Literature DB >> 2109578

Paradoxical response of Enterococcus faecalis to the bactericidal activity of penicillin is associated with reduced activity of one autolysin.

R Fontana1, M Boaretti, A Grossato, E A Tonin, M M Lleò, G Satta.   

Abstract

Ten clinical isolates of Enterococcus faecalis were examined for susceptibility to the bactericidal activity of penicillin. Four of these had MBCs of penicillin equal to 2 to 4 x the MIC, and six exhibited a paradoxical response to penicillin, i.e., the bactericidal activity of the antibiotic had a concentration optimum at 2 to 4 x the MIC and decreased significantly at concentrations above this. We found that the paradoxical response to penicillin was an intrinsic and stable property of a strain, but that its phenotypic expression was not homogeneous; only a fraction of the cell population that died at low concentrations was able to survive at high penicillin concentrations. The size of this fraction increased with increasing antibiotic concentration and reached a maximum in the late-log phase of growth. All 10 strains produced a lytic enzyme that was active on Micrococcus luteus heat-killed cells, whereas only some strains lysed E. faecalis heat-killed cells. Strains producing large amounts of the latter enzyme did not show the paradoxical response to penicillin, whereas mutants of these strains that lacked this enzymatic activity paradoxically responded to the antibiotic activity. In addition, from strains that showed paradoxical response to penicillin and produced only the enzyme that was active on M. luteus, it was possible to isolate mutants that were also capable of lysing E. faecalis cells and that were killed with similar efficiency by all concentrations above the MBC. On the basis of these findings, the paradoxical response to penicillin is explained as a property of certain strains of E. faecalis; this property is genetically characterized by alterations in synthesis or activity of one autolysin but phenotypically expressed only by a few cells that are in a particular physiological condition when exposed to high concentrations of antibiotics.

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Year:  1990        PMID: 2109578      PMCID: PMC171579          DOI: 10.1128/AAC.34.2.314

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  17 in total

1.  Penicillin tolerance in Streptococcus faecium ATCC 9790.

Authors:  I Said; H Fletcher; A Volpe; L Daneo-Moore
Journal:  Antimicrob Agents Chemother       Date:  1987-07       Impact factor: 5.191

2.  Multiple antibiotic resistance in a bacterium with suppressed autolytic system.

Authors:  A Tomasz; A Albino; E Zanati
Journal:  Nature       Date:  1970-07-11       Impact factor: 49.962

3.  Some properties of two autolytic-defective mutants of Streptococcus faecalis ATCC 9790.

Authors:  H M Pooley; G D Shockman; M L Higgins; J Porres-Juan
Journal:  J Bacteriol       Date:  1972-01       Impact factor: 3.490

Review 4.  Antibiotic tolerance among clinical isolates of bacteria.

Authors:  S Handwerger; A Tomasz
Journal:  Rev Infect Dis       Date:  1985 May-Jun

5.  Recognition of group D streptococcal species of human origin by biochemical and physiological tests.

Authors:  R R Facklam
Journal:  Appl Microbiol       Date:  1972-06

6.  Identification of a streptococcal penicillin-binding protein that reacts very slowly with penicillin.

Authors:  R Fontana; R Cerini; P Longoni; A Grossato; P Canepari
Journal:  J Bacteriol       Date:  1983-09       Impact factor: 3.490

7.  Role of autolysins in the killing of bacteria by some bactericidal antibiotics.

Authors:  H J Rogers; C W Forsberg
Journal:  J Bacteriol       Date:  1971-12       Impact factor: 3.490

8.  Streptococcus faecium ATCC 9790 penicillin-binding proteins and penicillin sensitivity are heavily influenced by growth conditions: proposal for an indirect mechanism of growth inhibition by beta-lactams.

Authors:  R Fontana; P Canepari; G Satta; J Coyette
Journal:  J Bacteriol       Date:  1983-05       Impact factor: 3.490

9.  Determination of minimum bactericidal concentrations of oxacillin for Staphylococcus aureus: influence and significance of technical factors.

Authors:  P C Taylor; F D Schoenknecht; J C Sherris; E C Linner
Journal:  Antimicrob Agents Chemother       Date:  1983-01       Impact factor: 5.191

10.  Inhibition of beta-lactam antibiotics at two different times in the cell cycle of Streptococcus faecium ATCC 9790.

Authors:  M J Pucci; E T Hinks; D T Dicker; M L Higgins; L Daneo-Moore
Journal:  J Bacteriol       Date:  1986-03       Impact factor: 3.490

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  13 in total

1.  Prevalence of vancomycin-resistant enterococci in fecal samples from hospitalized patients and nonhospitalized controls in a cattle-rearing area of France.

Authors:  K Gambarotto; M C Ploy; P Turlure; C Grélaud; C Martin; D Bordessoule; F Denis
Journal:  J Clin Microbiol       Date:  2000-02       Impact factor: 5.948

2.  Mechanism of action of BAY v 3522, a new cephalosporin with unusually good activity against enterococci.

Authors:  G Amalfitano; A Grossato; R Fontana
Journal:  Antimicrob Agents Chemother       Date:  1991-09       Impact factor: 5.191

3.  Functional analysis of AtlA, the major N-acetylglucosaminidase of Enterococcus faecalis.

Authors:  Catherine Eckert; Maxime Lecerf; Lionel Dubost; Michel Arthur; Stéphane Mesnage
Journal:  J Bacteriol       Date:  2006-10-13       Impact factor: 3.490

4.  Cloning, sequencing, and expression in Escherichia coli of a Streptococcus faecalis autolysin.

Authors:  C Béliveau; C Potvin; J Trudel; A Asselin; G Bellemare
Journal:  J Bacteriol       Date:  1991-09       Impact factor: 3.490

5.  Penicillin tolerance and modification of lipoteichoic acid associated with expression of vancomycin resistance in VanB-type Enterococcus faecium D366.

Authors:  L Gutmann; S Al-Obeid; D Billot-Klein; E Ebnet; W Fischer
Journal:  Antimicrob Agents Chemother       Date:  1996-01       Impact factor: 5.191

6.  Host lysozyme-mediated lysis of Lactococcus lactis facilitates delivery of colitis-attenuating superoxide dismutase to inflamed colons.

Authors:  Sonia A Ballal; Patrick Veiga; Kathrin Fenn; Monia Michaud; Jason H Kim; Carey Ann Gallini; Jonathan N Glickman; Gaëlle Quéré; Peggy Garault; Chloé Béal; Muriel Derrien; Pascal Courtin; Saulius Kulakauskas; Marie-Pierre Chapot-Chartier; Johan van Hylckama Vlieg; Wendy S Garrett
Journal:  Proc Natl Acad Sci U S A       Date:  2015-06-08       Impact factor: 11.205

7.  In vitro response to bactericidal activity of cell wall-active antibiotics does not support the general opinion that enterococci are naturally tolerant to these antibiotics.

Authors:  R Fontana; A Grossato; M Ligozzi; E A Tonin
Journal:  Antimicrob Agents Chemother       Date:  1990-08       Impact factor: 5.191

8.  Identification of a gene (arpU) controlling muramidase-2 export in Enterococcus hirae.

Authors:  M M Lleò; R Fontana; M Solioz
Journal:  J Bacteriol       Date:  1995-10       Impact factor: 3.490

9.  Effect of disruption of a gene encoding an autolysin of Enterococcus faecalis OG1RF.

Authors:  X Qin; K V Singh; Y Xu; G M Weinstock; B E Murray
Journal:  Antimicrob Agents Chemother       Date:  1998-11       Impact factor: 5.191

10.  Role of the Enterococcus faecalis GelE protease in determination of cellular chain length, supernatant pheromone levels, and degradation of fibrin and misfolded surface proteins.

Authors:  Christopher M Waters; Michelle H Antiporta; Barbara E Murray; Gary M Dunny
Journal:  J Bacteriol       Date:  2003-06       Impact factor: 3.490

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