An anti-infective synthetic peptide with dual antimicrobial and immunomodulatory activities
Year: 2016
Type: article
Abstract: Antibiotic-resistant infections are predicted to kill 10 million people per year by 2050, costing the global economy $100 trillion. Therefore, there is an urgent need to develop alternative technologies. We have engineered a synthetic peptide called clavanin-MO, derived from a marine tunicate antimicrobial peptide, which exhibits potent antimicrobial and immunomodulatory properties both in vitro and in vivo. The peptide effectively killed a panel of representative bacterial strains, including multidrug-resistant hospital isolates. Antimicrobial activity of the peptide was demonstrated in animal models, reducing bacterial counts by six orders of magnitude, and contributing to infection clearance. In addition, clavanin-MO was capable of modulating innate immunity by stimulating leukocyte recruitment to the site of infection, and production of immune mediators GM-CSF, IFN-γ and MCP-1, while suppressing an excessive and potentially harmful inflammatory response by increasing synthesis of anti-inflammatory cytokines such as IL-10 and repressing the levels of pro-inflammatory cytokines IL-12 and TNF-α. Finally, treatment with the peptide protected mice against otherwise lethal infections caused by both Gram-negative and -positive drug-resistant strains. The peptide presented here directly kills bacteria and further helps resolve infections through its immune modulatory properties. Peptide anti-infective therapeutics with combined antimicrobial and immunomodulatory properties represent a new approach to treat antibiotic-resistant infections.
Source: Scientific Reports
DOI: 10.1038/srep35465
Language: English
Subfield: Microbiology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,690
Funders: Fundación Ramón Areces, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação de Apoio ao Desenvolvimento do Ensino, Ciência e Tecnologia do Estado de Mato Grosso do Sul, National Institutes of Health, Defense Threat Reduction Agency, National Institute of Biomedical Imaging and Bioengineering, Army Research Office, Army Research Laboratory
Awards: G1614988657, G2803563960, G3429140574, G3491862500, G3732666562, G4306803201, G4950536974, G5259331294, Engineering “Phagebody” Antimicrobials for Carbapenem-Resistant Enterobacteriaceae, G5841114617, G611330818, G6274897657, Mucin Glycans in the Regulation of Microbial Virulence, G6541015203, G6682268439, G7452299184
OpenAlex ID: W2548197444
