Dynamics of adaptive immunity against phage in bacterial populations.

The CRISPR (clustered regularly interspaced short palindromic repeats) mechanism allows bacteria to adaptively defend against phages by acquiring short genomic sequences (spacers) that target specific sequences in the viral genome. We propose a population dynamical model where immunity can be both a...

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Main Authors: Serena Bradde, Marija Vucelja, Tiberiu Teşileanu, Vijay Balasubramanian
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-04-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC5411097?pdf=render
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spelling doaj-3b922a3ae5d342f58db5fe0200dd66aa2020-11-24T21:51:48ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582017-04-01134e100548610.1371/journal.pcbi.1005486Dynamics of adaptive immunity against phage in bacterial populations.Serena BraddeMarija VuceljaTiberiu TeşileanuVijay BalasubramanianThe CRISPR (clustered regularly interspaced short palindromic repeats) mechanism allows bacteria to adaptively defend against phages by acquiring short genomic sequences (spacers) that target specific sequences in the viral genome. We propose a population dynamical model where immunity can be both acquired and lost. The model predicts regimes where bacterial and phage populations can co-exist, others where the populations exhibit damped oscillations, and still others where one population is driven to extinction. Our model considers two key parameters: (1) ease of acquisition and (2) spacer effectiveness in conferring immunity. Analytical calculations and numerical simulations show that if spacers differ mainly in ease of acquisition, or if the probability of acquiring them is sufficiently high, bacteria develop a diverse population of spacers. On the other hand, if spacers differ mainly in their effectiveness, their final distribution will be highly peaked, akin to a "winner-take-all" scenario, leading to a specialized spacer distribution. Bacteria can interpolate between these limiting behaviors by actively tuning their overall acquisition probability.http://europepmc.org/articles/PMC5411097?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Serena Bradde
Marija Vucelja
Tiberiu Teşileanu
Vijay Balasubramanian
spellingShingle Serena Bradde
Marija Vucelja
Tiberiu Teşileanu
Vijay Balasubramanian
Dynamics of adaptive immunity against phage in bacterial populations.
PLoS Computational Biology
author_facet Serena Bradde
Marija Vucelja
Tiberiu Teşileanu
Vijay Balasubramanian
author_sort Serena Bradde
title Dynamics of adaptive immunity against phage in bacterial populations.
title_short Dynamics of adaptive immunity against phage in bacterial populations.
title_full Dynamics of adaptive immunity against phage in bacterial populations.
title_fullStr Dynamics of adaptive immunity against phage in bacterial populations.
title_full_unstemmed Dynamics of adaptive immunity against phage in bacterial populations.
title_sort dynamics of adaptive immunity against phage in bacterial populations.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2017-04-01
description The CRISPR (clustered regularly interspaced short palindromic repeats) mechanism allows bacteria to adaptively defend against phages by acquiring short genomic sequences (spacers) that target specific sequences in the viral genome. We propose a population dynamical model where immunity can be both acquired and lost. The model predicts regimes where bacterial and phage populations can co-exist, others where the populations exhibit damped oscillations, and still others where one population is driven to extinction. Our model considers two key parameters: (1) ease of acquisition and (2) spacer effectiveness in conferring immunity. Analytical calculations and numerical simulations show that if spacers differ mainly in ease of acquisition, or if the probability of acquiring them is sufficiently high, bacteria develop a diverse population of spacers. On the other hand, if spacers differ mainly in their effectiveness, their final distribution will be highly peaked, akin to a "winner-take-all" scenario, leading to a specialized spacer distribution. Bacteria can interpolate between these limiting behaviors by actively tuning their overall acquisition probability.
url http://europepmc.org/articles/PMC5411097?pdf=render
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AT tiberiutesileanu dynamicsofadaptiveimmunityagainstphageinbacterialpopulations
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