Literature DB >> 22729924

Oncocin derivative Onc72 is highly active against Escherichia coli in a systemic septicaemia infection mouse model.

Daniel Knappe1, Stefanie Fritsche, Gottfried Alber, Gabriele Köhler, Ralf Hoffmann, Uwe Müller.   

Abstract

OBJECTIVES: The antimicrobial oncocin derivative Onc72 is highly active against a number of Gram-negative bacteria, including resistant strains. Here we study its toxicity and efficacy in a lethal mouse infection model.
METHODS: In an acute toxicity study, purified Onc72 was administered to NMRI mice in four consecutive injections within a period of 24 h as an intraperitoneal bolus. The animals' behaviour was monitored for 5 days, before several organs were examined by histopathology. A lethal Escherichia coli infection model was established and the efficacy of Onc72 was evaluated for different peptide doses considering the survival rates of each dose group and the bacterial counts in blood, lavage and organs.
RESULTS: Intraperitoneal bolus injections with single doses of 20 or 40 mg of Onc72 per kg of body weight did not result in any abnormal animal behaviour. No mouse became moribund or died within the studied period. Histopathological examinations revealed no toxic effects. When infected with E. coli at a lethal dose, none of the untreated animals survived the next 24 h, whereas all animals treated three times with Onc72 at doses of ≥5 mg/kg survived the observation period of 5 days. No bacteria were detected in the blood of treated animals after day 5 post-infection. The effective dose (ED(50)) was ∼2 mg/kg.
CONCLUSIONS: No toxic effects were observed for Onc72 within the studied dose range up to 40 mg/kg, indicating a safety margin of >20.

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Year:  2012        PMID: 22729924     DOI: 10.1093/jac/dks241

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  10 in total

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3.  Introduction of a lysine residue promotes aggregation of temporin L in lipopolysaccharides and augmentation of its antiendotoxin property.

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5.  Intracellular toxicity of proline-rich antimicrobial peptides shuttled into mammalian cells by the cell-penetrating peptide penetratin.

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6.  N-Terminal Ile-Orn- and Trp-Orn-Motif Repeats Enhance Membrane Interaction and Increase the Antimicrobial Activity of Apidaecins against Pseudomonas aeruginosa.

Authors:  Martina E C Bluhm; Viktoria A F Schneider; Ingo Schäfer; Stefania Piantavigna; Tina Goldbach; Daniel Knappe; Peter Seibel; Lisandra L Martin; Edwin J A Veldhuizen; Ralf Hoffmann
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9.  Synergy Between Proline-Rich Antimicrobial Peptides and Small Molecule Antibiotics Against Selected Gram-Negative Pathogens in vitro and in vivo.

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Journal:  Med Drug Discov       Date:  2020-12-30
  10 in total

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