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. 2017 Jan 19;2017:5470241. doi: 10.1155/2017/5470241

Table 3.

Characteristics of E. coli strains used in the study.

Strain Specimen Sero-
group
Phylo-
genetic group
MLST MICa(μg/mL) Growth on
M9 agar supplemented with:
uhpT expression induced by G6Pb Amino acid residue alternations in proteins encoded by glpT, ptsI, cyaA, murA, uhpA, and uhpT genesc
G6P − G6P + G6P+
cAMP+
G3P G6P cyaA glpT murA ptsI uhpA uhpT
SRE257 Urine O1 B2 95 1024 1024 1024 + 1.24 Val399Leu 163~188 deletion
SRE91 Aspiration tube O1 D 648 128 128 32 3.78 155~158 deletion
Phe176Leu
Thr3Ala
SRE49 Urine O25b:H4 B2 131 128 128 128 + NT His716Leu Lys410Arg ND ND
SRE54 Urine O25b:H4 B2 131 64 64 64 + 1.59 His716Leu Ala443Thr
Gly452Asp
SRE237 Urine O25b:H4 B2 131 64 64 64 + 1.59 His716Leu
SRE29 Urine O25b:H4 B2 131 32 32 32 + + 1226.22
SRE252 Urine O25a D 73 32 32 4 3.68 ND Ile171Thr Lys145Asn
SRE280 Ascites O12 D 1486 32 32 32 + 0.56 Ser142Asn
SRE18 Urine ND D 405 16 16 16 + 2.22 Met1Ile
SRE253 Urine O18 B2 95 8 8 8 198.09 His716Leu
SRE40 Decubitus O25a D 501 32 0.5 NT + + 284.05
SRE41 Catheter urine O1 D 648 8 0.5 NT + + 328.56
SRE110 Catheter urine O25b:H4 B2 131 8 0.5 NT + + 190.02
SRE205 Urine ND A 131 8 0.5 NT + + 734.19
SRE227 Pus O1 B2 95 8 0.5 NT + + 247.28
SRE30 Urine O1 D 648 8 0.25 NT + + 719.08
ATCC 25922 NT NT 32 0.5 NT + + 308.69

aFOM MICs were determined in the presence (+) or absence (−) of glucose-6-phosphate (G6P) and/or cAMP.

b E. coli cells were incubated in M9 minimum salt solution in the presence or absence of G6P. The uhpT mRNA levels were determined by real-time RT-PCR, and the data were normalized to rpoD mRNA levels. Induction of uhpT expression by G6P was calculated by dividing the uhpT mRNA level in the presence of G6P by the uhpT mRNA level in the absence of G6P.

cAmino acid mutations found only in strains with reduced FOM susceptibility (MIC ≥ 8 μg/mL) compared with strains with FOM MIC < 1 μg/mL.

ND: not detected. NT: not tested.