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Carbapenemase-producing Enterobacteriaceae, U.S. Rivers

机译:美国河流生产碳青霉烯酶的肠杆菌科

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Our study was initiated by previous isolation of 30imipenem-resistant, gram-negative rods from 7 of 16 U.S.rivers sampled from 1999 to 2001. Imipenem hydrolysiswas detected in 22 of those isolates identified asEnterobacter asburiae. Random amplified polymorphismDNA analysis showed that these E. asburiae isolates weregenetically indistinguishable. An identical clavulanicacid–inhibited β-lactamase IMI-2 was identified from eachisolate that shared 99% and 97% amino acid identity withthe chromosome-encoded β-lactamases IMI-1 and NmcA,respectively, from E. cloacae clinical isolates. The blaIMI-2gene was located on a self-transferable 66-kb plasmid.Sequence analysis of a cloned 5.5-kb DNA fragmentobtained from 1 of the imipenem-resistant E. asburiae iso-lates identified an upstream LysR-type regulator gene thatexplained inducibility of IMI-2 expression. β-Lactamase IMI-2 is the first inducible and plasmid-encoded carbapene-mase. Identification of clonally related E. asburiae isolatesfrom distant rivers indicates an environmental and enter-obacterial reservoir for carbapenemase genes
机译:我们的研究始于先前从1999年至2001年采样的16个美国河流中的7个中分离出30个对亚胺培南具有抗药性的革兰氏阴性杆菌。在鉴定为白色肠杆菌的22个分离物中检测到亚胺培南水解。随机扩增多态性DNA分析表明,这些分离的白僵菌在遗传上是无法区分的。从每株分离株中鉴定出了一种相同的棒酸抑制的β-内酰胺酶IMI-2,它们与阴沟肠杆菌临床分离株分别与染色体编码的β-内酰胺酶IMI-1和NmcA共享99%和97%的氨基酸同一性。 blaIMI-2基因位于一个可自我转移的66kb质粒上,对从1个对亚胺培南耐药的阿斯伯酵母菌株的克隆获得的5.5kb DNA片段进行序列分析,确定了上游LysR型调控基因,该基因解释了该基因的诱导能力。 IMI-2表达。 β-内酰胺酶IMI-2是第一个可诱导的,质粒编码的卡宾烯酶。从远处河系中分离出与克隆相关的阿斯巴肠埃希氏菌的鉴定表明了碳青霉烯酶基因的环境和肠细菌贮藏

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