Wang Yu, Li Zhen-hua
Respiratory Diseases Research Institute, First Affiliated Hospital, China Medical University, Shenyang 110001, China.
Zhonghua Jie He He Hu Xi Za Zhi. 2005 Oct;28(10):685-8.
To investigate the susceptibility and genotype characteristics of Escherichia coli and Klebsiella pneumoniae producing plasmid-mediated AmpC beta lactamase.
A total of 110 strains of Escherichia coli and Klebsiella pneumoniae were collected from patients hospitalized in our respiratory ward during January 2002-May 2004. The isolates harboring AmpC beta-lactamase were detected by three-dimensional test, and isoelectric focusing analysis, electroporation, PCR and DNA sequencing were performed to determine the genotypes.
AmpC enzyme was detected in 9.30% (4/43) of the Escherichia coli isolates and 4.48% (3/67) of the Klebsiella pneumoniae isolates. The susceptibility test showed 7 isolates tested were all resistant to cefoxitin, and part of these strains were resistant to the third-generation cephalosporins, beta-lactams/beta-lactamase inhibitors, aztreonam, amikacin and ciprofloxacin, but most of them were susceptible to cefepime and imipenem. Three strains of Klebsiella pneumoniae and 2 strains of Escherichia coli transferred cefoxitin-resistance to recipients by electroporation. Results of PCR and DNA sequencing defined them to be DHA-1 AmpC beta-lactamase.
Escherichia coli and Klebsiella pneumoniae producing plasmid-mediated AmpC beta lactamase were isolated from clinical strains in this hospital, and its gene can be transferred horizontally.
研究产质粒介导AmpCβ-内酰胺酶的大肠埃希菌和肺炎克雷伯菌的药敏特性及基因型特征。
收集2002年1月至2004年5月在我院呼吸内科住院患者的110株大肠埃希菌和肺炎克雷伯菌。采用三维试验检测产AmpCβ-内酰胺酶的菌株,并用等电聚焦分析、电穿孔、聚合酶链反应(PCR)及DNA测序确定基因型。
在大肠埃希菌分离株中AmpC酶检出率为9.30%(4/43),肺炎克雷伯菌分离株中为4.48%(3/67)。药敏试验显示,7株检测菌均对头孢西丁耐药,部分菌株对第三代头孢菌素、β-内酰胺类/β-内酰胺酶抑制剂、氨曲南、阿米卡星和环丙沙星耐药,但多数对头孢吡肟和亚胺培南敏感。3株肺炎克雷伯菌和2株大肠埃希菌通过电穿孔将头孢西丁耐药性传递给受体菌。PCR及DNA测序结果确定它们为DHA-1 AmpCβ-内酰胺酶。
从本院临床菌株中分离出产质粒介导AmpCβ-内酰胺酶的大肠埃希菌和肺炎克雷伯菌,其基因可水平转移。