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Pieulle, L.

Publications and source records attributed to Pieulle, L..

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

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, 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 in bacteria, which results from the capture of extracellular DNA by surface-exposed pili belonging to the superfamily of type 4 filament (T4F). How T4F - that are composed of major and minor pilins - interact with DNA remains poorly understood, especially in competent 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 many different T4F - have been functionalized in monoderms to capture DNA. This is an evolutionary strategy used by bacteria to promote the exceptional functional versatility of T4F.

microbiology↗

Systematic functional analysis of the Com pilus in Streptococcus sanguinis: a minimalistic type 4 filament dedicated to DNA uptake in monoderm bacteria

Type 4 filaments (T4F) are a superfamily of functionally versatile nanomachines, ubiquitous in prokaryotes, which use similar multi-protein machineries to assemble and operate filamentous polymers of type 4 pilins. The best studied T4F use very complex machineries, which has posed challenges to understanding the mechanisms of both filament assembly and the roles they facilitate. Here, we report the systematic functional analysis of the Com pilus, a widespread T4F mediating DNA uptake during natural transformation in monoderm bacteria. Using Streptococcus sanguinis as a model, we show that Com pili are bona fide type 4 pili (T4P), which represent a new pilus sub-type. We show that with only eight components necessary for their assembly and functioning - all "core" poteins universally conserved across this superfamily - the Com pilus epitomises a minimalistic T4F. We demonstrate that core T4F components are sufficient for filament assembly. Intriguingly, akin to more elaborate T4F, the Com pilus contains four minor pilins forming a complex likely to be situated at the apex of the filaments. Our results have global implications for T4F and make Com pili a model for elucidating the fundamental processes underpinning filament assembly.

microbiology↗

Structure of a heteropolymeric type 4 pilus from a monoderm bacterium

Type 4 pili (T4P) are important virulence factors, which belong to a superfamily of nanomachines ubiquitous in prokaryotes, called type 4 filaments (T4F). T4F are defined as helical polymers of type 4 pilins. Recent advances in cryo-electron microscopy (cryo-EM) led to structures of several T4F. This revealed that the long N-terminal -helix, the trademark of pilins, packs in the centre of the filaments to form a hydrophobic core, which in bacteria is accompanied by the melting (unfolding) of a portion of 1. Since all available bacterial T4F structures are from diderm species, we tested whether this architecture is conserved in phylogenetically distant species by determining the structure of the T4P of the monoderm Streptococcus sanguinis. Our 3.7 A resolution cryo-EM structure of this heteropolymeric T4P, and the resulting full atomic model including all minor pilins, highlight universal features of bacterial T4F and have widespread implications in understanding their biology.

microbiology↗