Unraveling the molecular mechanisms of DNA capture by the Com pilus in naturally transformable monoderm bacteria

ABSTRACT Transformation is a mechanism of horizontal gene transfer widespread in bacteria. The first step in transformation—capture of exogenous DNA—is mediated by surface-exposed filaments belonging to the type 4 filament (T4F) superfamily. How these protein polymers, composed of major and minor pi...

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Main Authors: Jérémy Mom, Odile Valette, Laetitia Pieulle, Vladimir Pelicic
Format: Article
Language:English
Published: American Society for Microbiology 2025-06-01
Series:mBio
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Online Access:https://journals.asm.org/doi/10.1128/mbio.00851-25
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author Jérémy Mom
Odile Valette
Laetitia Pieulle
Vladimir Pelicic
author_facet Jérémy Mom
Odile Valette
Laetitia Pieulle
Vladimir Pelicic
author_sort Jérémy Mom
collection DOAJ
description ABSTRACT Transformation is a mechanism of horizontal gene transfer widespread in bacteria. The first step in transformation—capture of exogenous DNA—is mediated by surface-exposed filaments belonging to the type 4 filament (T4F) superfamily. How these protein polymers, composed of major and minor pilin subunits, interact with DNA remains poorly understood. Here, we address this question for the Com pilus, a widespread T4F mediating DNA capture in competent monoderm species. Our functional analysis, performed in Streptococcus sanguinis, was guided by a complete structural model of the Com pilus. We show that the major pilin ComGC does not bind DNA. In contrast, a systematic mutational analysis of electropositive residues exposed at the filament surface in the four minor pilins (ComGD, ComGE, ComGF, and ComGG) reveals that the interface between ComGD and ComGF is important for DNA capture. Sequential mutations in these two interacting subunits lead to complete abolition of transformation, without affecting piliation. We further demonstrate the physical interaction between ComGD and ComGF using disulfide crosslinking, upon mutagenesis of two strategically positioned residues into cysteines. A structural model of the Com pilus tip interacting with DNA recapitulates all these findings and highlights a novel mode of DNA-binding, conserved in hundreds of monoderm species.IMPORTANCEBacteria are capable of evolving and diversifying very rapidly by acquiring new genetic material via horizontal gene transfer (HGT). Transformation is a widespread mechanism of HGT, which results from the capture of extracellular DNA by surface-exposed pili belonging to the type 4 filament (T4F) superfamily. How T4F—composed of major and minor pilins—interact with DNA remains poorly understood, especially in monoderm species that use a unique T4F for DNA capture, known as Com pilus or T4dP. The significance of this work is in characterizing a novel mode of DNA-binding by showing that the interface between two minor pilins, part of a tip-located complex of four pilins—found in different T4F—has been functionalized in monoderms to capture DNA. This is an evolutionary mechanism promoting the exceptional functional versatility of T4F.
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spelling doaj-art-a8d6f5a814474c6180daf1371490d8782025-08-20T03:25:44ZengAmerican Society for MicrobiologymBio2150-75112025-06-0116610.1128/mbio.00851-25Unraveling the molecular mechanisms of DNA capture by the Com pilus in naturally transformable monoderm bacteriaJérémy Mom0Odile Valette1Laetitia Pieulle2Vladimir Pelicic3Laboratoire de Chimie Bactérienne, Aix-Marseille Université/CNRS (UMR7283), Institut de Microbiologie de la Méditerranée, Marseille, FranceLaboratoire de Chimie Bactérienne, Aix-Marseille Université/CNRS (UMR7283), Institut de Microbiologie de la Méditerranée, Marseille, FranceLaboratoire de Chimie Bactérienne, Aix-Marseille Université/CNRS (UMR7283), Institut de Microbiologie de la Méditerranée, Marseille, FranceLaboratoire de Chimie Bactérienne, Aix-Marseille Université/CNRS (UMR7283), Institut de Microbiologie de la Méditerranée, Marseille, FranceABSTRACT Transformation is a mechanism of horizontal gene transfer widespread in bacteria. The first step in transformation—capture of exogenous DNA—is mediated by surface-exposed filaments belonging to the type 4 filament (T4F) superfamily. How these protein polymers, composed of major and minor pilin subunits, interact with DNA remains poorly understood. Here, we address this question for the Com pilus, a widespread T4F mediating DNA capture in competent monoderm species. Our functional analysis, performed in Streptococcus sanguinis, was guided by a complete structural model of the Com pilus. We show that the major pilin ComGC does not bind DNA. In contrast, a systematic mutational analysis of electropositive residues exposed at the filament surface in the four minor pilins (ComGD, ComGE, ComGF, and ComGG) reveals that the interface between ComGD and ComGF is important for DNA capture. Sequential mutations in these two interacting subunits lead to complete abolition of transformation, without affecting piliation. We further demonstrate the physical interaction between ComGD and ComGF using disulfide crosslinking, upon mutagenesis of two strategically positioned residues into cysteines. A structural model of the Com pilus tip interacting with DNA recapitulates all these findings and highlights a novel mode of DNA-binding, conserved in hundreds of monoderm species.IMPORTANCEBacteria are capable of evolving and diversifying very rapidly by acquiring new genetic material via horizontal gene transfer (HGT). Transformation is a widespread mechanism of HGT, which results from the capture of extracellular DNA by surface-exposed pili belonging to the type 4 filament (T4F) superfamily. How T4F—composed of major and minor pilins—interact with DNA remains poorly understood, especially in monoderm species that use a unique T4F for DNA capture, known as Com pilus or T4dP. The significance of this work is in characterizing a novel mode of DNA-binding by showing that the interface between two minor pilins, part of a tip-located complex of four pilins—found in different T4F—has been functionalized in monoderms to capture DNA. This is an evolutionary mechanism promoting the exceptional functional versatility of T4F.https://journals.asm.org/doi/10.1128/mbio.00851-25natural transformation systemsgenetic competencetype 4 piliDNA-binding proteinsgram-positive bacteria
spellingShingle Jérémy Mom
Odile Valette
Laetitia Pieulle
Vladimir Pelicic
Unraveling the molecular mechanisms of DNA capture by the Com pilus in naturally transformable monoderm bacteria
mBio
natural transformation systems
genetic competence
type 4 pili
DNA-binding proteins
gram-positive bacteria
title Unraveling the molecular mechanisms of DNA capture by the Com pilus in naturally transformable monoderm bacteria
title_full Unraveling the molecular mechanisms of DNA capture by the Com pilus in naturally transformable monoderm bacteria
title_fullStr Unraveling the molecular mechanisms of DNA capture by the Com pilus in naturally transformable monoderm bacteria
title_full_unstemmed Unraveling the molecular mechanisms of DNA capture by the Com pilus in naturally transformable monoderm bacteria
title_short Unraveling the molecular mechanisms of DNA capture by the Com pilus in naturally transformable monoderm bacteria
title_sort unraveling the molecular mechanisms of dna capture by the com pilus in naturally transformable monoderm bacteria
topic natural transformation systems
genetic competence
type 4 pili
DNA-binding proteins
gram-positive bacteria
url https://journals.asm.org/doi/10.1128/mbio.00851-25
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AT laetitiapieulle unravelingthemolecularmechanismsofdnacapturebythecompilusinnaturallytransformablemonodermbacteria
AT vladimirpelicic unravelingthemolecularmechanismsofdnacapturebythecompilusinnaturallytransformablemonodermbacteria