Affiliation:
1. Department of Microbiology and Molecular Genetics1 and
2. Molecular Biology Institute,2 University of California, Los Angeles, Los Angeles, California 90095
Abstract
ABSTRACT
The
Yersinia enterocolitica inv
gene encodes the primary invasion factor invasin, which has been previously shown to be critical in the initial stages of infection. The expression of
inv
is influenced by growth phase and temperature and is maximal during late exponential-early stationary phase at 23°C. In addition, motility of
Y. enterocolitica
is regulated by temperature.
Y. enterocolitica
cells are motile when grown at lower temperatures (30°C or below), while bacteria grown at 37°C are nonmotile. This study was initiated to determine the molecular basis for the temperature regulation of
inv
expression. Two mutants were isolated that both showed a significant decrease in invasin expression but are hypermotile when grown at 23°C. The first mutant (JB1A8v) was a result of a random mTn
5
Km insertion into the
uvrC
gene. The
uvrC
mutant JB1A8v demonstrated a significant decrease in
inv
and an increase in
fleB
(encodes flagellin) expression. These results suggest that expression of
inv
and flagellin genes is coordinated at the level of transcription. The second regulatory mutant, JB16v, was a result of a targeted insertion into a locus similar to
sspA
which in
E. coli
encodes a stationary-phase regulator. The
E. coli sspA
gene was cloned and assayed for complementation in both of the regulatory mutants. It was determined that
E. coli sspA
restored invasin expression in both the
uvrC
mutant and the
sspA
mutant. In addition, the complementing clone decreased flagellin levels in these mutants.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
61 articles.
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