Research Article

Mechanism of Reduced Susceptibility to Fosfomycin in Escherichia coli Clinical Isolates

Table 3

Characteristics of E. coli strains used in the study.

StrainSpecimenSero-
group
Phylo-
genetic group
MLSTMIC(μg/mL)Growth on
M9 agar supplemented with:
uhpT expression induced by G6P Amino acid residue alternations in proteins encoded by glpT, ptsI, cyaA, murA, uhpA, and uhpT genes
G6P −G6P +G6P+
cAMP+
G3PG6PcyaAglpTmurAptsIuhpAuhpT

SRE257UrineO1B295102410241024+1.24Val399Leu163~188 deletion
SRE91Aspiration tubeO1D648128128323.78155~158 deletion
Phe176Leu
Thr3Ala
SRE49UrineO25b:H4B2131128128128+NTHis716LeuLys410ArgNDND
SRE54UrineO25b:H4B2131646464+1.59His716LeuAla443Thr
Gly452Asp
SRE237UrineO25b:H4B2131646464+1.59His716Leu
SRE29UrineO25b:H4B2131323232++1226.22
SRE252UrineO25aD73323243.68NDIle171ThrLys145Asn
SRE280AscitesO12D1486323232+0.56Ser142Asn
SRE18UrineNDD405161616+2.22Met1Ile
SRE253UrineO18B295888198.09His716Leu
SRE40DecubitusO25aD501320.5NT++284.05
SRE41Catheter urineO1D64880.5NT++328.56
SRE110Catheter urineO25b:H4B213180.5NT++190.02
SRE205UrineNDA13180.5NT++734.19
SRE227PusO1B29580.5NT++247.28
SRE30UrineO1D64880.25NT++719.08
ATCC 25922NTNT320.5NT++308.69

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