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Evolution of H9N2 avian influenza virus in embryonated chicken eggs with or without homologous vaccine antibodies

机译:含或不含同源疫苗抗体的鸡胚鸡蛋中H9N2禽流感病毒的进化

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Vaccines constitute a unique selective pressure, different from natural selection, drives the evolution of influenza virus. In this study, A/Chicken/Shanghai/F/1998 (H9N2) was continually passaged in specific pathogen-free embryonated chicken eggs with or without selective pressures from antibodies induced by homologous maternal antibodies. Genetic mutations, antigenic drift, replication, and pathogenicity of the passaged virus were evaluated. Antigenic drift of the passaged viruses occurred in the 47th generation (vF47) under selective pressure on antibodies and in the 52nd generation (nF52) without selective pressure from antibodies. Seven mutations were observed in the vF47 virus, with three in PB2 and four in HA, whereas 12 mutations occurred in the nF52 virus, with three in PB2, two in PB1, four in HA, one in NP, one in NA, and one in NS. Remarkably, the sequences of the HA segment from vF47 were 100% homologous with those of the nF52 virus. Both the vF47 and nF52 viruses showed enhanced replication compared to the parental virus F/98, but higher levels of replication and pathogenicity were displayed by nF52 than by vF47. An inactive vaccine derived from the parental virus F/98 did not confer protection against challenges by either the vF47 or nF52 virus, but inactive vaccines derived from the vF47 or nF52 virus were able to provide protection against a challenge using F/98. Taken together, the passage of H9N2 viruses with or without selective pressure of the antibodies induced by homologous maternal antibodies showed genetic variation, enhanced replication, and variant antigenicity. Selective pressure of the antibody does not seem to play a key role in antigenic drift in the egg model but may impact the genetic variation and replication ability of H9N2 viruses. These results improve understanding of the evolution of the H9N2 influenza virus and may aid in selecting appropriate vaccine seeds.
机译:与自然选择不同,疫苗构成独特的选择压力,可驱动流感病毒的进化。在这项研究中,A / Chicken / Shanghai / F / 1998(H9N2)在有或没有来自同源母体抗体诱导的抗体的选择性压力下,在无特定病原体的胚鸡蛋中连续传代。评估了传代病毒的遗传突变,抗原漂移,复制和致病性。传代病毒的抗原性漂移发生在第47代(vF47)受到抗体的选择性压力下,而第52代(nF52)则没有抗体的选择性压力。在vF47病毒中发现了7个突变,在PB2中出现了3个突变,在HA中出现了4个突变,而在nF52病毒中出现了12个突变,在PB2中出现了3个突变,在PB1中出现了2个突变,在HA中出现了4个突变,在HA中出现了4个突变,在NP中出现了一个突变,在NA中出现了一个突变,在NA中出现了一个突变。在NS中。明显地,来自vF47的HA片段的序列与nF52病毒的序列100%同源。与亲代病毒F / 98相比,vF47和nF52病毒均显示出增强的复制,但nF52比vF47显示出更高水平的复制和致病性。衍生自亲本病毒F / 98的无活性疫苗未赋予vF47或nF52病毒抵抗攻击的保护,但衍生自vF47或nF52病毒的无活性疫苗能够提供针对F / 98攻击的保护。综上所述,在有或没有由同源母源抗体诱导的抗体选择性压力下,H9N2病毒的传代均显示出遗传变异,增强的复制和变异抗原性。抗体的选择压力似乎在卵模型中的抗原漂移中并不起关键作用,但可能会影响H9N2病毒的遗传变异和复制能力。这些结果增进了对H9N2流感病毒进化的了解,并可能有助于选择合适的疫苗种子。

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