Infection and Immunity, January 2001, p. 508-517, Vol. 69, No. 1
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.1.508-517.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Department of Veterinary and Biomedical Sciences, University of Nebraska, Lincoln, Nebraska 68583,1 and Kuzell Institute for Arthritis and Infectious Diseases, California Pacific Medical Center, San Francisco, California 941152
Received 14 July 2000/Returned for modification 21 September 2000/Accepted 3 October 2000
Successful parasitism of host cells by intracellular pathogens
involves adherence, entry, survival, intracellular replication, and
cell-to-cell spread. Our laboratory has been examining the role of
early events, adherence and entry, in the pathogenesis of the
facultative intracellular pathogen Legionella pneumophila. Currently, the mechanisms used by L. pneumophila to gain
access to the intracellular environment are not well understood. We
have recently isolated three loci, designated enh1,
enh2, and enh3, that are involved in the
ability of L. pneumophila to enter host cells. One of the
genes present in the enh1 locus, rtxA, is
homologous to repeats in structural toxin genes (RTX) found in many
bacterial pathogens. RTX proteins from other bacterial species are
commonly cytotoxic, and some of them have been shown to bind to
2 integrin receptors. In the current study, we
demonstrate that the L. pneumophila rtxA gene is involved
in adherence, cytotoxicity, and pore formation in addition to its role
in entry. Furthermore, an rtxA mutant does not replicate as
well as wild-type L. pneumophila in monocytes and is less
virulent in mice. Thus, we conclude that the entry gene
rtxA is an important virulence determinant in L. pneumophila and is likely to be critical for the production of
Legionnaires' disease in humans.
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