XRE transcription factors conserved in Caulobacter and φCbK modulate adhesin development and phage production.

The xenobiotic response element (XRE) family of transcription factors (TFs), which are commonly encoded by bacteria and bacteriophage, regulate diverse features of bacterial cell physiology and impact phage infection dynamics. Through a pangenome analysis of Caulobacter species isolated from soil an...

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Main Authors: Maeve McLaughlin, Aretha Fiebig, Sean Crosson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-11-01
Series:PLoS Genetics
Online Access:https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1011048&type=printable
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author Maeve McLaughlin
Aretha Fiebig
Sean Crosson
author_facet Maeve McLaughlin
Aretha Fiebig
Sean Crosson
author_sort Maeve McLaughlin
collection DOAJ
description The xenobiotic response element (XRE) family of transcription factors (TFs), which are commonly encoded by bacteria and bacteriophage, regulate diverse features of bacterial cell physiology and impact phage infection dynamics. Through a pangenome analysis of Caulobacter species isolated from soil and aquatic ecosystems, we uncovered an apparent radiation of a paralogous XRE TF gene cluster, several of which have established functions in the regulation of holdfast adhesin development and biofilm formation in C. crescentus. We further discovered related XRE TFs throughout the class Alphaproteobacteria and its phages, including the φCbK Caulophage, suggesting that members of this cluster impact host-phage interactions. Here we show that a closely related group of XRE transcription factors encoded by both C. crescentus and φCbK can physically interact and function to control the transcription of a common gene set, influencing processes including holdfast development and the production of φCbK virions. The φCbK-encoded XRE paralog, tgrL, is highly expressed at the earliest stages of infection and can directly inhibit transcription of host genes including hfiA, a potent holdfast inhibitor, and gafYZ, an activator of prophage-like gene transfer agents (GTAs). XRE proteins encoded from the C. crescentus chromosome also directly repress gafYZ transcription, revealing a functionally redundant set of host regulators that may protect against spurious production of GTA particles and inadvertent cell lysis. Deleting the C. crescentus XRE transcription factors reduced φCbK burst size, while overexpressing these host genes or φCbK tgrL rescued this burst defect. We conclude that this XRE TF gene cluster, shared by C. crescentus and φCbK, plays an important role in adhesion regulation under phage-free conditions, and influences host-phage dynamics during infection.
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spelling doaj.art-9a40e14491cc426d9cef2b41670d266b2023-12-16T05:31:31ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042023-11-011911e101104810.1371/journal.pgen.1011048XRE transcription factors conserved in Caulobacter and φCbK modulate adhesin development and phage production.Maeve McLaughlinAretha FiebigSean CrossonThe xenobiotic response element (XRE) family of transcription factors (TFs), which are commonly encoded by bacteria and bacteriophage, regulate diverse features of bacterial cell physiology and impact phage infection dynamics. Through a pangenome analysis of Caulobacter species isolated from soil and aquatic ecosystems, we uncovered an apparent radiation of a paralogous XRE TF gene cluster, several of which have established functions in the regulation of holdfast adhesin development and biofilm formation in C. crescentus. We further discovered related XRE TFs throughout the class Alphaproteobacteria and its phages, including the φCbK Caulophage, suggesting that members of this cluster impact host-phage interactions. Here we show that a closely related group of XRE transcription factors encoded by both C. crescentus and φCbK can physically interact and function to control the transcription of a common gene set, influencing processes including holdfast development and the production of φCbK virions. The φCbK-encoded XRE paralog, tgrL, is highly expressed at the earliest stages of infection and can directly inhibit transcription of host genes including hfiA, a potent holdfast inhibitor, and gafYZ, an activator of prophage-like gene transfer agents (GTAs). XRE proteins encoded from the C. crescentus chromosome also directly repress gafYZ transcription, revealing a functionally redundant set of host regulators that may protect against spurious production of GTA particles and inadvertent cell lysis. Deleting the C. crescentus XRE transcription factors reduced φCbK burst size, while overexpressing these host genes or φCbK tgrL rescued this burst defect. We conclude that this XRE TF gene cluster, shared by C. crescentus and φCbK, plays an important role in adhesion regulation under phage-free conditions, and influences host-phage dynamics during infection.https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1011048&type=printable
spellingShingle Maeve McLaughlin
Aretha Fiebig
Sean Crosson
XRE transcription factors conserved in Caulobacter and φCbK modulate adhesin development and phage production.
PLoS Genetics
title XRE transcription factors conserved in Caulobacter and φCbK modulate adhesin development and phage production.
title_full XRE transcription factors conserved in Caulobacter and φCbK modulate adhesin development and phage production.
title_fullStr XRE transcription factors conserved in Caulobacter and φCbK modulate adhesin development and phage production.
title_full_unstemmed XRE transcription factors conserved in Caulobacter and φCbK modulate adhesin development and phage production.
title_short XRE transcription factors conserved in Caulobacter and φCbK modulate adhesin development and phage production.
title_sort xre transcription factors conserved in caulobacter and φcbk modulate adhesin development and phage production
url https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1011048&type=printable
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AT arethafiebig xretranscriptionfactorsconservedincaulobacterandphcbkmodulateadhesindevelopmentandphageproduction
AT seancrosson xretranscriptionfactorsconservedincaulobacterandphcbkmodulateadhesindevelopmentandphageproduction