Clonal spread of fluoroquinolone non-susceptible Streptococcus pyogenes

被引:33
作者
Malhotra-Kumar, S
Lammens, C
Chapelle, S
Mallentjer, C
Weyler, J
Goossens, H
机构
[1] Univ Antwerp, Dept Epidemiol & Community Med, B-2610 Antwerp, Belgium
[2] Univ Antwerp, Belgian Reference Ctr Grp A Streptococcus, B-2610 Antwerp, Belgium
关键词
S; pyogenes; antibiotic resistance; molecular mechanisms;
D O I
10.1093/jac/dki011
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Fluoroquinolones are an important group of antibiotics widely used in adults, and, despite the absence of official approval, these drugs are also used in children. So far, resistance to fluoroquinolones in Streptococcus pyogenes is very rare. Methods: During a national surveillance programme in Belgium from 1999 to 2002, 2793 non-duplicate S. pyogenes recovered from tonsillopharyngitis patients were screened for fluoroquinolone resistance. Mutations in topoisomerase genes and the presence of any efflux pump activity were investigated to elucidate the fluoroquinolone resistance mechanisms. Clonality was assessed by pulsed-field gel electrophoresis (PFGE) and emm typing. Results: Non-susceptibility to fluoroquinolones, defined as ciprofloxacin MIC greater than or equal to 2 mg/L, was identified in 152 (5.4%) of 2793 S. pyogenes. Fifty-five (36%) fluoroquinolone non-susceptible isolates were investigated for known resistance mechanisms; all showed mutations in parC, and 29 (19%) isolates also in parE; antibiotic efflux was not noted. Two major PFGE types comprised 88% of fluoroquinolone non-susceptible S. pyogenes and belonged to serotypes emm6 and emm75. Overall, emm6 and emm75 constituted >90% of all fluoroquinolone non-susceptible isolates and showed a significant temporal and geographical shift within Belgian provinces. Although fluoroquinolone-susceptible S. pyogenes also showed fluctuations in the predominant S. pyogenes serotypes, emm6 or emm75 were under-represented in this population. Approx. 55% of the fluoroquinolone non-susceptible isolates were recovered from children ( less than or equal to16 years). Conclusions: We show here, for the first time, a multi-clonal spread of fluoroquinolone non-susceptible S. pyogenes exhibiting a known resistance mechanism. Non-susceptibility to fluoroquinolones in paediatric isolates is of concern.
引用
收藏
页码:320 / 325
页数:6
相关论文
共 28 条
[21]   Penicillin treatment failure in group a streptococcal tonsillopharyngitis:: No genetic difference found between strains isolated from failures and nonfailures [J].
Orrling, A ;
Karlsson, E ;
Melhus, Å ;
Stjernquist-Desatnik, A .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 2001, 110 (07) :690-695
[22]   Incidence of streptococcal carriers in private pediatric practice [J].
Pichichero, ME ;
Marsocci, SM ;
Murphy, AML ;
Hoeger, W ;
Green, JL ;
Sorrento, A .
ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE, 1999, 153 (06) :624-628
[23]   High-level fluoroquinolone resistance in a clinical Streptoccoccus pyogenes isolate in Germany [J].
Reinert, RR ;
Lütticken, R ;
Al-Lahham, A .
CLINICAL MICROBIOLOGY AND INFECTION, 2004, 10 (07) :659-662
[24]   Fluoroquinolone resistance in Streptococcus pyogenes [J].
Richter, SS ;
Diekema, DJ ;
Heilmann, KP ;
Almer, LS ;
Shortridge, VD ;
Zeitler, R ;
Flamm, RK ;
Doern, GV .
CLINICAL INFECTIOUS DISEASES, 2003, 36 (03) :380-383
[25]   Topical ciprofloxacin/dexamethasone otic suspension is superior to ofloxacin otic solution in the treatment of children with acute otitis media with otorrhea through tympanostomy tubes [J].
Roland, PS ;
Kreisler, LS ;
Reese, B ;
Anon, JB ;
Lanier, B ;
Conroy, PJ ;
Wall, GM ;
Dupre, SJ ;
Potts, S ;
Hogg, G ;
Stroman, DW ;
McLean, C .
PEDIATRICS, 2004, 113 (01) :E40-E46
[26]   INTERPRETING CHROMOSOMAL DNA RESTRICTION PATTERNS PRODUCED BY PULSED-FIELD GEL-ELECTROPHORESIS - CRITERIA FOR BACTERIAL STRAIN TYPING [J].
TENOVER, FC ;
ARBEIT, RD ;
GOERING, RV ;
MICKELSEN, PA ;
MURRAY, BE ;
PERSING, DH ;
SWAMINATHAN, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (09) :2233-2239
[27]   Resistance to multiple fluoroquinolones in a clinical isolate of Streptococcus pyogenes:: Identification of gyrA and parC and specification of point mutations associated with resistance [J].
Yan, SS ;
Fox, ML ;
Holland, SM ;
Stock, F ;
Gill, VJ ;
Fedorko, DP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (11) :3196-3198
[28]  
Zhanel George G., 2001, Current Opinion in Pharmacology, V1, P459, DOI 10.1016/S1471-4892(01)00080-7