Influenza Division, NCIRD, Centers for Disease Control and Prevention (CDC), Atlanta, GA, USA.
Influenza Division, NCIRD, Centers for Disease Control and Prevention (CDC), Atlanta, GA, USA; Chippewa Government Solutions, Sault Sainte Marie, MI, USA.
Antiviral Res. 2023 Oct;218:105719. doi: 10.1016/j.antiviral.2023.105719. Epub 2023 Sep 15.
Influenza virus neuraminidase (NA) can act as a receptor-binding protein, a role commonly attributed to hemagglutinin (HA). In influenza A(H3N2) viruses, three NA amino acid residues have previously been associated with NA-mediated hemagglutination: T148, D151, and more recently, H150. These residues are part of the 150-loop of the NA monomer. Substitutions at 148 and 151 arise from virus propagation in laboratory cell cultures, whereas changes at 150 occurred during virus evolution in the human host. In this study, we examined the effect of natural amino acid polymorphism at position 150 on NA-mediated hemagglutination. Using the A/Puerto Rico/8/34 backbone, we generated a comprehensive panel of recombinant A(H3N2) viruses that have different NAs but shared an HA that displays poor binding to red blood cells (RBCs). None of the tested substitutions at 150 (C, H, L, R, and S) promoted NA-binding. However, we identified two new determinants of NA-binding, Q136K and T439R, that emerged during virus culturing. Similar to T148I, both Q136K and T439R reduced NA enzyme activity by 48-86% and inhibition (14- to 173-fold) by the NA inhibitor zanamivir. NA-binding was observed when a virus preparation contained approximately 10% of NA variants with either T148I or T439R, highlighting the benefit of using deep sequencing in virus characterization. Taken together, our findings provide new insights into the molecular mechanisms underlying the ability of NA to function as a binding protein. Information gained may aid in the design of new and improved NA-targeting antivirals.
流感病毒神经氨酸酶(NA)可以作为一种受体结合蛋白,其作用通常归因于血凝素(HA)。在甲型流感病毒(H3N2)中,以前有三个 NA 氨基酸残基与 NA 介导的血凝有关:T148、D151,以及最近的 H150。这些残基是 NA 单体 150 环的一部分。148 和 151 的取代来自于实验室细胞培养中的病毒繁殖,而 150 的变化发生在人类宿主中的病毒进化过程中。在这项研究中,我们研究了位置 150 处天然氨基酸多态性对 NA 介导的血凝的影响。使用 A/Puerto Rico/8/34 骨架,我们生成了一个全面的重组 A(H3N2)病毒面板,这些病毒具有不同的 NA,但共享一种对红细胞(RBC)结合不良的 HA。在 150 位测试的取代(C、H、L、R 和 S)均未促进 NA 结合。然而,我们确定了两个新的 NA 结合决定因素,Q136K 和 T439R,它们在病毒培养过程中出现。与 T148I 相似,Q136K 和 T439R 使 NA 酶活性降低了 48-86%,并使 NA 抑制剂扎那米韦的抑制作用降低了 14-173 倍。当病毒制剂中含有大约 10%的具有 T148I 或 T439R 的 NA 变体时,观察到了 NA 结合,这突出了在病毒表征中使用深度测序的好处。总之,我们的发现为 NA 作为结合蛋白发挥作用的分子机制提供了新的见解。获得的信息可能有助于设计新的和改进的针对 NA 的抗病毒药物。