Literature DB >> 9276414

Molecular epidemiology and antibiotic susceptibility of enterococci in Cincinnati, Ohio: a prospective citywide survey.

D E Perlada1, A G Smulian, M T Cushion.   

Abstract

To determine patterns of antimicrobial susceptibility among enterococci and to assess molecular characteristics of vancomycin-resistant enterococci, 157 clinical blood isolates of enterococci from 10 hospitals in Cincinnati, Ohio, were prospectively collected during a 6-month period from February to July 1995. The isolates included 108 (69%) E. faecalis isolates, 46 (29%) E. faecium isolates, and 1 isolate each of E. avium, E. durans, and E. gallinarum. The E. faecalis and E. faecium isolates differed in their susceptibilities to ampicillin (100 versus 20%), ampicillin-sulbactam (100 versus 13%), vancomycin (100 versus 57%), imipenem (94 versus 2%), and high levels of gentamicin (59 versus 83%). Supplemental susceptibility testing of the 21 vancomycin-resistant isolates showed that 21 (100%) were susceptible to chloramphenicol and that only 7 (33%) were susceptible to doxycycline. Nineteen (90%) of the vancomycin-resistant E. faecium isolates were of the VanB phenotype, with vanB resistance genes detected by PCR and hybridization with gene-specific probes; and the E. gallinarum isolates demonstrated the VanC phenotype with the vanC1 gene. One vancomycin-resistant E. faecium isolate was highly resistant to both teicoplanin and vancomycin, corresponding to the VanA phenotype; however, it was found to have the vanB gene. Pulsed-field gel electrophoresis (PFGE) revealed that all of the 19 E. faecium isolates with the VanB phenotype had identical to closely related banding patterns. Hybridization of restriction enzyme-digested DNA separated by PFGE with a vanB gene probe demonstrated differences in the locations of vanB genes that corresponded closely to the PFGE banding patterns. Our study has documented that the emerging vancomycin resistance in our city was mainly due to the clonal dissemination of a single strain of E. faecium VanB.

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Year:  1997        PMID: 9276414      PMCID: PMC229966          DOI: 10.1128/jcm.35.9.2342-2347.1997

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  22 in total

1.  Detection of glycopeptide resistance genotypes and identification to the species level of clinically relevant enterococci by PCR.

Authors:  S Dutka-Malen; S Evers; P Courvalin
Journal:  J Clin Microbiol       Date:  1995-01       Impact factor: 5.948

Review 2.  Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing.

Authors:  F C Tenover; R D Arbeit; R V Goering; P A Mickelsen; B E Murray; D H Persing; B Swaminathan
Journal:  J Clin Microbiol       Date:  1995-09       Impact factor: 5.948

Review 3.  Genetics and mechanisms of glycopeptide resistance in enterococci.

Authors:  M Arthur; P Courvalin
Journal:  Antimicrob Agents Chemother       Date:  1993-08       Impact factor: 5.191

4.  Clinical and molecular epidemiology of vancomycin-resistant Enterococcus faecium during its emergence in a city in southern Texas.

Authors:  F Moreno; P Grota; C Crisp; K Magnon; G P Melcher; J H Jorgensen; J E Patterson
Journal:  Clin Infect Dis       Date:  1995-11       Impact factor: 9.079

5.  Emergence of vancomycin-resistant enterococci in New York City.

Authors:  T R Frieden; S S Munsiff; D E Low; B M Willey; G Williams; Y Faur; W Eisner; S Warren; B Kreiswirth
Journal:  Lancet       Date:  1993-07-10       Impact factor: 79.321

Review 6.  Meropenem: a microbiological overview.

Authors:  J R Edwards
Journal:  J Antimicrob Chemother       Date:  1995-07       Impact factor: 5.790

7.  Enterococci resistant to multiple antimicrobial agents, including vancomycin. Establishment of endemicity in a university medical center.

Authors:  J G Morris; D K Shay; J N Hebden; R J McCarter; B E Perdue; W Jarvis; J A Johnson; T C Dowling; L B Polish; R S Schwalbe
Journal:  Ann Intern Med       Date:  1995-08-15       Impact factor: 25.391

8.  Inducible, transferable resistance to vancomycin in Enterococcus faecalis A256.

Authors:  D M Shlaes; A Bouvet; C Devine; J H Shlaes; S al-Obeid; R Williamson
Journal:  Antimicrob Agents Chemother       Date:  1989-02       Impact factor: 5.191

9.  Comparison of pigment production and motility tests with PCR for reliable identification of intrinsically vancomycin-resistant enterococci.

Authors:  C P Cartwright; F Stock; G A Fahle; V J Gill
Journal:  J Clin Microbiol       Date:  1995-07       Impact factor: 5.948

10.  Use of primers selective for vancomycin resistance genes to determine van genotype in enterococci and to study gene organization in VanA isolates.

Authors:  A Miele; M Bandera; B P Goldstein
Journal:  Antimicrob Agents Chemother       Date:  1995-08       Impact factor: 5.191

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  15 in total

1.  Improved pulsed-field gel electrophoresis for typing vancomycin-resistant enterococci.

Authors:  D Turabelidze; M Kotetishvili; A Kreger; J G Morris; A Sulakvelidze
Journal:  J Clin Microbiol       Date:  2000-11       Impact factor: 5.948

2.  Isolation and characterization of glycopeptide-resistant enterococci from hospitalized patients over a 30-month period.

Authors:  R R Nelson; K F McGregor; A R Brown; S G Amyes; H Young
Journal:  J Clin Microbiol       Date:  2000-06       Impact factor: 5.948

3.  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

4.  Prevalence of vancomycin-resistant enterococcus in prenatal screening cultures.

Authors:  Melissa B Miller; Sonia L Allen; Mary Ellen Mangum; Anastassia Doutova; Peter H Gilligan
Journal:  J Clin Microbiol       Date:  2004-02       Impact factor: 5.948

5.  Local genetic patterns within a vancomycin-resistant Enterococcus faecalis clone isolated in three hospitals in Portugal.

Authors:  Carla Novais; Teresa M Coque; João Carlos Sousa; Fernando Baquero; Luisa Peixe
Journal:  Antimicrob Agents Chemother       Date:  2004-09       Impact factor: 5.191

6.  Outbreak of vancomycin-resistant Enterococcus faecium of the phenotype VanB in a hospital in Warsaw, Poland: probable transmission of the resistance determinants into an endemic vancomycin-susceptible strain.

Authors:  M Kawalec; M Gniadkowski; M Zaleska; T Ozorowski; L Konopka; W Hryniewicz
Journal:  J Clin Microbiol       Date:  2001-05       Impact factor: 5.948

7.  Use of molecular and reference susceptibility testing methods in a multicenter evaluation of MicroScan dried overnight gram-positive MIC panels for detection of vancomycin and high-level aminoglycoside resistances in enterococci.

Authors:  Y S Chen; S A Marshall; P L Winokur; S L Coffman; W W Wilke; P R Murray; C A Spiegel; M A Pfaller; G V Doern; R N Jones
Journal:  J Clin Microbiol       Date:  1998-10       Impact factor: 5.948

Review 8.  Two-component signal transduction as a target for microbial anti-infective therapy.

Authors:  J F Barrett; J A Hoch
Journal:  Antimicrob Agents Chemother       Date:  1998-07       Impact factor: 5.191

9.  Present and future problems of antibiotic resistance in gram-positive cocci.

Authors:  J Jeljaszewicz; G Młynarczyk; A Młynarczyk
Journal:  Infection       Date:  1998 Jan-Feb       Impact factor: 3.553

Review 10.  Diversity among multidrug-resistant enterococci.

Authors:  B E Murray
Journal:  Emerg Infect Dis       Date:  1998 Jan-Mar       Impact factor: 6.883

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