Opis projektu
Uderzenie w czuły punkt bakterii
Gronkowiec złocisty to powszechnie występująca bakteria, która może egzystować na Twojej skórze czy nawet w nosie i być przy tym nieszkodliwa. Jednakże może się ona stać śmiertelnie groźna, jeśli znajdzie drogę do Twojego krwiobiegu, stawów, kości, płuc lub serca. Zakażenia gronkowcem powodują zatrucia pokarmowe, posocznicę, zespół wstrząsu toksycznego, a nawet septyczne zapalenie stawów. Gronkowiec złocisty znany jest ze swej zdolności do wytworzenia antybiotykooporności i z tego względu jest on doskonałym systemem modelowym dla wyjaśnienia mechanizmów tolerancji na antybiotyki. W projekcie CheckBacZ wykorzystano zaawansowane technicznie metody oceny różnych etapów cyklu komórkowego tej bakterii w celu znalezienia sposobów uczynienia jej podatną na leki.
Cel
The occurrence of multiple-drug resistant bacteria constitutes an important threat to healthy lives, signifying the importance of alternative strategies to combat bacterial infections. This research project bears the potential to significantly contribute to overcome antibiotic resistances that occur during the treatment of bacterial infections, as it combines the studies of cell division, cell cycle regulation and antibiotic resistance in the clinically relevant model Staphylococcus aureus. Given that the tubulin homologue FtsZ is essential for cell division and serves as an antibiotic resistance determinant in this organism, the proposed research activity focuses on the cytokinetic Z-ring, more precisely its role in driving the staphylococcal cell cycle. Super-resolution microscopy will be used to determine if FtsZ treadmilling controls the rate of cytokinesis and if it organizes the peptidoglycan synthesis proteins during cell division, aiming to provide evidence for a FtsZ-dependent checkpoint in the cell cycle. Profiting from a mutant screen currently ongoing in the host laboratory, mutants impaired in the timing of septum formation will be identified to study the functional integration of corresponding genes into FtsZ-driven septum synthesis. In view of the fact that bacteria at different stages of the cell cycle are phenotypically distinct, microfluidics will be used to test if the degree of antibiotic tolerance varies during the cell cycle, which would enforce the vision for re-sensitizing resistant bacteria by manipulating their cell cycle.
The strong expertise and the availability of cutting-edge techniques in the host group together with my professional experience will generate an ideal synergy within this work programme. I will generate valuable scientific knowledge, acquire transferrable skills and create new collaborations in the international bacterial cell biology community, thus paving the way for establishing myself as an independent researcher.
Dziedzina nauki
- natural sciencesbiological sciencesmicrobiologybacteriology
- natural sciencesphysical sciencesopticsmicroscopysuper resolution microscopy
- natural sciencesbiological sciencescell biology
- medical and health sciencesbasic medicinepharmacology and pharmacypharmaceutical drugsantibiotics
- medical and health sciencesbasic medicinepharmacology and pharmacydrug resistanceantibiotic resistance
Słowa kluczowe
Program(-y)
Temat(-y)
System finansowania
MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)Koordynator
1099 085 Lisboa
Portugalia