Biology subjects

Ellison, T. J.

Publications and source records attributed to Ellison, T. J..

5 recordsLinked to original sources

bioRxiv2026

A broad-spectrum phage-encoded mechanism to disarm bacterial type IV filaments

Phages can modify host cell physiology to thwart competitors. The Pseudomonas aeruginosa-specific phage DMS3 encodes Aqs1, a protein inhibitor of type IV pilus (T4P) function to prevent host cell recognition by other phages that leverage these filaments for infection. Aqs1 disrupts T4P by binding to the hexameric ATPase PilB, required to power pilus filament extension, though several mechanistic details remain unclear. We show that Aqs1 has broad-spectrum activity and can disrupt T4P function in a variety of Gram negative bacteria. This protein inhibits PilB by binding to a solvent-exposed hydrophobic patch on the N2-domain, distal to the active site. Binding destabilizes the hexamer, preventing PilB accumulation at T4P machines. Aqs1 likely disrupts PilB oligomerization by displacing a flexible linker segment between the PilB N1- and N2-domains required for inter-subunit contact. Together, the Aqs1 mode of action provides a design template for broad-spectrum inhibitors of diverse bacterial virulence factors. SignificanceThe phage-encoded protein Aqs1 disables type IV pilus (T4P) production in Pseudomonas aeruginosa by targeting the hexameric ATPase responsible for assembling pilus fibers. We show that despite originating from a P. aeruginosa-specific phage, Aqs1 can also disable T4 ATPase-dependent phenotypes across other pathogenic bacteria and homologous systems. Mechanistically, Aqs1 binds to a conserved patch on the PilB N2-domain away from the active site. Binding here breaks apart the PilB oligomer, preventing it from acting on T4P machines. Aqs1 binding at the N2-domain patch likely displaces a flexible PilB linker segment that binds to this site to stabilize the hexamer. Our work highlights a novel and conserved PilB allosteric site which is exploited by the phage-encoded protein Aqs1 to disrupt diverse T4 systems in multiple bacteria.

microbiology↗

bioRxiv2026

β-strand complementation within tip initiation complexes licenses assembly of diverse type IV filaments

PilC/PilY1 proteins are tip-located adhesins of type IV pili (T4P) that are critical for T4P function in diverse behaviors including twitching motility, DNA uptake, and host cell adhesion. PilC and PilY1 adhesins are proposed to interact with initiation complexes composed of minor pilins (PilIJK family proteins) to aid in initiation of T4P polymerization, but it has been unclear how PilC/PilY1 proteins promote fiber assembly. We combined structural modeling, genetic, and biochemical experiments using Neisseria gonorrhoeae and Acinetobacter baylyi to delineate how PilC/PilY1 control T4P assembly: a short peptide at the C-terminus of PilC/PilY1 initiates T4P assembly via {beta}-strand complementation with PilK-family minor pilins. This {beta}-strand is necessary and partially sufficient to trigger fiber assembly. In a working model, the PilK-PilC/PilY1 complex is recognized by a preformed PilI-PilJ heterodimer to form a quaternary "licensing complex" that then templates and initiates fiber assembly. In type II secretion systems (T2SS) lacking PilC/PilY1, PilK homologs directly incorporate the terminal {beta}-strand provided by PilC/PilY1 in T4P. Moreover, phylogenetically distinct Tad T4P lack a canonical PilK homolog and instead contain a structurally similar minor pilin-like protein called TadG/CpaL that is important for fiber assembly. We show that CpaL of Caulobacter crescentus Tad T4P acts similarly to the T2SS PilK homolog to provide the C-terminal {beta}-strand required for assembly. Our results explain how PilC/PilY1 can be retained on the fiber tip under enormous tensile loads generated during mechanical shear and T4P retraction and demonstrate how diverse T4P systems employ {beta}-strand complementation to license fiber assembly. SIGNIFICANCEProkaryotic type IV filaments are ancient, diverse, and broadly distributed nanomachines that assemble and retract to execute diverse microbial functions. They include type IV pili and type II secretion systems, mediating toxin secretion, motility, surface adhesion, biofilm formation, DNA uptake, and other functions. Here, we show that two widely conserved subunits of the tip, PilI and PilJ, form a module that recognizes the folding of a {beta}-sheet in a third subunit, PilK. The final {beta}-strand in this sheet can be supplied in trans by the last [~]10 aminoacyl residues of large PilC/PilY1 adhesins, or in cis by PilK itself. In a working model, this recognition results in formation of a PilIJK trimer, which then licenses fiber polymerization through a templating mechanism.

microbiology↗

bioRxiv2025

Twitching motility suppressors reveal a role for FimX in type IV pilus extension dynamics

In Pseudomonas aeruginosa, retractable protein filaments called type IV pili (T4P) facilitate surface adherence, sensing, and directional movement known as twitching motility. T4P are necessary for the bacteria to engage in surface-associated behaviors, including establishing acute infections. Pilus extension is driven by the hexameric ATPase, PilB, at the base of the T4P nanomachine in coordination with various protein regulatory effectors. The cyclic-di-GMP binding protein, FimX, works with PilB to mediate normal extension processes, though how this effector controls pilus assembly remains unclear. To explore the role of FimX in T4P function, we leveraged the significant {Delta}fimX twitching motility deficit to screen for mutants capable of overcoming this phenotype. We identified suppressor mutations that increase twitching in {Delta}fimX background, mapping primarily to cyclic-AMP homeostatic machinery or to PilB, the FimX target. Distinct suppressor mutations in PilB increased ATP hydrolysis in vitro and this activity was subject to modulation by FimX. Using microscopy to monitor the extension dynamics of fluorescently labelled T4P, we showed that {Delta}fimX mutants produce slow-to-extend, short pili, a phenotype that is rescued by mutations enhancing PilB ATP hydrolysis and/or re-introduction of FimX. Together, these data implicate FimX as a regulator of PilB enzymatic function, potentially enabling P. aeruginosa to fine-tune pilus extension dynamics in response to environmental cues. SummaryType IV pili enable Pseudomonas aeruginosa to attach to surfaces, move (twitch), and form biofilms. Pilus extension is powered by the motor protein PilB, which is regulated by other factors, including FimX, a protein that binds cyclic-di-GMP. Although FimX is important for twitching, how it influences PilB was unclear. We deleted fimX, which severely reduces motility, and searched for mutants that regained movement. We identified two types: some had mutations in PilB that increased its ATPase activity, allowing it to function without FimX, while others affected the cyclic-AMP signaling pathway and increased overall production of pilus components, showing that motility can also be improved through changes in quantity versus quality. Our results suggest that FimX normally fine-tunes PilB enzymatic activity, enabling dynamic control of pilus extension in response to surface signals. This work helps explain how P. aeruginosa adapts to different environments, a process crucial for infection and biofilm development.

microbiology↗

bioRxiv2025

FimX regulates type IV pilus localization via the Pil-Chp chemosensory system in Acinetobacter baylyi

Type IV pili (T4P) are widespread dynamic appendages required for diverse prokaryotic behaviors including twitching motility, biofilm formation, and DNA uptake leading to natural transformation. Although the components involved in T4P assembly and dynamics are largely conserved across divergent clades of bacteria, the mechanisms underlying T4P function and regulation differ significantly and remain poorly characterized outside of a select few model organisms. One understudied characteristic of T4P includes the spatial organization of T4P envelope-spanning nanomachines and how organizational patterns contribute to single cell behaviors. The bacterial species Acinetobacter baylyi localizes its T4P nanomachines in a unique pattern along the long axis of the cell, making it a robust model to study the mechanisms underlying the regulation of intracellular organization in single cell organisms. In this work, we find that the T4P regulatory protein FimX has been co-opted away from regulating T4P dynamics to instead control T4P positioning through a chemosensory Pil-Chp pathway. We show FimX directly interacts with the Pil-Chp histidine kinase ChpA which likely influences Pil-Chp signaling and the subsequent positioning of T4P machines. These data contribute to our understanding of how bacterial regulatory systems can evolve to function in diverse biological processes. SIGNIFICANCE STATEMENTSubcellular organization of protein complexes plays a vital role in their function in all domains of life, yet the molecular mechanisms underlying subcellular organization in bacteria remain poorly understood. This work shows the T4P regulatory component FimX directly interacts with a chemosensory signaling protein to regulate the positioning of T4P nanomachines. These data provide insight into how signaling systems can evolve to regulate diverse processes, and they establish a direct connection between environmental signaling cascades and the regulation of bacterial cell biology.

microbiology↗

bioRxiv2024

DNA binding is rate-limiting for natural transformation

Bacteria take up environmental DNA using dynamic appendages called type IV pili (T4P) to elicit horizontal gene transfer in a process called natural transformation. Natural transformation is widespread amongst bacteria yet determining how different factors universally contribute to or limit this process across species has remained challenging. Here we show that Acinetobacter baylyi, the most naturally transformable species, is highly transformable due to its ability to robustly bind nonspecific DNA via a dedicated orphan minor pilin, FimT. We show that, compared to its homologues, A. baylyi FimT contains multiple positively charged residues that additively promote DNA binding efficiency. Expression of A. baylyi FimT in a closely related Acinetobacter pathogen is sufficient to substantially improve its capacity for natural transformation, demonstrating that T4P-DNA binding is a rate-limiting step in this process. These results demonstrate the importance of T4P-DNA binding efficiency in driving natural transformation, establishing a key factor limiting horizontal gene transfer. ImportanceNatural transformation is a multi-step, broadly conserved mechanism for horizontal gene transfer in which bacteria take up exogenous DNA from the environment and integrate it into their genome by homologous recombination. A complete picture of the factors that limit this behavior remain unclear due to variability between bacterial systems. In this manuscript, we provide clear and direct evidence that DNA binding by type IV pili prior to DNA uptake is a rate-limiting step of natural transformation. We show that increasing DNA binding in antibiotic resistant Acinetobacter pathogens can boost their transformation rates by 100-fold. In addition to expanding our understanding of the factors that limit transformation in the environment, these results will also contribute to a deeper understanding of the spread of antibiotic resistance genes in relevant human pathogens.

microbiology↗