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Huwiler, S. G.

Publications and source records attributed to Huwiler, S. G..

3 recordsLinked to original sources

Modulating gene expression and protein secretion in the bacterial predator Bdellovibrio bacteriovorus

The predatory bacterium Bdellovibrio bacteriovorus kills and consumes other bacteria, thrives in diverse environments and holds great potential to address major challenges in medicine, agriculture, and biotechnology. As a bacterial predator it represents an alternative to traditional antimicrobial strategies to combat multidrug-resistant bacterial pathogens and prevent food waste, while the multitude of predatory enzymes it produces hold potential for biotechnological applications. However, the limited availability of versatile genetic tools and secretion assays constrain both fundamental studies and bioengineering of B. bacteriovorus. Here, we developed a molecular toolbox for B. bacteriovorus by systematically tuning gene expression and secretion of a reporter protein. We investigated functional native and synthetic promoters from the Anderson library with varying expression levels and demonstrated their efficacy in driving expression of the fluorescent reporter protein mScarletI3 at both the population and single-cell level. Additionally, we evaluated different ribosomal binding sites (RBS) to fine-tune gene expression. To examine secretion, we established a novel protocol to quantify extracellular release of a Nanoluc luciferase reporter protein in B. bacteriovorus using different native Sec-dependent signal sequences. We anticipate that the newly developed genetic toolkit and techniques will advance research on this fundamental predator-prey system, laying the foundation for its broader application and future bioengineering efforts. This work will pave the way for tailored applications of B. bacteriovorus in microbial ecology, agriculture, biotechnology, and medicine.

microbiology↗

Quantitative proteome of bacterial periplasmic predation reveals a prey damaging protease

The rise of antimicrobial resistant pathogens calls for novel ways to kill and damage bacteria. A rich source for bacterial cell-damaging proteins is periplasmic predatory bacterium Bdellovibrio bacteriovorus, which invades, kills and subsequently exits the Gram-negative prey cell. An increased understanding of predatory protein function can be achieved by analyzing their relative abundance at key stages of predation. Here, we present the first quantitative proteome covering the complete predatory life cycle of the bacterial predator B. bacteriovorus killing Escherichia coli, quantifying 2195 predator proteins. From these proteins, nine protein clusters sharing similar expression patterns were identified. Towards the end of the life cycle when the predator exits prey remnants, we identified significant amounts of protease Bd2269. Gene knockout and heterologous expression experiments revealed that Bd2269 is involved in the prey exit process and damages E. coli from within. This quantitative predator proteome is a valuable resource to unravel bacterial predator-prey interactions and advances the search for novel antimicrobial enzymes.

microbiology↗

Outer membrane changes enable evolutionary escape from bacterial predation

To combat antimicrobial resistant pathogens, natural predatory bacteria, like Bdellovibrio bacteriovorus, represent potential alternatives. B. bacteriovorus could be particularly potent as it kills a broad range of human bacterial pathogens, however, it remains unclear whether prey can evolve genetically-determined resistance against predation. Here, we show that the model bacterium Escherichia coli K-12 consistently evolves resistance against B. bacteriovorus during experimental evolution. Selection for resistance scaled positively with predation pressure and was widespread after two cycles of predator exposure. Like antibiotics, predation resistance was costly, manifesting in a trade-off between predation resistance and fitness in the absence of predators. Genetic analysis identified changes in outer membrane porin OmpF as common resistance mechanism, while a mutation in cell envelope lipopolysaccharide-modifying enzyme WaaF was rarer but also conferred predation resistance. Our study uncovers evolutionary and mechanistic aspects of prey escape from predation, generating important knowledge on predator-prey interactions and to advance sustainable treatments.

evolutionary biology↗