Literature DB >> 6643343

Effects of subinhibitory concentrations of antibiotics on Staphylococcus aureus interactions with fibronectin.

R A Proctor, R J Hamill, D F Mosher, J A Textor, P J Olbrantz.   

Abstract

Bacterial adherence to host tissues relies on interactions between tissue macromolecules and bacterial surface molecules. One of the major predisposing factors to infection with Staphylococcus aureus is trauma to tissues. A common element in traumatized tissues is fibronectin. In previous studies, we have shown that fibronectin binds to Staph. aureus. In this paper, we have investigated the effects of subinhibitory concentrations of antibiotics on fibronectin interactions with Staph. aureus. Exposure of Staph. aureus to 1/4 MIC of penicillin increases the number of binding sites and enhances adherence of Staph. aureus to a collagen-fibronectin matrix. Chloramphenicol, erythromycin, clindamycin, and U57,930E all decreased the number of binding sites. Also, U57,930E reduced Staph. aureus adherence to a collagen-fibronectin matrix. Taken together, these data suggest that penicillin may enhance Staph. aureus adherence to tissue fibronectin whereas U57,930E might reduce such binding.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6643343     DOI: 10.1093/jac/12.suppl_c.85

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


  12 in total

1.  Influence of antibiotics on fibronectin binding and phagocytosis of staphylococci by human polymorphonuclear leukocytes.

Authors:  J E Doran
Journal:  Eur J Clin Microbiol       Date:  1987-04       Impact factor: 3.267

2.  Increased expression of fibronectin-binding proteins by fluoroquinolone-resistant Staphylococcus aureus exposed to subinhibitory levels of ciprofloxacin.

Authors:  C Bisognano; P E Vaudaux; D P Lew; E Y Ng; D C Hooper
Journal:  Antimicrob Agents Chemother       Date:  1997-05       Impact factor: 5.191

3.  Efficacies of ofloxacin, rifampin, and clindamycin in treatment of Staphylococcus aureus abscesses and correlation with results of an in vitro assay of intracellular bacterial killing.

Authors:  D M Bamberger; B L Herndon; M Dew; R P Chern; H Mitchell; L E Summers; R F Marcus; S C Kim; P R Suvarna
Journal:  Antimicrob Agents Chemother       Date:  1997-05       Impact factor: 5.191

4.  Induction of fibronectin-binding proteins and increased adhesion of quinolone-resistant Staphylococcus aureus by subinhibitory levels of ciprofloxacin.

Authors:  C Bisognano; P Vaudaux; P Rohner; D P Lew; D C Hooper
Journal:  Antimicrob Agents Chemother       Date:  2000-06       Impact factor: 5.191

5.  Adsorption of fibronectin onto polymethylmethacrylate and promotion of Staphylococcus aureus adherence.

Authors:  P E Vaudaux; F A Waldvogel; J J Morgenthaler; U E Nydegger
Journal:  Infect Immun       Date:  1984-09       Impact factor: 3.441

6.  Ultrastructural studies of adherence of Staphylococcus aureus in experimental acute hematogenous osteomyelitis.

Authors:  D J Speers; S M Nade
Journal:  Infect Immun       Date:  1985-08       Impact factor: 3.441

7.  Role of fibronectin in human monocyte and macrophage bactericidal activity.

Authors:  R A Proctor; J A Textor; J M Vann; D F Mosher
Journal:  Infect Immun       Date:  1985-03       Impact factor: 3.441

8.  Phagocytosis of Staphylococcus aureus by cultured bovine aortic endothelial cells: model for postadherence events in endovascular infections.

Authors:  R J Hamill; J M Vann; R A Proctor
Journal:  Infect Immun       Date:  1986-12       Impact factor: 3.441

9.  Release of fibronectin-lipoteichoic acid complexes from group A streptococci with penicillin.

Authors:  T J Nealon; E H Beachey; H S Courtney; W A Simpson
Journal:  Infect Immun       Date:  1986-02       Impact factor: 3.441

10.  C1q, a subunit of the first component of complement, enhances binding of plasma fibronectin to bacteria.

Authors:  J M Sorvillo; E Pearlstein
Journal:  Infect Immun       Date:  1985-09       Impact factor: 3.441

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.