Growth characteristics of experimental live influenza vaccine strains with modified NP and NS genes

P. Prokopenko, Виктория A. Matyushenko, I. Isakova-Sivak, L. Rudenko
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Abstract

BACKGROUND: Vaccination is the most effective means of fighting influenza epidemics, but the immunogenicity of licensed influenza vaccines is not always satisfactory. One of the ways to increase the immunogenicity of an attenuated live influenza vaccine is to shorten the open reading frame of the NS1 protein, a modulator of innate antiviral immunity. In addition, the T-cell response to vaccination can be optimized by including the NP gene from the epidemic parental virus into the genome of vaccine strains. MATERIALS AND METHODS: The open reading frame of the NS1 protein of the master donor virus A/Leningrad/134/17/57 was truncated to 126 amino acids by site-directed mutagenesis. The HA, NA, and NP genes of the model virus A/Anhui/1/2013 (H7N9) were cloned into the pCIPolISapIT vector. The rescue of recombinant influenza viruses was performed by transfection of Vero cells with a desired set of plasmids. The growth properties of the recombinant viruses were determined in embryonated chicken eggs incubated at different temperatures, as well as in the tissues of the respiratory tract of mice (nasal turbinates, lungs). RESULTS: Experimental live influenza vaccine strains of subtype H7N9 with genome compositions 6:2 and 5:3 and carrying a full-length or truncated NS1 gene were actively replicated in eggs under optimal conditions, while maintaining the temperature-sensitive and cold-adapted phenotypes characteristic of classical live influenza vaccine strains. All viruses lacked the ability to grow in the lungs of C57BL/6J mice, which confirms the attenuated phenotype of the viruses. In the nasal passages of mice, only viruses with the full-length NS1 gene replicated, while viruses expressing the truncated NS1 protein were not detected in the respiratory tract of animals. CONCLUSIONS: The results indicate that modification of the NS1 gene of the vaccine virus and the inclusion of wild-type NP gene in its genome does not affect its growth characteristics in eggs. A decrease in the activity of viral replication in the upper respiratory tract of mice with a shortening of the NS1 open reading frame indicates an increase in the attenuating properties of modified vaccines, which opens up prospects for the use of new vaccines in children under three years of age.
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NP和NS基因修饰流感活疫苗实验株的生长特性
背景:疫苗接种是对抗流感流行最有效的手段,但已获得许可的流感疫苗的免疫原性并不总是令人满意。增加流感减毒活疫苗免疫原性的方法之一是缩短NS1蛋白的开放阅读框,NS1蛋白是先天抗病毒免疫的调节剂。此外,通过将流行亲本病毒的NP基因加入疫苗株基因组中,可以优化t细胞对疫苗接种的反应。材料与方法:采用定点诱变法将主供体病毒A/Leningrad/134/17/57的NS1蛋白开放阅读框截断为126个氨基酸。将模型病毒A/Anhui/1/2013 (H7N9)的HA、NA和NP基因克隆到pCIPolISapIT载体中。重组流感病毒的拯救是通过用一组所需的质粒转染Vero细胞来完成的。在不同温度下孵育的鸡胚和小鼠呼吸道组织(鼻鼻甲、肺)中测定了重组病毒的生长特性。结果:基因组组成为6:2和5:3、携带全长或截断的NS1基因的H7N9亚型流感活疫苗实验株在最佳条件下可在鸡蛋中积极复制,同时保持了经典流感活疫苗株的温度敏感和冷适应表型特征。所有病毒都缺乏在C57BL/6J小鼠肺中生长的能力,这证实了病毒的减毒表型。在小鼠鼻道中,只复制了全长NS1基因的病毒,而在动物呼吸道中未检测到表达截断NS1蛋白的病毒。结论:疫苗病毒NS1基因的修饰和野生型NP基因在其基因组中的包含不影响其在蛋中的生长特性。NS1开放阅读框缩短导致小鼠上呼吸道病毒复制活性降低,表明改性疫苗的减毒特性增强,这为3岁以下儿童使用新疫苗开辟了前景。
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