Development of a novel short 12-meric papiliocin-derived peptide that is effective against Gram-negative sepsis

  • Sci Rep. 2019 Mar 7;9(1):3817. doi: 10.1038/s41598-019-40577-8.
Jieun Kim  1 ,  Binu Jacob  1 ,  Mihee Jang  1 ,  Chulhee Kwak  1 ,  Yeongjoon Lee  1 ,  Kkabi Son  1 ,  Sujin Lee  2 ,  In Duk Jung  2 ,  Myeong Seon Jeong  3 ,  Seung-Hae Kwon  3 ,  Yangmee Kim  4
Affiliations
  • 1. Department of Bioscience and Biotechnology, Konkuk University, Seoul, 05029, South Korea.
  • 2. Department of Immunology, Lab of Dendritic Cell Differentiation and Regulation, School of Medicine, Konkuk University, Chungju, 27478, South Korea.
  • 3. Chuncheon Center, Korea Basic Science Institute, Chuncheon, 24341, South Korea.
  • 4. Department of Bioscience and Biotechnology, Konkuk University, Seoul, 05029, South Korea. [email protected].
PMID: 30846839 DOI: 10.1038/s41598-019-40577-8
Abstract

The development of novel peptide Antibiotics with potent activity against multidrug-resistant Gram-negative bacteria and anti-septic activity is urgently needed. In this study, we designed short, 12-meric antimicrobial peptides by substituting Amino acids from the N-terminal 12 residues of the papiliocin (Pap12-1) peptide to alter cationicity and amphipathicity and improve Antibacterial activity and Bacterial membrane interactions. Pap12-6, with an amphipathic α-helical structure and Trp12 at the C-terminus, showed broad-spectrum Antibacterial activity, especially against multidrug-resistant Gram-negative bacteria. Dye leakage, membrane depolarization, and electron microscopy data proved that Pap12-6 kills bacteria by permeabilizing the Bacterial membrane. Additionally, Pap12-6 significantly reduced the secretion of NO, TNF-α, and IL-6 and secreted Alkaline Phosphatase reporter gene activity confirmed that Pap12-6 shows anti-inflammatory activity via a TLR4-mediated NF-κB signaling pathway. In a mouse sepsis model, Pap12-6 significantly improved survival, reduced Bacterial growth in organs, and reduced LPS and inflammatory cytokine levels in the serum and organs. Pap12-6 showed minimal cytotoxicity towards mammalian cells and controlled liver and kidney damage, proving its high Bacterial selectivity. Our results suggest that Pap12-6 is a promising peptide Antibiotic for the therapeutic treatment of Gram-negative sepsis via dual bactericidal and immunomodulatory effects on the host.

Products