期刊文献+

大肠埃希氏菌O157:H7能力验证结果分析及讨论 被引量:1

Analysis and Discussion on the Verification Results of Escherichia coli O157:H7
下载PDF
导出
摘要 目的:从FAPAS能力验证样品(沙拉)中分离、鉴定大肠埃希氏菌O157:H7,分别判定两个样品是否检出目标菌。方法:本实验采用国家标准《食品安全国家标准 食品微生物学检验 大肠埃希氏菌O157:H7/NM检验》(GB 4789.36—2016)第一法和基质辅助激光解吸电离飞行时间质谱法(Matrix-assisted Laser Desorption Ionization-time of Flight Mass Spectrometry,MALDI-TOF MS)对能力验证样品进行鉴定。结果:样品M248d11A中未检出大肠埃希氏菌O157:H7,鉴定干扰菌株为大肠埃希氏菌;样品M248d11B中检出大肠埃希氏菌O157:H7,结果为满意。结论:在进行能力验证实验中,为避免交叉污染,尽量选择不同生物安全柜进行试验;MALDI-TOF MS对于血清型的鉴定可以参考聚类树状谱系图,但不建议作为判定的主要依据。 Objective:To isolate and identify Escherichia coli O157:H7 from FAPAS ability verification sample (salad),and determine whether the target bacteria are detected in the two samples.Method:The first method of GB 4789.36—2016 and matrix assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF MS) were used to identify the ability verification samples.Result:Escherichia coli O157:H7 was not detected in sample M248d11A,and the interfering strain was identified as Escherichia coli.Escherichia coli O157:H7 was detected in sample M248d11B.Conclusion:In the capacity verification experiment,in order to avoid cross contamination,different biosafety cabinets should be selected as far as possible;MALDI-TOF MS can refer to the clustering tree pedigree for the identification of serotypes,but it is not recommended as the main basis for judgment.
作者 刘霓 LIU Ni(Liaoning Inspection Examination and Certification Center,Shenyang 110000,China)
出处 《食品安全导刊》 2022年第6期105-107,共3页 China Food Safety Magazine
关键词 能力验证 大肠埃希氏菌O157:H7 基质辅助激光解吸电离飞行时间质谱法 proficiency test Escherichia coli O157:H7 matrix-assisted laser desorption ionization-time of flight mass spectrometry
  • 相关文献

参考文献2

二级参考文献34

  • 1王晓萌.肠出血性大肠埃希菌O157:H7不同分型方法比较[J].中国公共卫生,2005,21(4):451-452. 被引量:3
  • 2张渊魁,张中直,甘孟侯.用质粒DNA指纹图谱分析法研究鸡源大肠杆菌的流行病学特征[J].畜牧兽医学报,1995,26(5):473-480. 被引量:10
  • 3潘玲,吴信法.肠出血性大肠杆菌(EHEC)O157∶H7的研究近况[J].中国动物检疫,1996,13(6):37-38. 被引量:3
  • 4Krishnan C, Fitzgerald V A, Dakin S J, et al.Laboratory investigation of out break of hemorrhagic colitis caused by Escherichia coli O157:H7[J].J Clin Microbiol, 1987, 25 (6) : 1043-1047.
  • 5Haldane D J M,Damn M A S,Anderson J D.Improved biochemical screening procedure for small clinical laboratories forvero (Shiga-like)-toxin-produceing strains of Escherichia coli O 157:H7[J].J Clin Microbiol, 1986,24 (4) : 652-653.
  • 6Karen C,Ken J,Stephen D.Multiplex Real-Time PCR method to identify Shiga toxin genes stxl, stx2 and Escherichia coli O157:H7/H-serotype [J].Appl Environ Microbiol, 2003, 69 (10) : 6327-6334.
  • 7Call D R,Broekman F J, Chandler D P.Detecting and genotyping Escheriehia coli O157:H7 using mutiplex PCR and nucleic acidmieroarrays [J].J Food Microbiol, 2001, 67 (1/2) : 71-80.
  • 8Demareo D R, Lira D V.Detection of Escheriehia coli O157:H7 in 10 and 25 gram ground beef samples with an evanescent-wave biosensor with silica and polystyrene waveguides [J].Jounal of Food Protection, 2002,65 (4) : 596-602.
  • 9Wong S, Srdjan Jelacic B S, Rebecca L H, et al.The risk of the hemolytic uremic syndrome after antibiotic Ixeatment of Escheichia coli O157:H7 infections [J].The New England Journal of Medicine, 2000, 342: 1930-1936.
  • 10Shimada O, Ishikawa H, Tosaka-Shimada H, et al.Exocytotic secretion of toxins from. macrophages infected with Escherichia coli O 157:H7[J].Cell Struct and Func, 1999, 24 (5) : 247-253.

共引文献26

同被引文献7

引证文献1

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