莫尔努皮拉维尔增加了SARS-CoV-2基因组的多样性和复杂性:一个病例控制队列研究
Cesare Ernesto Maria Gruber1, Fabio Giovanni Tucci2, Emanuela Giombini1
1Laboratory of Virology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Rome, Italy.
Journal of medical virology
|May 6, 2024
概括
摩尔努皮拉维尔治疗增加了SARS-CoV-2突变,特别是更高的过渡/转换比率和G->A变化,表明药物活性. 这种抗病毒药物还增加了COVID-19患者的病毒准物种多样性.
科学领域:
- 病毒学 病毒学
- 药理学 药理学是指药理学的学科.
- 基因组学就是基因组学.
背景情况:
- 莫尔努皮拉维尔是一种口服抗病毒药,用于对抗SARS-CoV-2.
- 营销后监测显示,SARS-CoV-2的血统具有增加的过渡/转变比率,这是已知的molnupiravir特征.
研究的目的:
- 为了评估molnupiravir对SARS-CoV-2患者的突变效应.
- 调查molnupiravir对病毒类物种多样性的影响.
主要方法:
- 来自接受莫尔努皮拉维尔治疗的患者的SARS-CoV-2全基因组测序.
- 与用 tixagevimab/cilgavimab 治疗的对照组进行比较分析.
- 突变分析侧重于转变/转变比率和G->A变化.
主要成果:
- 摩尔努皮拉维尔治疗导致SARS-CoV-2的转变/转变比率显著增加,在启动后7天.
- 观察到高G->A突变率,独立于APOBEC活动.
- 证明了病毒类物种的多样性和复杂性增加.
结论:
- 莫尔努皮拉维尔诱导了SARS-CoV-2中特有的突变特征.
- 药物的影响扩展到病毒遗传多样性的增加.
- 这些发现提供了关于molnupiravir体内抗病毒活性和潜在的进化后果的见解.
相关概念视频
Single Nucleotide Polymorphisms-SNPs
15.0K
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,...
15.0K
Viral Mutations
32.3K
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...
32.3K
Retroviruses
12.2K
Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
12.2K
Viral Recombination
23.4K
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.
23.4K
Mechanisms of Retrovirus-induced Cancers
5.1K
Retroviruses are RNA viruses that have been shown to cause cancers in diverse species, including chickens, mice, cats, and monkeys. The RNA genomes of these viruses are first reverse-transcribed into single and then double-stranded DNA (dsDNA) copies. This dsDNA called proviral DNA then integrates into the host genome. Subsequently, the host cell transcribes the proviral DNA in concert with the chromosomal DNA. This leads to the production of viral RNA and proteins that assemble at the host...
5.1K
Comparing Copy Number Variations and SNPs
17.7K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
17.7K


