BactDrugConj · Bacteriocin-mediated Import of Active Molecules
„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“
- Период
- 2022-05-03 → 2024-05-02
- Финансиране от ЕС
- 184 708 €
- Участници
- 1
- Схема
- MSCA-IF
Линиите свързват координатора с партньорите.
Накратко на български
Бактериоцините се изследват като средство за транспортиране на активни молекули в бактерии като Pseudomonas aeruginosa. Това е важно, защото много патогени стават устойчиви на антибиотици, което затруднява лечението на тежки инфекции при болни хора.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Bacteriocin-mediated Import of Active Molecules
The discovery and improvement of antibiotics has transformed human and veterinary medicine and saved millions of lives in the last decades. Nevertheless, the evolutionary pressure on bacteria during antibiotic treatment and the low genetic barrier to resistance has led to the appearance of bacterial strains insensitive to certain classes of antibiotics. Antibiotic resistant bacteria pose a severe threat to healthcare systems around the world. The situation is particularly urgent for multidrug resistant (MDR) Gram-negative bacteria, making some of these organisms untreatable in a near future. According to the recently published estimation from the European Centre for Disease Prevention and Control, about 33,000 people die every year due to infections with antibiotic-resistant bacteria within the European Union. The mortality associated with the MDR bacteria is now higher than in 2007 and 39 % of the burden is caused by infections against which the last-line antibiotics are inefficient. These data highlight the importance of developing new strategies to overcome the antibiotic resistance in pathogenic bacteria. The opportunistic pathogen Pseudomonas aeruginosa is a major problem in hospitals. This Gram-negative bacterial pathogen causes ventilator-associated pneumonia, complicated urinary tract infection, and post-operative infections of soft tissues. These bacteria represent a threat for immunocompromised patients, where infections following surgery can be fatal.1 Besides, P. aeruginosa chronical infections are often deadly for patients suffering from rare diseases, such as cystic fibrosis (CF). P. aeruginosa colonises the lungs of CF patients resulting in higher rates of mortality than the disease itself. Some strains of P. aeruginosa are resistant to nearly all of the available antibiotics, both due to their capacity to acquire resistance genes via horizontal transfer and their intrinsic resistance mechanisms. This project will explore biotechnological approaches against antibioresistance in P.aeruginosa. Bacteriocins are ribosomally synthesised antimicrobial peptides that are produced by various bacteria to kill or inhibit growth of their competitors during the fight for resources. They can be effective against antibiotic-resistant bacteria. Pyocins are bacteriocins secreted by P. aeruginosa to kill closely related Pseudomonas strains. They simply highjack the nutrient-import systems of vulnerable bacteria to make their way into the cell. However, their killing ¬potential is low compared to some chemically-synthesised antibiotics. Therefore, coupling the vector properties of bacteriocins and the cytotoxicity of synthetic drugs represents a novel and potentially revolutionary antibacterial chemotherapeutic approach following a Trojan Horse strategy.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
Bacterial antibiotic resistance has become a massive threat to the public health. The situation with the opportunistic pathogen P.aeruginosa is particularly worrying because this major cause of nosocomial infections in immunocompromised patients becomes resistant to nearly all antibiotics available. Pyocin S2 is a bacteriocin, a natural protein able to kill several P.aeruginosa strains. The pyocin highjacks a nutrient transport system of the bacteria to get across the cell envelop. My project aims to develop chimeric bacteriocin-antibiotic conjugates to overcome the resistance mechanisms of P.aeruginosa by combining the vector potency of the pyocin and the bacteriotoxic activity of known synthetic antibiotics. Using the bacteriocin as a Trojan horse will be beneficial because: i) the active uptake of the drug; ii) reduced susceptibility to the efflux-mediated resistance; iii) specific targeting the pathogenic bacteria in the presence of healthy commensal microbiota. Preliminary results with organic fluorophores have revealed the feasibility of the pyocin S2-mediated vectorization of small molecules. In my work I will combine synthetic chemistry, biochemistry, microbiology and pharmacology approaches to synthesise defined antibiotic-pyocin conjugates and to create a new class of antibacterial molecules urgently needed in the post-antibiotic era.
Оригинален текст от CORDIS (на английски).
Участници
- UNIVERSITE DE STRASBOURG · StrasbourgКоординаторФранция
Връзки
Данни: CORDIS, © Европейски съюз
