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Antimicrobial Agents and Chemotherapy, November 1998, p. 2919-2922, Vol. 42, No. 11
Department of Infectious Diseases and
Microbiology,
Received 11 May 1998/Returned for modification 24 June
1998/Accepted 26 August 1998
Ciprofloxacin, 500 mg, was introduced as the first-line therapy for
gonorrhea at St. Mary's Hospital, London, in 1989, when a surveillance
program was initiated to detect the emergence of resistance. Isolates
of Neisseria gonorrhoeae from consecutive patients
attending the Jefferiss Wing, Genitourinary Medicine Clinic at St.
Mary's Hospital, between 1989 and 1997 have been tested for
susceptibility to ciprofloxacin by using an agar dilution breakpoint
technique. Isolates considered potentially resistant (MIC, >0.12
µg/ml) were further characterized by determination of the MICs of
ciprofloxacin, nalidixic acid, and penicillin, auxotyped and serotyped,
and screened for mutations in the DNA gyrase gene, gyrA,
and the topoisomerase IV gene, parC. A total of 4,875 isolates were tested. While the majority of isolates were highly
susceptible (MIC,
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Drift in Susceptibility of Neisseria
gonorrhoeae to Ciprofloxacin and Emergence of Therapeutic
Failure
and
0.008 µg of ciprofloxacin/ml), there was a drift
toward reduced susceptibility in N. gonorrhoeae isolated between 1993 and 1996 (P < 0.001). In 1997 this drift was reduced but remained above pre-1993 levels. Isolates
from 18 patients were classed as potentially resistant (MIC, >0.12 µg/ml); all of these belonged to serogroup B, and NR/IB-1 was the
most common auxotype/serovar class. The infections in 14 of the 18 patients were known to be acquired abroad, and 5 were known to result
in therapeutic failure. The surveillance program has established
that ciprofloxacin is still a highly effective antibiotic against
N. gonorrhoeae in this population. However, it
has identified a drift in susceptibility which may have resulted
from increased usage of ciprofloxacin. High-level resistance
has now emerged, although treatment failure is still uncommon.
*
Corresponding author. Mailing address: Medical
Microbiology, ICSM, St. Mary's Campus, Norfolk Place, Paddington,
London W2 1PG, United Kingdom. Phone: 44-171-594-3965. Fax:
44-171-262-6299. E-mail: c.ison{at}ic.ac.uk.
Present address: Immunobiology Unit, Institute of Child Health,
London WC1N 1EH, United Kingdom.
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