Banoun Helene
Independent researcher, Former research fellow at INSERM (French Institute for Health and Medical Research), Marseille, France.
Nephron. 2021;145(4):392-403. doi: 10.1159/000515417. Epub 2021 Apr 28.
Since the reporting of the first cases of coronavirus in China and the publication of the first sequence of SARS-CoV-2 in December 2019, the virus has undergone numerous mutations. In Europe, the spring outbreak (March-April) was followed by a drop in the number of cases and deaths. The disease may have evolved into a milder form. The increase in PCR-positive cases in late summer 2020 did not lead to the expected increase in hospitalizations, ICU admissions, and deaths, based on the severity of the disease in the spring. This difference in disease severity could be due to factors independent of the virus or to the evolution of the virus. This review attempts to identify the mutations that have appeared since the beginning of the pandemic and their role in the temporal evolution of the pandemic. There are a cell and humoral type cross-reactivity in a large part of the population to common cold coronaviruses (HCoVs) and SARS-CoV-2. Evolutionarily important mutations and deletions have emerged in the SARS-CoV-2 genes encoding proteins that interact with the host immune system. In addition, one of the major mutations (in viral polymerase) is logically associated with a higher frequency of mutations throughout the genome. This frequency fluctuates over time and shows a peak at the time when the epidemic was most active. The rate of mutations in proteins involved in the relationship to the immune system continues to increase after the first outbreak. The cross-reactivity on the 1 hand and the viral mutations observed on the other hand could explain the evolution of the pandemic until the summer of 2020, partly due to the evolution of the virus in relation to the host immune system. The immunization campaign began in December 2020: concerns are emerging about a possible escape of the circulating variants vaccines in early 2021. These variants could also escape immunity acquired through infection with the 2020 strains.
自中国报告首例冠状病毒病例以及2019年12月公布严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的首个序列以来,该病毒已发生多次突变。在欧洲,春季疫情爆发(3月至4月)之后,病例数和死亡人数有所下降。该疾病可能已演变为一种较轻的形式。基于春季疾病的严重程度,2020年夏末聚合酶链反应(PCR)阳性病例的增加并未导致住院、重症监护病房(ICU)收治人数和死亡人数出现预期的增加。疾病严重程度的这种差异可能是由于与病毒无关的因素,也可能是由于病毒的进化。本综述试图确定自疫情开始以来出现的突变及其在疫情时间演变中的作用。很大一部分人群对普通感冒冠状病毒(HCoVs)和SARS-CoV-2存在细胞和体液类型的交叉反应。在编码与宿主免疫系统相互作用的蛋白质的SARS-CoV-2基因中出现了具有进化重要性的突变和缺失。此外,一个主要突变(在病毒聚合酶中)在逻辑上与整个基因组中更高的突变频率相关。这种频率随时间波动,并在疫情最活跃时达到峰值。首次爆发后,与免疫系统相关的蛋白质中的突变率持续上升。一方面的交叉反应和另一方面观察到的病毒突变可以解释直到2020年夏季疫情的演变,部分原因是病毒相对于宿主免疫系统的进化。免疫接种运动于2020年12月开始:人们开始担心2021年初正在传播的变异株可能会逃避疫苗的作用。这些变异株也可能逃避通过感染2020年毒株获得的免疫力。