A thermolabile extracellular entero-cytolysin (EC) from Vibrio cholera
e non-01 was purified by ammonium sulphate fractionation, DE-52 cellul
ose ion exchange chromatography, gel-filtration on Ultrogel AcA-44 and
high performance liquid chromatography on a Mono Q. The purified EC h
ad a molecular weight of 63 kD and an isoelectric point of 6.2. It was
not inactivated by cholesterol or 5.5'-dithio-bis(2-nitrobenzoic acid
), nor activated by dithiothreitol. EC had no immunological cross-reac
tivity with cholera toxin. The EC caused fluid accumulation in the int
estines of infant rabbits, death of mice by intravenous injection, and
increased vascular permeability in the paw oedema test in mice. V. ch
olerae non-01 EC lysed erythrocytes from various species and cultured
cells (CHO, L-929, L-41, HEp-2, Vero, MDCK and BHK-21). In contrast to
cholera toxin, EC caused crude destruction of target cells. The EC ca
used hemolysis by a colloid-osmotic mechanism due to the formation of
hydrophilic pores of 1.8-2.0 nm diameter in the cell membrane. This EC
also was able to open pores in lipid membranes. The induced channels
were anion-selective and had a diameter of 1.8-2.0 nm.