School of Medical Sciences, Faculty of Medicine, UNSW, Sydney, New South Wales, Australia.
The Kirby Institute, UNSW, Sydney, New South Wales, Australia.
Rev Med Virol. 2022 Sep;32(5):e2381. doi: 10.1002/rmv.2381. Epub 2022 Jul 20.
The first dominant SARS-CoV-2 Omicron variant BA.1 harbours 35 mutations in its Spike protein from the original SARS-CoV-2 variant that emerged late 2019. Soon after its discovery, BA.1 rapidly emerged to become the dominant variant worldwide and has since evolved into several variants. Omicron is of major public health concern owing to its high infectivity and antibody evasion. This review article examines the theories that have been proposed on the evolution of Omicron including zoonotic spillage, infection in immunocompromised individuals and cryptic spread in the community without being diagnosed. Added to the complexity of Omicron's evolution are the multiple reports of recombination events occurring between co-circulating variants of Omicron with Delta and other variants such as XE. Current literature suggests that the combination of the novel mutations in Omicron has resulted in the variant having higher infectivity than the original Wuhan-Hu-1 and Delta variant. However, severity is believed to be less owing to the reduced syncytia formation and lower multiplication in the human lung tissue. Perhaps most challenging is that several studies indicate that the efficacy of the available vaccines have been reduced against Omicron variant (8-127 times reduction) as compared to the Wuhan-Hu-1 variant. The administration of booster vaccine, however, compensates with the reduction and improves the efficacy by 12-35 fold. Concerningly though, the broadly neutralising monoclonal antibodies, including those approved by FDA for therapeutic use against previous SARS-CoV-2 variants, are mostly ineffective against Omicron with the exception of Sotrovimab and recent reports suggest that the Omicron BA.2 is also resistant to Sotrovimab. Currently two new Omicron variants BA.4 and BA.5 are emerging and are reported to be more transmissible and resistant to immunity generated by previous variants including Omicron BA.1 and most monoclonal antibodies. As new variants of SARS-CoV-2 will likely continue to emerge it is important that the evolution, and biological consequences of new mutations, in existing variants be well understood.
最早出现的 SARS-CoV-2 奥密克戎变异株 BA.1 其刺突蛋白相较于 2019 年末出现的原始 SARS-CoV-2 变异株有 35 处突变。在被发现后不久,BA.1 迅速成为全球主要流行变异株,并进一步进化出多种变异株。奥密克戎变异株由于其高传染性和对抗体的逃避能力而引起了极大的公共卫生关注。本文综述了关于奥密克戎变异株进化的理论,包括从动物传播到人、在免疫功能低下个体中感染以及在未被诊断的情况下在社区中隐匿传播。奥密克戎变异株进化的复杂性在于,在奥密克戎与德尔塔以及其他变异株如 XE 等共同流行的变异株之间,有多次报道发生重组事件。目前的文献表明,奥密克戎变异株的新型突变组合导致其比原始的武汉株和德尔塔变异株具有更高的传染性。然而,由于合胞体形成减少和在人肺组织中的繁殖减少,严重程度被认为较低。也许最具挑战性的是,几项研究表明,与武汉株相比,现有的疫苗针对奥密克戎变异株的有效性降低了(8-127 倍)。然而,接种加强疫苗可以弥补这种降低,并将有效性提高 12-35 倍。令人担忧的是,包括美国食品药品监督管理局批准用于治疗以前的 SARS-CoV-2 变异株的那些在内的广泛中和单克隆抗体,对奥密克戎变异株大多无效,除了 Sotrovimab 和最近的报告表明,奥密克戎 BA.2 也对 Sotrovimab 具有耐药性。目前,两种新的奥密克戎变异株 BA.4 和 BA.5 正在出现,据报道它们的传染性更强,并且对以前的变异株包括奥密克戎 BA.1 和大多数单克隆抗体产生的免疫力具有耐药性。随着新的 SARS-CoV-2 变异株的出现,了解现有变异株中新型突变的进化和生物学后果非常重要。