Genetic heterogeneity of CTX-M type extended-spectrum ß-lactamase producing Escherichia coli strains from diverse sources in Saudi Arabia

S. Hassan, Y. Gherbawy, A. Altalhi
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引用次数: 1

Abstract

Background: The rise of CTX-M extended spectrum β-lactamase (ESBLs)-producing E. coli in non-human sources is a growing concern of public health. Understanding the extent of public health risk attributed to CTX-M type ESBLs-producing strains from different sources is critical for effective control. Objective: This study focuses on detection and molecular typing of CTX-M type ESBL-producing E. coli isolated from various sources in Taif, Western Saudi Arabia.  Material and Methods: A total of 24 E. coli ESBLs-producing isolates from multiple sources were assessed for the presence of CTX-M groups gene by PCR, and subsequently their clonal relatedness by random amplifid of polymorphic DNA (RAPD) analysis. Isolates were selected according to a resistance phenotype consistent with production of ESBL-type beta-lactamase using double disk diffusion method. Results: A CTX-M gene was detected in all 24 isolates. RAPD typing of E. coli isolates bearing CTX-M gene showed 24 patterns verifid into two major clusters (A, B) and three sub-clusters (A1 – A3). Phylogenetic analysis indicating a degree of similarity among clustering isolates from human, sheep and raw milk origins. Identical profie was observed between three isolates obtained from pet bird and chicken.
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沙特阿拉伯不同来源产ß-内酰胺酶的CTX-M型大肠杆菌菌株的遗传异质性
背景:在非人类来源产生CTX-M扩展谱β-内酰胺酶(ESBLs)的大肠杆菌的兴起是一个日益关注的公共卫生问题。了解来自不同来源的CTX-M型产生esbls的菌株造成的公共卫生风险程度对于有效控制至关重要。目的:研究沙特西部塔伊夫不同来源产esbl的CTX-M型大肠杆菌的检测及分子分型。材料与方法:采用PCR方法对24株产esbls的大肠杆菌分离株进行CTX-M群基因检测,并通过RAPD分析其克隆亲缘性。采用双盘扩散法,根据与生产esbl型β -内酰胺酶一致的抗性表型选择分离株。结果:24株分离株均检出CTX-M基因。对携带CTX-M基因的大肠杆菌进行RAPD分型,发现24种模式,分为A、B两大聚类和A1 ~ A3三个亚聚类。系统发育分析表明,来自人、羊和原料奶的聚类分离株具有一定程度的相似性。从家禽鸟和鸡中分离得到的三株分离株具有相同的特征。
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