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Pf bacteriophages hinder sputum antibiotic diffusion via electrostatic binding.
Chen, Qingquan; Cai, Pam; Chang, Tony Hong Wei; Burgener, Elizabeth; Kratochvil, Michael J; Gupta, Aditi; Hargil, Aviv; Secor, Patrick R; Nielsen, Josefine Eilsø; Barron, Annelise E; Milla, Carlos; Heilshorn, Sarah C; Spakowitz, Andy; Bollyky, Paul L.
Afiliação
  • Chen Q; Division of Infectious Diseases and Geographic Medicine, Dept. of Medicine, Stanford University School of Medicine, Beckman Center, 279 Campus Drive, Stanford, CA 94305.
  • Cai P; Department of Chemical Engineering, Stanford University, Stanford, CA, 94305.
  • Chang THW; Division of Infectious Diseases and Geographic Medicine, Dept. of Medicine, Stanford University School of Medicine, Beckman Center, 279 Campus Drive, Stanford, CA 94305.
  • Burgener E; Center for Excellence in Pulmonary Biology, Department of Pediatrics, Stanford University, Stanford, CA 94305.
  • Kratochvil MJ; Children's Hospital of Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, CA 90027.
  • Gupta A; Division of Infectious Diseases and Geographic Medicine, Dept. of Medicine, Stanford University School of Medicine, Beckman Center, 279 Campus Drive, Stanford, CA 94305.
  • Hargil A; Department of Materials Science and Engineering, Stanford University, 476 Lomita Mall, Stanford, CA 94305.
  • Secor PR; Division of Infectious Diseases and Geographic Medicine, Dept. of Medicine, Stanford University School of Medicine, Beckman Center, 279 Campus Drive, Stanford, CA 94305.
  • Nielsen JE; Division of Infectious Diseases and Geographic Medicine, Dept. of Medicine, Stanford University School of Medicine, Beckman Center, 279 Campus Drive, Stanford, CA 94305.
  • Barron AE; Division of Biological Sciences, University of Montana, United States.
  • Milla C; Department of Bioengineering, School of Medicine & School of Engineering, Stanford University, Stanford, CA 94305, United States.
  • Heilshorn SC; Department of Science and Environment, Roskilde University, 4000 Roskilde, Denmark.
  • Spakowitz A; Department of Bioengineering, School of Medicine & School of Engineering, Stanford University, Stanford, CA 94305, United States.
  • Bollyky PL; Center for Excellence in Pulmonary Biology, Department of Pediatrics, Stanford University, Stanford, CA 94305.
bioRxiv ; 2024 Mar 10.
Article em En | MEDLINE | ID: mdl-38496625
ABSTRACT
Despite great progress in the field, chronic Pseudomonas aeruginosa (Pa) infections remain a major cause of morbidity and mortality in patients with cystic fibrosis, necessitating treatment with inhaled antibiotics. Pf phage is a filamentous bacteriophage produced by Pa that has been reported to act as a structural element in Pa biofilms. Pf presence has been associated with resistance to antibiotics and poor outcomes in cystic fibrosis, though the underlying mechanisms are unclear. Here, we have investigated how Pf phages and sputum biopolymers impede antibiotic diffusion using human sputum samples and fluorescent recovery after photobleaching. We demonstrate that tobramycin interacts with Pf phages and sputum polymers through electrostatic interactions. We also developed a set of mathematical models to analyze the complex observations. Our analysis suggests that Pf phages in sputum reduce the diffusion of charged antibiotics due to a greater binding constant associated with organized liquid crystalline structures formed between Pf phages and sputum polymers. This study provides insights into antibiotic tolerance mechanisms in chronic Pa infections and may offer potential strategies for novel therapeutic approaches.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article