Peptide polymer displaying potent activity against clinically isolated multidrug resistant Pseudomonas aeruginosa in vitro and in vivo.

Multidrug resistant (MDR) Pseudomonas aeruginosa has caused serious nosocomial infections owing to its high intrinsic resistance and ease of acquiring resistance to common antibiotics. There is an urgent need to develop antimicrobial agents against MDR Pseudomonas aeruginosa. Here we report a 27-mer peptide polymer 90 : 10 DLL : BLG, as a synthetic mimic of a host defense peptide, that displayed potent in vitro and in vivo activities against multiple strains of clinically isolated MDR Pseudomonas aeruginosa, performing even better than antibiotics within our study. This peptide polymer also showed negligible hemolysis and low cytotoxicity, as well as quick bacterial killing efficacy. The structural diversity of peptide polymers, their easy synthesis from lithium hexamethyldisilazide-initiated fast N-carboxyanhydride polymerization, and the excellent reproducibility of their chemical structure and biological profiles altogether suggested great potential for antimicrobial applications of peptide polymers as synthetic mimics of host defense peptides.

[1]  Runhui Liu,et al.  Efficient synthesis of amino acid polymers for protein stabilization. , 2019, Biomaterials science.

[2]  A. Wan,et al.  pH-Degradable imidazolium oligomers as antimicrobial materials with tuneable loss of activity. , 2019, Biomaterials science.

[3]  K. Fukushima,et al.  Modulating bioactivities of primary ammonium-tagged antimicrobial aliphatic polycarbonates by varying length, sequence and hydrophobic side chain structure. , 2019, Biomaterials science.

[4]  Runhui Liu,et al.  Host defense peptide mimicking poly-β-peptides with fast, potent and broad spectrum antibacterial activities. , 2019, Biomaterials science.

[5]  Runhui Liu,et al.  Lithium hexamethyldisilazide initiated superfast ring opening polymerization of alpha-amino acid N-carboxyanhydrides , 2018, Nature Communications.

[6]  Runhui Liu,et al.  Versatile Antibacterial Materials: An Emerging Arsenal for Combatting Bacterial Pathogens , 2018, Advanced Functional Materials.

[7]  Chunsheng Xiao,et al.  From Antimicrobial Peptides to Antimicrobial Poly(α‐amino acid)s , 2018, Advanced healthcare materials.

[8]  Collins Wenhan Chu,et al.  A macromolecular approach to eradicate multidrug resistant bacterial infections while mitigating drug resistance onset , 2018, Nature Communications.

[9]  Lichen Yin,et al.  Bacteria-Assisted Activation of Antimicrobial Polypeptides by a Random-Coil to Helix Transition. , 2017, Angewandte Chemie.

[10]  Daniel N. Wilson,et al.  Proline-rich antimicrobial peptides targeting protein synthesis. , 2017, Natural product reports.

[11]  Guangshun Wang,et al.  Host defense antimicrobial peptides as antibiotics: design and application strategies. , 2017, Current opinion in chemical biology.

[12]  G. Wong,et al.  Interactions between Membranes and "Metaphilic" Polypeptide Architectures with Diverse Side-Chain Populations. , 2017, ACS nano.

[13]  Qiang Gao,et al.  Rationally designed dual functional block copolymers for bottlebrush-like coatings: In vitro and in vivo antimicrobial, antibiofilm, and antifouling properties. , 2017, Acta biomaterialia.

[14]  G. Qiao,et al.  Combating multidrug-resistant Gram-negative bacteria with structurally nanoengineered antimicrobial peptide polymers , 2016, Nature Microbiology.

[15]  M. Brockhurst,et al.  Pseudomonas aeruginosa Evolutionary Adaptation and Diversification in Cystic Fibrosis Chronic Lung Infections , 2016, Trends in microbiology.

[16]  Jinbao Xu,et al.  Cationic polycarbonate-grafted superparamagnetic nanoparticles with synergistic dual-modality antimicrobial activity. , 2016, Biomaterials science.

[17]  Peng Sang,et al.  γ-AApeptides: Design, Structure, and Applications. , 2016, Accounts of chemical research.

[18]  Lifeng Kang,et al.  High durability and low toxicity antimicrobial coatings fabricated by quaternary ammonium silane copolymers. , 2016, Biomaterials science.

[19]  Andrew L. Ferguson,et al.  Helical antimicrobial polypeptides with radial amphiphilicity , 2015, Proceedings of the National Academy of Sciences.

[20]  Carlos Juan,et al.  The increasing threat of Pseudomonas aeruginosa high-risk clones. , 2015, Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy.

[21]  Analette I. Lopez,et al.  Antimicrobial peptide LL-37 on surfaces presenting carboxylate anions. , 2015, Biomaterials science.

[22]  J. Chen,et al.  Multifunctional biocompatible and biodegradable folic acid conjugated poly(ε-caprolactone)-polypeptide copolymer vesicles with excellent antibacterial activities. , 2015, Bioconjugate chemistry.

[23]  K. Sanyal,et al.  Broad spectrum antibacterial and antifungal polymeric paint materials: synthesis, structure-activity relationship, and membrane-active mode of action. , 2015, ACS applied materials & interfaces.

[24]  Gerard C. L. Wong,et al.  Ternary Nylon-3 Copolymers as Host-Defense Peptide Mimics: Beyond Hydrophobic and Cationic Subunits , 2014, Journal of the American Chemical Society.

[25]  S. Gellman,et al.  Tuning the Biological Activity Profile of Antibacterial Polymers via Subunit Substitution Pattern , 2014, Journal of the American Chemical Society.

[26]  J. Haldar,et al.  Polymers with tunable side-chain amphiphilicity as non-hemolytic antibacterial agents. , 2013, Chemical communications.

[27]  L. Shaw,et al.  Lipo-γ-AApeptides as a new class of potent and broad-spectrum antimicrobial agents. , 2012, Journal of medicinal chemistry.

[28]  L. Shaw,et al.  Non-hemolytic α-AApeptides as antimicrobial peptidomimetics. , 2011, Chemical communications.

[29]  R. Hancock,et al.  Pseudomonas aeruginosa: all roads lead to resistance. , 2011, Trends in microbiology.

[30]  J. Hedrick,et al.  Biodegradable nanostructures with selective lysis of microbial membranes. , 2011, Nature chemistry.

[31]  C. M. Li,et al.  A polycationic antimicrobial and biocompatible hydrogel with microbe membrane suctioning ability. , 2011, Nature materials.

[32]  K. Kuroda,et al.  Structural determinants of antimicrobial activity and biocompatibility in membrane-disrupting methacrylamide random copolymers. , 2009, Biomacromolecules.

[33]  Nancy D. Hanson,et al.  Antibacterial-Resistant Pseudomonas aeruginosa: Clinical Impact and Complex Regulation of Chromosomally Encoded Resistance Mechanisms , 2009, Clinical Microbiology Reviews.

[34]  W. DeGrado,et al.  De novo design and in vivo activity of conformationally restrained antimicrobial arylamide foldamers , 2009, Proceedings of the National Academy of Sciences.

[35]  A. Barron,et al.  Peptoids that mimic the structure, function, and mechanism of helical antimicrobial peptides , 2008, Proceedings of the National Academy of Sciences.

[36]  T. Deming Synthetic polypeptides for biomedical applications , 2007 .

[37]  R. Hancock,et al.  Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies , 2006, Nature Biotechnology.

[38]  W. DeGrado,et al.  Amphiphilic polymethacrylate derivatives as antimicrobial agents. , 2005, Journal of the American Chemical Society.

[39]  G. Tew,et al.  Tuning the hemolytic and antibacterial activities of amphiphilic polynorbornene derivatives. , 2004, Journal of the American Chemical Society.

[40]  M. Zasloff Antimicrobial peptides of multicellular organisms , 2002, Nature.

[41]  S. Gellman,et al.  Antibiotics: Non-haemolytic β-amino-acid oligomers , 2000, Nature.

[42]  H. G. Boman,et al.  Antibacterial peptides: Key components needed in immunity , 1991, Cell.