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改进的从粉状婴儿配方食品中分离和检测阪崎肠杆菌(克罗诺杆菌属)的方法的建立。

Development of an improved protocol for the isolation and detection of Enterobacter sakazakii (Cronobacter) from powdered infant formula.

机构信息

U.S. Food and Drug Administration, 5100 Paint Branch Parkway HFS-711, College Park, Maryland 20740, USA.

出版信息

J Food Prot. 2010 Jun;73(6):1016-22. doi: 10.4315/0362-028x-73.6.1016.

DOI:10.4315/0362-028x-73.6.1016
PMID:20537255
Abstract

Enterobacter sakazakii causes severe maladies and, in some cases, is fatal among infants. Powdered infant formula (PIF) contaminated with E. sakazakii has been documented as a potential cause of several outbreaks involving infants. This study describes the development of a method for the isolation and detection of E. sakazakii from PIF. It combines Taqman real-time PCR, Brilliance E. sakazakii and R&F chromogenic agars, and RAPID ID 32E biochemical tests. This method provides an expedient analysis within 1 to 2 days depending on the amount and stress status of E. sakazakii organisms and competing microorganisms in PIF. The real-time PCR has bifunctional applications, including both screening and culture confirmation of E. sakazakii.

摘要

阪崎肠杆菌可引起严重疾病,在某些情况下可导致婴儿死亡。受阪崎肠杆菌污染的配方粉已被证实是几起涉及婴儿的暴发事件的潜在原因。本研究描述了一种从配方粉中分离和检测阪崎肠杆菌的方法。它结合了 Taqman 实时 PCR、 Brilliance 阪崎肠杆菌和 R&F 显色琼脂,以及 RAPID ID 32E 生化测试。该方法可根据配方粉中阪崎肠杆菌和其他微生物的数量和应激状态,在 1 至 2 天内提供便捷的分析。实时 PCR 具有双重应用,包括阪崎肠杆菌的筛查和培养确认。

相似文献

1
Development of an improved protocol for the isolation and detection of Enterobacter sakazakii (Cronobacter) from powdered infant formula.改进的从粉状婴儿配方食品中分离和检测阪崎肠杆菌(克罗诺杆菌属)的方法的建立。
J Food Prot. 2010 Jun;73(6):1016-22. doi: 10.4315/0362-028x-73.6.1016.
2
Rapid, specific detection of Enterobacter sakazakii in infant formula using a real-time PCR assay.使用实时荧光定量聚合酶链反应法快速、特异性检测婴儿配方奶粉中的阪崎肠杆菌。
J Food Prot. 2005 Jan;68(1):59-63. doi: 10.4315/0362-028x-68.1.59.
3
Comparison of three chromogenic media and evaluation of two molecular-based identification systems for the detection of Enterobacter sakazakii from environmental samples from infant formulae factories.三种显色培养基的比较以及两种基于分子的鉴定系统对婴儿配方奶粉厂环境样本中阪崎肠杆菌检测的评估
J Food Prot. 2007 Jul;70(7):1678-84. doi: 10.4315/0362-028x-70.7.1678.
4
Incorporation of an internal control into the PCR assay published in "Development of an improved protocol for the isolation and detection of Enterobacter sakazakii (Cronobacter) from powdered infant formula," J. Food Prot. 73(6):1016-1022 (2010).将内部控制纳入发表于《改进从婴儿配方奶粉中分离和检测阪崎肠杆菌(克罗诺杆菌)的方案的制定》(《食品保护杂志》73(6):1016 - 1022,2010年)中的聚合酶链反应检测方法。
J Food Prot. 2011 Jun;74(6):872-3. doi: 10.4315/0362-028X.74.6.872.
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Detection of Enterobacter sakazakii strains by real-time PCR.实时 PCR 检测阪崎肠杆菌。
J Food Prot. 2005 Aug;68(8):1623-7. doi: 10.4315/0362-028x-68.8.1623.
6
Evaluation of a new one-step enrichment in conjunction with a chromogenic medium for the detection of Cronobacter spp. (Enterobacter sakazakii) in powdered infant formula.评估一种新型一步富集法结合显色培养基用于检测婴儿配方奶粉中的阪崎肠杆菌属(阪崎肠杆菌)。
J Food Prot. 2009 Jul;72(7):1472-5. doi: 10.4315/0362-028x-72.7.1472.
7
Direct real-time PCR with ethidium monoazide: a method for the rapid detection of viable Cronobacter sakazakii in powdered infant formula.直接实时聚合酶链反应结合吖啶橙:一种快速检测粉状婴儿配方食品中阪崎克罗诺杆菌的方法。
J Food Prot. 2012 Sep;75(9):1572-9. doi: 10.4315/0362-028X.JFP-12-015.
8
Evaluation of a revised U.S. Food and Drug Administration method for the detection of Cronobacter in powdered infant formula: a collaborative study.评价美国食品和药物管理局修订的粉状婴儿配方食品中克罗诺杆菌检测方法:一项协作研究。
J Food Prot. 2012 Jun;75(6):1144-7. doi: 10.4315/0362-028X.JFP-11-388.
9
A robotic DNA purification protocol and real-time PCR for the detection of Enterobacter sakazakii in powdered infant formulae.一种用于检测婴儿配方奶粉中阪崎肠杆菌的机器人DNA纯化方案及实时PCR方法。
BMC Microbiol. 2006 Dec 13;6:100. doi: 10.1186/1471-2180-6-100.
10
"Development of an improved protocol for the isolation and detection of Enterobacter sakazakii (Cronobacter) from powdered infant formula," a comment on: J. Food Prot. 73(6):1016-1022 (2010).“关于改进从婴儿配方奶粉中分离和检测阪崎肠杆菌(克罗诺杆菌属)的方案的研究”,对《食品保护杂志》73(6):1016 - 1022(2010年)一文的评论
J Food Prot. 2010 Nov;73(11):1964-6; author reply 1965-6. doi: 10.4315/0362-028x-73.11.1964.

引用本文的文献

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Bacteremia caused by Enterobacter asburiae misidentified biochemically as Cronobacter sakazakii and accurately identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry: a case report.肠杆菌属aspergillus 引起的菌血症被生化错误鉴定为阪崎克罗诺杆菌,并通过基质辅助激光解吸/电离飞行时间质谱准确鉴定:一例报告。
J Med Case Rep. 2022 Jan 19;16(1):19. doi: 10.1186/s13256-021-03241-2.
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Molecular Surveillance of Cronobacter spp. Isolated from a Wide Variety of Foods from 44 Different Countries by Sequence Typing of 16S rRNA, rpoB and O-Antigen Genes.
通过对16S rRNA、rpoB和O抗原基因进行序列分型,对从44个不同国家的多种食品中分离出的阪崎肠杆菌进行分子监测。
Foods. 2017 May 11;6(5):36. doi: 10.3390/foods6050036.
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Genetic Characterization of Cronobacter sakazakii Recovered from the Environmental Surveillance Samples During a Sporadic Case Investigation of Foodborne Illness.在食源性疾病散发病例调查期间从环境监测样本中分离出的阪崎肠杆菌的基因特征分析
Curr Microbiol. 2016 Aug;73(2):273-9. doi: 10.1007/s00284-016-1059-z. Epub 2016 May 7.
5
Strategies for the identification and tracking of cronobacter species: an opportunistic pathogen of concern to neonatal health.鉴定和追踪克罗诺杆菌属策略:一种与新生儿健康相关的机会致病菌。
Front Pediatr. 2015 May 5;3:38. doi: 10.3389/fped.2015.00038. eCollection 2015.
6
Pan-genome analysis of the emerging foodborne pathogen Cronobacter spp. suggests a species-level bidirectional divergence driven by niche adaptation.泛基因组分析表明,食源性新兴致病菌克罗诺杆菌属(Cronobacter spp.)在生态位适应的驱动下发生了种水平的双向分歧。
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