Literature DB >> 399365

Antibiotic-associated pseudomembranous colitis.

J G Bartlett.   

Abstract

C. difficile was originally described in 1935 but was of minimal clinical interest until recently, when studies showed it to be the cause of antibiotic-associated PMC. Intestinal complications caused by C. difficile appear almost exclusively in conjunction with exposure to antibiotics. Evidence that supports the etiologic role of this organism in antibiotic-associated PMC comes from both bacteriological studies and tissue culture assays. Tissue culture assays have been used to demonstrate that the stool supernate from nearly all patients with anatomically confirmed PMC contains a cytotoxin that is neutralized with Clostridium sordellii antitoxin. The cytotoxin has rarely been found in persons without gastro-intestinal complications related to antibiotic usage. Cultures of stool from patients with anti-biotic-associated PMC usually yield C. difficile, which is encountered only infrequently in the fecal flora of healthy persons. Strains of C. difficile have been shown to cause a similar disease in experimental animals administered antibiotics or intracecal injections of broth cultures of C. difficile. According to the antitoxin neutralization tests and biochemical purification studies done to date, C. difficile is the only organism that produces a cytotoxin similar or identical to the cytotoxin encountered in stools of patients with PMC. The toxin is a high-molecular-weight protein that appears to cause changes in the permeability of cells in tissue culture. However, the mechanism of its action on intestinal mucosa and the cause of its production with antibiotic exposure in clinical settings have not been well defined.

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Year:  1979        PMID: 399365     DOI: 10.1093/clinids/1.3.530

Source DB:  PubMed          Journal:  Rev Infect Dis        ISSN: 0162-0886


  56 in total

Review 1.  Antibiotic-associated diarrhoea. A costly problem.

Authors:  T V Riley
Journal:  Pharmacoeconomics       Date:  1996-07       Impact factor: 4.981

2.  Clostridium difficile toxin A induces a specific antisecretory factor which protects against intestinal mucosal damage.

Authors:  J Torres; E Jennische; S Lange; I Lönnroth
Journal:  Gut       Date:  1991-07       Impact factor: 23.059

3.  Clostridium difficile: a pathogen of the nineties.

Authors:  T V Riley
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1998-03       Impact factor: 3.267

4.  Application of whole-cell DNA restriction endonuclease profiles to the epidemiology of Clostridium difficile-induced diarrhea.

Authors:  E J Kuijper; J H Oudbier; W N Stuifbergen; A Jansz; H C Zanen
Journal:  J Clin Microbiol       Date:  1987-04       Impact factor: 5.948

5.  Clostridium difficile colitis secondary to intravenous vancomycin.

Authors:  J R Hecht; E J Olinger
Journal:  Dig Dis Sci       Date:  1989-01       Impact factor: 3.199

6.  Effective and reduced-cost modified selective medium for isolation of Clostridium difficile.

Authors:  Michelle M Nerandzic; Curtis J Donskey
Journal:  J Clin Microbiol       Date:  2008-12-10       Impact factor: 5.948

7.  Lincomycin increases the half-life of beta-lactamase mRNA.

Authors:  O Matsushita; A Okabe; H Hayashi; Y Kanemasa
Journal:  Antimicrob Agents Chemother       Date:  1989-06       Impact factor: 5.191

8.  Rapid method to detect shiga toxin and shiga-like toxin I based on binding to globotriosyl ceramide (Gb3), their natural receptor.

Authors:  S Ashkenazi; T G Cleary
Journal:  J Clin Microbiol       Date:  1989-06       Impact factor: 5.948

9.  Colonization of the large bowel by Clostridium difficile in healthy infants: quantitative study.

Authors:  P L Stark; A Lee; B D Parsonage
Journal:  Infect Immun       Date:  1982-03       Impact factor: 3.441

10.  Comparison of methods for recovery of Clostridium difficile from an environmental surface.

Authors:  B P Buggy; K H Wilson; R Fekety
Journal:  J Clin Microbiol       Date:  1983-08       Impact factor: 5.948

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