The clonal diversity of extended-spectrum-β-lactamase (ESBL)-producing Escherichia coli isolates from nine different species of wild animals from distinct regions of Portugal and Spain and their content in replicon plasmids were analyzed. Among the initial 53 ESBL-producing E. coli isolates that were studied (from previous studies), 28 were selected, corresponding to different animal origins with distinct ESBL types and pulsed-field gel electrophoresis (PFGE) patterns. These 28 isolates produced different ESBLs ascribed to the following families: CTX-M, SHV and TEM. The isolates were classified into three phylogenetic groups: B1 (n = 11), A (n = 10) and D (n = 7). The seven E. coli of phylogroup D were then typed by multilocus sequence typing and ascribed to four distinct sequence types: ST117, ST115, ST2001 and ST69. The clonal diversity and relationship between isolates was studied by PFGE. Lastly, the plasmids were analyzed according to their incompatibility group using the PCR-based-replicon-typing scheme. A great diversity of replicon types was identified, with up to five per isolate. Most of the CTX-M-1 and SHV-12 producing E. coli isolates carried IncI1 or IncN replicons. The diversity of ESBL-producing E. coli isolates in wild animals, which can be disseminated in the environment, emphasizes the environmental and health problems that we face nowadays.

译文

分析了来自葡萄牙和西班牙不同地区的9种不同野生动物的产超广谱 β-内酰胺酶 (ESBL) 大肠杆菌的克隆多样性及其在复制子质粒中的含量。在最初研究的53种产生ESBL的大肠杆菌分离株中 (来自先前的研究),选择了28种,分别对应于具有不同ESBL类型和脉冲场凝胶电泳 (PFGE) 模式的不同动物来源。这28个分离株产生了不同的ESBLs,这些ESBLs归因于以下家族: ctx-m,SHV和TEM。分离株分为三个系统发育组: B1 (n = 11),A (n = 10) 和D (n = 7)。然后通过多基因座序列分型对系统组D的七个大肠杆菌进行分型,并归因于四种不同的序列类型: ST117,ST115,ST2001和st69。通过PFGE研究了分离株之间的克隆多样性和关系。最后,使用基于PCR的复制子分型方案根据其不相容性组分析质粒。鉴定出复制子类型的多样性,每个分离株最多5种。大多数产生大肠杆菌的CTX-M-1和SHV-12分离株都带有IncI1或IncN复制子。野生动物中产生ESBL的大肠杆菌分离物的多样性,可以在环境中传播,这强调了我们当今面临的环境和健康问题。

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