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1 Escherichia coli strains, O157:H7 Sakai and uropathogenic 536, and we use DLA mapping to identify mi
2 s comprised of 22 isolates, all belonging to uropathogenic and bacteremic E. coli strains previously
4 TE protein produced by Shigella flexneri 2a, uropathogenic and enteroaggregative Escherichia coli str
7 al and avian pathogenic E. coli strains, and uropathogenic and neonatal meningitis E. coli strains.
8 erates a soluble molecular net that captures uropathogenic bacteria and facilitates their clearance.
10 as traditional clinical thinking would hold, uropathogenic bacteria direct a complex, intracellular c
12 pecies-specific detection of as few as 2,600 uropathogenic bacteria in culture, inoculated urine, and
13 y available probiotic capable of eradicating uropathogenic bacteria make targeted probiotic preventio
14 ulate that urea can potentially be sensed by uropathogenic bacteria to initiate infection program.
18 own by PFGE to be closely related to a human uropathogenic CgA strain, was found to cluster with the
19 n of the antimicrobial resistant profiles of uropathogenic clinical isolates in Mueller-Hinton media
20 etically distant strains of E. coli, from an uropathogenic clonal complex ST14 and fluoroquinolone-re
24 pathogenic E. coli (ExPEC) and include human uropathogenic E. coli (UPEC) and avian pathogenic E. col
25 del and was significantly less virulent than uropathogenic E. coli (UPEC) CFT073 in a mouse sepsis mo
26 totransporter that is known to contribute to uropathogenic E. coli (UPEC) colonisation of the urinary
31 nic pathotypes of E. coli, the definition of uropathogenic E. coli (UPEC) remains phenomenologic, wit
32 ins from enteropathogenic E. coli (EPEC) and uropathogenic E. coli (UPEC) shows that the EPEC protein
33 analysis of the draft genome sequences of 11 uropathogenic E. coli (UPEC) strains isolated from two t
34 lated proteins is critical in the ability of uropathogenic E. coli (UPEC) to colonize and invade the
35 on markedly reduced the ability of infecting uropathogenic E. coli (UPEC) to grow and sustain infecti
37 erichia coli (ExPEC) strains, referred to as uropathogenic E. coli (UPEC), causes most uncomplicated
38 morrhagic E. coli (EHEC) and extraintestinal uropathogenic E. coli (UPEC), despite being very highly
39 easurements were conducted on 837 samples of uropathogenic E. coli (UPEC), including 268 ESBL(+) and
40 genic Escherichia coli (EHEC), and UpaG from uropathogenic E. coli (UPEC), we present three represent
41 recently identified as a vaccine target for uropathogenic E. coli (UPEC)-mediated urinary tract infe
47 e urinary tract infection model, A-ICs bound uropathogenic E. coli and responded by acidifying the ur
49 c sensor to selectively and sensitive detect uropathogenic E. coli cells (E. coli UTI89) using artifi
52 against Escherichia coli strains, including uropathogenic E. coli CFT073 and UTI89, enterohemorrhagi
53 ry concentration (MIC) value is observed for uropathogenic E. coli CFT073 relative to Amp/Amx, and ti
55 d by the urinary tract mucosa in response to uropathogenic E. coli challenge and acts in innate immun
57 to urinary catheters and ability to prevent uropathogenic E. coli from colonizing urinary catheters
61 erric iron in the growth medium of wild-type uropathogenic E. coli induced the expression of qseBC in
62 ced by injecting 100 million HlyA-producing, uropathogenic E. coli into the urinary bladder of BALB/c
63 nst challenge with a broad range of clinical uropathogenic E. coli isolates and produced immunity tha
64 genes to a well-characterized collection of uropathogenic E. coli isolates to compare the discrimina
68 ke inflammation suppressor genes A and B) of uropathogenic E. coli strain CFT073, homologs of the Shi
72 antly less prevalent or functional among the uropathogenic E. coli strains (both in 6% of strains) th
73 fecal-commensal, intestinal pathogenic, and uropathogenic E. coli strains all displayed similar grow
74 linked next to the dsdCXA locus in 24 of 67 uropathogenic E. coli strains but are found in only 1 of
76 vat, fyuA, and chuA, highly associated with uropathogenic E. coli strains that can distinguish three
81 s for the subversion of TLR signaling by the uropathogenic E. coli virulence factor TcpC and furnish
83 r the generation of a protective response to uropathogenic E. coli, its importance in innate immunity
84 iofilms formed by 3 diverse human pathogens, uropathogenic E. coli, nontypeable Haemophilus influenza
85 ture to FimH, the type 1 fimbrial adhesin of uropathogenic E. coli, which shows shear-dependent bindi
94 of the O antigen ligase gene, waaL, from the uropathogenic E. coliisolate NU14 results in a strain th
95 t ineffective, inflammatory response against uropathogenic, E. coli-induced, acute pyelonephritis.
96 ladder epithelial cells were challenged with uropathogenic Escherichia coli (CFT073) and microbial PA
97 ession and attenuates enterohaemorrhagic and uropathogenic Escherichia coli (EHEC and UPEC), Salmonel
99 the FmlH adhesin, has been shown to provide uropathogenic Escherichia coli (UPEC) a fitness advantag
101 Urinary tract infections (UTIs) caused by uropathogenic Escherichia coli (UPEC) affect 150 million
102 Urinary tract infections (UTIs) caused by uropathogenic Escherichia coli (UPEC) are a significant
106 mmon and in general are caused by intestinal uropathogenic Escherichia coli (UPEC) ascending via the
108 ction of the prostate by clinically relevant uropathogenic Escherichia coli (UPEC) can initiate and e
114 Invasion of bladder epithelial cells by uropathogenic Escherichia coli (UPEC) contributes to ant
116 describe the whole bladder transcriptome of uropathogenic Escherichia coli (UPEC) cystitis in mice u
118 The metV genomic island in the chromosome of uropathogenic Escherichia coli (UPEC) encodes a putative
119 While in transit within and between hosts, uropathogenic Escherichia coli (UPEC) encounters multipl
120 Here, we show in a murine model of UTI that uropathogenic Escherichia coli (UPEC) established quiesc
121 elial cells (BECs) that expels intracellular uropathogenic Escherichia coli (UPEC) from their intrace
122 binding, invasion, and biofilm formation of uropathogenic Escherichia coli (UPEC) in the host urothe
123 s bladder epithelial binding and invasion by uropathogenic Escherichia coli (UPEC) in the initial sta
127 Urinary tract infection (UTI) caused by uropathogenic Escherichia coli (UPEC) is a substantial e
128 The pathogenesis of pyelonephritis caused by uropathogenic Escherichia coli (UPEC) is not well unders
142 is isolate TOP52 was compared to that of the uropathogenic Escherichia coli (UPEC) isolate UTI89 in a
143 Here, we show that Hfq is critical for the uropathogenic Escherichia coli (UPEC) isolate UTI89 to e
147 urinary tract infections (UTI), cystitis by uropathogenic Escherichia coli (UPEC) occurs through an
149 rostatitis cases are caused by Gram-negative uropathogenic Escherichia coli (UPEC) or Gram-positive E
150 tandem mass spectrometry to characterize the uropathogenic Escherichia coli (UPEC) outer membrane sub
153 ated urinary tract infection (UTI) caused by uropathogenic Escherichia coli (UPEC) represents a preva
156 ed transurethrally with the cystitis-derived uropathogenic Escherichia coli (UPEC) strain UTI89.
165 usly shown to contribute to the virulence of uropathogenic Escherichia coli (UPEC) within the urinary
168 (UTIs), the majority of which are caused by uropathogenic Escherichia coli (UPEC), afflict nearly 60
169 tract infections (UTIs), primarily caused by uropathogenic Escherichia coli (UPEC), annually affect o
170 tract infections (UTI), primarily caused by uropathogenic Escherichia coli (UPEC), are one of the le
171 t infections (UTIs), predominantly caused by uropathogenic Escherichia coli (UPEC), belong to the mos
172 re fundamental for keeping kidneys free from uropathogenic Escherichia coli (UPEC), but we have shown
173 (CNF1), a toxin produced by many strains of uropathogenic Escherichia coli (UPEC), constitutively ac
177 cal for colonization of the urinary tract by uropathogenic Escherichia coli (UPEC), mediate opposing
178 formation and remove established biofilms of uropathogenic Escherichia coli (UPEC), Pseudomonas aerug
179 nfections (UTIs) have complex dynamics, with uropathogenic Escherichia coli (UPEC), the major causati
180 estigated deployment of this pathway against uropathogenic Escherichia coli (UPEC), the major cause o
185 haracterize the adaptive immune responses to uropathogenic Escherichia coli (UPEC), the predominant u
187 ulator of stress resistance and virulence in uropathogenic Escherichia coli (UPEC), the principal cau
191 1 pili (T1P) are major virulence factors for uropathogenic Escherichia coli (UPEC), which cause both
192 pe 1 pili are important virulence factors in uropathogenic Escherichia coli (UPEC), which cause the m
193 a key event in the pathogenesis mediated by uropathogenic Escherichia coli (UPEC), yet the mechanism
210 e show that purified CdiA-CT(536) toxin from uropathogenic Escherichia coli 536 translocates into bac
211 ArdB encoded on a pathogenicity island from uropathogenic Escherichia coli and a KlcA from an IncP-1
212 o interfere with adhesive fiber formation in uropathogenic Escherichia coli and oligomerization of am
213 antivirulence strategies aimed at targeting uropathogenic Escherichia coli and potentially other Qse
216 nt communication pathway by which strains of uropathogenic Escherichia coli can inhibit the growth of
221 iae are homopolymeric adhesive organelles of uropathogenic Escherichia coli composed of DraE subunits
222 Type 1 fimbrial phase-locked mutants of uropathogenic Escherichia coli cystitis isolate F11 were
223 he otherwise healthy host is the movement of uropathogenic Escherichia coli from the intestinal tract
229 h this platform, we observed the growth of a uropathogenic Escherichia coli isolate, with an initial
233 s study was to determine whether OMVs from a uropathogenic Escherichia coli strain can induce cardiac
235 e gene encoding d-serine deaminase, dsdA, in uropathogenic Escherichia coli strain CFT073 results in
237 vic pain behavior elicited by infection with uropathogenic Escherichia coli strain NU14 and ASB strai
238 ide triggers rugose biofilm formation by the uropathogenic Escherichia coli strain UTI89 and by enter
239 tions between the fimbrial adhesin FimH from uropathogenic Escherichia coli strains and its natural h
240 tal insights into the adhesion properties of uropathogenic Escherichia coli strains to their target r
243 the P pilus, a key virulence factor used by uropathogenic Escherichia coli to adhere to the host uri
244 onserved chaperone/usher pathway and used by uropathogenic Escherichia coli to attach to bladder cell
245 Pyelonephritis-associated pili (pap) allow uropathogenic Escherichia coli to bind to epithelial cel
247 mH, which would otherwise mediate binding of uropathogenic Escherichia coli to the host urothelium to
249 polymeric structures that mediate binding of uropathogenic Escherichia coli to the surface of the kid
250 copolymer nanoparticles are conjugated with uropathogenic Escherichia coli type 1 pilus adhesin FimH
251 in-containing protein C (TcpC) from virulent uropathogenic Escherichia coli, a common human pathogen.
253 nsporter toxin (Sat), found predominantly in uropathogenic Escherichia coli, is a member of the SPATE
254 t infections (UTIs), predominantly caused by uropathogenic Escherichia coli, is the adhesion of bacte
256 of fimbriae are the type 1 and P fimbriae of uropathogenic Escherichia coli, the major causative agen
259 Using the P and type 1 pilus systems of uropathogenic Escherichia coli, we show that a conserved
269 natonium), umami (monosodium glutamate), and uropathogenic Escherichia coli; and release acetylcholin
270 and Tap, were determined for a collection of uropathogenic, fecal-commensal, and diarrheagenic Escher
272 y infected mice revealed superior fitness of uropathogenic GBS for bladder colonization and potent ur
275 enic GBS for bladder colonization and potent uropathogenic GBS-specific up-regulation of interleukin
277 ostatitis (category II) are characterized by uropathogenic infections of the prostate gland that resp
279 t to the betABIT locus was found in 42 of 67 uropathogenic isolates and 8 of 15 of the commensal stra
285 S. agalactiae (ABSA) that was not seen among uropathogenic S. agalactiae (UPSA) strains isolated from
287 and marker], pap [P fimbriae] elements, usp [uropathogenic-specific protein], and fyuA [yersiniabacti
289 egulator of motility in E. coli K12 and in a uropathogenic strain; surface attachment assays revealed
290 type 1 pili (adhesive organelles produced by uropathogenic strains of E. coli and assembled by the ch
292 tract infections are most commonly caused by uropathogenic strains of Escherichia coli (UPEC), which
295 s expressed by the majority of commensal and uropathogenic strains of Escherichia coli on the tips of
296 und that certain Escherichia coli, including uropathogenic strains, contained a bacterial growth-inhi
297 the B2 phylogroup, which contains primarily uropathogenic strains, suggesting that the E. coli/Shige
299 s observation of disease progression and the uropathogenic virulence cascade using a variety of micro
300 electrophoresis analysis) with a profile of uropathogenic virulence genes similar to that of the tes