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Integron-mediated Antibiotic Resistance In Shiga Toxin-producing Escherichia Coli

机译:产志贺毒素大肠杆菌中整合子介导的抗生素抗性

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This study was undertaken to characterize the integrons present in a group of Shiga toxin-producing Escherichia coli (STEC) isolates and the ability of these integrons to transfer antibiotic resistance genes from STEC to E. coli K-12 MG1655. A total of 177 STEC isolates were analyzed for antibiotic susceptibility and the presence of integrons. Class 1 integrons were detected in 14 STEC isolates, and a class 2 integron was identified in 1 STEC isolate. The STEC isolates positive for class 1 integrons were resistant to streptomycin (MICs > 128μg/ml) and sulfisoxazole (MICs > 1,024 μg/ml), and the isolate positive for the class 2 integron was resistant to streptomycin (MIC of 128 μg/ml), trimethoprim (MIC > 256 μg/ml), and streptothricin (MIC > 32 μg/ml). Results of restriction digestion and nucleotide sequencing revealed that the cassette regions of the class 1 integrons had a uniform size of 1.1 kb and contained a nucleotide sequence identical to that of aadAl. The class 2 integron cassette region was 2.0 kb and carried nucleotide sequences homologous to those of aadAl, satl, and dfrAl. Results of the conjugation experiments revealed that horizontal transfers of conjugative plasmids are responsible for the dissemination of class 1 integron-mediated antibiotic resistance genes from STEC to E. coli K-12 MG1655. Antibiotic resistance traits not mediated by integrons, such as resistance to tetracycline and oxytetracycline, were cotransferred with the integron-mediated antibiotic resistance genes. The study suggested a possible role of integron and conjugative plasmid in dissemination of genes conferring resistance to antibiotics from pathogenic to generic E. coli cells.
机译:进行这项研究的目的是鉴定一组产志贺毒素的大肠杆菌(STEC)分离物中存在的整合素,以及这些整合素将抗生素抗性基因从STEC转移至大肠杆菌K-12 MG1655的能力。总共分析了177种STEC分离株的抗生素敏感性和整联体的存在。在14个STEC分离物中检测到1类整合素,在1个STEC分离物中鉴定出2个整合子。对1类整合素呈阳性的STEC分离株对链霉素(MICs>128μg/ ml)和磺胺异恶唑(对MICs> 1,024μg/ ml)呈耐药性,对2类整联体呈阳性的菌株对链霉素(MIC为128μg/ ml ),甲氧苄啶(MIC> 256μg/ ml)和链霉菌素(MIC> 32μg/ ml)。限制性酶切消化和核苷酸测序的结果表明,第1类整联蛋白的盒区具有1.1kb的统一大小,并且包含与aadA1相同的核苷酸序列。第2类整合子盒区域为2.0kb,并携带与aadA1,sat1和dfrA1的核苷酸序列同源的核苷酸序列。结合实验的结果表明,结合质粒的水平转移是导致1类整倍体介导的抗生素抗性基因从STEC传播到大肠杆菌K-12 MG1655的原因。不受整合素介导的抗生素抗性特征,例如对四环素和土霉素的抗性与整合子介导的抗生素抗性基因共转移。这项研究表明整合子和共轭质粒可能在传播赋予从致病性大肠杆菌到普通大肠杆菌细胞对抗生素具有抗性的基因中发挥作用。

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