间歇性病毒驱动的继承产生了CRISPR介导的微生物-病毒共同进化的动态交替
Armun Liaghat1,2, Jiayue Yang3, Rachel Whitaker3,4
1Department of Ecology and Evolution, University of Chicago, Chicago, IL, USA.
Journal of the Royal Society, Interface
|August 21, 2024
概括
当宿主竞争削弱微生物对抗病毒的防御能力时,病毒流行病就会出现. 这项研究模拟了宿主-病原体动态如何从控制转向广泛爆发,由生态和进化反驱动.
科学领域:
- 生态生态学 生态生态学
- 进化生物学 进化生物学
- 微生物学 微生物学
- 流行病学 流行病学
背景情况:
- 在模型中,病毒和微生物与CRISPR-Cas免疫力之间的共同进化显示了宿主控制和病毒流行病的交替动态.
- 这些交替动态尚未在其他宿主-病原体系统中观察到.
- 了解从受控的宿主-病原体相互作用过渡到大规模爆发至关重要.
研究的目的:
- 用一个随机生态进化模型研究宿主控制的崩和向大病毒爆发的过渡.
- 确定宿主密度依赖的竞争在病毒驱动的继承和多样性中的作用.
- 根据关键参数推导出病毒出现的概率,并探索基于关键参数的交替概率.
主要方法:
- 开发了一个随机的生态进化模型,包括宿主密度依赖的竞争.
- 利用感染和逃脱网络来分析宿主-病原体相互作用.
- 导出病毒出现概率和分析的交替概率作为非维度参数的函数.
主要成果:
- 宿主密度依赖的竞争驱动着由病毒驱动的间歇继承,并在控制阶段集中病毒逃生途径.
- 病毒出现概率的波动,大小和频率的增加,标志着大规模爆发的方法.
- 宿主竞争和病毒多样化之间的新兴反会产生一个脆弱的宿主免疫结构.
结论:
- 该研究表明,生态因素 (宿主竞争) 和进化动态 (病毒多样化) 如何相互作用,破坏宿主免疫力.
- 这些相互作用促进了从受控的宿主-病原体相互作用到大规模流行病的动态过渡.
- 这些发现强调了考虑生态进化反对于理解流行病动态的重要性.
相关概念视频
Viral Mutations
32.2K
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...
32.2K
Viral Recombination
23.3K
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.
23.3K
CRISPR and crRNAs
16.9K
Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
16.9K
CRISPR
50.0K
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
50.0K
Retrovirus Life Cycles
45.8K
Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the...
45.8K
Conservative Site-specific Recombination and Phase Variation
6.0K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
The recognition sites for Cre recombinase called LoxP...
6.0K


