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新CMY型头孢菌素酶在大肠埃希菌中的流行 被引量:22

A new member of CMY type cephalosporinase prevailing in Escherichia coli
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摘要 目的 对临床产质粒介导AmpC酶大肠埃希菌的耐药表型以及分子生物学特性进行研究 ,以期发现新的头孢菌素酶。方法 对从临床分离的大肠埃希氏菌先后用纸片扩散法、三维试验、等电聚焦试验以及微量稀释法等进行表型检测。然后用接合试验、多重PCR以及基因测序等方法进行分子生物学研究。结果  719株受试的大肠埃希菌经三维试验 ,等电聚焦以及酶抑制试验表明有 6株细菌都能够产一种等电点 (PI)为 8 9的能够被氯唑西林抑制而不能被克拉维酸抑制的 β 内酰胺酶。用微量稀释法检测表明这些菌株对多种三代头孢菌素耐药 ,但对头孢吡肟、亚胺培南和美洛培南均敏感。接合试验表明它们携带的AmpC酶具有转移性 ,多重PCR检测表明这些基因来源于费氏枸橼酸杆菌家族 ,DNA测序表明该基因和CMY 2以及CMY 7有 99%的同源性 ,为一种新的CMY型头孢菌素酶。结论 发现了一种新的CMY型头孢菌素酶 ,它介导了高产AmpC酶大肠埃希菌对多种抗生素的耐药 。 Objective To study the resistant phenotype and molecular biology character of plasmid mediated high AmpC-producing clinical isolates of Escherichia coli and to find new AmpC genotype. Methods The cefoxitin highly resistant clinical isolates of Escherichia coli were studied by K-B method, three-dimensional method, Isoelectric Focusing (IEF) and the MIC of these strains were examined by micro-dilution method. The conjugation experiment, multiplex PCR and DNA sequencing methods were used in further study. Results Above 719 strains studied, there are 6 isolates were showed as high AmpC-producing by three-dimensional method and IEF found they could produce a β-Lactamase which PI was 8.9 and could be inhibited by cloxacillin but not by clavulnate. The strains were resistant to most of third generation cephalosporins, but were susceptible to cefepime,meropenem and imipenem. The experiment also showed that the gene which express this AmpC like β-Lactamase could be transferable. Multiplex PCR indicated they belong to Citrobacter freundii family. Sequencing of corresponding DNA revealed 99% identities of the deduced amino acid sequence with CMY-2 and CMY-7 respectively. It is a new CMY type cephalosporinase.Conclusion A new CMY type cephalosporinase has been found in clinical strains of Escherichia coli in our hospital. It was resistant to many antibiotics and its resistance could be transferred horizontally.
出处 《中华医学杂志》 CAS CSCD 北大核心 2004年第22期1872-1875,共4页 National Medical Journal of China
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  • 1She DY, Liu YN. The expression of AmpC and extended-spectrum (beta)-lactamases among clinical isolates of Enterobacter cloacae and its impact on antibiotics susceptibility. Natl Med J China, 2002,82: 1355-1358.佘丹阳, 刘又宁. AmpC酶和超广谱β-内酰胺酶在阴
  • 2National Committee for Clinical Laboratory Standards. Performance standards for antimicrobial susceptibility testing,10th informational supplement (aerobic dilution), 2002. M100-S10.
  • 3Philippon A, Arlet G, Jacoby GA. Plasmid determined AmpC-type β-lactamases. Antimicrob Agents Chemother, 2002,46: 1-11.
  • 4Sanders DD, Sanders WE ,Moland ES. Characterization of β-lactamases in situ on polyacylamide gels. Antimicrob Agents Chemother, 1986, 30: 951-952.
  • 5Thomson KS, Sanders CC. Detection of extended-spectrum β-lactamaes in members of the family Enterobacteriaceae: comparison of the double-disk and three-dimensional tests. Antimicrob Agents Chemother, 1992, 36:1877-1882.
  • 6Ellen SM, Jennifer AB, Jason O. Occurrence of newer beta-Lactamases in Klebsiella pneumoniae isolates from 24 U.S. hospitals. Antimicrob Agents Chemother, 2002, 46: 3837-3842.
  • 7Nelson EC, Elisa BG. Molecular basis of AmpC hyperproduction in clinical isolates of Escherichia coli. Antimicrob Agents Chemother, 1999, 43: 957-959.
  • 8Pitout JD, Reisbig MD, Mulvey M. Association between handling of pet treats and infection with Salmonella enterica serotype newport expressing the AmpC beta-lactamase, CMY-2. J Clin Microbiol, 2003, 41: 4578-82.
  • 9Yan JJ, Chiu CH, Ko WC, et al. Ceftriaxone-resistant Salmonella enterica serovar Hadar: evidence for interspecies transfer of blaCMY-2 in a Taiwan Residents university hospital. J Formos Med Assoc, 2002, 101: 665-668.
  • 10Hoyen CM, Hujer AM, Hujer KM, et al. A clinical strain of Escherichia coli possessing CMY-2 plasmid-mediated amp C beta-lactamase: an emerging concern in pediatrics? Microb Drug Resist, 2002, 8: 329-33.

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