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Non-classical Phase Diagram for Virus Bacterial Coevolution Mediated by Clustered Regularly Interspaced Short Palindromic Repeats

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Date 2017 Feb 17
PMID 28202591
Citations 7
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Abstract

CRISPR is a newly discovered prokaryotic immune system. Bacteria and archaea with this system incorporate genetic material from invading viruses into their genomes, providing protection against future infection by similar viruses. The condition for coexistence of prokaryots and viruses is an interesting problem in evolutionary biology. In this work, we show an intriguing phase diagram of the virus extinction probability, which is more complex than that of the classical predator-prey model. As the CRISPR incorporates genetic material, viruses are under pressure to evolve to escape recognition by CRISPR. When bacteria have a small rate of deleting spacers, a new parameter region in which bacteria and viruses can coexist arises, and it leads to a more complex coexistence patten for bacteria and viruses. For example, when the virus mutation rate is low, the virus extinction probability changes non-montonically with the bacterial exposure rate. The virus and bacteria coevolution not only alters the virus extinction probability, but also changes the bacterial population structure. Additionally, we show that recombination is a successful strategy for viruses to escape from CRISPR recognition when viruses have multiple proto-spacers, providing support for a recombination-mediated escape mechanism suggested experimentally. Finally, we suggest that the re-entrant phase diagram, in which phages can progress through three phases of extinction and two phases of abundance at low spacer deletion rates as a function of exposure rate to bacteria, is an experimentally testable phenomenon.

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References
1.
Paez-Espino D, Morovic W, Sun C, Thomas B, Ueda K, Stahl B . Strong bias in the bacterial CRISPR elements that confer immunity to phage. Nat Commun. 2013; 4:1430. DOI: 10.1038/ncomms2440. View

2.
Przybilski R, Richter C, Gristwood T, Clulow J, Vercoe R, Fineran P . Csy4 is responsible for CRISPR RNA processing in Pectobacterium atrosepticum. RNA Biol. 2011; 8(3):517-28. DOI: 10.4161/rna.8.3.15190. View

3.
Swarts D, Mosterd C, van Passel M, Brouns S . CRISPR interference directs strand specific spacer acquisition. PLoS One. 2012; 7(4):e35888. PMC: 3338789. DOI: 10.1371/journal.pone.0035888. View

4.
van der Oost J, Jore M, Westra E, Lundgren M, Brouns S . CRISPR-based adaptive and heritable immunity in prokaryotes. Trends Biochem Sci. 2009; 34(8):401-7. DOI: 10.1016/j.tibs.2009.05.002. View

5.
Westra E, van Houte S, Oyesiku-Blakemore S, Makin B, Broniewski J, Best A . Parasite Exposure Drives Selective Evolution of Constitutive versus Inducible Defense. Curr Biol. 2015; 25(8):1043-9. DOI: 10.1016/j.cub.2015.01.065. View