Affiliation:
1. College of Veterinary Medicine, North Carolina State University, 4700 Hillsborough Street, Raleigh, North Carolina 27606
Abstract
ABSTRACT
The csr regulatory system of
Salmonella
regulates the expression of the genes of
Salmonella
pathogenicity island 1 (SPI1) required for the invasion of epithelial cells. This system consists of the posttranscriptional regulator CsrA and an untranslated regulatory RNA, CsrB, that opposes the action of CsrA. Here we identify and characterize the role of a second regulatory RNA, CsrC, whose ortholog was discovered previously in
Escherichia coli
. We show that a mutant of
csrC
has only mild defects in invasion and the expression of SPI1 genes, as does a mutant of
csrB
, but that a double
csrB csrC
mutant is markedly deficient in these properties, suggesting that the two regulatory RNAs play redundant roles in the control of invasion. We further show that CsrC, like CsrB, is controlled by the BarA/SirA two-component regulator but that a
csrB csrC
mutant exhibits a loss of invasion equivalent to that of a
barA
or
sirA
mutant, indicating that much of the effect of BarA/SirA on invasion functions through its control of CsrB and CsrC. In addition to their control by BarA/SirA, each regulatory RNA is also controlled by other components of the csr system. The loss of
csrB
was found to increase the level of CsrC by sevenfold, while the loss of
csrC
increased CsrB by nearly twofold. Similarly, the overexpression of
csrA
increased CsrC by nearly 11-fold and CsrB by 3-fold and also significantly increased the stability of both RNAs.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
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