Clostridium difficile toxin A perturbs cytoskeletal structure and tight junction permeability of cultured human intestinal epithelial monolayers.

Abstract

Toxin A of Clostridium difficile causes severe inflammatory enterocolitis in man and animals that appears to be mediated in part by acute inflammatory cells that migrate into the toxin A-exposed mucosa. To determine the direct effects of toxin A on intestinal epithelial permeability and structure in the ab- sence of other modulating factors, we used cultured mono- layers of a human intestinal epithelial cell line (T84). A toxin A concentration of 7 X 10-1 ,ug/ml (3 X i0-' M) nearly abolished monolayer transepithelial resistance within 6-8 h. This marked permeability defect occurred while the monolayers were still confluent. Dual sodium-mannitol flux studies local- ized the permeability defect to the intercellular tight junction. Cytotoxicity assays and morphological evaluation using No- marski optics and electron microscopy failed to demonstrate any evidence of cell damage at the time the maximum resis- tance response was observed. Fluorescent staining for F actin, however, revealed a marked decrease in fluorescent intensity in toxin-treated monolayers versus controls. These data show that toxin A can directly affect the barrier function of this model intestinal epithelium and initially does so by selectively enhancing tight junction permeability. Furthermore, cytoskeletal structure is markedly altered over the same time course, although the integrity of individual cells is maintained. Be- cause the cytoskeleton of intestinal epithelial cells is known to be capable of regulating tight junction permeability, we specu- late that the above effects of toxin A on epithelial barrier function result from alterations of the cytoskeleton. Purification oftoxin A. Toxin A was purified to homogeneity (sin- gle band at 229 kD by SDS-PAGE) from broth culture supernatants of 1516