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本文引用的文献

1
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.
2
Antibiotics in early life alter the murine colonic microbiome and adiposity.生命早期使用抗生素会改变小鼠结肠微生物群组成和肥胖。
Nature. 2012 Aug 30;488(7413):621-6. doi: 10.1038/nature11400.
3
Suppression of Clostridium difficile in the gastrointestinal tracts of germfree mice inoculated with a murine isolate from the family Lachnospiraceae.无菌小鼠接种来自毛螺菌科的鼠源分离株后,其胃肠道中艰难梭菌的抑制作用。
Infect Immun. 2012 Nov;80(11):3786-94. doi: 10.1128/IAI.00647-12. Epub 2012 Aug 13.
4
Burden of Clostridium difficile on the healthcare system.艰难梭菌对医疗体系的负担。
Clin Infect Dis. 2012 Aug;55 Suppl 2(Suppl 2):S88-92. doi: 10.1093/cid/cis335.
5
Relapse versus reinfection: recurrent Clostridium difficile infection following treatment with fidaxomicin or vancomycin.复发与再感染: fidaxomicin 或万古霉素治疗后的复发性艰难梭菌感染。
Clin Infect Dis. 2012 Aug;55 Suppl 2(Suppl 2):S104-9. doi: 10.1093/cid/cis357.
6
The Clostridium difficile spo0A gene is a persistence and transmission factor.艰难梭菌 spo0A 基因是一个持续存在和传播的因素。
Infect Immun. 2012 Aug;80(8):2704-11. doi: 10.1128/IAI.00147-12. Epub 2012 May 21.
7
Interaction between the intestinal microbiota and host in Clostridium difficile colonization resistance.艰难梭菌定植抵抗中肠道微生物群与宿主的相互作用。
Trends Microbiol. 2012 Jul;20(7):313-9. doi: 10.1016/j.tim.2012.04.001. Epub 2012 May 15.
8
Models for the study of Clostridium difficile infection.艰难梭菌感染的研究模型。
Gut Microbes. 2012 Mar-Apr;3(2):145-67. doi: 10.4161/gmic.19526. Epub 2012 Mar 1.
9
Systematic review of intestinal microbiota transplantation (fecal bacteriotherapy) for recurrent Clostridium difficile infection.系统评价肠道微生物群移植(粪便细菌治疗)治疗复发性艰难梭菌感染。
Clin Infect Dis. 2011 Nov;53(10):994-1002. doi: 10.1093/cid/cir632.
10
Acquisition of spores on gloved hands after contact with the skin of patients with Clostridium difficile infection and with environmental surfaces in their rooms.接触艰难梭菌感染患者皮肤和其病房环境表面后,手套上会获得孢子。
Am J Infect Control. 2012 Aug;40(6):556-8. doi: 10.1016/j.ajic.2011.08.002. Epub 2011 Oct 7.

用于研究艰难梭菌感染和传播的鼠类模型。

Murine models to study Clostridium difficile infection and transmission.

机构信息

Bacterial Pathogenesis Laboratory, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK.

出版信息

Anaerobe. 2013 Dec;24:94-7. doi: 10.1016/j.anaerobe.2013.09.008. Epub 2013 Sep 25.

DOI:10.1016/j.anaerobe.2013.09.008
PMID:24076318
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4089867/
Abstract

Clostridium difficile is the leading cause of antibiotic-associated diarrhea in healthcare facilities worldwide. C. difficile infections are difficult to treat because of the high rate of disease recurrence after antibiotic therapy, leaving few treatment options for patients. C. difficile is also difficult to contain within a healthcare setting due to a highly-transmissible, resistant spore form that challenges standard infection control measures. The recent development of murine infection models to study the interactions between C. difficile, the host and the microbiota are providing novel insight into the mechanisms of pathogenesis and transmission that should guide the development of therapies and intervention measures.

摘要

艰难梭菌是全球医疗保健机构中抗生素相关性腹泻的主要原因。由于抗生素治疗后疾病复发率高,艰难梭菌感染难以治疗,患者的治疗选择有限。由于具有高度传染性和耐药性的孢子形式,艰难梭菌在医疗环境中也难以控制,这给标准的感染控制措施带来了挑战。最近开发的用于研究艰难梭菌、宿主和微生物组之间相互作用的小鼠感染模型,为发病机制和传播机制提供了新的见解,这些见解应指导治疗和干预措施的开发。