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Innate and adaptive immunity in bacteria: Mechanisms of programmed genetic variation to fight bacteriophages

机译:细菌的先天性和适应性免疫:抵抗细菌噬菌体的程序化遗传变异机制

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摘要

Bacteria are constantly challenged by bacteriophages (viruses that infect bacteria), the most abundant microorganism on earth. Bacteria have evolved a variety of immunity mechanisms to resist bacteriophage infection. In response, bacteriophages can evolve counter-resistance mechanisms and launch a 'virus versus host' evolutionary arms race. In this context, rapid evolution is fundamental for the survival of the bacterial cell. Programmed genetic variation mechanisms at loci involved in immunity against bacteriophages generate diversity at a much faster rate than random point mutation and enable bacteria to quickly adapt and repel infection. Diversity-generating retroelements (DGRs) and phase variation mechanisms enhance the generic (innate) immune response against bacteriophages. On the other hand, the integration of small bacteriophage sequences in CRISPR loci provide bacteria with a virus-specific and sequence-specific adaptive immune response. Therefore, although using different molecular mechanisms, both prokaryotes and higher organisms rely on programmed genetic variation to increase genetic diversity and fight rapidly evolving infectious agents.
机译:细菌不断受到噬菌体(感染细菌的病毒)的挑战,噬菌体是地球上最丰富的微生物。细菌已经进化出多种免疫机制来抵抗噬菌体感染。作为响应,噬菌体可以进化出抗药性机制并发起“病毒与宿主”进化军备竞赛。在这种情况下,快速进化对于细菌细胞的生存至关重要。参与针对噬菌体免疫的基因座上的程序化遗传变异机制以比随机点突变快得多的速率产生多样性,并使细菌能够快速适应和排斥感染。产生多样性的逆向元件(DGR)和相变机制增强了针对噬菌体的通用(先天)免疫应答。另一方面,在CRISPR基因座中小的噬菌体序列的整合为细菌提供了病毒特异性和序列特异性的适应性免疫应答。因此,尽管使用不同的分子机制,但原核生物和高级生物都依赖于程序化的遗传变异来增加遗传多样性并与迅速发展的传染原作斗争。

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