A. Ritter et al., TRANSFER-RNA GENES AND PATHOGENICITY ISLANDS - INFLUENCE ON VIRULENCEAND METABOLIC PROPERTIES OF UROPATHOGENIC ESCHERICHIA-COLI, Molecular microbiology, 17(1), 1995, pp. 109-121
The uropathogenic Escherichia coli strain 536 (O6:K15:H31) carries two
unstable DNA regions on its chromosome which were termed pathogenicit
y islands (Pais). Both pathogenicity islands, Pai I and Pai II, are in
corporated into tRNA specific loci: Pai I is located in the tRNA gene
for selenocysteine (selC), and Pai II is integrated in the leucine-spe
cific tRNA locus leuX. Mutant strain 536-21 has lost the two pathogeni
city islands together with the intact tRNA genes. While 536 is a virul
ent strain, 536-21 has lost a number of properties, including in vivo
virulence. In previous publications we reported that the genes coding
for two haemolysins (hlyI, hlyII) and P-related fimbria (prf) are loca
ted on the Pais. In this paper, we demonstrate that the expression of
other gene products influencing metabolic properties in addition to in
vivo virulence are strongly dependent on the intact tRNA loci selC an
d leuX. In order to determine the influence of the two tRNAs on the ex
pression of these properties, the genes selC and leuX were cloned from
the genome of strain 536 and then introduced into the mutant 536-21.
Our results clearly show that the selenocysteine-specific tRNA (tRNA(S
ec)) directly influences the ability of the bacteria to grow under ana
erobic conditions, because selenocysteine is part of the enzyme format
e dehydrogenase (FDH) which is involved in mixed acid fermentation. Th
e rare leucine-specific tRNA(5)(Leu), encoded by leuX, influences a nu
mber of properties including type 1 fimbria production, flagellation a
nd motility, production of enterobactin and serum resistance, and is a
lso necessary for full in vivo virulence. While the tRNA(Sec) is direc
tly involved in the production of FDHs, the leuX specific tRNA(5)(Leu)
appears to influence the expression of various factors through specif
ic transcriptional or translational control mechanisms.