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An outbreak of toxin A negative, toxin B positive Clostridium difficile-associated diarrhea in a Canadian tertiary-care hospital.加拿大一家三级护理医院爆发了毒素A阴性、毒素B阳性的艰难梭菌相关性腹泻。
Can Commun Dis Rep. 1999 Apr 1;25(7):65-9.
2
Increasing hospitalization and death possibly due to Clostridium difficile diarrheal disease.艰难梭菌腹泻病可能导致住院率和死亡率上升。
Emerg Infect Dis. 1998 Oct-Dec;4(4):619-25. doi: 10.3201/eid0404.980412.
3
A novel toxinotyping scheme and correlation of toxinotypes with serogroups of Clostridium difficile isolates.一种新型艰难梭菌分离株毒素分型方案及毒素型与血清型的相关性
J Clin Microbiol. 1998 Aug;36(8):2240-7. doi: 10.1128/JCM.36.8.2240-2247.1998.
4
Identification of toxin A-negative, toxin B-positive Clostridium difficile by PCR.通过聚合酶链反应鉴定毒素A阴性、毒素B阳性的艰难梭菌。
J Clin Microbiol. 1998 Aug;36(8):2178-82. doi: 10.1128/JCM.36.8.2178-2182.1998.
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Clostridium difficile: a pathogen of the nineties.
Eur J Clin Microbiol Infect Dis. 1998 Mar;17(3):137-41. doi: 10.1007/BF01691108.
6
Survey of incidence of Clostridium difficile infection in Canadian hospitals and diagnostic approaches.加拿大医院艰难梭菌感染发病率及诊断方法调查。
J Clin Microbiol. 1998 Jul;36(7):2076-80. doi: 10.1128/JCM.36.7.2076-2080.1998.
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Clostridium difficile--associated diarrhea.艰难梭菌相关性腹泻
Clin Infect Dis. 1998 May;26(5):1027-34; quiz 1035-6. doi: 10.1086/520276.
8
Antibodies to recombinant Clostridium difficile toxins A and B are an effective treatment and prevent relapse of C. difficile-associated disease in a hamster model of infection.针对重组艰难梭菌毒素A和B的抗体在艰难梭菌感染的仓鼠模型中是一种有效的治疗方法,可预防艰难梭菌相关疾病的复发。
Infect Immun. 1998 May;66(5):2018-25. doi: 10.1128/IAI.66.5.2018-2025.1998.
9
Clostridium difficile-associated diarrhea: epidemiology, risk factors, and infection control.艰难梭菌相关性腹泻:流行病学、危险因素及感染控制
Infect Control Hosp Epidemiol. 1997 Sep;18(9):628-32. doi: 10.1086/647687.
10
Characterization of polymorphisms in the toxin A and B genes of Clostridium difficile.艰难梭菌毒素A和B基因多态性的特征分析
FEMS Microbiol Lett. 1997 Mar 15;148(2):197-202. doi: 10.1111/j.1574-6968.1997.tb10288.x.

一株导致艰难梭菌相关性腹泻医院感染暴发的艰难梭菌毒素A阴性、毒素B阳性菌株的特征分析

Characterization of a toxin A-negative, toxin B-positive strain of Clostridium difficile responsible for a nosocomial outbreak of Clostridium difficile-associated diarrhea.

作者信息

Alfa M J, Kabani A, Lyerly D, Moncrief S, Neville L M, Al-Barrak A, Harding G K, Dyck B, Olekson K, Embil J M

机构信息

Department of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.

出版信息

J Clin Microbiol. 2000 Jul;38(7):2706-14. doi: 10.1128/JCM.38.7.2706-2714.2000.

DOI:10.1128/JCM.38.7.2706-2714.2000
PMID:10878068
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC87004/
Abstract

Clostridium difficile-associated diarrhea (CAD) is a very common nosocomial infection that contributes significantly to patient morbidity and mortality as well as to the cost of hospitalization. Previously, strains of toxin A-negative, toxin B-positive C. difficile were not thought to be associated with clinically significant disease. This study reports the characterization of a toxin A-negative, toxin B-positive strain of C. difficile that was responsible for a recently described nosocomial outbreak of CAD. Analysis of the seven patient isolates from the outbreak by pulsed-field gel electrophoresis indicated that this outbreak was due to transmission of a single strain of C. difficile. Our characterization of this strain (HSC98) has demonstrated that the toxin A gene lacks 1.8 kb from the carboxy repetitive oligopeptide (CROP) region but apparently has no other major deletions from other regions of the toxin A or toxin B gene. The remaining 1.3-kb fragment of the toxin A CROP region from strain HSC98 showed 98% sequence homology with strain 1470, previously reported by M. Weidmann in 1997 (GenBank accession number Y12616), suggesting that HSC98 is toxinotype VIII. The HSC98 strain infecting patients involved in this outbreak produced the full spectrum of clinical illness usually associated with C. difficile-associated disease. This pathogenic spectrum was manifest despite the inability of this strain to alter tight junctions as determined by using in vitro tissue culture testing, which suggested that no functional toxin A was produced by this strain.

摘要

艰难梭菌相关性腹泻(CAD)是一种非常常见的医院感染,对患者的发病率和死亡率以及住院费用有重大影响。以前,毒素A阴性、毒素B阳性的艰难梭菌菌株被认为与临床上显著的疾病无关。本研究报告了一株毒素A阴性、毒素B阳性的艰难梭菌菌株的特征,该菌株导致了最近描述的一次医院内CAD暴发。通过脉冲场凝胶电泳对此次暴发中7例患者分离株的分析表明,此次暴发是由单一菌株的艰难梭菌传播所致。我们对该菌株(HSC98)的特征分析表明,毒素A基因在羧基重复寡肽(CROP)区域缺失了1.8 kb,但毒素A或毒素B基因的其他区域显然没有其他主要缺失。来自HSC98菌株的毒素A CROP区域剩余的1.3 kb片段与M. Weidmann在1997年报道的1470菌株(GenBank登录号Y12616)显示出98%的序列同源性,表明HSC98是毒素型VIII。感染此次暴发中患者的HSC98菌株产生了通常与艰难梭菌相关性疾病相关的全谱临床病症。尽管通过体外组织培养试验确定该菌株无法改变紧密连接,这表明该菌株未产生功能性毒素A,但这种致病谱仍然存在。