FFC#22/2020

Role of viable but non culturable (VBNC) bacterial forms in CF patients in a clinical setting: a translational research

AREA 5 Clinical and Epidemiological research

FFC#22/2020

Role of viable but non culturable (VBNC) bacterial forms in CF patients in a clinical setting: a translational research
€ 0 still needed
0%
€ 70.000 goal

pRINCIPAL INVESTIGATOR

Natalia Cirilli (Ospedali Riuniti, Dip. Materno Infantile, Centro FC, Ancona)

Partner

Luca Tiano (Università Politecnica delle Marche, Dip. di Scienze della Vita e dell’Ambiente); Rosaria Gesuita (Università Politecnica delle Marche, Centro di Epidemiologia, Biostatistica e Informatica Medica)

Researchers

14

Category

AREA 5 Clinical and Epidemiological research

Duration

2 years

Goal

€ 70.000

Funds raised

€ 70.000

Objectives

Results of the project FFC#13/2017, have shown that the VBNCs (Viable Non-Cultivable Bacteria) are bacteria in the CF lung that can escape the classical diagnostic cultures, being inactive however still viable. Such bacteria are capable of interrupting their state of quiescence and reactivate, causing relapses and making the respiratory infection chronic. Having developed a specific method of investigation to identify them (a combined techniques of molecular biology-qPCR- and flow cytometry), now researchers want to understand their importance in the clinical history of CF patients. Through this two-year prospective study, which will involve a hundred patients, both VBCNs and other bacteria in the sputum samples collected at each follow-up will be investigated and the role of VBNCs will be evaluated in association with the clinical status of patients and with the evolution of their CF lung disease.

WHO ADOPTED THE PROJECT

Delegazione FFC di Ascoli Piceno con il Gruppo di sostegno FFC di Martinsicuro Teramo

€ 25.000

Delegazione FFC di Fabriano Ancona

€ 25.000

Delegazione FFC di Umbertide Città di Castello

€ 10.000

OTHER PROJECTS

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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