Membrane-active macromolecules kill antibiotic-tolerant bacteria and potentiate antibiotics towards Gram-negative bacteria

• Published in: PloS one 2017-08, Vol.12 (8), p.e0183263-e0183263
• Main Authors: Uppu, Divakara S S M, Konai, Mohini M, Sarkar, Paramita, Samaddar, Sandip, Fensterseifer, Isabel C M, Farias-Junior, Celio, Krishnamoorthy, Paramanandam, Shome, Bibek R, Franco, Octávio L, Haldar, Jayanta
• Format: Article
• Language: English
• Subjects: Animal models; Animals; Anti-Bacterial Agents - pharmacology; Antibacterial agents; Antibiotics; Bacteria; Bacterial infections; Biofilms; Biology; Biology and Life Sciences; Carbapenemase; Chemistry; Colistin; Colony Count, Microbial; Dispersion; Disruption; Dosage and administration; Drug resistance; Drug Synergism; Drug therapy; Epidemiology; Erythromycin; Gram-negative bacteria; Gram-Negative Bacteria - drug effects; Gram-Negative Bacteria - isolation & purification; Health aspects; Health care; Infections; Informatics; Klebsiella; Laboratories; Linezolid; Lipopolysaccharides; Macromolecules; Medicine and Health Sciences; Mice; Microbial Sensitivity Tests; Nehru, Jawaharlal (1889-1964); Peptides; Pharmaceutical sciences; Physical Sciences; Polymers; Potentiation; Rifampin; Risk factors; Surgery; Surgical site infections; Vancomycin; Wound infection
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0183263

Chronic bacterial biofilms place a massive burden on healthcare due to the presence of antibiotic-tolerant dormant bacteria. Some of the conventional antibiotics such as erythromycin, vancomycin, linezolid, rifampicin etc. are inherently ineffective against Gram-negative bacteria, particularly in their biofilms. Here, we report membrane-active macromolecules that kill slow dividing stationary-phase and antibiotic tolerant cells of Gram-negative bacteria. More importantly, these molecules potentiate antibiotics (erythromycin and rifampicin) to biofilms of Gram-negative bacteria. These molecules eliminate planktonic bacteria that are liberated after dispersion of biofilms (dispersed cells). The membrane-active mechanism of these molecules forms the key for potentiating the established antibiotics. Further, we demonstrate that the combination of macromolecules and antibiotics significantly reduces bacterial burden in mouse burn and surgical wound infection models caused by Acinetobacter baumannii and Carbapenemase producing Klebsiella pneumoniae (KPC) clinical isolate respectively. Colistin, a well-known antibiotic targeting the lipopolysaccharide (LPS) of Gram-negative bacteria fails to kill antibiotic tolerant cells and dispersed cells (from biofilms) and bacteria develop resistance to it. On the contrary, these macromolecules prevent or delay the development of bacterial resistance to known antibiotics. Our findings emphasize the potential of targeting the bacterial membrane in antibiotic potentiation for disruption of biofilms and suggest a promising strategy towards developing therapies for topical treatment of Gram-negative infections.