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Evolution of the CRISPR-Cas adaptive immunity systems in prokaryotes: models and observations on virus-host coevolution.原核生物中CRISPR-Cas适应性免疫系统的进化:病毒-宿主共同进化的模型与观察
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Pseudo-chaotic oscillations in CRISPR-virus coevolution predicted by bifurcation analysis.分支分析预测的 CRISPR-病毒共进化中的拟混沌振荡。
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本文引用的文献

1
Nasty viruses, costly plasmids, population dynamics, and the conditions for establishing and maintaining CRISPR-mediated adaptive immunity in bacteria.恶劣的病毒、昂贵的质粒、种群动态,以及在细菌中建立和维持 CRISPR 介导的适应性免疫的条件。
PLoS Genet. 2010 Oct 28;6(10):e1001171. doi: 10.1371/journal.pgen.1001171.
2
A minimal model for multiple epidemics and immunity spreading.用于多重传染病和免疫传播的最小模型。
PLoS One. 2010 Oct 18;5(10):e13326. doi: 10.1371/journal.pone.0013326.
3
Heterogeneous diversity of spacers within CRISPR (clustered regularly interspaced short palindromic repeats).CRISPR(成簇规律间隔短回文重复序列)内间隔区的异质多样性。
Phys Rev Lett. 2010 Sep 17;105(12):128102. doi: 10.1103/PhysRevLett.105.128102. Epub 2010 Sep 14.
4
Impact of CRIPSR immunity on the emergence of bacterial pathogens.CRISPR免疫对细菌病原体出现的影响。
Future Microbiol. 2010 May;5(5):693-5. doi: 10.2217/fmb.10.38.
5
CRISPR-mediated phage resistance and the ghost of coevolution past.CRISPR 介导的噬菌体抗性与协同进化的幽灵。
Proc Biol Sci. 2010 Jul 22;277(1691):2097-103. doi: 10.1098/rspb.2010.0055. Epub 2010 Mar 17.
6
The CRISPR system: small RNA-guided defense in bacteria and archaea.CRISPR 系统:细菌和古菌中 RNA 引导的小片段干扰防御系统。
Mol Cell. 2010 Jan 15;37(1):7-19. doi: 10.1016/j.molcel.2009.12.033.
7
Self versus non-self discrimination during CRISPR RNA-directed immunity.CRISPR RNA 指导的免疫过程中的自我与非我区分。
Nature. 2010 Jan 28;463(7280):568-71. doi: 10.1038/nature08703. Epub 2010 Jan 13.
8
Sustainability of virulence in a phage-bacterial ecosystem.噬菌体-细菌生态系统中毒力的可持续性。
J Virol. 2010 Mar;84(6):3016-22. doi: 10.1128/JVI.02326-09. Epub 2010 Jan 13.
9
CRISPR/Cas, the immune system of bacteria and archaea.CRISPR/Cas,细菌和古菌的免疫系统。
Science. 2010 Jan 8;327(5962):167-70. doi: 10.1126/science.1179555.
10
RNA-guided RNA cleavage by a CRISPR RNA-Cas protein complex.CRISPR RNA-Cas蛋白复合物介导的RNA引导的RNA切割
Cell. 2009 Nov 25;139(5):945-56. doi: 10.1016/j.cell.2009.07.040.

靶向细菌免疫缓冲噬菌体多样性。

Targeted bacterial immunity buffers phage diversity.

机构信息

Center for Models of Life, Niels Bohr Institute, University of Copenhagen, Blegdamsvej 17, 2100 Copenhagen Ø, Denmark.

出版信息

J Virol. 2011 Oct;85(20):10554-60. doi: 10.1128/JVI.05222-11. Epub 2011 Aug 3.

DOI:10.1128/JVI.05222-11
PMID:21813617
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3187494/
Abstract

Bacteria have evolved diverse defense mechanisms that allow them to fight viral attacks. One such mechanism, the clustered, regularly interspaced, short palindromic repeat (CRISPR) system, is an adaptive immune system consisting of genetic loci that can take up genetic material from invasive elements (viruses and plasmids) and later use them to reject the returning invaders. It remains an open question how, despite the ongoing evolution of attack and defense mechanisms, bacteria and viral phages manage to coexist. Using a simple mathematical model and a two-dimensional numerical simulation, we found that CRISPR adaptive immunity allows for robust phage-bacterium coexistence even when the number of virus species far exceeds the capacity of CRISPR-encoded genetic memory. Coexistence is predicted to be a consequence of the presence of many interdependent species that stress but do not overrun the bacterial defense system.

摘要

细菌已经进化出多种防御机制,使它们能够抵御病毒攻击。其中一种机制是成簇、规律间隔、短回文重复序列(CRISPR)系统,这是一种适应性免疫系统,由能够摄取来自入侵元素(病毒和质粒)的遗传物质的遗传基因座组成,然后利用这些物质来抵御再次入侵的外来物质。尽管攻击和防御机制在不断进化,但细菌和病毒噬菌体是如何设法共存的,这仍然是一个悬而未决的问题。通过使用简单的数学模型和二维数值模拟,我们发现,即使病毒种类的数量远远超过 CRISPR 编码的遗传记忆能力,CRISPR 适应性免疫也可以允许噬菌体和细菌稳定共存。共存是由于存在许多相互依存的物种而导致的,这些物种对细菌防御系统施加压力,但不会使其崩溃。