Infection and Immunity, February 1999, p. 817-825, Vol. 67, No. 2
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Microbiology II,
Received 11 August 1998/Returned for modification 18 September
1998/Accepted 1 November 1998
Incubation of human epithelial cells with nanomolar concentrations
of chromatographically purified Serratia marcescens
hemolysin (ShlA) caused irreversible vacuolation and subsequent lysis
of the cells. Vacuolation differed from vacuole formation by
Helicobacter pylori VacA. Sublytic doses of ShlA led to a
reversible depletion of intracellular ATP. Restoration to the initial
ATP level was presumably due to the repair of the toxin damage and was
inhibited by cycloheximide. Pores formed in epithelial cells and
fibroblasts without disruption of the plasma membrane, and the pores
appeared to be considerably smaller than those observed in artificial
lipid membranes and in erythrocytes and did not allow the influx of propidium iodide or trypan blue. All cytotoxic effects induced by
isolated recombinant ShlA were also obtained with exponentially growing
S. marcescens cells. The previously suggested role
of the hemolysin in the pathogenicity of S. marcescens is supported by these data.
*
Corresponding author. Mailing address: Mikrobiologie
II, Auf der Morgenstelle 28, D-72076 Tübingen, Germany. Phone:
49-7071-2978848. Fax: 49-7071-294634. E-mail:
ralf.hertle{at}mikrobio.uni-tuebingen.de.
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