Literature DB >> 10681338

Flow cytometric investigation of filamentation, membrane patency, and membrane potential in Escherichia coli following ciprofloxacin exposure.

H J Wickens1, R J Pinney, D J Mason, V A Gant.   

Abstract

Ninety-eight percent of the cells in a population of Escherichia coli in log-phase growth lost colony-forming ability after being exposed for 3 h to the quinolone antibiotic ciprofloxacin at four times the MIC in nutrient broth, a concentration easily reached in vivo. Flow cytometric analysis, however, demonstrated that only 68% of this bacterial population had lost membrane potential, as judged by the membrane potential-sensitive dye bis-(1,3-dibutylbarbituric acid) trimethine oxonol [DiBAC(4)(3)], and only 30% could no longer exclude the nucleic acid-binding dye propidium iodide (PI), reflecting lost membrane integrity, efflux mechanisms, or both. Subsequent removal of ciprofloxacin and resuspension in nutrient broth resulted in renewed cell division after 2 h, with a calculated postantibiotic effect (PAE) time of 57 min. The proportion of DiBAC- and PI-fluorescent cells in this recovering population remained stable for more than 4 h after antibiotic removal. Eighty percent of cells present at drug removal were filamentous. Their number subsequently decreased with time, and the increase in particle count seen at the end of the PAE resulted from the division of short cells. Exposure to ciprofloxacin in the presence of the protein synthesis inhibitor chloramphenicol increased colony-forming ability to 60% of starting population numbers. In contrast to ciprofloxacin alone, this antibiotic combination resulted in insignificant filamentation and no dye uptake. Subsequent drug removal and resuspension in nutrient broth resulted in the appearance of filaments within 1 h, with 69% of the population forming filaments at 3 h. Dye uptake was also seen, with 20% of the population fluorescing with either dye after 4 h. We were unable to relate dye uptake to the viable count. Cell division resumed 240 min after removal of both drugs, yielding a PAE calculated at 186 min. Inhibition of protein synthesis with chloramphenicol prevented ciprofloxacin-induced changes in bacterial morphology, cell membrane potential, and ability to exclude nucleic acid-binding dye. These changes persisted beyond the end of the classically defined PAE and were not a definite indicator of cell death as defined by loss of colony formation, which related at least in part to filamentation.

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Year:  2000        PMID: 10681338      PMCID: PMC89746          DOI: 10.1128/AAC.44.3.682-687.2000

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


  19 in total

1.  Morphological and biochemical changes in Escherichia coli after exposure to ciprofloxacin.

Authors:  J M Diver; R Wise
Journal:  J Antimicrob Chemother       Date:  1986-11       Impact factor: 5.790

2.  Induction of the SOS response by new 4-quinolones.

Authors:  I Phillips; E Culebras; F Moreno; F Baquero
Journal:  J Antimicrob Chemother       Date:  1987-11       Impact factor: 5.790

3.  The application of flow cytometry to the study of bacterial responses to antibiotics.

Authors:  V A Gant; G Warnes; I Phillips; G F Savidge
Journal:  J Med Microbiol       Date:  1993-08       Impact factor: 2.472

4.  Flow cytometry of bacteria: a promising tool in experimental and clinical microbiology.

Authors:  E Boye; H B Steen; K Skarstad
Journal:  J Gen Microbiol       Date:  1983-04

5.  Correlation of quinolone MIC and inhibition of DNA, RNA, and protein synthesis and induction of the SOS response in Escherichia coli.

Authors:  L J Piddock; R N Walters; J M Diver
Journal:  Antimicrob Agents Chemother       Date:  1990-12       Impact factor: 5.191

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Authors:  B M Howard; R J Pinney; J T Smith
Journal:  Arzneimittelforschung       Date:  1993-10

7.  Function of the SOS process in repair of DNA damage induced by modern 4-quinolones.

Authors:  B M Howard; R J Pinney; J T Smith
Journal:  J Pharm Pharmacol       Date:  1993-07       Impact factor: 3.765

8.  Postantibiotic effect of CI-960, enoxacin and ciprofloxacin on Escherichia coli: effect on morphology and haemolysin activity.

Authors:  L Guan; J C Burnham
Journal:  J Antimicrob Chemother       Date:  1992-05       Impact factor: 5.790

9.  Bactericidal activities of five quinolones for Escherichia coli strains with mutations in genes encoding the SOS response or cell division.

Authors:  L J Piddock; R N Walters
Journal:  Antimicrob Agents Chemother       Date:  1992-04       Impact factor: 5.191

10.  4-quinolones and the SOS response.

Authors:  C S Lewin; B M Howard; N T Ratcliffe; J T Smith
Journal:  J Med Microbiol       Date:  1989-06       Impact factor: 2.472

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5.  Incorporation of exogenous fatty acids protects Enterococcus faecalis from membrane-damaging agents.

Authors:  Holly E Saito; John R Harp; Elizabeth M Fozo
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6.  Time course of microbiologic outcome and gene expression in Candida albicans during and following in vitro and in vivo exposure to fluconazole.

Authors:  A Lepak; J Nett; L Lincoln; K Marchillo; D Andes
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7.  The Global Regulatory Cyclic AMP Receptor Protein (CRP) Controls Multifactorial Fluoroquinolone Susceptibility in Salmonella enterica Serovar Typhimurium.

Authors:  Stefani C Kary; Joshua R K Yoneda; Stephen C Olshefsky; Laura A Stewart; Steven B West; Andrew D S Cameron
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8.  Xenobiotics shape the physiology and gene expression of the active human gut microbiome.

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10.  Sub-Inhibitory Concentration of Piperacillin-Tazobactam May be Related to Virulence Properties of Filamentous Escherichia coli.

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