Veterinary Science Department, University of Trás-os-Montes and Alto Douro, Vila Real, Portugal.
Foodborne Pathog Dis. 2010 Aug;7(8):991-4. doi: 10.1089/fpd.2009.0494.
The main aim of this study was to determine the frequency of antibiotic resistance among Escherichia coli isolates recovered in Levine agar plates from 54 fecal samples of captive ostriches from a farm in the South of Portugal. Fifty-four nonselected E. coli isolates were obtained (one/sample) and the phenotypes and genotypes of antibiotic resistance were characterized. The following numbers of isolates showed antibiotic resistance: ampicillin (nine), tetracycline (seven), streptomycin (three), amoxicillin-clavulanic acid, cefoxitin, or gentamicin (one), and cefotaxime, ceftazidime, azthreonam, imipenem, nalidixic acid, ciprofloxacin, and trimethoprim/sulfamethoxazole (zero). The bla(TEM) gene was identified in six out of nine ampicillin-resistant isolates, and the tet(A) or tet(B) genes in five out of seven tetracycline-resistant isolates. Mutations at positions -42, -18, -1, and +58 of ampC promoter region were identified in one cefoxitin-resistant isolate. Further, the occurrence of extended-spectrum beta-lactamase (ESBL)-producing E. coli isolates was estimated in the 54 fecal samples of ostriches using cefotaxime-supplemented Levine agar plates for ESBL-positive E. coli recovery. Three samples contained ESBL-positive E. coli isolates of which one isolate/sample was characterized, leading to the detection of the following beta-lactamases: bla(CTX-M-14a) + bla(TEM-1b) (two isolates) and bla(TEM-52c) (one isolate). The three ESBL-positive isolates were classified into the phylogroup B1, and contained class 1 integrons with the gene cassettes dfrA17 + aadA5 (one isolate) and aadA1 (two isolates). This study adds to our knowledge about the wide dissemination of ESBL-producing E. coli isolates in different ecosystems, including captive ostriches, that could be transferred to humans through the food chain.
本研究的主要目的是确定从葡萄牙南部一个农场的 54 份圈养鸵鸟粪便样本中在 Levine 琼脂平板上回收的大肠杆菌分离株的抗生素耐药频率。获得了 54 个非选择性大肠杆菌分离株(一个/样本),并对其抗生素耐药表型和基因型进行了特征描述。以下是显示抗生素耐药的分离株数量:氨苄西林(9 个)、四环素(7 个)、链霉素(3 个)、阿莫西林-克拉维酸、头孢西丁或庆大霉素(1 个)和头孢噻肟、头孢他啶、氨曲南、亚胺培南、萘啶酸、环丙沙星和甲氧苄啶/磺胺甲恶唑(0 个)。在 9 个氨苄西林耐药分离株中鉴定出 bla(TEM)基因,在 7 个四环素耐药分离株中鉴定出 tet(A)或 tet(B)基因。在 1 个头孢西丁耐药分离株中鉴定出 ampC 启动子区域-42、-18、-1 和 +58 位置的突变。此外,使用头孢噻肟补充的 Levine 琼脂平板从 54 份鸵鸟粪便样本中估计了产超广谱β-内酰胺酶(ESBL)大肠杆菌分离株的发生情况,以回收 ESBL 阳性大肠杆菌。三个样本含有 ESBL 阳性大肠杆菌分离株,其中一个分离株/样本进行了特征描述,检测到以下β-内酰胺酶:bla(CTX-M-14a) + bla(TEM-1b)(两个分离株)和 bla(TEM-52c)(一个分离株)。三个 ESBL 阳性分离株被分类为 B1 群,含有带有 dfrA17 + aadA5(一个分离株)和 aadA1(两个分离株)基因盒的 1 类整合子。本研究增加了我们对包括圈养鸵鸟在内的不同生态系统中 ESBL 产生大肠杆菌分离株广泛传播的认识,这些分离株可能通过食物链转移到人类身上。