4.7 Article

Disruption of biofilms and killing of Burkholderia cenocepacia from cystic fibrosis lung using an antioxidant-antibiotic combination therapy

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ELSEVIER
DOI: 10.1016/j.ijantimicag.2021.106372

Keywords

Antioxidants; Burkholderia cenocepacia; Biofilms; Antibiotic resistance; N-acetyl cysteine

Funding

  1. Commercial Development & Industry Partnership (CDIP) grant (University of Sydney) [CT20584]
  2. Commercial Development & Industry Partnership (CDIP) grant (Whiteley Corporation) [CT20584]
  3. Department of Industry, Innovation and Science (Innovative Manufacturing CRC Ltd)
  4. Whiteley Corporation [IMCRC/WLY/08052019.1]

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Cystic fibrosis is a genetic disease that results in thick lung mucus which can be colonised by bacteria, leading to biofilm formation. This study found that a combination therapy of NAC and ciprofloxacin can significantly disrupt B. cenocepacia biofilms and reduce the necessity for high concentrations of antibiotics.
Cystic fibrosis (CF) is a disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR). The resulting chloride and bicarbonate imbalance produces a thick, static lung mucus. This mucus is not easily expelled from the lung and can be colonised by bacteria, leading to biofilm formation. CF lung infection with Burkholderia cepacia complex (BCC), particularly the subspecies B. cenocepacia, results in higher morbidity and mortality. Patients infected with BCC can rapidly progress to cepacia syndrome, a fatal necrotising pneumonia. The aim of this study was to identify whether a combination therapy (CT) of selected antioxidants and antibiotics significantly disrupts B. cenocepacia biofilms and to determine the optimum CT level for treatment. Using controlled in vitro spectrophotometry, colony-forming unit and microscopy assays, three antioxidants (N-acetylcysteine [NAC], glutathione and vitamin C) and three antibiotics (ciprofloxacin, ceftazidime and tobramycin) were screened and assessed for their ability to disrupt the early and mature biofilms of six B. cenocepacia CF isolates. A combination of NAC and ciprofloxacin produced a statistically significant biofilm disruption in all strains tested, with growth inhibition (>5-8 log(10)) observed when exposed to 4890 or 8150 mu g/mL NAC in combination with 32 or 64 mu g/mL ciprofloxacin. NAC-mediated biofilm disruption may be aided by the acidic pH of NAC at higher concentrations. This study showed that NAC is an effective disruptor that reduces the necessity for high concentrations of antibiotic. Further research will focus on the host toxicity and efficacy in ex vivo CF models. (C) 2021 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.

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