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Antimicrobial Agents and Chemotherapy, March 2000, p. 682-687, Vol. 44, No. 3
Microbiology Section, Department of
Pharmaceutics, The School of Pharmacy, University of London, London
WC1N 1AX,1 Department of Microbiology,
University College Hospitals Trust, London WC1E
6DB,3 and Department of Biological
Sciences, Warwick University, Coventry CV4 7AL,2
United Kingdom
Received 19 July 1999/Returned for modification 14 October
1999/Accepted 16 December 1999
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
[DiBAC4(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.
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Flow Cytometric Investigation of Filamentation,
Membrane Patency, and Membrane Potential in Escherichia
coli following Ciprofloxacin Exposure
*
Corresponding author. Mailing address: Department of
Microbiology, University College Hospitals Trust, Grafton Way, London WC1E 6DB, United Kingdom. Phone: 44-171-380 9517. Fax: 44-171-388 8514. E-mail: v.gant{at}academic.uclh.nthames.nhs.uk.
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