Affiliation:
1. Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, California 93106
Abstract
ABSTRACT
Escherichia coli ssrA
encodes a small stable RNA molecule, tmRNA, that has many diverse functions, including tagging abnormal proteins for degradation, supporting phage growth, and modulating the activity of DNA binding proteins. Here we show that
ssrA
plays a role in
Salmonella enterica
serovar Typhimurium pathogenesis and in the expression of several genes known to be induced during infection. Moreover, the phage-like attachment site,
attL
, encoded within
ssrA
, serves as the site of integration of a region of
Salmonella
-specific sequence; adjacent to the 5′ end of
ssrA
is another region of
Salmonella
-specific sequence with extensive homology to predicted proteins encoded within the unlinked
Salmonella
pathogenicity island SPI4.
S. enterica
serovar Typhimurium
ssrA
mutants fail to support the growth of phage P22 and are delayed in their ability to form viable phage particles following induction of a phage P22 lysogen. These data indicate that
ssrA
plays a role in the pathogenesis of
Salmonella
, serves as an attachment site for
Salmonella
-specific sequences, and is required for the growth of phage P22.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
101 articles.
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