Literature DB >> 2184160

The emergence and mechanisms of trimethoprim resistance in Escherichia coli isolated from outpatients in Finland.

E Heikkilä1, O V Renkonen, R Sunila, P Uurasmaa, P Huovinen.   

Abstract

Trimethoprim (TMP), either alone or in combination with sulphonamides, is commonly used for treating urinary tract infections. In Finland, TMP alone has been in clinical use since 1973. TMP resistance in the major outpatient urinary tract pathogen, Escherichia coli, increased during 1978-1988 from 5% to 16% in the Turku area, during 1980-1988 from 3% to 19% in the Helsinki area and also during 1980-1988 from 3% to 14% in the Rovaniemi area. The majority (91%) of TMP-resistant strains were highly-resistant to TMP (MIC greater than or equal to 1024 mg/l). The most common (57%) TMP resistance gene, detected by DNA hybridization, was the type I dihydrofolate (DHFR) gene. The type II DHFR genes were found in less than 3% of the strains studied. No positive hybridizations were detected with the type III DHFR probe, and only a few positive hybridizations were found with the type V DHFR probe. Forty percent of the isolates did not hybridize with any of the DHFR probes used, suggesting additional unknown resistance mechanisms responsible for the high-level TMP resistance. These unknown TMP resistance mechanisms, together with the type I DHFR-mediated resistance, were responsible for the increase of TMP resistance among the E. coli strains studied.

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Year:  1990        PMID: 2184160     DOI: 10.1093/jac/25.2.275

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


  12 in total

1.  New gene cassettes for trimethoprim resistance, dfr13, and Streptomycin-spectinomycin resistance, aadA4, inserted on a class 1 integron.

Authors:  P V Adrian; C J Thomson; K P Klugman; S G Amyes
Journal:  Antimicrob Agents Chemother       Date:  2000-02       Impact factor: 5.191

2.  Synergism of trimethoprim and ciprofloxacin in vitro against clinical bacterial isolates.

Authors:  P Huovinen; J S Wolfson; D C Hooper
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1992-03       Impact factor: 3.267

3.  Mutations in the dihydrofolate reductase gene of trimethoprim-resistant isolates of Streptococcus pneumoniae.

Authors:  P V Adrian; K P Klugman
Journal:  Antimicrob Agents Chemother       Date:  1997-11       Impact factor: 5.191

Review 4.  Trimethoprim and sulfonamide resistance.

Authors:  P Huovinen; L Sundström; G Swedberg; O Sköld
Journal:  Antimicrob Agents Chemother       Date:  1995-02       Impact factor: 5.191

5.  The prevalence of antimicrobial resistance in human faecal flora in South Africa.

Authors:  P M Shanahan; B A Wylie; P V Adrian; H J Koornhof; C J Thomson; S G Amyes
Journal:  Epidemiol Infect       Date:  1993-10       Impact factor: 2.451

6.  Antibiotic resistance in bacterial urinary tract infections, 1991 to 1997.

Authors:  I E Dyer; T M Sankary; J A Dawson
Journal:  West J Med       Date:  1998-11

7.  Analysis of genetic localization of the type I trimethoprim resistance gene from Escherichia coli isolated in Finland.

Authors:  E Heikkilä; L Sundström; M Skurnik; P Huovinen
Journal:  Antimicrob Agents Chemother       Date:  1991-08       Impact factor: 5.191

8.  Trimethoprim resistance in Escherichia coli isolates from a geriatric unit.

Authors:  E Heikkilä; L Sundström; P Huovinen
Journal:  Antimicrob Agents Chemother       Date:  1990-10       Impact factor: 5.191

9.  Trimethoprim resistant dihydrofolate reductases in normal faecal flora isolated in India.

Authors:  S Tait; S G Amyes
Journal:  Epidemiol Infect       Date:  1994-10       Impact factor: 2.451

10.  Transferable high-level trimethoprim resistance among isolates of Escherichia coli from urinary tract infections in Ontario, Canada.

Authors:  N Harnett
Journal:  Epidemiol Infect       Date:  1992-12       Impact factor: 2.451

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