Literature DB >> 16122911

In vitro activity of MSI-78 alone and in combination with antibiotics against bacteria responsible for bloodstream infections in neutropenic patients.

Andrea Giacometti1, Oscar Cirioni, Wojciech Kamysz, Giuseppina D'Amato, Carmela Silvestri, Alberto Licci, Piotr Nadolski, Alessandra Riva, Jerzy Lukasiak, Giorgio Scalise.   

Abstract

MSI-78 is a 22 amino acid amphipathic peptide with potent antimicrobial activity against Gram-positive and Gram-negative organisms, including antibiotic-resistant strains. In this study, we assessed the in vitro activity of MSI-78 alone and in combination with eight clinically used antimicrobial agents against several strains of Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis and Escherichia coli isolated from blood of neutropenic febrile patients. Antimicrobial activity of MSI-78 was measured by minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), time-kill studies and checkerboard titration method. The Gram-negative isolates were susceptible to the peptide at concentrations in the range 0.50-16 mg/L, while staphylococci showed lower susceptibility. MSI-78 demonstrated a higher antimicrobial activity than colistin against Gram-negative organisms. The checkerboard titration method demonstrated synergy when the peptide was combined with beta-lactams. These results provide evidence for the potential use of MSI-78 in the management of severe infections in neutropenic patients.

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Year:  2005        PMID: 16122911     DOI: 10.1016/j.ijantimicag.2005.06.011

Source DB:  PubMed          Journal:  Int J Antimicrob Agents        ISSN: 0924-8579            Impact factor:   5.283


  6 in total

1.  Membrane interaction of antimicrobial peptides using E. coli lipid extract as model bacterial cell membranes and SFG spectroscopy.

Authors:  Lauren Soblosky; Ayyalusamy Ramamoorthy; Zhan Chen
Journal:  Chem Phys Lipids       Date:  2015-02-20       Impact factor: 3.329

2.  Structural features governing the activity of lactoferricin-derived peptides that act in synergy with antibiotics against Pseudomonas aeruginosa in vitro and in vivo.

Authors:  Susana Sánchez-Gómez; Bostjan Japelj; Roman Jerala; Ignacio Moriyón; Mirian Fernández Alonso; José Leiva; Sylvie E Blondelle; Jörg Andrä; Klaus Brandenburg; Karl Lohner; Guillermo Martínez de Tejada
Journal:  Antimicrob Agents Chemother       Date:  2010-10-18       Impact factor: 5.191

3.  Does cholesterol suppress the antimicrobial peptide induced disruption of lipid raft containing membranes?

Authors:  Austin J McHenry; Michele F M Sciacca; Jeffrey R Brender; Ayyalusamy Ramamoorthy
Journal:  Biochim Biophys Acta       Date:  2012-08-01

Review 4.  Structure, membrane orientation, mechanism, and function of pexiganan--a highly potent antimicrobial peptide designed from magainin.

Authors:  Lindsey M Gottler; Ayyalusamy Ramamoorthy
Journal:  Biochim Biophys Acta       Date:  2008-10-29

5.  Efficacy of Mastoparan-AF alone and in combination with clinically used antibiotics on nosocomial multidrug-resistant Acinetobacter baumannii.

Authors:  Chun-Hsien Lin; Mong-Chuan Lee; Jason T C Tzen; Hsien-Ming Lee; Sam-Min Chang; Wu-Chun Tu; Chuen-Fu Lin
Journal:  Saudi J Biol Sci       Date:  2016-12-23       Impact factor: 4.219

6.  Synergistic effects of antimicrobial peptide DP7 combined with antibiotics against multidrug-resistant bacteria.

Authors:  Xiaozhe Wu; Zhan Li; Xiaolu Li; Yaomei Tian; Yingzi Fan; Chaoheng Yu; Bailing Zhou; Yi Liu; Rong Xiang; Li Yang
Journal:  Drug Des Devel Ther       Date:  2017-03-22       Impact factor: 4.162

  6 in total

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