SARS-CoV CH.1.1 变种:基因组和结构洞察力
Liliana Bazzani1, Elena Imperia2,3, Fabio Scarpa4
1Sciences and Technologies for Sustainable Development and One Health, University Campus Bio-Medico of Rome, 00128 Rome, Italy.
Infectious disease reports
|June 27, 2023
概括
一种新的COVID-19变种,Omicron CH.1.1 "Orthrus",显示了与L452R.类似的突变. 早期分析表明,可能会增加严重程度和传播,需要加强全球监测.
科学领域:
- 病毒学和分子流行病学.
- 新兴病原体的基因组监测
背景情况:
- 这种Omicron亚变体XBB.1.5 (
- 克拉肯 (Kraken) 是一个巨大的动物.
- ) 在2023年初的全球COVID-19病例中占主导地位.
- 一个新的Omicron亚型,CH.1.1 (
- 这就是Orthrus Orthrus.
- ),出现了L452R突变,此前在Delta和BA.4/BA.5变种中见过.
研究的目的:
- 为了初步了解新出现的SARS-CoV-2 CH.1.1变种的全球分布.
- 分析CH.1.1突变在疾病严重程度,疫苗耐药性和传播方面的潜在功能意义.
- 调查CH.1.1变种的遗传起源和循环模式.
主要方法:
- 基因组数据分析与结构分子建模相结合.
- 同性学建模以评估与ACE2和静电电位的相互作用.
- 遗传学分析以确定进化关系和神秘循环.
主要成果:
- 这种CH.1.1变种与其他Omicron菌株共享约73%的突变.
- 同性学建模表明,与祖先菌株相比,CH.1.1可能表现出弱化的ACE2相互作用和更积极的静电电位表面.
- 遗传学分析表明,CH.1.1在正式检测之前已经在欧洲神秘地传播.
结论:
- CH.1.1变种具有突变,需要积极监测,因为它可能对疾病严重程度,疫苗有效性和传染性产生潜在影响.
- 基因组和结构分析为这种新兴的SARS-CoV-2变种的潜在生物行为提供了洞察力.
- 全基因组测序对于有效检测和控制新出现的病毒菌株,如CH.1.1.1.1,至关重要.
相关概念视频
Single Nucleotide Polymorphisms-SNPs
15.3K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.3K
Size and Structure of Viral Genomes
67
Viral genomes exhibit remarkable diversity in size, structure, and composition, influencing their replication strategies and interactions with host cells. These genomes consist of either DNA or RNA and may be linear or circular. Additionally, they can be single-stranded or double-stranded, with each configuration affecting how the virus propagates within a host. RNA viruses, for instance, generally have smaller genomes than DNA viruses, a factor that contributes to their high mutation rates and...
67
Viral Mutations
32.5K
A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
32.5K
Viral Recombination
23.6K
Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
23.6K
Viral Structure
62.6K
Viruses are extraordinarily diverse in shape and size, but they all have several structural features in common. All viruses have a core that contains a DNA- or RNA-based genome. The core is surrounded by a protective coat of proteins called the capsid. The capsid is composed of subunits called capsomeres. The capsid and genome-containing core are together known as the nucleocapsid.
62.6K
Leaky Scanning
5.2K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA. Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.2K


