jia Liu, Xiyan Li, Jianfang Zhou, Ning Xiao, Lei Yang, Dayan Wang
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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.</p></div>","PeriodicalId":43021,"journal":{"name":"Vaccine: X","volume":"19 ","pages":"Article 100531"},"PeriodicalIF":2.7000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590136224001049/pdfft?md5=f7cdf2466fc67d18eea671a1e35c55b6&pid=1-s2.0-S2590136224001049-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Effects of different HA and NA gene combinations on the growth characteristics of the H3N8 influenza candidate vaccine virus\",\"authors\":\"Liqi Liu, Zi Li, Jia Liu, Xiyan Li, Jianfang Zhou, Ning Xiao, Lei Yang, Dayan Wang\",\"doi\":\"10.1016/j.jvacx.2024.100531\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>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.</p></div>\",\"PeriodicalId\":43021,\"journal\":{\"name\":\"Vaccine: X\",\"volume\":\"19 \",\"pages\":\"Article 100531\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2590136224001049/pdfft?md5=f7cdf2466fc67d18eea671a1e35c55b6&pid=1-s2.0-S2590136224001049-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Vaccine: X\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2590136224001049\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vaccine: X","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590136224001049","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
自 2022 年以来,中国三个省份报告了三例人感染新型 H3N8 禽流感病毒的病例。特异性疫苗是应对潜在流感大流行的重要手段。因此,我们从感染者身上分离出 H3N8 病毒 [A/河南/cnic410/2022(HN410)和 A/长沙/1000/2022(CS1000)],作为利用反向遗传学(RG)技术开发候选疫苗病毒(CVV)的原型病毒。以这两种病毒为基础,构建了5种不同HA和NA组合的变种病毒,以获得高产、安全的候选疫苗病毒。结果表明,所有病毒的抗原性相似,但生长特性不同。与携带 HN410 NA 的病毒相比,携带 CS1000 NA 的后裔病毒具有更好的生长能力和 NA 酶活性。此外,与 HN410 相比,CS1000 的 NA 基因在第 46 位多了一个潜在的 N-糖基化位点。第 46 位的替换表明,在不同的变种病毒中添加或去除 N-糖基化位点对其生长能力有不同的影响。一种携带 HN410 HA 和 CS1000 NA、生长能力强的重交病毒被选为 CVV,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。
Effects of different HA and NA gene combinations on the growth characteristics of the H3N8 influenza candidate vaccine virus
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.