Singh Ruby, Schroeder Carl M, Meng Jianghong, White David G, McDermott Patrick F, Wagner David D, Yang Hanchun, Simjee Shabbir, Debroy Chitrita, Walker Robert D, Zhao Shaohua
Division of Animal and Food Microbiology, Office of Research, Center for Veterinary Medicine, U.S. Food & Drug Administration, Laurel, MD 20708, USA.
J Antimicrob Chemother. 2005 Jul;56(1):216-9. doi: 10.1093/jac/dki161. Epub 2005 May 23.
The objective of this study was to identify antimicrobial resistance and class 1 integrons among Shiga toxin-producing Escherichia coli (STEC).
Two-hundred and seventy-four STEC recovered from poultry, cattle, swine and humans were characterized by antimicrobial susceptibility testing, screened for the presence of class 1 integrons by PCR, and assayed for integron transfer by conjugation.
Ninety-three (34%) of the isolates were resistant to streptomycin, followed by 89 (32%) to sulfamethoxazole, 83 (30%) to tetracycline, 48 (18%) to ampicillin, 29 (11%) to cefalothin, 22 (8%) to trimethoprim/sulfamethoxazole, 18 (7%) to gentamicin, 13 (5%) to chloramphenicol and 10 (4%) to cefoxitin. Class 1 integrons were detected in 43 (16%) of the 274 isolates. The adenyl acetyltransferase gene, aadA, which confers resistance to streptomycin, was identified in integrons from 41 (95%) of these 43 isolates, and the dfrA12 gene, which confers resistance to trimethoprim, was identified in integrons from eight (19%) of the isolates. The sat1 gene, which confers resistance to streptothricin, an antimicrobial that has never been approved for use in the United States, was identified in integrons from three (7%) of the isolates. Transfer of integrons by conjugation between strains of E. coli resulted in transfer of antimicrobial-resistant phenotypes for ampicillin, chloramphenicol, cefalothin, gentamicin, tetracycline, trimethoprim, sulfamethoxazole and streptomycin.
Antimicrobial resistance is common in STEC. Class 1 integrons located on mobile plasmids have facilitated the emergence and dissemination of antimicrobial resistance among STEC in humans and food animals.
本研究的目的是鉴定产志贺毒素大肠杆菌(STEC)中的抗菌药物耐药性及1类整合子。
从家禽、牛、猪和人类中分离出274株STEC,通过抗菌药物敏感性试验进行鉴定,采用聚合酶链反应(PCR)筛选1类整合子的存在,并通过接合试验检测整合子转移情况。
93株(34%)分离株对链霉素耐药,其次是89株(32%)对磺胺甲恶唑耐药、83株(30%)对四环素耐药、48株(18%)对氨苄西林耐药、29株(11%)对头孢噻吩耐药、22株(8%)对甲氧苄啶/磺胺甲恶唑耐药、18株(7%)对庆大霉素耐药、13株(5%)对氯霉素耐药、10株(4%)对头孢西丁耐药。在274株分离株中有43株(16%)检测到1类整合子。在这43株分离株中,有41株(95%)的整合子中鉴定出赋予链霉素耐药性的腺苷乙酰转移酶基因aadA,8株(19%)的整合子中鉴定出赋予甲氧苄啶耐药性的dfrA12基因。在3株(7%)分离株的整合子中鉴定出赋予链丝菌素耐药性的sat1基因,链丝菌素是一种从未在美国获批使用的抗菌药物。大肠杆菌菌株之间通过接合转移整合子,导致氨苄西林、氯霉素、头孢噻吩、庆大霉素、四环素、甲氧苄啶、磺胺甲恶唑和链霉素的抗菌药物耐药表型转移。
抗菌药物耐药性在STEC中很常见。位于可移动质粒上的1类整合子促进了人类和食用动物中STEC抗菌药物耐药性的出现和传播。