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 prote
ins. Here we show that ssrA plays a role in Salmonella enterica serovar Typ
himurium pathogenesis and in the expression of several genes known to be in
duced during infection, Moreover, the phage-like attachment site, attL, enc
oded within ssrA, serves as the site of integration of a region of Salmonel
la-specific sequence; adjacent to the 5' end of ssrA is another region of S
almonella-specific sequence with extensive homology to predicted proteins e
ncoded within the unlinked Salmonella pathogenicity island SPI4. S. enteric
a serovar Typhimurium ssrA mutants fail to support the growth of phage P22
and are delayed in their ability to form viable phage particles following i
nduction of a phage P22 lysogen, These data indicate that ssrA plays a role
in the pathogenesis of Salmonella, serves as an attachment site for Salmon
ella-specific sequences, and is required for the growth of phage P22.