Department of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State Universitygrid.36567.31, Manhattan, Kansas, USA.
Microbiol Spectr. 2022 Jun 29;10(3):e0178921. doi: 10.1128/spectrum.01789-21. Epub 2022 May 31.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a zoonotic agent capable of infecting humans and a wide range of animal species. Over the duration of the pandemic, mutations in the SARS-CoV-2 spike (S) protein have arisen, culminating in the spread of several variants of concern (VOCs) with various degrees of altered virulence, transmissibility, and neutralizing antibody escape. In this study, we used pseudoviruses that express specific SARS-CoV-2 S protein substitutions and cell lines that express angiotensin-converting enzyme 2 (ACE2) from nine different animal species to gain insights into the effects of VOC mutations on viral entry and antibody neutralization capability. All animal ACE2 receptors tested, except mink, support viral cell entry for pseudoviruses expressing the ancestral prototype S at levels comparable to human ACE2. Most single S substitutions did not significantly change virus entry, although 614G and 484K resulted in a decreased efficiency. Conversely, combinatorial VOC substitutions in the S protein were associated with increased entry of pseudoviruses. Neutralizing titers in sera from various animal species were significantly reduced against pseudoviruses expressing the S proteins of Beta, Delta, or Omicron VOCs compared to the parental S protein. Especially, substitutions in the S protein of the Omicron variant significantly reduced the neutralizing titers of the sera. This study reveals important insights into the host range of SARS-CoV-2 and the effect of recently emergent S protein substitutions on viral entry, virus replication, and antibody-mediated viral neutralization. The ongoing coronavirus disease 2019 (COVID-19) pandemic, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), continues to have devastating impacts on global health and socioeconomics. The recent emergence of SARS-CoV-2 variants of concern, which contain mutations that can affect the virulence, transmission, and effectiveness of licensed vaccines and therapeutic antibodies, are currently becoming the common strains circulating in humans worldwide. In addition, SARS-CoV-2 has been shown to infect a wide variety of animal species, which could result in additional mutations of the SARS-CoV-2 virus. In this study, we investigate the effect of mutations present in SARS-CoV-2 variants of concern and determine the effects of these mutations on cell entry, virulence, and antibody neutralization activity in humans and a variety of animals that might be susceptible to SARS-CoV-2 infection. This information is essential to understand the effects of important SARS-CoV-2 mutations and to inform public policy to create better strategies to control the COVID-19 pandemic.
严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 是一种能够感染人类和多种动物的人畜共患病原体。在大流行期间,SARS-CoV-2 刺突 (S) 蛋白发生了突变,最终导致几种具有不同程度毒力、传染性和中和抗体逃逸能力的关注变体 (VOCs) 的传播。在这项研究中,我们使用表达特定 SARS-CoV-2 S 蛋白取代的假病毒和表达来自 9 种不同动物物种的血管紧张素转换酶 2 (ACE2) 的细胞系,深入了解 VOC 突变对病毒进入和抗体中和能力的影响。除了水貂,所有测试的动物 ACE2 受体都支持表达原始原型 S 的假病毒对细胞的进入,其水平与人类 ACE2 相当。大多数单一的 S 取代并没有显著改变病毒进入,尽管 614G 和 484K 导致效率降低。相反,S 蛋白中的组合 VOC 取代与假病毒进入的增加有关。与亲本 S 蛋白相比,来自不同动物物种的血清对表达 Beta、Delta 或 Omicron VOCs 的 S 蛋白的假病毒的中和滴度显著降低。特别是,Omicron 变体 S 蛋白中的取代显著降低了血清的中和滴度。这项研究揭示了 SARS-CoV-2 的宿主范围以及最近出现的 S 蛋白取代对病毒进入、病毒复制和抗体介导的病毒中和的重要影响。由严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 引起的持续的 2019 年冠状病毒病 (COVID-19) 大流行继续对全球健康和社会经济造成破坏性影响。最近出现的 SARS-CoV-2 关注变体,其中包含可能影响已授权疫苗和治疗性抗体的毒力、传播和有效性的突变,目前已成为全球人类中常见的循环菌株。此外,SARS-CoV-2 已被证明感染了多种动物物种,这可能导致 SARS-CoV-2 病毒的额外突变。在这项研究中,我们研究了 SARS-CoV-2 关注变体中存在的突变的影响,并确定了这些突变对人类和可能易感染 SARS-CoV-2 的多种动物的细胞进入、毒力和抗体中和活性的影响。这些信息对于了解 SARS-CoV-2 重要突变的影响以及为控制 COVID-19 大流行制定更好的策略以告知公共政策至关重要。