期刊文献+

产酶的革兰阴性杆菌对抗生素的耐药性分析 被引量:2

Assay on Drug-Resistance of Gram-Negative Bacilli Producing Enzymes
下载PDF
导出
摘要 目的:探讨G-杆菌的产酶情况与耐药模式,并比较产酶菌与非产酶菌对9种抗生素的耐药率。方法:应用头孢西丁三维试验检测AmpC酶,采用美国国家临床实验室标准委员会(NCCLS)表型筛选和确认试验检测超广谱酶β内酰胺酶(ESBLs)菌株,以K-B琼脂扩散法做药敏试验。结果:在149株G-杆菌中,16株(10.7%)产AmpC酶,32株(21.1%)产ESBLs,2株(2.0%)同时产AmpC酶和ESBLs。产酶株对亚胺培南、头孢吡肟、阿米卡星耐药率低。结论:产AmpC酶和产ESBLs的G-杆菌为多重耐药菌株,治疗产2种β内酰胺酶细菌引起的感染亚胺培南为首选,头孢吡肟和阿米卡星可作为选用药物之一。 Objective: To study the drug-resistance of gram-negative bacilli producing enzymes and compare the resistance rate of strains producing and non producing enzymes to 9 antibiotics.Method:A three-dimensional test of cefoxitin and E-test were used to detect AmpC enzyme and extended spectrum βlactamases(ESBLS) respectively.Simotanously,drug-susceptibility was meastured by disk diffusion method in 149 strains of gram-negative bacilli.Results:16(10.7%)strains were AmpC positive,32(21.1%)strains were ESBLS positive and 2(2.0%)strains AmpC+ ESBLS were found among 149 strains of Gram negative bacilli.The resistance rate of strains-producing enzymes were low to imipenem,cepepime and amikacin.Conclusion:Gram-negative bacilli producing AmpC and ESBLS is multidrug-resistance strains.Imipenem is the most effective antibiotic for the treatment of infection caused by ESBLS or AmpC producing strains.Cepepime and amikacin are also effective for the treatment of such infections.
作者 朱玉玫 王煜
出处 《中国误诊学杂志》 CAS 2008年第14期3288-3289,共2页 Chinese Journal of Misdiagnostics
关键词 革兰氏阴性菌/药物作用 抗药性 细菌 Gram-Negative Bacteria/drug effects Drug Resistance,Bacterial
  • 相关文献

参考文献4

  • 1Black JA,Moland ES,Thomson KS. AmpC disk test for detection of plasmid-mediated AmpC β-lactamases in Enterobacteriaceae lacking chromosomal AmpC β-lactamases [J]. J Clin Microbiol, 2005,43(7):3110-3113
  • 2吴伟元,陈民钧.阴沟肠杆菌ampD基因突变与去阻遏持续高产AmpC酶[J].中国抗感染化疗杂志,2001,1(2):65-69. 被引量:37
  • 3Deshpande LM,jones RN,Fritsche TR,et al. Occurrence of plasmidic AmpC type beta-lactamase-mediated resistance in Es cherichia coli:report from the SENTRY Antimicrobial Surveillance Program[J]. Int J Antimicrob Agents, 2006,28 : 578-581.
  • 4Yan J J, Hsueh PR, Lu JJ,et al. Extended-spectrum beta-lactamases and plasmid-mediated AmpC enzymes among clinical isolates of Escherichia coli and Klebsiella pneumoniae from seven medical centers in Taiwan[J]. Antimicrob Agents Chemother, 2006,50(5) :1861-1864.

二级参考文献8

  • 1Wiedemann B, Dietz H, Pfeifle D. Induction of β-lactamase in Enterobacter cloacae[J]. Clin Infect Dis, 1998, 27(Suppl 1): S42-47.
  • 2Ehrhardt AF, Sanders CC, Romero JR et al. Sequencing and analysis of four new Enterobacter ampD alleles[J]. Antimicrob Agents Chemother, 1996, 40(8): 1953-1956.
  • 3Stapleton P, Shannon K, Phillips I. DNA sequence differences of ampD mutants of Citrobacter freundii[J]. Antimicrob Agents Chemother, 1995, 39(11): 2494-2498.
  • 4Matthew M, Harris AM, Marshall MJ, et al. The use of analytical isoelectric focusing for detection and identification of β-lactamases[J]. J Gen Microbiol, 1975, 88:169-178.
  • 5Stapleton P, Shannon K, Phillips I. The ability of β-lactamse antibitics to select mutants with derepressed β-lactamase synthesis from Citrobacter freundii[J]. J Antimicrobial Chemother, 1995, 36:483-496.
  • 6Kopp U, Wiedemann B, Lindquist S et al. Sequences of wild-type and mutant ampD genes of Citrobacter freundii and Enterobacter cloacae[J]. Antimicrob Agents Chemother, 1993, 37(2): 224-228.
  • 7Bennett PM, Chopra I. Molecular basis of β-lactamase induction in bacteria[J]. Antimicrob Agents Chemother, 1993, 37(2): 153-158.
  • 8Korfmann G, Sanders CC, Moland ES. Alterd phenotypes associated with ampD mutations in E. cloacae[J]. Antimicrob Agents Chemother, 1991, 35(2): 358-364.

共引文献36

同被引文献8

引证文献2

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部