Affiliation:
1. Department of Microbiology and Immunology, Northwestern University Medical School, Chicago, Illinois 60611
Abstract
ABSTRACT
When
Legionella pneumophila
grows on agar plates, it secretes a surfactant that promotes flagellum- and pilus-independent “sliding” motility. We isolated three mutants that were defective for surfactant. The first two had mutations in genes predicted to encode cytoplasmic enzymes involved in lipid metabolism. These genes mapped to two adjacent operons that we designated
bbcABCDEF
and
bbcGHIJK
. Backcrossing and complementation confirmed the importance of the
bbc
genes and suggested that the
Legionella
surfactant is lipid containing. The third mutant had an insertion in
tolC
. TolC is the outer membrane part of various trimolecular complexes involved in multidrug efflux and type I protein secretion. Complementation of the
tolC
mutant restored sliding motility. Mutants defective for an inner membrane partner of TolC also lacked a surfactant, confirming that TolC promotes surfactant secretion.
L. pneumophila
(
lspF
) mutants lacking type II protein secretion (T2S) are also impaired for a surfactant. When the
tolC
and
lspF
mutants were grown next to each other, the
lsp
mutant secreted surfactant, suggesting that TolC and T2S conjoin to mediate surfactant secretion, with one being the conduit for surfactant export and the other the exporter of a molecule that is required for induction or maturation of surfactant synthesis/secretion. Although the surfactant was not required for the extracellular growth, intracellular infection, and intrapulmonary survival of
L. pneumophila
, it exhibited antimicrobial activity toward seven other species of
Legionella
but not toward various non-
Legionella
species. These data suggest that the surfactant provides
L. pneumophila
with a selective advantage over other legionellae in the natural environment.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
36 articles.
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