Affiliation:
1. Institute of Microbiology and Genetics, Vienna Biocenter, University of Vienna, A-1030 Vienna, Austria
Abstract
ABSTRACT
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.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
136 articles.
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