Literature DB >> 11020251

In vitro activity of new generation fluoroquinolones against genotypically distinct and indistinguishable Clostridium difficile isolates.

M H Wilcox1, W Fawley, J Freeman, J Brayson.   

Abstract

We compared the activities of ciprofloxacin and levofloxacin with those of the newer fluoroquinolones grepafloxacin, moxifloxacin, sparfloxacin and trovafloxacin against Clostridium difficile isolates. As there is good evidence of marked clonal spread of C. difficile, we studied both genotypically distinct (n = 26) and indistinguishable (n = 28) isolates as determined by random amplified polymorphic DNA and ribosomal spacer PCR fingerprinting. The indistinguishable strains examined represent the main UK epidemic C. difficile clone. For 17 of 54 strains (31%) we were unable to read MICs following inocula preparation using Mueller-Hinton broth. Using Schaedler's broth for inocula preparation 93% of strains had readable MICs, although geometric mean MICs were uniformly higher (2.5- to 5.4-fold) compared with results using Mueller-Hinton broth. Moxifloxacin and trovafloxacin, followed by grepafloxacin, were the most active fluoroquinolones tested and were 3- to 4-fold more active than older agents such as ciprofloxacin by both MIC methods. Unexpectedly, clonal C. difficile strains had markedly reduced susceptibility compared with the distinct strains to each of the fluoroquinolones tested. Clonal strains were more than seven-fold or 12- to 29-fold less susceptible (according to geometric mean MICs) than distinct strains to both moxifloxacin and trovafloxacin, depending on the MIC method used. It remains to be seen whether the enhanced activity of new fluoroquinolones such as moxifloxacin in comparison with other fluoroquinolones against C. difficile implies that these agents are unlikely to be associated with C. difficile infection. However, clinical use of new generation fluoroquinolones in elderly hospitalized patients where C. difficile is endemic requires further study, particularly given the reduced antibiotic susceptibility to all fluoroquinolones of the readily transmissible UK C. difficile clone.

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Year:  2000        PMID: 11020251     DOI: 10.1093/jac/46.4.551

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


  8 in total

1.  Polymorphism and intramolecular proton transfer in fluoroquinolone compounds.

Authors:  Anna V Polishchuk; Emilya T Karaseva; Tatyna B Emelina; Oana Cramariuc; Vladimir E Karasev
Journal:  J Fluoresc       Date:  2011-07-13       Impact factor: 2.217

2.  Molecular epidemiology of endemic Clostridium difficile infection and the significance of subtypes of the United Kingdom epidemic strain (PCR ribotype 1).

Authors:  Warren N Fawley; Peter Parnell; Paul Verity; Jane Freeman; Mark H Wilcox
Journal:  J Clin Microbiol       Date:  2005-06       Impact factor: 5.948

3.  gyrA and gyrB mutations are implicated in cross-resistance to Ciprofloxacin and moxifloxacin in Clostridium difficile.

Authors:  Larbi Dridi; Jacques Tankovic; Béatrice Burghoffer; Frédéric Barbut; Jean-Claude Petit
Journal:  Antimicrob Agents Chemother       Date:  2002-11       Impact factor: 5.191

4.  Spectral-luminescent properties and molecular orbital treatment of some mono- and difluoroquinolones.

Authors:  Anna V Polishchuk; Emilya T Karaseva; Tatyna B Emelina; Oanna Cramariuc; Vladimir E Karasev
Journal:  J Fluoresc       Date:  2011-01-13       Impact factor: 2.217

Review 5.  Levofloxacin: a review of its use in the treatment of bacterial infections in the United States.

Authors:  Katherine F Croom; Karen L Goa
Journal:  Drugs       Date:  2003       Impact factor: 9.546

6.  Genetically diverse Clostridium difficile strains harboring abundant prophages in an estuarine environment.

Authors:  K R Hargreaves; H V Colvin; K V Patel; J J P Clokie; M R J Clokie
Journal:  Appl Environ Microbiol       Date:  2013-08-02       Impact factor: 4.792

7.  Effects of exposure of Clostridium difficile PCR ribotypes 027 and 001 to fluoroquinolones in a human gut model.

Authors:  Katie Saxton; Simon D Baines; Jane Freeman; Rachael O'Connor; Mark H Wilcox
Journal:  Antimicrob Agents Chemother       Date:  2008-08-18       Impact factor: 5.191

8.  gyrA mutations in fluoroquinolone-resistant Clostridium difficile PCR-027.

Authors:  Denise Drudy; Lorraine Kyne; Rebecca O'Mahony; Séamus Fanning
Journal:  Emerg Infect Dis       Date:  2007-03       Impact factor: 6.883

  8 in total

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