Akkiz Hikmet
Department of Gastroenterology and Hepatology, The University of Çukurova, Adana, Turkey.
Front Med (Lausanne). 2021 May 7;8:636532. doi: 10.3389/fmed.2021.636532. eCollection 2021.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative virus of the coronavirus disease 2019 (COVID-19), has been identified in China in late December 2019. SARS-CoV-2 is an enveloped, positive-sense, single-stranded RNA betacoronavirus of the Coronaviridae family. Coronaviruses have genetic proofreading mechanism that corrects copying mistakes and thus SARS-CoV-2 genetic diversity is extremely low. Despite lower mutation rate of the virus, researchers have detected a total of 12,706 mutations in the SARS-CoV-2 genome, the majority of which were single nucleotide polymorphisms. Sequencing data revealed that the SARS-CoV-2 accumulates two-single nucleotide mutations per month in its genome. Recently, an amino acid aspartate (D) to glycine (G) (D614G) mutation due to an adenine to guanine nucleotide change at position 23,403 at the 614th amino-acid position of the spike protein in the original reference genotype has been identified. The SARS-CoV-2 viruses that carry the spike protein D614G mutation have become dominant variant around the world. The D614G mutation has been found to be associated with 3 other mutations in the spike protein. Clinical and pseudovirus experimental studies have demonstrated that the spike protein D614G mutation alters the virus phenotype. However, the impact of the mutation on the rate of transmission between people, disease severity and the vaccine and therapeutic development remains unclear. Three variants of SARS-CoV-2 have recently been identified. They are B.1.1.7 (UK) variant, B.1.351 (N501Y.V2, South African) variant and B.1.1.28 (Brazilian) variant. Epidemiological data suggest that they have a higher transmissibility than the original variant. There are reports that some vaccines are less efficacious against the B.1.351 variant. This review article discusses the effects of novel mutations in the SARS-CoV-2 genome on transmission, clinical outcomes and vaccine development.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)是2019冠状病毒病(COVID-19)的致病病毒,于2019年12月下旬在中国被发现。SARS-CoV-2是一种有包膜的、正链、单链RNAβ冠状病毒,属于冠状病毒科。冠状病毒具有校正复制错误的基因校对机制,因此SARS-CoV-2的基因多样性极低。尽管该病毒的突变率较低,但研究人员在SARS-CoV-2基因组中总共检测到12706个突变,其中大多数是单核苷酸多态性。测序数据显示,SARS-CoV-2基因组每月积累两个单核苷酸突变。最近,在原始参考基因型的刺突蛋白第614位氨基酸位置的23403位发生腺嘌呤到鸟嘌呤的核苷酸变化,导致氨基酸天冬氨酸(D)到甘氨酸(G)(D614G)的突变。携带刺突蛋白D614G突变的SARS-CoV-2病毒已成为全球主要变体。已发现D614G突变与刺突蛋白中的其他3种突变有关。临床和假病毒实验研究表明,刺突蛋白D614G突变改变了病毒表型。然而,该突变对人际传播率、疾病严重程度以及疫苗和治疗药物研发的影响仍不清楚。最近已鉴定出三种SARS-CoV-2变体。它们是B.1.1.7(英国)变体、B.1.351(N501Y.V2,南非)变体和B.1.1.28(巴西)变体。流行病学数据表明,它们的传播性比原始变体更高。有报道称,一些疫苗对B.1.351变体的效力较低。这篇综述文章讨论了SARS-CoV-2基因组中的新突变对传播、临床结果和疫苗研发的影响。