France Anne Marie, Kugeler Kiersten M, Freeman Alison, Zalewski Christy Ann, Blahna Matthew, Zhang Lixin, Marrs Carl F, Foxman Betsy
Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
Clin Infect Dis. 2005 Apr 15;40(8):1101-7. doi: 10.1086/428727. Epub 2005 Mar 15.
Antibiotic resistance is increasingly complicating the management of urinary tract infection. We investigated the extent to which a group of Escherichia coli called clonal group A (CGA), which is associated with resistance to trimethoprim-sulfamethoxazole (TMP-SMZ), accounted for TMP-SMZ resistance among a prospectively collected set of uropathogenic and rectal E. coli isolates from a university population in Michigan.
Resistant and susceptible uropathogenic E. coli isolates (45 each) and 79 randomly selected rectal E. coli isolates were evaluated for CGA status by use of 2 definitions of this group-- the enterobacterial repetitive intergenic consensus sequence 2 (ERIC2)-polymerase chain reaction (PCR) pattern A fingerprint and the C288T single nucleotide polymorphism (SNP) in the fumC gene. We compared virulence gene profiles and molecular mechanisms of resistance to TMP-SMZ between isolates classified as CGA by both approaches to better characterize the relationship between isolates.
Of the 45 isolates that exhibited ERIC2-PCR pattern A, one-half (23 of 45) were resistant to TMP-SMZ, and 16 contained the C288T SNP. The pattern A isolates were diverse, exhibiting multiple mechanisms of resistance to TMP-SMZ and various combinations of virulence factors. C288T SNP isolates showed less variation, with 15 of 16 resistant to TMP-SMZ and a 1.8-kb class I integron bearing the dfrA17 gene present in 14 of 15 resistant isolates. Twelve of 16 exhibited the same combination of virulence genes. Pulsed-field gel electrophoresis patterns for these 12 isolates were unique.
CGA, as defined by the fumC C288T SNP, appears to be distantly clonal but is not an outbreak-related group. The widespread group has likely evolved through lateral transfer of genes conferring virulence and antibiotic resistance.
抗生素耐药性正日益使尿路感染的治疗变得复杂。我们调查了一组名为克隆群A(CGA)的大肠杆菌在密歇根大学人群中前瞻性收集的尿路致病性和直肠大肠杆菌分离株中对甲氧苄啶-磺胺甲恶唑(TMP-SMZ)耐药情况所占的比例,该克隆群与对TMP-SMZ的耐药性有关。
通过使用该克隆群的两种定义——肠杆菌重复基因间共有序列2(ERIC2)-聚合酶链反应(PCR)模式A指纹图谱和fumC基因中的C288T单核苷酸多态性(SNP),对耐药和敏感的尿路致病性大肠杆菌分离株(各45株)以及79株随机选择的直肠大肠杆菌分离株进行CGA状态评估。我们比较了通过两种方法分类为CGA的分离株之间的毒力基因谱和对TMP-SMZ的耐药分子机制,以更好地描述分离株之间的关系。
在呈现ERIC2-PCR模式A的45株分离株中,一半(45株中的23株)对TMP-SMZ耐药,16株含有C288T SNP。模式A分离株具有多样性,表现出对TMP-SMZ的多种耐药机制和各种毒力因子组合。C288T SNP分离株的变异较少,16株中有15株对TMP-SMZ耐药,15株耐药分离株中有14株携带带有dfrA17基因的1.8kb I类整合子。16株中有12株表现出相同的毒力基因组合。这12株分离株的脉冲场凝胶电泳图谱是独特的。
由fumC C288T SNP定义的CGA似乎是远亲克隆,但不是与暴发相关的群体。这个广泛存在的群体可能是通过赋予毒力和抗生素耐药性的基因横向转移而进化的。