Toxin A of Clostridium difficile: production, purification and effect in mouse intestine

Acta Pathol Microbiol Immunol Scand B. 1983 Dec;91(6):395-400. doi: 10.1111/j.1699-0463.1983.tb00066.x.

Abstract

Clostridium difficile produces one diarrhoeogenic toxin designed A, and one cytopathogenic toxin designed B. Toxin A was purified in a four-step-fractionation procedure. In the last purification step the toxin was separated by elution with galactose from an agarose gel. The purified toxin A induced a clear and watery hypersecretion in intestinal loops of mouse, while mixtures of toxin A and B induced a haemorrhagic secretion. At an ED50 value for the purified toxin A of 0.5 microgram there was a brief, optimal hypersecretion after four hours. Like the fluid secretion induced by cholera toxin, that induced by toxin A could be inhibited by chlorpromazine or by depletion of intestinal bile. In contrast to cholera toxin, however, toxin A did not activate intestinal adenylate cyclase--at least not permanently. Antisera which neutralized cholera toxin did not neutralize toxin A, and vice versa.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenylyl Cyclases / metabolism
  • Animals
  • Bacterial Proteins*
  • Bacterial Toxins / biosynthesis
  • Bacterial Toxins / isolation & purification
  • Bacterial Toxins / pharmacology*
  • Bile / physiology
  • Chlorpromazine / pharmacology
  • Cholera Toxin / pharmacology
  • Clostridium / metabolism*
  • Diarrhea / etiology*
  • Enterotoxins / pharmacology
  • Escherichia coli Proteins*
  • Intestinal Mucosa / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL

Substances

  • Bacterial Proteins
  • Bacterial Toxins
  • Enterotoxins
  • Escherichia coli Proteins
  • toxB protein, Clostridium difficile
  • Cholera Toxin
  • heat-labile enterotoxin, E coli
  • Adenylyl Cyclases
  • Chlorpromazine