FFC#15/2021

Tackling phage resistance to increase the robustness of phage therapy for curing Pseudomonas aeruginosa infections in patients with cystic fibrosis (PhaCyf)

AREA 3 Bronchopulmonary infection

FFC#15/2021

Tackling phage resistance to increase the robustness of phage therapy for curing Pseudomonas aeruginosa infections in patients with cystic fibrosis (PhaCyf)
€ 0 still needed
0%
€ 21.000 goal

pRINCIPAL INVESTIGATOR

Federica Briani (Dip. di Bioscienze, Università degli Studi di Milano)

Researchers

5

Category

AREA 3 Bronchopulmonary infection

Duration

1 year

Goal

€ 21.000

Funds raised

€ 21.000

Objectives

Phage therapy consists in the use of phages (viruses that exclusively infect bacteria) to kill bacteria that cause an infection and represents a promising strategy for treating bacterial infections that are refractory to antibiotics. For the treatment of Pseudomonas aeruginosa pulmonary infections in persons with cystic fibrosis (CF), phage therapy may be a promising strategy. Even for phages, bacteria are able to develop resistance, a problem for phage therapy that can be limited by the use of phage cocktails. Researchers in this project will investigate the bacterial functions that cause resistance and the consequences of phage resistance on other aspects of the physiology of bacteria, in particular those relevant to infection. The general objective of this project is to evaluate which P. aeruginosa genes are involved in the origin of resistance to individual phages/cocktails and how the mutations that cause phage resistance impact on growth, virulence and antibiotic resistance. Researchers will also expand phage collections by including new phages capable of growing on cocktail-resistant mutants.


XIX Convention FFC Ricerca – download here a brief presentation of the project

WHO ADOPTED THE PROJECT

Associazione Trentina Fibrosi Cistica ODV “In ricordo di Pio Nicolini”

€ 21.000

Delegazione FFC Ricerca di Prato

€ 30.000

Emanuela Cricri e amici della ricerca

€ 20.000

OTHER PROJECTS

Discover the other projects

GMRF#1/2026

Exploring the role of PKD1 in promoting CFTR stability and function at the cell surface

FFC#1/2026

Mapping proteins regulating CFTR mRNA stability to identify new therapeutic targets for nonsense mutations

FFC#2/2026

Evaluating the potential of phosphodiesterase inhibitors to enhance the efficacy of CFTR modulators and support personalized therapeutic approaches