Literature DB >> 2302344

Inhibition of the bacteriolytic effect of beta-lactam-antibiotics on Staphylococcus aureus by the polyanionic drugs suramin and Evans Blue.

J Wecke1, M Franz, P Giesbrecht.   

Abstract

The anionic polyelectrolytes suramin and Evans Blue inhibited different autolytic systems involved in wall growth and wall turnover of growing staphylococci and in wall autolysis of resting bacteria. Moreover, both substances lowered the beta-lactam-induced pre-lytic release of cytoplasmic constituents from staphylococci, and inhibited the beta-lactam-induced bacteriolysis as well as the loss of viability. The protective effects of these sulfonated drugs against bacteriolysis were also monitored by electron microscopy. Some medical implications of our results are discussed.

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Year:  1990        PMID: 2302344

Source DB:  PubMed          Journal:  APMIS        ISSN: 0903-4641            Impact factor:   3.205


  5 in total

1.  Localized perforation of the cell wall by a major autolysin: atl gene products and the onset of penicillin-induced lysis of Staphylococcus aureus.

Authors:  M Sugai; S Yamada; S Nakashima; H Komatsuzawa; A Matsumoto; T Oshida; H Suginaka
Journal:  J Bacteriol       Date:  1997-05       Impact factor: 3.490

Review 2.  Staphylococcal cell wall: morphogenesis and fatal variations in the presence of penicillin.

Authors:  P Giesbrecht; T Kersten; H Maidhof; J Wecke
Journal:  Microbiol Mol Biol Rev       Date:  1998-12       Impact factor: 11.056

3.  Fan-shaped ejections of regularly arranged murosomes involved in penicillin-induced death of staphylococci.

Authors:  P Giesbrecht; T Kersten; J Wecke
Journal:  J Bacteriol       Date:  1992-04       Impact factor: 3.490

4.  From amino acids polymers, antimicrobial peptides, and histones, to their possible role in the pathogenesis of septic shock: a historical perspective.

Authors:  Isaac Ginsburg; Peter Vernon van Heerden; Erez Koren
Journal:  J Inflamm Res       Date:  2017-02-01

5.  Multi-drug strategies are necessary to inhibit the synergistic mechanism causing tissue damage and organ failure in post infectious sequelae.

Authors:  I Ginsburg
Journal:  Inflammopharmacology       Date:  1999       Impact factor: 5.093

  5 in total

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