UDP-glucose deficiency in a mutant cell line protects against glucosyltransferase toxins from Clostridium difficile and Clostridium sordellii

J Biol Chem. 1996 Mar 22;271(12):6925-32. doi: 10.1074/jbc.271.12.6925.

Abstract

We have previously isolated a fibroblast mutant cell with high resistance to the two Rho-modifying glucosyltransferase toxins A and B of Clostridium difficile. We demonstrate here a low level of UDP-glucose in the mutant, which explains its toxin resistance since: (i) to obtain a detectable toxin B-mediated Rho modification in lysates of mutant cells, addition of UDP-glucose was required, and it promoted the Rho modification dose-dependently; (ii) high pressure liquid chromatography analysis of nucleotide extracts of cells indicated that the level of UDP-glucose in the mutant (0.8 nmol/10(6) cells) was lower than in the wild type (3.7 nmol/10(6) cells); and (iii) sensitivity to toxin B was restored upon microinjection of UDP-glucose. Using the mutant as indicator cell we also found that the related Clostridium sordellii lethal toxin is a glucosyltransferase which requires UDP-glucose as a cofactor. Like toxin B it glucosylated 21-23-kDa proteins in cell lysates, but Rho was not a substrate for lethal toxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins*
  • Bacterial Toxins / toxicity*
  • Cell Line
  • Clostridioides difficile / metabolism*
  • Clostridium / metabolism*
  • Cricetinae
  • Cricetulus
  • GTP-Binding Proteins / metabolism
  • Glucosyltransferases / toxicity*
  • Microinjections
  • Mutation
  • Uridine Diphosphate Glucose / deficiency*

Substances

  • Bacterial Proteins
  • Bacterial Toxins
  • lethal toxin LT, Clostridium sordellii
  • toxB protein, Clostridium difficile
  • Glucosyltransferases
  • GTP-Binding Proteins
  • Uridine Diphosphate Glucose