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Viral Diversity Threshold for Adaptive Immunity in Prokaryotes

Bacteria and archaea face continual onslaughts of rapidly diversifying viruses and plasmids. Many prokaryotes maintain adaptive immune systems known as clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated genes (Cas). CRISPR-Cas systems are genomic sensors that se...

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Autores principales: Weinberger, Ariel D., Wolf, Yuri I., Lobkovsky, Alexander E., Gilmore, Michael S., Koonin, Eugene V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3517865/
https://www.ncbi.nlm.nih.gov/pubmed/23221803
http://dx.doi.org/10.1128/mBio.00456-12
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author Weinberger, Ariel D.
Wolf, Yuri I.
Lobkovsky, Alexander E.
Gilmore, Michael S.
Koonin, Eugene V.
author_facet Weinberger, Ariel D.
Wolf, Yuri I.
Lobkovsky, Alexander E.
Gilmore, Michael S.
Koonin, Eugene V.
author_sort Weinberger, Ariel D.
collection PubMed
description Bacteria and archaea face continual onslaughts of rapidly diversifying viruses and plasmids. Many prokaryotes maintain adaptive immune systems known as clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated genes (Cas). CRISPR-Cas systems are genomic sensors that serially acquire viral and plasmid DNA fragments (spacers) that are utilized to target and cleave matching viral and plasmid DNA in subsequent genomic invasions, offering critical immunological memory. Only 50% of sequenced bacteria possess CRISPR-Cas immunity, in contrast to over 90% of sequenced archaea. To probe why half of bacteria lack CRISPR-Cas immunity, we combined comparative genomics and mathematical modeling. Analysis of hundreds of diverse prokaryotic genomes shows that CRISPR-Cas systems are substantially more prevalent in thermophiles than in mesophiles. With sequenced bacteria disproportionately mesophilic and sequenced archaea mostly thermophilic, the presence of CRISPR-Cas appears to depend more on environmental temperature than on bacterial-archaeal taxonomy. Mutation rates are typically severalfold higher in mesophilic prokaryotes than in thermophilic prokaryotes. To quantitatively test whether accelerated viral mutation leads microbes to lose CRISPR-Cas systems, we developed a stochastic model of virus-CRISPR coevolution. The model competes CRISPR-Cas-positive (CRISPR-Cas+) prokaryotes against CRISPR-Cas-negative (CRISPR-Cas−) prokaryotes, continually weighing the antiviral benefits conferred by CRISPR-Cas immunity against its fitness costs. Tracking this cost-benefit analysis across parameter space reveals viral mutation rate thresholds beyond which CRISPR-Cas cannot provide sufficient immunity and is purged from host populations. These results offer a simple, testable viral diversity hypothesis to explain why mesophilic bacteria disproportionately lack CRISPR-Cas immunity. More generally, fundamental limits on the adaptability of biological sensors (Lamarckian evolution) are predicted.
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spelling pubmed-35178652013-01-09 Viral Diversity Threshold for Adaptive Immunity in Prokaryotes Weinberger, Ariel D. Wolf, Yuri I. Lobkovsky, Alexander E. Gilmore, Michael S. Koonin, Eugene V. mBio Research Article Bacteria and archaea face continual onslaughts of rapidly diversifying viruses and plasmids. Many prokaryotes maintain adaptive immune systems known as clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated genes (Cas). CRISPR-Cas systems are genomic sensors that serially acquire viral and plasmid DNA fragments (spacers) that are utilized to target and cleave matching viral and plasmid DNA in subsequent genomic invasions, offering critical immunological memory. Only 50% of sequenced bacteria possess CRISPR-Cas immunity, in contrast to over 90% of sequenced archaea. To probe why half of bacteria lack CRISPR-Cas immunity, we combined comparative genomics and mathematical modeling. Analysis of hundreds of diverse prokaryotic genomes shows that CRISPR-Cas systems are substantially more prevalent in thermophiles than in mesophiles. With sequenced bacteria disproportionately mesophilic and sequenced archaea mostly thermophilic, the presence of CRISPR-Cas appears to depend more on environmental temperature than on bacterial-archaeal taxonomy. Mutation rates are typically severalfold higher in mesophilic prokaryotes than in thermophilic prokaryotes. To quantitatively test whether accelerated viral mutation leads microbes to lose CRISPR-Cas systems, we developed a stochastic model of virus-CRISPR coevolution. The model competes CRISPR-Cas-positive (CRISPR-Cas+) prokaryotes against CRISPR-Cas-negative (CRISPR-Cas−) prokaryotes, continually weighing the antiviral benefits conferred by CRISPR-Cas immunity against its fitness costs. Tracking this cost-benefit analysis across parameter space reveals viral mutation rate thresholds beyond which CRISPR-Cas cannot provide sufficient immunity and is purged from host populations. These results offer a simple, testable viral diversity hypothesis to explain why mesophilic bacteria disproportionately lack CRISPR-Cas immunity. More generally, fundamental limits on the adaptability of biological sensors (Lamarckian evolution) are predicted. American Society of Microbiology 2012-12-04 /pmc/articles/PMC3517865/ /pubmed/23221803 http://dx.doi.org/10.1128/mBio.00456-12 Text en Copyright © 2012 Weinberger et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported (http://creativecommons.org/licenses/by-nc-sa/3.0/) license, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Weinberger, Ariel D.
Wolf, Yuri I.
Lobkovsky, Alexander E.
Gilmore, Michael S.
Koonin, Eugene V.
Viral Diversity Threshold for Adaptive Immunity in Prokaryotes
title Viral Diversity Threshold for Adaptive Immunity in Prokaryotes
title_full Viral Diversity Threshold for Adaptive Immunity in Prokaryotes
title_fullStr Viral Diversity Threshold for Adaptive Immunity in Prokaryotes
title_full_unstemmed Viral Diversity Threshold for Adaptive Immunity in Prokaryotes
title_short Viral Diversity Threshold for Adaptive Immunity in Prokaryotes
title_sort viral diversity threshold for adaptive immunity in prokaryotes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3517865/
https://www.ncbi.nlm.nih.gov/pubmed/23221803
http://dx.doi.org/10.1128/mBio.00456-12
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