首页> 外文期刊>Antimicrobial agents and chemotherapy. >Molecular characterization of resistance to extended-spectrum cephalosporins in clinical Escherichia coli isolates from companion animals in the United States.
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Molecular characterization of resistance to extended-spectrum cephalosporins in clinical Escherichia coli isolates from companion animals in the United States.

机译:美国伴侣动物临床大肠杆菌分离物中对广谱头孢菌素耐药的分子特征。

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Resistance to extended-spectrum cephalosporins (ESC) among members of the family Enterobacteriaceae occurs worldwide; however, little is known about ESC resistance in Escherichia coli strains from companion animals. Clinical isolates of E. coli were collected from veterinary diagnostic laboratories throughout the United States from 2008 to 2009. E. coli isolates (n = 54) with reduced susceptibility to ceftazidime or cefotaxime (MIC >/= 16 mug/ml) and extended-spectrum-beta-lactamase (ESBL) phenotypes were analyzed. PCR and sequencing were used to detect mutations in ESBL-encoding genes and the regulatory region of the chromosomal gene ampC. Conjugation experiments and plasmid identification were conducted to examine the transferability of resistance to ESCs. All isolates carried the bla(CTX-M-1)-group beta-lactamase genes in addition to one or more of the following beta-lactamase genes: bla(TEM), bla(SHV-3), bla(CMY-2), bla(CTX-M-14-like), and bla(OXA-1.) Different bla(TEM) sequence variants were detected in some isolates (n = 40). Three isolates harbored a bla(TEM-181) gene with a novel mutation resulting in an Ala184Val substitution. Approximately 78% of the isolates had mutations in promoter/attenuator regions of the chromosomal gene ampC, one of which was a novel insertion of adenine between bases -28 and -29. Plasmids ranging in size from 11 to 233 kbp were detected in the isolates, with a common plasmid size of 93 kbp identified in 60% of isolates. Plasmid-mediated transfer of beta-lactamase genes increased the MICs (>/= 16-fold) of ESCs for transconjugants. Replicon typing among isolates revealed the predominance of IncI and IncFIA plasmids, followed by IncFIB plasmids. This study shows the emergence of conjugative plasmid-borne ESBLs among E. coli strains from companion animals in the United States, which may compromise the effective therapeutic use of ESCs in veterinary medicine.
机译:肠杆菌科成员对广谱头孢菌素(ESC)的耐药性在世界范围内普遍存在。然而,关于伴随动物的大肠杆菌菌株中的ESC抗性知之甚少。从2008年至2009年,从美国各地的兽医诊断实验室收集了大肠杆菌的临床分离株。大肠杆菌分离株(n = 54)对头孢他啶或头孢噻肟的敏感性降低(MIC> / = 16杯/毫升),光谱-β-内酰胺酶(ESBL)表型进行了分析。 PCR和测序被用来检测ESBL编码基因和染色体ampC调控区的突变。进行缀合实验和质粒鉴定以检查抗ESC的转移能力。除以下一个或多个以下β-内酰胺酶基因外,所有分离株均携带bla(CTX-M-1)-betaβ-内酰胺酶基因:bla(TEM),bla(SHV-3),bla(CMY-2) ,bla(CTX-M-14-like)和bla(OXA-1。)。在某些分离物中检测到了不同的bla(TEM)序列变体(n = 40)。三个分离株带有一个带有新突变的bla(TEM-181)基因,导致Ala184Val取代。大约78%的分离物在染色体基因ampC的启动子/衰减子区域具有突变,其中之一是在-28和-29碱基之间新插入腺嘌呤。在分离物中检测到大小在11至233 kbp之间的质粒,在60%的分离物中鉴定出93 kbp的常见质粒大小。质粒介导的β-内酰胺酶基因转移增加了转接合子的ESC的MIC(> / = 16倍)。分离株之间的复制子分型显示了IncI和IncFIA质粒的优势,其次是IncFIB质粒。这项研究表明,在美国陪伴动物的大肠杆菌菌株中,结合质粒携带的ESBLs的出现,可能会损害ESC在兽药中的有效治疗用途。

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