» Articles » PMID: 8406734

Clostridium Difficile Colitis and Diarrhea

Overview
Specialty Gastroenterology
Date 1993 Sep 1
PMID 8406734
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Clostridium difficile is now regarded as the most prevalent nosocomial pathogen, infecting as many as a quarter of hospitalized patients. The pathophysiology of infection with this unusual enteric pathogen involves alteration of the normal enteric flora by antibiotics, ingestion of spores, and colonization by C. difficile. The organism then releases potent exotoxins that produce an inflammatory colitis and diarrhea. A spectrum of host responses occurs, ranging from the asymptomatic carrier state to life-threatening pseudomembranous colitis. Effective therapy with vancomycin or metronidazole is available, but relapses occur in 15% to 20% of patients and may necessitate multiple courses of therapy.

Citing Articles

Introducing the sporobiota and sporobiome.

Tetz G, Tetz V Gut Pathog. 2017; 9:38.

PMID: 28680484 PMC: 5493122. DOI: 10.1186/s13099-017-0187-8.


Practical considerations in the use of outpatient antimicrobial therapy for musculoskeletal infections.

Marculescu C, Berbari E, Cantey J, Osmon D Mayo Clin Proc. 2012; 87(1):98-105.

PMID: 22212975 PMC: 3498104. DOI: 10.1016/j.mayocp.2011.11.005.


The enterotoxicity of Clostridium difficile toxins.

Sun X, Savidge T, Feng H Toxins (Basel). 2011; 2(7):1848-80.

PMID: 22069662 PMC: 3153265. DOI: 10.3390/toxins2071848.


The insect peptide coprisin prevents Clostridium difficile-mediated acute inflammation and mucosal damage through selective antimicrobial activity.

Kang J, Hwang J, Nam H, Ahn K, Seok H, Kim S Antimicrob Agents Chemother. 2011; 55(10):4850-7.

PMID: 21807975 PMC: 3186999. DOI: 10.1128/AAC.00177-11.


Clostridium difficile toxin A decreases acetylation of tubulin, leading to microtubule depolymerization through activation of histone deacetylase 6, and this mediates acute inflammation.

Nam H, Kang J, Kim S, Ahn K, Seok H, Park S J Biol Chem. 2010; 285(43):32888-32896.

PMID: 20696758 PMC: 2963380. DOI: 10.1074/jbc.M110.162743.