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The European Union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2010.欧盟2010年人畜共患病、人畜共患病原体及食源性疾病暴发的趋势与来源总结报告
Euro Surveill. 2012 Mar 8;17(10):20113.
2
The formation of Staphylococcus aureus enterotoxin in food environments and advances in risk assessment.金黄色葡萄球菌肠毒素在食品环境中的形成与风险评估进展。
Virulence. 2011 Nov-Dec;2(6):580-92. doi: 10.4161/viru.2.6.18122. Epub 2011 Nov 1.
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Extended staphylococcal enterotoxin D expression in ham products.在火腿制品中表达扩展型葡萄球菌肠毒素 D。
Food Microbiol. 2011 May;28(3):617-20. doi: 10.1016/j.fm.2010.11.013. Epub 2010 Nov 24.
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Acetic acid increases the phage-encoded enterotoxin A expression in Staphylococcus aureus.乙酸增加金黄色葡萄球菌噬菌体编码肠毒素 A 的表达。
BMC Microbiol. 2010 May 20;10:147. doi: 10.1186/1471-2180-10-147.
5
Prolonged expression and production of Staphylococcus aureus enterotoxin A in processed pork meat.加工猪肉中金黄色葡萄球菌肠毒素 A 的长时间表达和产生。
Int J Food Microbiol. 2010 Jul 31;141 Suppl 1:S69-74. doi: 10.1016/j.ijfoodmicro.2010.03.028. Epub 2010 Mar 27.
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Transcription of the phage-encoded Panton-Valentine leukocidin of Staphylococcus aureus is dependent on the phage life-cycle and on the host background.金黄色葡萄球菌噬菌体编码的杀白细胞素的转录取决于噬菌体生命周期和宿主背景。
Microbiology (Reading). 2009 Nov;155(Pt 11):3491-3499. doi: 10.1099/mic.0.032466-0. Epub 2009 Aug 6.
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Diversity of prophages in dominant Staphylococcus aureus clonal lineages.金黄色葡萄球菌优势克隆谱系中前噬菌体的多样性
J Bacteriol. 2009 Jun;191(11):3462-8. doi: 10.1128/JB.01804-08. Epub 2009 Mar 27.
8
Microarray analysis of toxicogenomic effects of ortho-phenylphenol in Staphylococcus aureus.邻苯基苯酚对金黄色葡萄球菌毒理基因组学效应的微阵列分析
BMC Genomics. 2008 Sep 15;9:411. doi: 10.1186/1471-2164-9-411.
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Characterization of Staphylococcus aureus strains associated with food poisoning outbreaks in France.法国与食物中毒暴发相关的金黄色葡萄球菌菌株的特征分析。
Int J Food Microbiol. 2007 Apr 20;115(3):369-75. doi: 10.1016/j.ijfoodmicro.2006.10.050. Epub 2007 Jan 17.
10
Phage release from biofilm and planktonic Staphylococcus aureus cells.噬菌体从生物膜和浮游金黄色葡萄球菌细胞中的释放。
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金黄色葡萄球菌肠毒素 A 的表达和形成升高及其与前噬菌体诱导的关系。

Elevated enterotoxin A expression and formation in Staphylococcus aureus and its association with prophage induction.

机构信息

Applied Microbiology, Department of Chemistry, Faculty of Engineering, Lund University, Lund, Sweden.

出版信息

Appl Environ Microbiol. 2012 Jul;78(14):4942-8. doi: 10.1128/AEM.00803-12. Epub 2012 Apr 27.

DOI:10.1128/AEM.00803-12
PMID:22544256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3416385/
Abstract

Staphylococcus aureus strains producing the bacteriophage-encoded staphylococcal enterotoxin A (SEA) were divided into two groups, high- and low-SEA-producing strains, based on the amount of SEA produced. After growth under favorable conditions in batch cultures, 10 of the 21 strains tested produced more than 1,000 ng/ml SEA, and 9 strains produced less than 10 ng/ml SEA; two enterotoxigenic strains, MRSA252 and Newman, produced intermediate levels of SEA (around 450 ng/ml). The differences in the production of SEA were found to be associated with the expression level of sea and whether the strains hosted the sea(1) or sea(2) version. Furthermore, differences in nucleotide sequence in the Siphoviridae phage region showed two clonal lineages of the high-SEA-producing strains. One of these lines was correlated with the capacity for a massive increase in SEA levels by prophage induction as demonstrated using mitomycin C (MC). This was also confirmed by the occurrence of additional sea expression, presumed to be initiated by a latent phage promoter located upstream of the endogenous sea promoter. Remarkably, the SEA level was increased up to 10-fold in some strains due to prophage induction. The low-SEA-producing group and the high-SEA-producing subgroup lacking phage-activated sea transcription showed no increase in SEA formation after the addition of MC. This study demonstrates that sea expression in enterotoxigenic strains is correlated with the clonal lineage of sea-carrying phages. The high-SEA-producing group, in particular the prophage-inducible sea(1) group, may be more relevant to staphylococcal food poisoning than the low-SEA-producing group, harboring mainly sea(2).

摘要

金黄色葡萄球菌菌株根据其产生的噬菌体编码肠毒素 A (SEA) 的量分为高 SEA 产生菌株和低 SEA 产生菌株两组。在分批培养中生长条件良好后,21 株测试菌株中有 10 株产生超过 1000ng/ml SEA,9 株产生低于 10ng/ml SEA;两种肠毒素产生菌株 MRSA252 和 Newman 产生中间水平的 SEA(约 450ng/ml)。SEA 产生量的差异与 sea 的表达水平以及菌株是否携带 sea(1)或 sea(2)版本有关。此外,在 Siphoviridae 噬菌体区域的核苷酸序列差异表明,高 SEA 产生菌株存在两个克隆谱系。其中一条与通过丝裂霉素 C(MC)诱导前噬菌体来大量增加 SEA 水平的能力有关。这也通过发生额外的 sea 表达得到证实,据推测,这是由位于内源性 sea 启动子上游的潜伏噬菌体启动子引发的。值得注意的是,由于前噬菌体诱导,一些菌株中的 SEA 水平增加了 10 倍。低 SEA 产生组和缺乏噬菌体激活 sea 转录的高 SEA 产生亚组在添加 MC 后,SEA 形成没有增加。这项研究表明,肠毒素产生菌株中的 sea 表达与携带 sea 噬菌体的克隆谱系有关。特别是高 SEA 产生组,特别是可诱导前噬菌体的 sea(1)组,可能比低 SEA 产生组更与葡萄球菌食物中毒相关,后者主要携带 sea(2)。