Literature DB >> 10768947

Effects of Enterococcus faecalis fsr genes on production of gelatinase and a serine protease and virulence.

X Qin1, K V Singh, G M Weinstock, B E Murray.   

Abstract

Three agr-like genes (fsrA, fsrB, and fsrC, for Enterococcus faecalis regulator) were found upstream of the previously reported gelatinase gene (gelE) and a downstream putative serine protease gene (sprE; accession number Z12296) of Enterococcus faecalis OG1RF. The deduced amino acid sequence of fsrA shows 26% identity and 38% similarity to Staphylococcus aureus AgrA (the response regulator of the accessory gene regulator system in the agr locus), FsrB shows 23% identity and 41% similarity to S. aureus AgrB, and FsrC shows 23% identity and 36% similarity to S. aureus AgrC (the sensor transducer of Agr system). Northern blot analysis suggested that gelE and sprE are cotranscribed and that fsrB and fsrC are also cotranscribed in OG1RF. Northern blot analysis of fsrA, fsrB, fsrC, gelE, and sprE insertion mutants showed that fsrB, fsrC, gelE, and sprE are not expressed in fsrA, fsrB, and fsrC mutants, while insertion in an open reading frame further upstream of fsrA did not effect the expression of these genes, suggesting that agr-like genes may be autoregulated and that they regulate gelE and sprE expression, as further confirmed by complementation of fsr gene mutations with a 6-kb fragment which contains all three fsr genes in the shuttle vector, pAT18. Testing of 95 other isolates of E. faecalis showed that 62% produced gelatinase (Gel(+)), while 91% (including all Gel(+) strains) hybridized to a gelE probe; 71% (including all Gel(+) strains) hybridized to an fsr probe, corroborating the conclusion that both gelE and fsr are necessary for gelatinase production. Testing of fsrA, fsrB, and sprE mutants in a mouse peritonitis model showed that sprE and agr-like gene mutants resulted in highly significantly prolonged survival compared to the parent strain OG1RF, a finding similar to what we had previously shown for a gelE mutant. These results suggest that sprE and agr-like genes contribute to the virulence of E. faecalis OG1RF in this model.

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Year:  2000        PMID: 10768947      PMCID: PMC97462          DOI: 10.1128/IAI.68.5.2579-2586.2000

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  23 in total

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Authors:  M Otto; R Süssmuth; G Jung; F Götz
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2.  Bacterial interference caused by autoinducing peptide variants.

Authors:  G Ji; R Beavis; R P Novick
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3.  Regulation of exoprotein gene expression in Staphylococcus aureus by agar.

Authors:  P Recsei; B Kreiswirth; M O'Reilly; P Schlievert; A Gruss; R P Novick
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Journal:  Science       Date:  1987-10-16       Impact factor: 47.728

5.  Cell density control of staphylococcal virulence mediated by an octapeptide pheromone.

Authors:  G Ji; R C Beavis; R P Novick
Journal:  Proc Natl Acad Sci U S A       Date:  1995-12-19       Impact factor: 11.205

6.  Regulation of agr-dependent virulence genes in Staphylococcus aureus by RNAIII from coagulase-negative staphylococci.

Authors:  K Tegmark; E Morfeldt; S Arvidson
Journal:  J Bacteriol       Date:  1998-06       Impact factor: 3.490

7.  Generation and testing of mutants of Enterococcus faecalis in a mouse peritonitis model.

Authors:  K V Singh; X Qin; G M Weinstock; B E Murray
Journal:  J Infect Dis       Date:  1998-11       Impact factor: 5.226

8.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

9.  Cloning, characterization, and sequencing of an accessory gene regulator (agr) in Staphylococcus aureus.

Authors:  H L Peng; R P Novick; B Kreiswirth; J Kornblum; P Schlievert
Journal:  J Bacteriol       Date:  1988-09       Impact factor: 3.490

10.  Cloning and characterization of an accessory gene regulator (agr)-like locus from Staphylococcus epidermidis.

Authors:  W J Van Wamel; G van Rossum; J Verhoef; C M Vandenbroucke-Grauls; A C Fluit
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  135 in total

1.  Characterization of fsr, a regulator controlling expression of gelatinase and serine protease in Enterococcus faecalis OG1RF.

Authors:  X Qin; K V Singh; G M Weinstock; B E Murray
Journal:  J Bacteriol       Date:  2001-06       Impact factor: 3.490

Review 2.  Two-component signal transduction in Enterococcus faecalis.

Authors:  Lynn Hancock; Marta Perego
Journal:  J Bacteriol       Date:  2002-11       Impact factor: 3.490

3.  Distribution of fsr among Enterococcus faecalis isolates from the SENTRY antimicrobial surveillance program.

Authors:  Ronald N Jones; Lalitagauri M Deshpande
Journal:  J Clin Microbiol       Date:  2003-08       Impact factor: 5.948

Review 4.  Peptide signaling in the staphylococci.

Authors:  Matthew Thoendel; Jeffrey S Kavanaugh; Caralyn E Flack; Alexander R Horswill
Journal:  Chem Rev       Date:  2010-12-21       Impact factor: 60.622

5.  Comparison of OG1RF and an isogenic fsrB deletion mutant by transcriptional analysis: the Fsr system of Enterococcus faecalis is more than the activator of gelatinase and serine protease.

Authors:  Agathe Bourgogne; Susan G Hilsenbeck; Gary M Dunny; Barbara E Murray
Journal:  J Bacteriol       Date:  2006-04       Impact factor: 3.490

6.  The N-terminal domain of enterococcal surface protein, Esp, is sufficient for Esp-mediated biofilm enhancement in Enterococcus faecalis.

Authors:  Preeti M Tendolkar; Arto S Baghdayan; Nathan Shankar
Journal:  J Bacteriol       Date:  2005-09       Impact factor: 3.490

7.  Multiple roles for Enterococcus faecalis glycosyltransferases in biofilm-associated antibiotic resistance, cell envelope integrity, and conjugative transfer.

Authors:  Jennifer L Dale; Julian Cagnazzo; Chi Q Phan; Aaron M T Barnes; Gary M Dunny
Journal:  Antimicrob Agents Chemother       Date:  2015-04-27       Impact factor: 5.191

8.  Comparative genomics and transduction potential of Enterococcus faecalis temperate bacteriophages.

Authors:  Azra Yasmin; John G Kenny; Jayendra Shankar; Alistair C Darby; Neil Hall; Clive Edwards; Malcolm J Horsburgh
Journal:  J Bacteriol       Date:  2009-12-11       Impact factor: 3.490

9.  Siamycin attenuates fsr quorum sensing mediated by a gelatinase biosynthesis-activating pheromone in Enterococcus faecalis.

Authors:  Jiro Nakayama; Emi Tanaka; Reiko Kariyama; Koji Nagata; Kenzo Nishiguchi; Ritsuko Mitsuhata; Yumi Uemura; Masaru Tanokura; Hiromi Kumon; Kenji Sonomoto
Journal:  J Bacteriol       Date:  2006-10-27       Impact factor: 3.490

10.  Structure-activity relationship of gelatinase biosynthesis-activating pheromone of Enterococcus faecalis.

Authors:  Kenzo Nishiguchi; Koji Nagata; Masaru Tanokura; Kenji Sonomoto; Jiro Nakayama
Journal:  J Bacteriol       Date:  2008-11-07       Impact factor: 3.490

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