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Bacterial membrane vesicles a novel delivery system for the treatment of multi-drug resistant Gram-negative bacterial infections.

Project description

Bacterial membrane vesicles tackle antibiotic resistance

The emergence of antibiotic resistance alongside the very few drugs in the development pipeline means that gram-negative bacteria are now high on the list of medical priorities. The EU-funded BacDrug project proposes to overcome the barrier of the highly selective outer membrane of gram-negative pathogens through lipid-based bacterial membrane vesicles (BMVs). BMVs are produced by non-pathogenic Lactococcus lactis and serve as a delivery system for drugs. Due to their nanoscale size, BMVs can pass through the bacterial membrane and kill drug-resistant gram-negative pathogens. This therapeutic approach has the potential to tackle antibiotic resistance, with obvious benefits for human health.


"Bacterial infections are a significant public health challenge and a major cause of human mortality globally. Antibiotics are indispensable for the treatment and prevention of infections caused by bacteria. However, global spread of drug-resistant bacteria, coupled with a dearth of new antibiotics in development has led to an alarming shortage of effective drugs. Gram-negative bacteria, in particular, protect themselves against antibiotics with a highly selective outer membrane. The high burden of diseases caused by Gram-negative bacteria, combined with their frequent multi-drug resistance has placed them as world´s highest-priority pathogens by the World Health Organization. Consequently, there is an urgent need for novel therapeutic approaches that combat Gram-negative bacterial pathogens. The goal of ""BacDrug"" is to use lipid-based bacterial membrane vesicles (BMVs) produced by non-pathogenic Lactococcus lactis as delivery system. BMVs have great potential as nanocarriers to by-pass the outer membrane and deliver their toxic payload to kill drug-resistant Gram-negative pathogens. A range of strategies will be used to load BMVs with cargo, including genetic engineering of L. lactis as well as chemical treatments. This Fellowship will harness expertise and techniques across microbiology, molecular biology, nanotechnology and drug design to deliver a successful outcome. The collaborative, truly interdisciplinary, cross faculty setting within the groups of Prof Molly Stevens (materials and bioengineering) and Dr Andrew Edwards (molecular microbiology) at ICL combines world-class expertise and provides an environment to maximise the success of this Fellowship, both in terms of the delivering the project and the training opportunities provided. Moreover, this innovative, alternative strategy to tackle drug-resistant Gram-negative bacterial infections has a high translational potential, which will be exploited via the clinical and translational research clinics at ICL."



Net EU contribution
€ 212 933,76
South kensington campus exhibition road
SW7 2AZ London
United Kingdom

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London Inner London — West Westminster
Activity type
Higher or Secondary Education Establishments
Other funding
€ 0,00