Completed Infection & Immunity Cells, Biochemistry & Physiology

Combating Gram Negative AMR Pathogens by Understanding the Envelope-Breaching Mechanisms of Predatory Bacteria

In plain English

AI plain-English summary

A predatory bacterium called *Bdellovibrio* punches through the tough outer membrane of disease-causing bacteria and kills them from the inside. This matters because Gram-negative bacteria—which have an extra protective outer membrane—are a leading cause of drug-resistant infections. That outer membrane blocks most antibiotics, making these pathogens a major threat to healthcare. *Bdellovibrio* has evolved to breach this barrier effortlessly, but exactly how it does so at the molecular level remains unknown. The researchers will combine genetics, microscopy, and protein structure analysis to identify the specific proteins and physical structures—such as a central pore and a protein-tagged secretory vesicle—that the predator uses to invade its prey. If successful, this work could reveal new molecular tools for breaking through bacterial outer membranes. Those tools might eventually be used in isolation—without the live predator—to deliver existing antibiotics more effectively or to create entirely new classes of antimicrobial drugs. The project is fundamental science: it seeks to understand a natural mechanism of bacterial invasion. Past discoveries of how bacteria attack each other have led to antibiotics and enzymes used in medicine and industry; a deeper understanding here could open similar unexpected avenues.

View original technical description
We aim to determine the exact molecular mechanisms by which the bacterial predator Bdellovibrio invades Gram negative pathogen prey and whether components of its invasion machinery could be used in isolation as a new approach to the treatment of antimicrobially resistant (AMR) bacterial infections.Gram negative AMR pathogens are a major threat to healthcare. Their “extra” outer membrane is a barrier to effective drug delivery. We wish to learn from nature as Bdellovibrio is able to effortlessly pass through the envelope of pathogen, (but not host), cells and kill them from within. Whole-cell usage of live Bdellovibrio shows great therapeutic promise. However, a deeper understanding of the molecular mechanisms by which Bdellovibrio achieves invasion is essential to inform future therapeutic options. We will use our combined expertise (in microbial-genetics and microscopy, plus protein structure:function analysis of these unusual predators), and preparatory data including:- an RNAseq dataset from an invasion-stalled mutant -providing us with candidate proteins made during invasion; 3DSIM/fluorescence microscopy revealing a central pore, surrounding “collar” and a protein-tagged robust secretory vesicle at the predator-invasion site. Our end goal is to associate specific invasion protein function to these physical features of pore generation/entry, uncovering mechanisms used by nature to breach prey-envelopes.

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Researchers

Andrew Lovering (EPMC Awardee)Liz Sockett (EPMC Awardee)Magnus Rueping (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Characterising Bdellovibrio bacteriovorus membrane proteins
Characterising the role of cell envelope-modifying enzymes during predation by Bdellovibrio bacteriovorus
Understanding the Role of Peptidoglycan Metabolism in Bacterial Predation
Exploring the function and regulation of surface molecules in the reaction to predation by Gram-negative bacteria during predation by the predatory bacterium Bdellovibrio bacteriovorus in host-appropriate settings.
The Bacterial Invasion Port of Bdellovibrio

Original classification

Investigator Award in Science

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