Art-175 is a highly efficient antibacterial against multidrug-resistant strains and persisters of Pseudomonas aeruginosa

Yves Briers, Maarten Walmagh, Barbara Grymonprez, Manfred Biebl, Jean Paul Pirnay, Valerie Defraine, Jan Michiels, William Cenens, Abram Aertsen, Stefan Miller, Rob Lavigne

    Publikation: Beitrag in FachzeitschriftArtikelBegutachtung

    Abstract

    Artilysins constitute a novel class of efficient enzyme-based antibacterials. Specifically, they covalently combine a bacteriophage-encoded endolysin, which degrades the peptidoglycan, with a targeting peptide that transports the endolysin through the outer membrane of Gram-negative bacteria. Art-085, as well as Art-175, its optimized homolog with increased thermostability, are each composed of the sheep myeloid 29-amino acid (SMAP-29) peptide fused to the KZ144 endolysin. In contrast to KZ144, Art-085 and Art-175 pass the outer membrane and kill Pseudomonas aeruginosa, including multidrug-resistant strains, in a rapid and efficient (∼5 log units) manner. Time-lapse microscopy confirms that Art-175 punctures the peptidoglycan layer within 1 min, inducing a bulging membrane and complete lysis. Art-175 is highly refractory to resistance development by naturally occurring mutations. In addition, the resistance mechanisms against 21 therapeutically used antibiotics do not show cross-resistance to Art-175. Since Art-175 does not require an active metabolism for its activity, it has a superior bactericidal effect against P. aeruginosa persisters (up to >4 log units compared to that of the untreated controls). In summary, Art-175 is a novel antibacterial that is well suited for a broad range of applications in hygiene and veterinary and human medicine, with a unique potential to target persister-driven chronic infections.

    OriginalspracheEnglisch
    Seiten (von - bis)3774-3784
    Seitenumfang11
    FachzeitschriftAntimicrobial Agents and Chemotherapy
    Jahrgang58
    Ausgabenummer7
    DOIs
    PublikationsstatusVeröffentlicht - Juli 2014

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