期刊文献+

十字划线与三维试验法检测革兰阴性杆菌产AmpC酶的比较

Comparison of Detecting AmpC Produced by Gram-negative Bacilli with Modified Three-dimensional Extract Test and Three-dimensional Test
暂未订购
导出
摘要 目的建立一种简便可行的检测革兰阴性杆菌产AmpC酶的方法,并与三维试验比较。方法采用新建立的十字划线法,以三维试验为参考方法,对45株临床标本分离的革兰阴性杆菌产AmpC酶进行检测,用阴沟肠杆菌ATCC700323作阴性对照;阴沟肠杆菌029M产AmpC酶株作阳性对照,并以三维试验比较检测结果。结果十字划线和三维试验对45株革兰阴性杆菌作AmpC酶的检测,其两种方法检出率分别为35.6%(16/45)和22.2%(10/45),两者之间差异有统计学显著性意义(酽=13.72,P〈0.05),与三维试验比较十字划线假阳性7株、假阴性1株,准确度为82.2%,敏感度为90%,特异度为80%。结论十字划线法可作为临床检测革兰阴性杆菌产AmpC酶较为理想的筛查方法。 Objective To establish a simple and workable method of detecting AmpC β-lactamase from Gram-negative bacil- li. Methods AmpC from 45 Gram-negative isolates were measured by modified three-dimensional extract test and the re- sult was compared with three-dimensional test. E. cloacae ATCC700323 was used as negative control,and E. cloacae O29M was used as positive control. Results Conducted by modified three-dimensional extract test and three-dimensional test,45 isolates were tested and AmpC was found positive as 35.6 % (16/45) and 22.2% (10/45) respectively. There was the re- markable difference between two methods (x2=13.72,P〈0. 05). Compared with three-dimensional test,the concordance, sensitivities and specificities result of modified three-dimensional extract test were 82.2%, 80. 0% and 90. 0% respective- ly. Conclusion Modified three-dimensional extract test is a simple and adaptable method of clinical detecting to AmpC from Gram-negative bacilli.
出处 《现代检验医学杂志》 CAS 2009年第4期74-77,共4页 Journal of Modern Laboratory Medicine
基金 基金项目:广州市科技局重大攻关项目资助课题(z00621-E0141),广州医学院资助课题.
关键词 AMPC酶 三维试验 十字划线法 AmpC β-lactamase three-dimensional test modified three-dimensional extract test
  • 相关文献

参考文献12

二级参考文献28

  • 1多丽波,刘晶,闫立昕,孙琪,王孟滨,李垚.高产AmpC酶大肠埃希菌、肺炎克雷伯菌的实验室检测[J].中国实验诊断学,2006,10(4):412-415. 被引量:5
  • 2张乐海,马丽霞,伊长英.2002—2005年实验室检测AmpCβ内酰胺酶研究进展[J].中华检验医学杂志,2006,29(10):944-946. 被引量:2
  • 3王冬国,周铁丽.质粒介导产AmpC酶大肠埃希菌、肺炎克雷伯菌AmpC基因型检测与分析[J].中华医院感染学杂志,2007,17(7):782-785. 被引量:14
  • 4Jones RN. Important and emerging-lactamase resistances in hospital-based pathogens: the AmpC enzymes [J]. Biagn Microbiol Infect Dis,1998,31:461-466.
  • 5Moland ES, Sandhu K, Pincus M, et al. A simple phenotypic approach to the detection of inducible plasmid-mediated AmpC β-lactamase (PAmpC) production in two New York isolates of Klebsiella pneumoniae (KP) [C]. Saltlake: 102ND General Meeting American Soc
  • 6Thomson KS, Sanders CC. Detection of extended-spectrum β-lactamases in members of the family enterbacteriaceae: comparison of the double-disk and three-dimensional tests [J]. Antimicrob Agemts Chemother,1992,36:1877-1882.
  • 7Coudron PE, Moland ES, Thomson KS. Occurrence and detection of AmpC beta-lactamasses among Escherchia coli, Klebsiella pneumoniae and proteus mirabilis iso ates at a Veteran's medical canter [J]. Clin Microbiol,2000,38:1791-1796.
  • 8Thomson KS, Sanders CC, Moland ES, et al. Use of microdilution panels with and without β-lactanase inbibitors as a phenotypic test for β-lactamase production among Escherchia coli, Klebsiella SPP, Enterobacter SPP. Citrobacter freunaii and serratia marc
  • 9Bauernfeind A, Schneider JR. A novel type of Ampc β-lactamases Acc-1, produced by Klebsiella pneumoniae strain causing nosocomial pneumoniae [J]. Antimicrob Agents Chemother,1999,43:1924.
  • 10Philippon A, Arlet G, Jacoby GA. Plasmid-determined AmpC-type β-lactamases [J]. Antimicrob Agents Chemother,2002,46:1-11.

共引文献376

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