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Journal of Bacteriology, June 1999, p. 3433-3437, Vol. 181, No. 11
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Growth Phase-Regulated Induction of
Salmonella-Induced Macrophage Apoptosis Correlates with
Transient Expression of SPI-1 Genes
Urban
Lundberg,
Ursula
Vinatzer,
Daniela
Berdnik,§
Alexander
von Gabain, and
Manuela
Baccarini*
Institute of Microbiology and Genetics,
Vienna Biocenter, University of Vienna, A-1030 Vienna, Austria
Received 16 July 1998/Accepted 30 March 1999
Invasive Salmonella has been reported to induce
apoptosis in a fraction of infected macrophages within 2 to 14 h
from the time of infection by a mechanism involving the type III
secretion machinery encoded by the Salmonella pathogenicity
island 1 (SPI-1). Here, we show that bacteria in the transition from
logarithmic to stationary phase cause 90% of the macrophages to
undergo phagocytosis-independent, caspase-mediated apoptosis within 30 to 60 min of infection. The ability of Salmonella to induce
this rapid apoptosis was growth phase regulated and cell type
restricted, with epithelial cells being resistant. Apoptosis induction
was also abrogated by disruption of the hilA gene (encoding
a regulator of SPI-1 genes) and by the expression of a constitutively
active PhoPQ. hilA itself and a subset of SPI-1 genes were
transiently expressed during aerobic growth in liquid medium.
Interestingly, however, hilA was found to be required only
for the expression of the prgH gene, while sipB, invA, and invF were expressed
in a hilA-independent manner. The expression of SPI-1 genes
and the secretion of invasion-associated proteins correlated temporally
with the induction of apoptosis and are likely to represent its
molecular basis. Thus, growth phase transition regulates the expression
and secretion of virulence determinants and represents the most
efficient environmental cue for apoptosis induction reported to date.
*
Corresponding author. Mailing address: Vienna
Biocenter, Department of Cell- and Microbiology, Institute for
Microbiology and Genetics, Dr. Bohr Gasse 9, A-1030 Vienna, Austria.
Phone: 43 (1) 4277-54607. Fax: 43 (1) 4277-9546. E-mail:
manuela{at}gem.univie.ac.at.

Present address: Department of Bacteriology, Baxter Hyland-Immuno,
A-2304 Orth/Donau,
Austria.

Present address: Institute for Medical Biology, A-1090 Vienna,
Austria.
§
Present address: Institute of Molecular Pathology, A-1030 Vienna,
Austria.
Journal of Bacteriology, June 1999, p. 3433-3437, Vol. 181, No. 11
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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