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1
Variations in virulence and molecular biology among emerging strains of Clostridium difficile.艰难梭菌新菌株毒力和分子生物学的变异。
Microbiol Mol Biol Rev. 2013 Dec;77(4):567-81. doi: 10.1128/MMBR.00017-13.
2
The anti-sigma factor TcdC modulates hypervirulence in an epidemic BI/NAP1/027 clinical isolate of Clostridium difficile.抗σ因子 TcdC 调节艰难梭菌 BI/NAP1/027 临床分离株的超强毒力。
PLoS Pathog. 2011 Oct;7(10):e1002317. doi: 10.1371/journal.ppat.1002317. Epub 2011 Oct 13.
3
Variations in TcdB activity and the hypervirulence of emerging strains of Clostridium difficile.产肠毒素梭菌 TcdB 活性的变化与艰难梭菌新出现的高毒力菌株。
PLoS Pathog. 2010 Aug 19;6(8):e1001061. doi: 10.1371/journal.ppat.1001061.
4
The flagellin FliC of Clostridium difficile is responsible for pleiotropic gene regulation during in vivo infection.艰难梭菌的鞭毛蛋白 FliC 负责体内感染过程中的多效基因调控。
PLoS One. 2014 May 19;9(5):e96876. doi: 10.1371/journal.pone.0096876. eCollection 2014.
5
Hype or hypervirulence: a reflection on problematic C. difficile strains.是炒作还是超级毒力:对有问题的艰难梭菌菌株的反思。
Virulence. 2013 Oct 1;4(7):592-6. doi: 10.4161/viru.26297. Epub 2013 Sep 10.
6
Clostridium difficile infection: toxins and non-toxin virulence factors, and their contributions to disease establishment and host response.艰难梭菌感染:毒素和非毒素毒力因子,以及它们对疾病建立和宿主反应的贡献。
Gut Microbes. 2012 Mar-Apr;3(2):121-34. doi: 10.4161/gmic.19399. Epub 2012 Mar 1.
7
Human hypervirulent Clostridium difficile strains exhibit increased sporulation as well as robust toxin production.人源强毒力艰难梭菌表现出更高的孢子形成能力和旺盛的毒素产生。
J Bacteriol. 2010 Oct;192(19):4904-11. doi: 10.1128/JB.00445-10. Epub 2010 Jul 30.
8
Epidemic ribotypes of Clostridium (now Clostridioides) difficile are likely to be more virulent than non-epidemic ribotypes in animal models.在动物模型中,艰难梭菌(现为艰难梭状芽孢杆菌)的流行株比非流行株更具毒性。
BMC Microbiol. 2020 Feb 5;20(1):27. doi: 10.1186/s12866-020-1710-5.
9
Lack of association between clinical outcome of Clostridium difficile infections, strain type, and virulence-associated phenotypes.艰难梭菌感染的临床结果、菌株类型与毒力相关表型之间缺乏关联。
J Clin Microbiol. 2011 Dec;49(12):4040-6. doi: 10.1128/JCM.05053-11. Epub 2011 Sep 28.
10
The emergence of 'hypervirulence' in Clostridium difficile.艰难梭菌“超级毒力”的出现。
Int J Med Microbiol. 2010 Aug;300(6):387-95. doi: 10.1016/j.ijmm.2010.04.008. Epub 2010 May 23.

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Clostridioides difficile meets the adenosine system: the art of manipulating host homeostasis.艰难梭菌与腺苷系统:操纵宿主内稳态的技巧
J Biomed Sci. 2025 Jul 11;32(1):66. doi: 10.1186/s12929-025-01160-8.
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Clostridioides difficile evolution in a tertiary German hospital through a retrospective genomic characterization.通过回顾性基因组特征分析,对德国一家三级医院中艰难梭菌的进化情况进行研究。
Infection. 2025 Jun 8. doi: 10.1007/s15010-025-02576-y.
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Changing patterns and biological features of community-acquired infection in Southwest China: 7 years of surveillance data.中国西南部社区获得性感染的变化模式及生物学特征:7年监测数据
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Elevated risk of adverse effects from foodborne contaminants and drugs in inflammatory bowel disease: a review.炎症性肠病患者食用食物污染物和药物的不良反应风险升高:综述
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and Gut Microbiota: From Colonization to Infection and Treatment.以及肠道微生物群:从定植到感染与治疗
Pathogens. 2024 Jul 31;13(8):646. doi: 10.3390/pathogens13080646.
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PhosphoLipidome Alteration Induced by Toxin B in Enteric Glial Cells.毒素 B 诱导肠神经胶质细胞的磷酯质组改变。
Cells. 2024 Jun 26;13(13):1103. doi: 10.3390/cells13131103.
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Therap Adv Gastroenterol. 2023 Nov 28;16:17562848231207280. doi: 10.1177/17562848231207280. eCollection 2023.
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Polyamines and hypusination are important for toxin B (TcdB)-mediated activation of group 3 innate lymphocytes (ILC3s).多胺和高丝氨酸化对于毒素 B (TcdB) 介导的第三类固有淋巴细胞 (ILC3) 的激活很重要。
Infect Immun. 2023 Nov 16;91(11):e0023623. doi: 10.1128/iai.00236-23. Epub 2023 Oct 20.
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Role of the Alteration in Calcium Homeostasis in Cell Death Induced by Toxin A and Toxin B.钙稳态改变在毒素A和毒素B诱导的细胞死亡中的作用
Biology (Basel). 2023 Aug 10;12(8):1117. doi: 10.3390/biology12081117.
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Toxin B Induced Senescence: A New Pathologic Player for Colorectal Cancer?毒素 B 诱导的衰老:结直肠癌的新病理因素?
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本文引用的文献

1
Gut microbiota patterns associated with colonization of different Clostridium difficile ribotypes.与不同艰难梭菌核糖体型定植相关的肠道微生物群模式。
PLoS One. 2013;8(2):e58005. doi: 10.1371/journal.pone.0058005. Epub 2013 Feb 28.
2
A mixture of functionally oligoclonal humanized monoclonal antibodies that neutralize Clostridium difficile TcdA and TcdB with high levels of in vitro potency shows in vivo protection in a hamster infection model.一种具有功能的寡克隆人源化单克隆抗体混合物,能在体外高效中和艰难梭菌毒素A(TcdA)和毒素B(TcdB),在仓鼠感染模型中显示出体内保护作用。
Clin Vaccine Immunol. 2013 Mar;20(3):377-90. doi: 10.1128/CVI.00625-12. Epub 2013 Jan 16.
3
CD44 Promotes intoxication by the clostridial iota-family toxins.CD44 促进梭菌iota 家族毒素的中毒。
PLoS One. 2012;7(12):e51356. doi: 10.1371/journal.pone.0051356. Epub 2012 Dec 7.
4
Fecal microbiome transplantation for recurrent Clostridium difficile infection: report on a case series.粪便微生物群移植治疗复发性艰难梭菌感染:病例系列报告。
Anaerobe. 2013 Feb;19:22-6. doi: 10.1016/j.anaerobe.2012.11.004. Epub 2012 Nov 23.
5
Targeted restoration of the intestinal microbiota with a simple, defined bacteriotherapy resolves relapsing Clostridium difficile disease in mice.用简单、明确的细菌疗法靶向修复肠道微生物群可解决小鼠复发性艰难梭菌病。
PLoS Pathog. 2012;8(10):e1002995. doi: 10.1371/journal.ppat.1002995. Epub 2012 Oct 25.
6
Antibody against TcdB, but not TcdA, prevents development of gastrointestinal and systemic Clostridium difficile disease.抗 TcdB 抗体,而非 TcdA 抗体,可预防胃肠道和全身艰难梭菌疾病的发生。
J Infect Dis. 2013 Jan 15;207(2):323-30. doi: 10.1093/infdis/jis669. Epub 2012 Nov 2.
7
Diagnosis of Clostridium difficile-associated disease: examination of multiple algorithms using toxin EIA, glutamate dehydrogenase EIA and loop-mediated isothermal amplification.艰难梭菌相关性疾病的诊断:使用毒素酶免疫测定、谷氨酸脱氢酶酶免疫测定和环介导等温扩增对多种算法进行检测
Br J Biomed Sci. 2012;69(3):112-8.
8
Association of relapse of Clostridium difficile disease with BI/NAP1/027.艰难梭菌疾病复发与 BI/NAP1/027 的关联。
J Clin Microbiol. 2012 Dec;50(12):4078-82. doi: 10.1128/JCM.02291-12. Epub 2012 Oct 10.
9
The utility of repeat enzyme immunoassay testing for the diagnosis of Clostridium difficile infection: a systematic review of the literature.重复酶免疫测定法在艰难梭菌感染诊断中的应用:文献系统评价
J Postgrad Med. 2012 Jul-Sep;58(3):194-8. doi: 10.4103/0022-3859.101392.
10
Impact of the type of diagnostic assay on Clostridium difficile infection and complication rates in a mandatory reporting program.诊断检测类型对强制性报告程序中艰难梭菌感染和并发症发生率的影响。
Clin Infect Dis. 2013 Jan;56(1):67-73. doi: 10.1093/cid/cis840. Epub 2012 Sep 25.

艰难梭菌新菌株毒力和分子生物学的变异。

Variations in virulence and molecular biology among emerging strains of Clostridium difficile.

机构信息

Address correspondence to Jimmy D. Ballard,

出版信息

Microbiol Mol Biol Rev. 2013 Dec;77(4):567-81. doi: 10.1128/MMBR.00017-13.

DOI:10.1128/MMBR.00017-13
PMID:24296572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3973386/
Abstract

Clostridium difficile is a Gram-positive, spore-forming organism which infects and colonizes the large intestine, produces potent toxins, triggers inflammation, and causes significant systemic complications. Treating C. difficile infection (CDI) has always been difficult, because the disease is both caused and resolved by antibiotic treatment. For three and a half decades, C. difficile has presented a treatment challenge to clinicians, and the situation took a turn for the worse about 10 years ago. An increase in epidemic outbreaks related to CDI was first noticed around 2003, and these outbreaks correlated with a sudden increase in the mortality rate of this illness. Further studies discovered that these changes in CDI epidemiology were associated with the rapid emergence of hypervirulent strains of C. difficile, now collectively referred to as NAP1/BI/027 strains. The discovery of new epidemic strains of C. difficile has provided a unique opportunity for retrospective and prospective studies that have sought to understand how these strains have essentially replaced more historical strains as a major cause of CDI. Moreover, detailed studies on the pathogenesis of NAP1/BI/027 strains are leading to new hypotheses on how this emerging strain causes severe disease and is more commonly associated with epidemics. In this review, we provide an overview of CDI, discuss critical mechanisms of C. difficile virulence, and explain how differences in virulence-associated factors between historical and newly emerging strains might explain the hypervirulence exhibited by this pathogen during the past decade.

摘要

艰难梭菌是一种革兰氏阳性、产芽孢的生物体,它感染并定植于大肠,产生强效毒素,引发炎症,并导致严重的全身并发症。治疗艰难梭菌感染(CDI)一直很困难,因为这种疾病既是由抗生素治疗引起的,也是由抗生素治疗引起的。三十五年以来,艰难梭菌一直是临床医生面临的治疗挑战,大约 10 年前情况变得更糟。大约 2003 年首次注意到与 CDI 相关的流行疫情暴发有所增加,这些暴发与该病的死亡率突然上升有关。进一步的研究发现,CDI 流行病学的这些变化与产毒力更强的艰难梭菌(现在统称为 NAP1/BI/027 株)的快速出现有关。艰难梭菌新流行株的发现为回顾性和前瞻性研究提供了一个独特的机会,这些研究旨在了解这些菌株如何基本上取代了更多的历史菌株,成为 CDI 的主要病因。此外,对 NAP1/BI/027 株发病机制的详细研究提出了新的假说,解释了这种新兴菌株如何引起严重疾病,以及为何更常与流行有关。在这篇综述中,我们概述了 CDI,讨论了艰难梭菌毒力的关键机制,并解释了历史和新出现的菌株之间在毒力相关因素上的差异如何解释该病原体在过去十年中表现出的超强毒力。