Horizontal Gene Transfer of Functional Type VI Killing Genes by Natural Transformation

ABSTRACT Horizontal gene transfer (HGT) can have profound effects on bacterial evolution by allowing individuals to rapidly acquire adaptive traits that shape their strategies for competition. One strategy for intermicrobial antagonism often used by Proteobacteria is the genetically encoded contact-...

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Autores principales:	Jacob Thomas, Samit S. Watve, William C. Ratcliff, Brian K. Hammer
Formato:	article
Lenguaje:	EN
Publicado:	American Society for Microbiology 2017
Materias:	type VI secretion Vibrio cholerae genetics horizontal gene transfer natural transformation systems Microbiology QR1-502
Acceso en línea:	https://doaj.org/article/addfa87f959e491fac945887bfc80b14
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spelling	oai:doaj.org-article:addfa87f959e491fac945887bfc80b142021-11-15T15:51:44ZHorizontal Gene Transfer of Functional Type VI Killing Genes by Natural Transformation10.1128/mBio.00654-172150-7511https://doaj.org/article/addfa87f959e491fac945887bfc80b142017-09-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.00654-17https://doaj.org/toc/2150-7511ABSTRACT Horizontal gene transfer (HGT) can have profound effects on bacterial evolution by allowing individuals to rapidly acquire adaptive traits that shape their strategies for competition. One strategy for intermicrobial antagonism often used by Proteobacteria is the genetically encoded contact-dependent type VI secretion system (T6SS), a weapon used to kill heteroclonal neighbors by direct injection of toxic effectors. Here, we experimentally demonstrate that Vibrio cholerae can acquire new T6SS effector genes via horizontal transfer and utilize them to kill neighboring cells. Replacement of one or more parental alleles with novel effectors allows the recombinant strain to dramatically outcompete its parent. Using spatially explicit modeling, we examine how this process could affect the ecology and evolution of surface-attached microbial populations. HGT of T6SS effector-immunity pairs is risky: transformation brings a cell into conflict with its former clone mates but can be adaptive when superior T6SS alleles are acquired. More generally, we find that these costs and benefits are not symmetric and that high rates of HGT can act as a hedge against competitors with unpredictable T6SS efficacy. We conclude that antagonism and horizontal transfer drive successive rounds of weapon optimization and selective sweeps, dynamically shaping the composition of microbial communities. IMPORTANCE The contact-dependent type VI secretion system (T6SS) is frequently used by Proteobacteria to kill adjacent competitors. While DNA released by T6 killing can be horizontally acquired, it remains untested whether T6 genes themselves can be horizontally acquired and then utilized to compete with neighboring cells. Using naturally transformable Vibrio cholerae, we provide the first direct empirical support for the hypothesis that T6 genes are exchanged horizontally (e.g., from dead competitors) and functionally deployed to compete with neighboring cells. Using computational simulations, we also demonstrate that high rates of HGT can be adaptive, allowing V. cholerae to improve upon existing T6 weaponry and survive direct encounters with otherwise superior competitors. We anticipate that our evolutionary results are of broad microbiological relevance, applying to many bacteria capable of HGT that utilize the T6SS or similar antagonistic systems, and highlight the profound impact of HGT in shaping microbial community structure.Jacob ThomasSamit S. WatveWilliam C. RatcliffBrian K. HammerAmerican Society for Microbiologyarticletype VI secretionVibrio choleraegeneticshorizontal gene transfernatural transformation systemsMicrobiologyQR1-502ENmBio, Vol 8, Iss 4 (2017)
institution	DOAJ
collection	DOAJ
language	EN
topic	type VI secretion Vibrio cholerae genetics horizontal gene transfer natural transformation systems Microbiology QR1-502
spellingShingle	type VI secretion Vibrio cholerae genetics horizontal gene transfer natural transformation systems Microbiology QR1-502 Jacob Thomas Samit S. Watve William C. Ratcliff Brian K. Hammer Horizontal Gene Transfer of Functional Type VI Killing Genes by Natural Transformation
description	ABSTRACT Horizontal gene transfer (HGT) can have profound effects on bacterial evolution by allowing individuals to rapidly acquire adaptive traits that shape their strategies for competition. One strategy for intermicrobial antagonism often used by Proteobacteria is the genetically encoded contact-dependent type VI secretion system (T6SS), a weapon used to kill heteroclonal neighbors by direct injection of toxic effectors. Here, we experimentally demonstrate that Vibrio cholerae can acquire new T6SS effector genes via horizontal transfer and utilize them to kill neighboring cells. Replacement of one or more parental alleles with novel effectors allows the recombinant strain to dramatically outcompete its parent. Using spatially explicit modeling, we examine how this process could affect the ecology and evolution of surface-attached microbial populations. HGT of T6SS effector-immunity pairs is risky: transformation brings a cell into conflict with its former clone mates but can be adaptive when superior T6SS alleles are acquired. More generally, we find that these costs and benefits are not symmetric and that high rates of HGT can act as a hedge against competitors with unpredictable T6SS efficacy. We conclude that antagonism and horizontal transfer drive successive rounds of weapon optimization and selective sweeps, dynamically shaping the composition of microbial communities. IMPORTANCE The contact-dependent type VI secretion system (T6SS) is frequently used by Proteobacteria to kill adjacent competitors. While DNA released by T6 killing can be horizontally acquired, it remains untested whether T6 genes themselves can be horizontally acquired and then utilized to compete with neighboring cells. Using naturally transformable Vibrio cholerae, we provide the first direct empirical support for the hypothesis that T6 genes are exchanged horizontally (e.g., from dead competitors) and functionally deployed to compete with neighboring cells. Using computational simulations, we also demonstrate that high rates of HGT can be adaptive, allowing V. cholerae to improve upon existing T6 weaponry and survive direct encounters with otherwise superior competitors. We anticipate that our evolutionary results are of broad microbiological relevance, applying to many bacteria capable of HGT that utilize the T6SS or similar antagonistic systems, and highlight the profound impact of HGT in shaping microbial community structure.
format	article
author	Jacob Thomas Samit S. Watve William C. Ratcliff Brian K. Hammer
author_facet	Jacob Thomas Samit S. Watve William C. Ratcliff Brian K. Hammer
author_sort	Jacob Thomas
title	Horizontal Gene Transfer of Functional Type VI Killing Genes by Natural Transformation
title_short	Horizontal Gene Transfer of Functional Type VI Killing Genes by Natural Transformation
title_full	Horizontal Gene Transfer of Functional Type VI Killing Genes by Natural Transformation
title_fullStr	Horizontal Gene Transfer of Functional Type VI Killing Genes by Natural Transformation
title_full_unstemmed	Horizontal Gene Transfer of Functional Type VI Killing Genes by Natural Transformation
title_sort	horizontal gene transfer of functional type vi killing genes by natural transformation
publisher	American Society for Microbiology
publishDate	2017
url	https://doaj.org/article/addfa87f959e491fac945887bfc80b14
work_keys_str_mv	AT jacobthomas horizontalgenetransferoffunctionaltypevikillinggenesbynaturaltransformation AT samitswatve horizontalgenetransferoffunctionaltypevikillinggenesbynaturaltransformation AT williamcratcliff horizontalgenetransferoffunctionaltypevikillinggenesbynaturaltransformation AT briankhammer horizontalgenetransferoffunctionaltypevikillinggenesbynaturaltransformation
_version_	1718427360332611584

Horizontal Gene Transfer of Functional Type VI Killing Genes by Natural Transformation

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