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Appl. Environ. Microbiol., Mar 1997, 844-850, Vol 63, No. 3
SJ Clough, AB Flavier, MA Schell and TP Denny
A complex network regulates virulence in Ralstonia solanacearum (formerly
Pseudomonas solanacearum); central to this system is PhcA, a LysR-type
transcriptional regulator. We report here that two PhcA-regulated virulence
factors, endoglucanase (Egl) and acidic exopolysaccharide I (EPS I), and
motility are expressed differentially during exponential growth in batch
cultures. Tests with strains carrying lacZ fusions in a wild-type genetic
background revealed that expression (on a per-cell basis) of phcA was
constant but expression of egl and epsB increased 20- to 50-fold during
multiplication from 1 x 10(sup7) to 5 x 10(sup8) CFU/ml. Expression of
xpsR, an intermediate regulator downstream of PhcA in the regulatory
cascade for eps expression, was similar to that of epsB and egl. Motility
track photography revealed that all strains were essentially nonmotile at
10(sup6) CFU/ml. As cell density increased, 30 to 50% of wild-type cells
were motile between 10(sup7) and 10(sup8) CFU/ml, but this population was
again nonmotile at 10(sup9) CFU/ml. In contrast, about 60% of the cells of
phcB and phcA mutants remained motile at 10(sup9) CFU/ml. Expression of
phcB, which is not positively regulated by PhcA, was the inverse of epsB,
egl, and xpsR (i.e., it decreased 20-fold at high cell density). PhcB is
essential for production of an extracellular factor, tentatively identified
as 3-hydroxypalmitic acid methyl ester (3-OH PAME), that might act as an
exponential-phase signal to activate motility or expression of virulence
genes. However, growth of the lacZ fusion strains in medium containing
excess 3-OH PAME did not result in motility or expression of virulence
genes at dramatically lower cell densities, suggesting that 3-OH PAME is
not the only factor controlling these traits.
Copyright © 1997, American Society for Microbiology
Differential Expression of Virulence Genes and Motility in Ralstonia (Pseudomonas) solanacearum during Exponential Growth
Departments of Plant Pathology and Microbiology, University of Georgia, Athens, Georgia 30602
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