Over the course of a 20-month period, in a hospital respiratory ward in whi
ch ciprofloxacin was often used as empirical antimicrobial therapy for lowe
r respiratory tract infections (LRTIs), 16 patients with chronic bronchitis
developed nosocomial LRTIs caused by penicillin- and ciprofloxacin-resista
nt Streptococcus pneumoniae (serotype 23 F). The minimum inhibitory concent
ration (MIC) of ciprofloxacin for all isolates from the first 9 patients wa
s 4 mug/mL, in association with a parC mutation. Isolates from the subseque
nt 7 patients all had a ciprofloxacin MIC of 16 mug/mL, in association with
an additional mutation in gyrA. The MICs for this isolate were 8 mug/mL of
levofloxacin (resistant), 2 mug/mL of moxifloxacin and gatifloxacin (inter
mediately resistant), and 0.12 mug/mL of gemifloxacin. This outbreak demons
trates the ability of S. pneumoniae to acquire multiple mutations that resu
lt in increasing levels of resistance to the fluoroquinolones and to be tra
nsmitted from person to person.