Evolutionary Stabilization of Cooperative Toxin Production through a Bacterium-Plasmid-Phage Interplay

Bacteria are excellent model organisms to study mechanisms of social evolution. The production of public goods, e.g., toxin release by cell lysis in clonal bacterial populations, is a frequently studied example of cooperative behavior. Here, we analyze evolutionary stabilization of toxin release by...

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Main Authors: Stefanie Spriewald, Eva Stadler, Burkhard A. Hense, Philipp C. Münch, Alice C. McHardy, Anna S. Weiss, Nancy Obeng, Johannes Müller, Bärbel Stecher
Format: Article
Language:English
Published: American Society for Microbiology 2020-07-01
Series:mBio
Subjects:
Online Access:https://doi.org/10.1128/mBio.00912-20
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spelling doaj-e2dc3f535c5144d0ac574990a668bdab2021-07-02T12:55:59ZengAmerican Society for MicrobiologymBio2150-75112020-07-01114e00912-2010.1128/mBio.00912-20Evolutionary Stabilization of Cooperative Toxin Production through a Bacterium-Plasmid-Phage InterplayStefanie SpriewaldEva StadlerBurkhard A. HensePhilipp C. MünchAlice C. McHardyAnna S. WeissNancy ObengJohannes MüllerBärbel StecherBacteria are excellent model organisms to study mechanisms of social evolution. The production of public goods, e.g., toxin release by cell lysis in clonal bacterial populations, is a frequently studied example of cooperative behavior. Here, we analyze evolutionary stabilization of toxin release by the enteric pathogen Salmonella. The release of colicin Ib (ColIb), which is used by Salmonella to gain an edge against competing microbiota following infection, is coupled to bacterial lysis mediated by temperate phages. Here, we show that phage-dependent lysis and subsequent release of colicin and phage particles occurs only in part of the ColIb-expressing Salmonella population. This phenotypic heterogeneity in lysis, which represents an essential step in the temperate phage life cycle, has evolved as a bet-hedging strategy under fluctuating environments such as the gastrointestinal tract. Our findings suggest that prophages can thereby evolutionarily stabilize costly toxin release in bacterial populations.Colicins are toxins produced and released by Enterobacteriaceae to kill competitors in the gut. While group A colicins employ a division of labor strategy to liberate the toxin into the environment via colicin-specific lysis, group B colicin systems lack cognate lysis genes. In Salmonella enterica serovar Typhimurium (S. Tm), the group B colicin Ib (ColIb) is released by temperate phage-mediated bacteriolysis. Phage-mediated ColIb release promotes S. Tm fitness against competing Escherichia coli. It remained unclear how prophage-mediated lysis is realized in a clonal population of ColIb producers and if prophages contribute to evolutionary stability of toxin release in S. Tm. Here, we show that prophage-mediated lysis occurs in an S. Tm subpopulation only, thereby introducing phenotypic heterogeneity to the system. We established a mathematical model to study the dynamic interplay of S. Tm, ColIb, and a temperate phage in the presence of a competing species. Using this model, we studied long-term evolution of phage lysis rates in a fluctuating infection scenario. This revealed that phage lysis evolves as bet-hedging strategy that maximizes phage spread, regardless of whether colicin is present or not. We conclude that the ColIb system, lacking its own lysis gene, is making use of the evolutionary stable phage strategy to be released. Prophage lysis genes are highly prevalent in nontyphoidal Salmonella genomes. This suggests that the release of ColIb by temperate phages is widespread. In conclusion, our findings shed new light on the evolution and ecology of group B colicin systems.https://doi.org/10.1128/mBio.00912-20bacteriophagelysogenvirusevolutiontoxinbacteriocinregulationheterogeneityadaptive dynamicsevolutionary stable strategyspiteful interactionbistabilitycheatercolicingastrointestinal infectionphenotypic noise
collection DOAJ
language English
format Article
sources DOAJ
author Stefanie Spriewald
Eva Stadler
Burkhard A. Hense
Philipp C. Münch
Alice C. McHardy
Anna S. Weiss
Nancy Obeng
Johannes Müller
Bärbel Stecher
spellingShingle Stefanie Spriewald
Eva Stadler
Burkhard A. Hense
Philipp C. Münch
Alice C. McHardy
Anna S. Weiss
Nancy Obeng
Johannes Müller
Bärbel Stecher
Evolutionary Stabilization of Cooperative Toxin Production through a Bacterium-Plasmid-Phage Interplay
mBio
bacteriophage
lysogen
virus
evolution
toxin
bacteriocin
regulation
heterogeneity
adaptive dynamics
evolutionary stable strategy
spiteful interaction
bistability
cheater
colicin
gastrointestinal infection
phenotypic noise
author_facet Stefanie Spriewald
Eva Stadler
Burkhard A. Hense
Philipp C. Münch
Alice C. McHardy
Anna S. Weiss
Nancy Obeng
Johannes Müller
Bärbel Stecher
author_sort Stefanie Spriewald
title Evolutionary Stabilization of Cooperative Toxin Production through a Bacterium-Plasmid-Phage Interplay
title_short Evolutionary Stabilization of Cooperative Toxin Production through a Bacterium-Plasmid-Phage Interplay
title_full Evolutionary Stabilization of Cooperative Toxin Production through a Bacterium-Plasmid-Phage Interplay
title_fullStr Evolutionary Stabilization of Cooperative Toxin Production through a Bacterium-Plasmid-Phage Interplay
title_full_unstemmed Evolutionary Stabilization of Cooperative Toxin Production through a Bacterium-Plasmid-Phage Interplay
title_sort evolutionary stabilization of cooperative toxin production through a bacterium-plasmid-phage interplay
publisher American Society for Microbiology
series mBio
issn 2150-7511
publishDate 2020-07-01
description Bacteria are excellent model organisms to study mechanisms of social evolution. The production of public goods, e.g., toxin release by cell lysis in clonal bacterial populations, is a frequently studied example of cooperative behavior. Here, we analyze evolutionary stabilization of toxin release by the enteric pathogen Salmonella. The release of colicin Ib (ColIb), which is used by Salmonella to gain an edge against competing microbiota following infection, is coupled to bacterial lysis mediated by temperate phages. Here, we show that phage-dependent lysis and subsequent release of colicin and phage particles occurs only in part of the ColIb-expressing Salmonella population. This phenotypic heterogeneity in lysis, which represents an essential step in the temperate phage life cycle, has evolved as a bet-hedging strategy under fluctuating environments such as the gastrointestinal tract. Our findings suggest that prophages can thereby evolutionarily stabilize costly toxin release in bacterial populations.Colicins are toxins produced and released by Enterobacteriaceae to kill competitors in the gut. While group A colicins employ a division of labor strategy to liberate the toxin into the environment via colicin-specific lysis, group B colicin systems lack cognate lysis genes. In Salmonella enterica serovar Typhimurium (S. Tm), the group B colicin Ib (ColIb) is released by temperate phage-mediated bacteriolysis. Phage-mediated ColIb release promotes S. Tm fitness against competing Escherichia coli. It remained unclear how prophage-mediated lysis is realized in a clonal population of ColIb producers and if prophages contribute to evolutionary stability of toxin release in S. Tm. Here, we show that prophage-mediated lysis occurs in an S. Tm subpopulation only, thereby introducing phenotypic heterogeneity to the system. We established a mathematical model to study the dynamic interplay of S. Tm, ColIb, and a temperate phage in the presence of a competing species. Using this model, we studied long-term evolution of phage lysis rates in a fluctuating infection scenario. This revealed that phage lysis evolves as bet-hedging strategy that maximizes phage spread, regardless of whether colicin is present or not. We conclude that the ColIb system, lacking its own lysis gene, is making use of the evolutionary stable phage strategy to be released. Prophage lysis genes are highly prevalent in nontyphoidal Salmonella genomes. This suggests that the release of ColIb by temperate phages is widespread. In conclusion, our findings shed new light on the evolution and ecology of group B colicin systems.
topic bacteriophage
lysogen
virus
evolution
toxin
bacteriocin
regulation
heterogeneity
adaptive dynamics
evolutionary stable strategy
spiteful interaction
bistability
cheater
colicin
gastrointestinal infection
phenotypic noise
url https://doi.org/10.1128/mBio.00912-20
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