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Shiga toxin-producing Escherichia coli O104:H4: a new challenge for microbiology.产志贺毒素大肠杆菌 O104:H4:微生物学的新挑战。
Appl Environ Microbiol. 2012 Jun;78(12):4065-73. doi: 10.1128/AEM.00217-12. Epub 2012 Apr 13.
2
Outbreak of Shiga toxin-producing Escherichia coli O104:H4 associated with organic fenugreek sprouts, France, June 2011.2011 年 6 月法国因食用有机葫芦巴芽而爆发的产志贺毒素大肠杆菌 O104:H4 疫情。
Clin Infect Dis. 2012 Jun;54(11):1588-94. doi: 10.1093/cid/cis255. Epub 2012 Mar 28.
3
Epidemiology of Shiga toxin producing Escherichia coli in Australia, 2000-2010.澳大利亚 2000-2010 年产志贺毒素大肠杆菌的流行病学研究。
BMC Public Health. 2012 Jan 21;12:63. doi: 10.1186/1471-2458-12-63.
4
A rapid procedure for the detection and isolation of enterohaemorrhagic Escherichia coli (EHEC) serogroup O26, O103, O111, O118, O121, O145 and O157 strains and the aggregative EHEC O104:H4 strain from ready-to-eat vegetables.一种快速检测和分离即食蔬菜中肠出血性大肠杆菌(EHEC)血清群 O26、O103、O111、O118、O121、O145 和 O157 菌株以及聚集性 EHEC O104:H4 菌株的快速程序。
Int J Food Microbiol. 2012 Jan 3;152(1-2):19-30. doi: 10.1016/j.ijfoodmicro.2011.10.009. Epub 2011 Oct 21.
5
Human infections with non-O157 Shiga toxin-producing Escherichia coli, Switzerland, 2000-2009.瑞士 2000-2009 年非 O157 产志贺毒素大肠埃希菌感染。
Emerg Infect Dis. 2011 Feb;17(2):180-5. doi: 10.3201/eid1702.100909.
6
Laboratory practices for the identification of Shiga toxin-producing Escherichia coli in the United States, FoodNet sites, 2007.美国食品网监测点 2007 年志贺毒素产生型大肠埃希氏菌检测的实验室实践。
Foodborne Pathog Dis. 2011 Apr;8(4):555-60. doi: 10.1089/fpd.2010.0764. Epub 2010 Dec 27.
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Shiga-toxigenic Escherichia coli detection in stool samples screened for viral gastroenteritis in Alberta, Canada.在加拿大艾伯塔省对病毒性肠胃炎进行粪便样本筛查中检测出产志贺毒素大肠杆菌。
J Clin Microbiol. 2011 Feb;49(2):574-8. doi: 10.1128/JCM.01693-10. Epub 2010 Dec 8.
8
Phylogenetic analysis and Shiga toxin production profiling of Shiga toxin-producing/enterohemorrhagic Escherichia coli clinical isolates.产志贺毒素/肠出血性大肠杆菌临床分离株的系统进化分析及志贺毒素产生谱分析。
Microb Pathog. 2010 Nov;49(5):246-51. doi: 10.1016/j.micpath.2010.06.005. Epub 2010 Jun 15.
9
Enhanced surveillance of non-O157 verotoxin-producing Escherichia coli in human stool samples from Manitoba.曼尼托巴省人类粪便样本中非 O157 型肠出血性大肠杆菌的强化监测。
Can J Infect Dis Med Microbiol. 2005 Nov;16(6):329-34. doi: 10.1155/2005/859289.
10
Shiga toxin-producing Escherichia coli, Idaho.产志贺毒素大肠杆菌,爱达荷州
Emerg Infect Dis. 2007 Aug;13(8):1262-4. doi: 10.3201/eid1308.070189.

评价一种新型显色琼脂培养基对产志贺毒素大肠杆菌(STEC)的检测效果,以及加拿大马尼托巴省 O157 和非 O157 STEC 的相对流行率。

Evaluation of a new chromogenic agar medium for detection of Shiga toxin-producing Escherichia coli (STEC) and relative prevalences of O157 and non-O157 STEC in Manitoba, Canada.

机构信息

Cadham Provincial Laboratory, Winnipeg, Manitoba, Canada.

出版信息

J Clin Microbiol. 2013 Feb;51(2):466-71. doi: 10.1128/JCM.02329-12. Epub 2012 Nov 21.

DOI:10.1128/JCM.02329-12
PMID:23175263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3553920/
Abstract

This study assesses the detection performance of CHROMagar STEC medium relative to a reference cytotoxin assay and describes the current relative prevalence of O157 and non-O157 Shiga toxin-producing Escherichia coli (STEC) serotypes within the province of Manitoba, Canada. Over a 10-month period, 205 nonfrozen routine stool submissions to Cadham Provincial Laboratory (CPL) were used to assess the performance of CHROMagar STEC. Of the 205 stools, 14 were identified as true positives by a cytotoxin assay, with resultant CHROMagar STEC sensitivity, specificity, and positive predictive and negative predictive values of 85.7%, 95.8%, 60.0%, and 98.9%, respectively. Using a separate panel of 111 STEC strains, CHROMagar STEC was shown to support the growth of 96 (86.5%) isolates. To assess relative prevalence, attempts were made to isolate by any means all STEC strains identified at CPL over a 17-month period. Of 49 isolates (representing 86.0% of all STEC infections detected), only 28.6% were O157 STEC strains. Of the 35 non-O157 STEC strains, 29 were subjected to further molecular analysis. In contrast to earlier results from our area, carriage of stx(2) appears to have increased. Overall, although CHROMagar STEC is not recommended as a primary screen, our results indicate that it is an effective supplemental medium for the isolation of probable STEC strains. Increased isolation of these serotypes is warranted to better understand their prevalence, clinical characteristics, and epidemiology and aid in the development or enhancement of food safety control programs targeting all STEC serotypes.

摘要

本研究评估了 CHROMagar STEC 培养基相对于参考细胞毒素检测的检测性能,并描述了加拿大马尼托巴省目前 O157 和非 O157 志贺毒素产生大肠杆菌 (STEC) 血清型的相对流行率。在 10 个月的时间里,使用 Cadham 省级实验室(CPL)的 205 份非冷冻常规粪便送检样本评估 CHROMagar STEC 的性能。在 205 份粪便中,有 14 份通过细胞毒素检测被确认为真正的阳性,CHROMagar STEC 的灵敏度、特异性、阳性预测值和阴性预测值分别为 85.7%、95.8%、60.0%和 98.9%。使用 111 株 STEC 菌株的单独面板,CHROMagar STEC 被证明支持 96(86.5%)株的生长。为了评估相对流行率,尝试通过任何手段分离 CPL 在 17 个月期间发现的所有 STEC 菌株。在 49 株分离株(代表所有检测到的 STEC 感染的 86.0%)中,只有 28.6%是 O157 STEC 菌株。在 35 株非 O157 STEC 菌株中,有 29 株进行了进一步的分子分析。与我们地区早期的结果相比,stx(2)的携带似乎有所增加。总的来说,尽管 CHROMagar STEC 不建议作为首选筛查方法,但我们的结果表明它是一种有效的辅助培养基,可用于分离可能的 STEC 菌株。需要增加这些血清型的分离,以更好地了解它们的流行率、临床特征和流行病学,并有助于制定或加强针对所有 STEC 血清型的食品安全控制计划。