Abstract

Clustered regularly interspaced short palindromic repeats (CRISPR) in bacterial and archaeal DNA have recently been shown to be a new type of antiviral immune system in these organisms. We here study the diversity of spacers in CRISPR under selective pressure. We propose a population dynamics model that explains the biological observation that the leader-proximal end of CRISPR is more diversified and the leader-distal end of CRISPR is more conserved. This result is shown to be in agreement with recent experiments. Our results show that the CRISPR spacer structure is influenced by and provides a record of the viral challenges that bacteria face.

Highlights

  • Clustered regularly interspaced short palindromic repeats (CRISPR) in bacteria and archaea have recently been suggested to provide adaptable immunity in these organisms [1,2,3]

  • Clustered regularly interspaced short palindromic repeats (CRISPR) in bacterial and archaeal DNA have recently been shown to be a new type of antiviral immune system in these organisms

  • Our results show that the CRISPR spacer structure is influenced by and provides a record of the viral challenges that bacteria face

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Summary

CRISPR with a new spacer

New spacers are always added to the leader-proximal end [9]. To avoid infinite growth of CRISPR, an old spacer is dropped when CRISPR is longer than a certain length [10]. The Kronecker delta function i;k is 1 if spacer type i matches virus strain k; otherwise, it is 0 This model is modified from the classic immune response model with antigenic variation [13]. The initial value for the differential equations are naive bacteria whose CRISPR provide no resistance to viruses because their spacers are empty. At the beginning, both positions have high diversity of spacers.

Shannon entropy Shannon Entropy
Position of spacers
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