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本文引用的文献

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Probiotics and gastrointestinal infections.益生菌与胃肠道感染
Interdiscip Perspect Infect Dis. 2008;2008:290769. doi: 10.1155/2008/290769. Epub 2009 Feb 4.
2
Aetiology of community-acquired, acute gastroenteritis in hospitalised adults: a prospective cohort study.住院成人社区获得性急性胃肠炎的病因:一项前瞻性队列研究。
BMC Infect Dis. 2008 Oct 22;8:143. doi: 10.1186/1471-2334-8-143.
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Updated guidelines for evaluating public health surveillance systems: recommendations from the Guidelines Working Group.《公共卫生监测系统评估更新指南:指南工作组的建议》
MMWR Recomm Rep. 2001 Jul 27;50(RR-13):1-35; quiz CE1-7.
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Molecular analysis of shiga toxin-producing Escherichia coli strains isolated from hemolytic-uremic syndrome patients and dairy samples in France.对从法国溶血尿毒综合征患者和乳制品样本中分离出的产志贺毒素大肠杆菌菌株的分子分析。
Appl Environ Microbiol. 2008 Apr;74(7):2118-28. doi: 10.1128/AEM.02688-07. Epub 2008 Feb 1.
5
Feasibility of a molecular screening method for detection of Salmonella enterica and Campylobacter jejuni in a routine community-based clinical microbiology laboratory.在一个基于社区的常规临床微生物实验室中,一种用于检测肠炎沙门氏菌和空肠弯曲菌的分子筛查方法的可行性。
J Clin Microbiol. 2007 Nov;45(11):3692-700. doi: 10.1128/JCM.00896-07. Epub 2007 Sep 5.
6
The use of a combined enrichment-filtration technique for the isolation of Campylobacter spp. from clinical samples.一种用于从临床样本中分离弯曲杆菌属的富集-过滤联合技术的应用。
Clin Microbiol Infect. 2007 Jun;13(6):643-4. doi: 10.1111/j.1469-0691.2007.01712.x. Epub 2007 Mar 19.
7
Single multiplex assay to identify simultaneously enteropathogenic, enteroaggregative, enterotoxigenic, enteroinvasive and Shiga toxin-producing Escherichia coli strains in Brazilian children.用于同时鉴定巴西儿童中致病性大肠杆菌、聚集性大肠杆菌、产肠毒素大肠杆菌、侵袭性大肠杆菌和产志贺毒素大肠杆菌菌株的单一多重检测法。
FEMS Microbiol Lett. 2007 Feb;267(2):145-50. doi: 10.1111/j.1574-6968.2006.00580.x.
8
Rapid identification and differentiation of clinical isolates of enteropathogenic Escherichia coli (EPEC), atypical EPEC, and Shiga toxin-producing Escherichia coli by a one-step multiplex PCR method.通过一步多重聚合酶链反应方法快速鉴定和区分致病性大肠杆菌(EPEC)、非典型EPEC和产志贺毒素大肠杆菌的临床分离株。
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9
Estimating foodborne gastroenteritis, Australia.澳大利亚食源性肠胃炎的估算
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10
Costs of gastroenteritis in The Netherlands.荷兰肠胃炎的成本。
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比较 EntericBio 多重 PCR 系统与常规培养检测肠道细菌病原体的效果。

Comparison of the EntericBio multiplex PCR system with routine culture for detection of bacterial enteric pathogens.

机构信息

Department of Medical Microbiology, Cork University Hospital, Wilton, Cork, Ireland.

出版信息

J Clin Microbiol. 2009 Nov;47(11):3449-53. doi: 10.1128/JCM.01026-09. Epub 2009 Sep 2.

DOI:10.1128/JCM.01026-09
PMID:19726596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2772650/
Abstract

The EntericBio system uses a multiplex PCR assay for the simultaneous detection of Campylobacter spp., Salmonella enterica, Shigella spp., and Escherichia coli O157 from feces. It combines overnight broth enrichment with PCR amplification and detection by hybridization. An evaluation of this system was conducted by comparing the results obtained with the system with those obtained by routine culture, supplemented with alternative PCR detection methods. In a study of 773 samples, routine culture and the EntericBio system yielded 94.6 and 92.4% negative results, respectively. Forty-two samples had positive results by culture, and all of these were positive with the EntericBio system. This system detected an additional 17 positive samples (Campylobacter spp., n = 12; Shigella spp., n = 1; E. coli O157, n = 4), but the results for 5 samples (Campylobacter spp., n = 2; Shigella spp., n = 1; E. coli O157, n = 2) could not be confirmed. The target for Shigella spp. detected by the EntericBio system is the ipaH gene, and the molecular indication of the presence of Shigella spp. was investigated by sequence analysis, which confirmed that the ipaH gene was present in a Klebsiella pneumoniae isolate from the patient. The sensitivity, specificity, positive predictive value, and negative predictive value were 100%, 99.3%, 91.5%, and 100%, respectively. Turnaround times were significantly reduced with the EntericBio system, and a result was available between 24 and 32 h after receipt of the sample in the laboratory. In addition, the amount of laboratory waste was significantly reduced by use of this system. In summary, the EntericBio system proved convenient to use, more sensitive than the conventional culture used in this study, and highly specific; and it generated results significantly faster than routine culture for the pathogens tested.

摘要

肠道生物系统使用多重 PCR 检测法同时从粪便中检测弯曲菌属、沙门氏菌属、志贺氏菌属和大肠杆菌 O157。它将过夜肉汤富集与 PCR 扩增和杂交检测相结合。通过将该系统的结果与常规培养的结果进行比较,并辅以替代 PCR 检测方法,对该系统进行了评估。在一项对 773 个样本的研究中,常规培养和肠道生物系统的阴性结果率分别为 94.6%和 92.4%。42 个样本经培养呈阳性,所有这些样本均经肠道生物系统呈阳性。该系统还检测到 17 个额外的阳性样本(弯曲菌属,n = 12;志贺氏菌属,n = 1;大肠杆菌 O157,n = 4),但其中 5 个样本(弯曲菌属,n = 2;志贺氏菌属,n = 1;大肠杆菌 O157,n = 2)的结果无法得到确认。肠道生物系统检测到的志贺氏菌属的靶标是 ipaH 基因,通过序列分析研究了存在志贺氏菌属的分子指标,证实了患者分离的肺炎克雷伯菌中存在 ipaH 基因。灵敏度、特异性、阳性预测值和阴性预测值分别为 100%、99.3%、91.5%和 100%。使用肠道生物系统显著缩短了周转时间,在实验室收到样本后的 24 至 32 小时内即可获得结果。此外,该系统显著减少了实验室废物的产生。总之,肠道生物系统使用方便,比本研究中使用的常规培养更敏感,特异性更高;并且与常规培养相比,该系统产生结果的速度明显更快。