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本文引用的文献

1
Clostridium difficile: progress and challenges.艰难梭菌:进展与挑战。
Ann N Y Acad Sci. 2010 Dec;1213:62-9. doi: 10.1111/j.1749-6632.2010.05863.x.
2
The role of toxin A and toxin B in Clostridium difficile infection.艰难梭菌感染中毒素 A 和毒素 B 的作用。
Nature. 2010 Oct 7;467(7316):711-3. doi: 10.1038/nature09397. Epub 2010 Sep 15.
3
Molecular characterization of toxin A-negative, toxin B-positive variant strains of Clostridium difficile isolated in Korea.韩国分离的产毒 A 阴性、产毒 B 阳性艰难梭菌变异株的分子特征。
Diagn Microbiol Infect Dis. 2010 Jun;67(2):198-201. doi: 10.1016/j.diagmicrobio.2010.01.007. Epub 2010 Mar 24.
4
Piglet models of acute or chronic Clostridium difficile illness.急性或慢性艰难梭菌病的小猪模型。
J Infect Dis. 2010 Feb 1;201(3):428-34. doi: 10.1086/649799.
5
The ClosTron: Mutagenesis in Clostridium refined and streamlined.ClosTron:改良和精简的梭菌诱变。
J Microbiol Methods. 2010 Jan;80(1):49-55. doi: 10.1016/j.mimet.2009.10.018. Epub 2009 Nov 3.
6
Antibiotic treatment of clostridium difficile carrier mice triggers a supershedder state, spore-mediated transmission, and severe disease in immunocompromised hosts.对艰难梭菌携带小鼠进行抗生素治疗会引发超级排菌状态、孢子介导的传播以及免疫功能低下宿主的严重疾病。
Infect Immun. 2009 Sep;77(9):3661-9. doi: 10.1128/IAI.00558-09. Epub 2009 Jun 29.
7
Toxin B is essential for virulence of Clostridium difficile.毒素B对于艰难梭菌的毒力至关重要。
Nature. 2009 Apr 30;458(7242):1176-9. doi: 10.1038/nature07822. Epub 2009 Mar 1.
8
Clostridium difficile toxin synthesis is negatively regulated by TcdC.艰难梭菌毒素的合成受到TcdC的负调控。
J Med Microbiol. 2008 Jun;57(Pt 6):685-689. doi: 10.1099/jmm.0.47775-0.
9
Structure and mode of action of clostridial glucosylating toxins: the ABCD model.梭菌属糖基化毒素的结构与作用模式:ABCD模型
Trends Microbiol. 2008 May;16(5):222-9. doi: 10.1016/j.tim.2008.01.011. Epub 2008 Apr 18.
10
Repression of Clostridium difficile toxin gene expression by CodY.CodY对艰难梭菌毒素基因表达的抑制作用。
Mol Microbiol. 2007 Oct;66(1):206-19. doi: 10.1111/j.1365-2958.2007.05906.x. Epub 2007 Aug 28.

产毒A 和产毒 B 在艰难梭菌感染中都很重要。

Both, toxin A and toxin B, are important in Clostridium difficile infection.

机构信息

Clostridia Research Group, Centre for Biomolecular Sciences, School of Molecular Medical Sciences, University of Nottingham, Nottingham NG7 2RD, UK.

出版信息

Gut Microbes. 2011 Jul-Aug;2(4):252-5. doi: 10.4161/gmic.2.4.16109. Epub 2011 Jul 1.

DOI:10.4161/gmic.2.4.16109
PMID:21804353
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3260544/
Abstract

The bacterium is the leading cause of healthcare associated diarrhoea in the developed world and thus presents a major financial burden. The main virulence factors of are two large toxins, A and B. Over the years there has been some debate over the respective roles and importance of these two toxins. To address this, we recently constructed stable toxin mutants of and found that they were virulent if either toxin A or toxin B was functional. This underlined the importance of each toxin and the necessity to consider both when developing countermeasures against infection (CDI). In this article we discuss our findings in the context of previous work and outline some of the challenges which face the field as a result.

摘要

这种细菌是发达国家医疗保健相关性腹泻的主要病原体,因此给医疗保健带来了巨大的经济负担。的主要毒力因子是两种大型毒素,A 和 B。多年来,这两种毒素的相对作用和重要性一直存在争议。为了解决这个问题,我们最近构建了的稳定毒素突变体,发现只要毒素 A 或毒素 B 具有功能,它们就是有毒的。这突出了每种毒素的重要性,并且在开发针对感染(CDI)的对策时,有必要同时考虑这两种毒素。在本文中,我们将根据以前的工作讨论我们的发现,并概述该领域目前面临的一些挑战。