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本文引用的文献

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Antibiotic resistance in gram-negative bacteria: the role of gene cassettes and integrons.革兰氏阴性菌中的抗生素耐药性:基因盒与整合子的作用
Drug Resist Updat. 1998;1(2):109-19. doi: 10.1016/s1368-7646(98)80026-5.
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Nosocomial spread of multi-resistant Klebsiella pneumoniae containing a plasmid encoding multiple beta-lactamases.携带编码多种β-内酰胺酶质粒的多重耐药肺炎克雷伯菌的医院内传播。
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Spread of a Klebsiella pneumoniae strain producing a plasmid-mediated ACC-1 AmpC beta-lactamase in a teaching hospital admitting disabled patients.一株产质粒介导的ACC-1 AmpCβ-内酰胺酶的肺炎克雷伯菌在一家收治残疾患者的教学医院中的传播。
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Complexity of Klebsiella pneumoniae isolates resistant to both cephamycins and extended-spectrum cephalosporins at a teaching hospital in Taiwan.台湾一家教学医院中对头孢霉素和超广谱头孢菌素均耐药的肺炎克雷伯菌分离株的复杂性。
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First report of Salmonella isolates with the DHA-1 AmpC beta-lactamase in the United Kingdom.英国首次报告携带DHA-1 AmpCβ-内酰胺酶的沙门氏菌分离株。
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Complex multiple antibiotic and mercury resistance region derived from the r-det of NR1 (R100).源自NR1(R100)的r-det的复杂多重抗生素和汞抗性区域。
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Epidemiology and clinical features of bloodstream infections caused by AmpC-type-beta-lactamase-producing Klebsiella pneumoniae.产AmpC型β-内酰胺酶肺炎克雷伯菌所致血流感染的流行病学及临床特征
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CMY-13, a novel inducible cephalosporinase encoded by an Escherichia coli plasmid.CMY-13,一种由大肠杆菌质粒编码的新型诱导型头孢菌素酶。
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9
Case report: Bacteremia due to Salmonella enterica Serotype Montevideo producing plasmid-mediated AmpC beta-lactamase (DHA-1).病例报告:由产质粒介导的AmpCβ-内酰胺酶(DHA-1)的肠炎沙门氏菌蒙得维的亚血清型引起的菌血症。
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10
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巴黎地区产DHA-1的克雷伯菌属的出现:源自摩根摩根菌的ampC和ampR基因的遗传结构

Emergence of DHA-1-producing Klebsiella spp. in the Parisian region: genetic organization of the ampC and ampR genes originating from Morganella morganii.

作者信息

Verdet Charlotte, Benzerara Yahia, Gautier Valérie, Adam Olivier, Ould-Hocine Zahia, Arlet Guillaume

机构信息

Service de Bactériologie, Hôpital Tenon, 4, rue de la Chine, Paris 75970 cedex, France.

出版信息

Antimicrob Agents Chemother. 2006 Feb;50(2):607-17. doi: 10.1128/AAC.50.2.607-617.2006.

DOI:10.1128/AAC.50.2.607-617.2006
PMID:16436717
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1366880/
Abstract

Eleven Klebsiella pneumoniae clinical isolates and one Klebsiella oxytoca clinical isolate showing various pulsed-field gel electrophoresis types and producing an inducible DHA-1 class C beta-lactamase were isolated in the Parisian region between 1998 and 2003. The aim of this study was to compare the genetic organization of the bla(DHA-1) genes in this collection of clinical isolates. In four isolates, the Morganella morganii-derived genomic region containing bla(DHA-1) was inserted in an entire complex sul1-type integron, including a region common to In6-In7 (CR1), as previously described in a bla(DHA-1)-producing Salmonella enterica serovar Enteritidis KF92 isolate from Saudi Arabia in 1992. Different gene cassette arrays were characterized in each of these integrons. In two of them, an additional 10-kb fragment was inserted between the CR1 and the M. morganii-derived region and was similar to the sap (ABC transporter family) and psp (phage shock protein) operons originated from Salmonella enterica serovar Typhimurium. The length of the M. morganii region was variable, suggesting that several independent recombination events have occurred and that open reading frame orf513 encodes a recombinase involved in the mobilization of the resistance genes. The genetic organization of bla(DHA-1) was identical in the eight other isolates. This structure is likely derived from a complex integron following the insertion of IS26, leading to the deletion of the first part of integron. The horizontal transfer of one plasmid carrying that truncated integron was shown for seven of these isolates.

摘要

1998年至2003年期间,在巴黎地区分离出了11株肺炎克雷伯菌临床分离株和1株产酸克雷伯菌临床分离株,它们呈现出不同的脉冲场凝胶电泳类型,并产生可诱导的DHA-1型C类β-内酰胺酶。本研究的目的是比较这组临床分离株中bla(DHA-1)基因的遗传结构。在4株分离株中,含有bla(DHA-1)的摩根氏摩根菌来源的基因组区域插入到一个完整的复合sul1型整合子中,包括In6-In7的共同区域(CR1),这与1992年从沙特阿拉伯分离出的一株产bla(DHA-1)的肠炎沙门氏菌血清型肠炎菌株KF92中所描述的情况相同。在每个这些整合子中鉴定出了不同的基因盒阵列。其中两株在CR1和摩根氏摩根菌来源的区域之间插入了一个额外的10kb片段,该片段与源自鼠伤寒沙门氏菌的sap(ABC转运蛋白家族)和psp(噬菌体休克蛋白)操纵子相似。摩根氏摩根菌区域的长度是可变的,这表明发生了几次独立的重组事件,并且开放阅读框orf513编码一种参与抗性基因移动的重组酶。在其他8株分离株中,bla(DHA-1)的遗传结构是相同的。这种结构可能是在IS26插入后从一个复合整合子衍生而来,导致整合子的第一部分缺失。其中7株分离株显示携带该截短整合子的一个质粒发生了水平转移。