Evaluating the effects of ivacaftor exposure on Staphylococcus aureus small colony variant development and antibiotic tolerance
Open Access
- 30 October 2024
- journal article
- research article
- Published by Oxford University Press (OUP) in JAC-Antimicrobial Resistance
- Vol. 6 (6) , dlae185
Abstract
Background: Ivacaftor exhibits anti-staphylococcal properties but does not clear Staphylococcus aureus from the lungs of people with cystic fibrosis (pwCF). We assessed whether exposure to therapeutic concentrations of ivacaftor could allow S. aureus to form small colony variants (SCVs), a phenotype commonly associated with bacterial persistence. Methods: Humanized G551D-CFTR (hG551D) rats were treated with ivacaftor for 7 days. Concentrations in the plasma, epithelial lining fluid and lung tissue lysate were measured using LC-MS/MS. Survival of S. aureus during ivacaftor treatment was assessed in an hG551D rat model of lung infection. S. aureus adaptation to therapeutic concentrations of ivacaftor was investigated in vitro by serial passage in the presence of 10 µM ivacaftor. Bacterial survival in the presence of antimicrobials was evaluated using growth curves and density assays. Results: Ivacaftor plasma concentrations of treated hG551D rats reached 3.488 ± 1.118 µM, with more variable concentrations in the epithelial lining fluid and lung tissue lysate. During S. aureus infection, ivacaftor-treated hG551D rats returned similar numbers of bacteria from the lung, compared with vehicle-treated controls. Exposure of S. aureus to ivacaftor in vitro led to the formation of ivacaftor-tolerant SCVs with an unstable phenotype and increased antibiotic tolerance. Conclusions: Treatment with ivacaftor did not alter S. aureus burden in the cystic fibrosis rat and led to the formation of tolerant SCVs in vitro, suggesting that development of an SCV phenotype may allow S. aureus to persist in the cystic fibrosis lung during ivacaftor therapy.Keywords
Funding Information
- National Heart, Lung, and Blood Institute
- National Institutes of Health (1K08HL131867, 1R01HL153079)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK072482)
- Cystic Fibrosis Foundation (ROWE19R0, BIRKET20A0)
This publication has 47 references indexed in Scilit:
- Small colony variants: a pathogenic form of bacteria that facilitates persistent and recurrent infectionsNature Reviews Microbiology, 2006
- Cystic FibrosisNew England Journal of Medicine, 2005
- Allometric scaling of pharmacokinetic parameters in drug discovery: Can human CL, Vss and t1/2 be predicted fromin-vivo rat data?European Journal of Drug Metabolism and Pharmacokinetics, 2004
- Population Dynamics of Persistent Staphylococcus aureus Isolated from the Airways of Cystic Fibrosis Patients during a 6-Year Prospective StudyJournal of Clinical Microbiology, 2003
- Small-Colony Mutants of Staphylococcus aureus Allow Selection of Gyrase-Mediated Resistance to Dual-Target FluoroquinolonesAntimicrobial Agents and Chemotherapy, 2002
- Phenotypic switching of antibiotic resistance circumvents permanent costs in Staphylococcus aureusCurrent Biology, 2001
- Persistent Infection with Small Colony Variant Strains of Staphylococcus aureus in Patients with Cystic FibrosisThe Journal of Infectious Diseases, 1998
- Characteristics of quinolone-induced small colony variants in Staphylococcus aureusJournal of Antimicrobial Chemotherapy, 1997
- Identification of glycoproteins on nitrocellulose membranes and gelsMolecular Biotechnology, 1996
- Estimation of volume of epithelial lining fluid recovered by lavage using urea as marker of dilutionJournal of Applied Physiology, 1986