Are fluoroquinolone-susceptible isolates of Streptococcus pneumoniae really susceptible?: A comparison of resistance mechanisms in Canadian isolates from 1997 and 2003

被引:14
作者
Schurek, KN
Adam, HJ
Siemens, CG
Hoban, CJ
Hoban, DJ
Zhanel, GG
机构
[1] Univ Manitoba, Fac Med, Dept Med Microbiol, Winnipeg, MB R3E 0W3, Canada
[2] Hlth Sci Ctr, Winnipeg, MB R3A 1R9, Canada
基金
加拿大健康研究院;
关键词
levofloxacin; mutations; efflux;
D O I
10.1093/jac/dki315
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To assess the prevalence of efflux and amino acid substitutions in ParC and GyrA in Canadian clinical isolates of fluoroquinolone-susceptible Streptococcus pneumoniae with levofloxacin MICs of 1 mg/L collected before the introduction of the respiratory fluoroquinolones (1995-1997) and after 7 years of use (2003). Methods: Quinolone resistance determining regions of parC and gyrA were sequenced for 111 clinical isolates collected from 1995 to 1997 and 665 isolates collected in 2003. Efflux was assessed using a reserpine agar dilution method. Results: No isolates exhibited efflux. No significant increase in isolates harbouring amino acid substitutions was observed over time (0.9% in 1995-1997 to 2.1% in 2003, P = 0.32). However, the proportion of isolates with a ciprofloxacin MIC = 2 mg/L and a levofloxacin MIC = 1 mg/L versus ciprofloxacin MIC = 1 mg/L and a levofloxacin MIC = 1 mg/L increased over time (3.6% to 6.5%, P = 0.0021). Conclusions: No increase in prevalence of first-step parC mutations was observed among all fluoroquinolone-susceptible clinical isolates of S. pneumoniae with levofloxacin MICs of 1 mg/L after the introduction of the respiratory fluoroquinolones; however, fluoroquinolones appear to be selecting for isolates with elevated ciprofloxacin MICs.
引用
收藏
页码:769 / 772
页数:4
相关论文
共 14 条
[1]   Fluoroquinolone resistance in clinical isolates of Streptococcus pneumoniae:: Contributions of type II topoisomerase mutations and efflux to levels of resistance [J].
Bast, DJ ;
Low, DE ;
Duncan, CL ;
Kilburn, L ;
Mandell, LA ;
Davidson, RJ ;
de Azavedo, JCS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (11) :3049-3054
[2]  
CLSI-Clinical Laboratory Standard Institute, 2005, M100S15 CLSI
[3]   Brief report: Resistance to levofloxacin and failure of treatment of pneumococcal pneumonia. [J].
Davidson, R ;
Cavalcanti, R ;
Brunton, JL ;
Bast, DJ ;
de Azavedo, JCS ;
Kibsey, P ;
Fleming, C ;
Low, DE .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (10) :747-750
[4]   Prevalence of single mutations in topoisomerase type II genes among levofloxacin-susceptible clinical strains of Streptococcus pneumoniae isolated in the United States in 1992 to 1996 and 1999 to 2000 [J].
Davies, TA ;
Evangelista, A ;
Pfleger, S ;
Bush, K ;
Sahm, DF ;
Goldschmidt, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (01) :119-124
[5]   A review of Streptococcus pneumoniae infection treatment failures associated with fluoroquinolone resistance [J].
Fuller, JD ;
Low, DE .
CLINICAL INFECTIOUS DISEASES, 2005, 41 (01) :118-121
[6]  
Lim S, 2003, EMERG INFECT DIS, V9, P833
[7]   Activities of fluoroquinolones against Streptococcus pneumoniae type II topoisomerases purified as recombinant proteins [J].
Morrissey, I ;
George, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (11) :2579-2585
[8]   Mechanisms of fluoroquinolone resistance: An update 1994-1998 [J].
Piddock, LJV .
DRUGS, 1999, 58 (Suppl 2) :11-18
[9]   Designing fluoroquinolone breakpoints for Streptococcus pneumoniae by using genetics instead of pharmacokinetics-pharmacodynamics [J].
Smith, HJ ;
Noreddin, AM ;
Siemens, CG ;
Schurek, KN ;
Greisman, J ;
Hoban, CJ ;
Hoban, DJ ;
Zhanel, GG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (09) :3630-3635
[10]  
Standards NCfCL, 2000, M7A5 NCCLS