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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
3 riation by phase variation were described in uropathogenic and commensal Enterobacteriaceae.
4                                              Uropathogenic and diarrheal Escherichia coli strains exp
5 TE protein produced by Shigella flexneri 2a, uropathogenic and enteroaggregative Escherichia coli str
6 c hybridization (CGH) analysis of a panel of uropathogenic and fecal/commensal E. coli isolates.
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.
9 of prostatitis induced by infection from the uropathogenic bacteria CP9.
10 as traditional clinical thinking would hold, uropathogenic bacteria direct a complex, intracellular c
11 pecies-specific detection of as few as 2,600 uropathogenic bacteria in culture, inoculated urine, and
12 y available probiotic capable of eradicating uropathogenic bacteria make targeted probiotic preventio
13 ulate that urea can potentially be sensed by uropathogenic bacteria to initiate infection program.
14        This is in part due to the ability of uropathogenic bacteria to invade, replicate, and persist
15 y susceptible to infection of the kidneys by uropathogenic bacteria, indicating a potentially importa
16  ligands but instead respond specifically to uropathogenic bacteria.
17  a role in permeability barrier function and uropathogenic bacterial binding.
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                                              Uropathogenic E coli containing prsG-adhesin-encoding pl
21 pathogenic E. coli (ExPEC) and include human uropathogenic E. coli (UPEC) and avian pathogenic E. col
22 del and was significantly less virulent than uropathogenic E. coli (UPEC) CFT073 in a mouse sepsis mo
23                     Here, we show that, when uropathogenic E. coli (UPEC) infect bladder epithelial c
24                                              Uropathogenic E. coli (UPEC) is the dominant cause of ur
25                                              Uropathogenic E. coli (UPEC) must adapt to life in sever
26 ins from enteropathogenic E. coli (EPEC) and uropathogenic E. coli (UPEC) shows that the EPEC protein
27 lated proteins is critical in the ability of uropathogenic E. coli (UPEC) to colonize and invade the
28 on markedly reduced the ability of infecting uropathogenic E. coli (UPEC) to grow and sustain infecti
29                      During murine cystitis, uropathogenic E. coli (UPEC) utilizes type 1 pili to bin
30 erichia coli (ExPEC) strains, referred to as uropathogenic E. coli (UPEC), causes most uncomplicated
31 genic Escherichia coli (EHEC), and UpaG from uropathogenic E. coli (UPEC), we present three represent
32  recently identified as a vaccine target for uropathogenic E. coli (UPEC)-mediated urinary tract infe
33                          We studied QseBC in uropathogenic E. coli (UPEC).
34  a plasmid and pathogenicity island of human uropathogenic E. coli (UPEC).
35 17A in response to in vitro stimulation with uropathogenic E. coli Ags.
36 e urinary tract infection model, A-ICs bound uropathogenic E. coli and responded by acidifying the ur
37 sfolded proteins derived from the P pilus of uropathogenic E. coli and that mutations in either cpxP
38                        Indeed, CdiA-CTs from uropathogenic E. coli and the plant pathogen Dickeya dad
39                                              Uropathogenic E. coli are more likely than commensal E.
40 h codes for the pilus proteins necessary for uropathogenic E. coli cellular adhesion.
41                                We found that uropathogenic E. coli CFT073 and enteropathogenic E. col
42  against Escherichia coli strains, including uropathogenic E. coli CFT073 and UTI89, enterohemorrhagi
43 ry concentration (MIC) value is observed for uropathogenic E. coli CFT073 relative to Amp/Amx, and ti
44 s are homologous to regions in the sequenced uropathogenic E. coli CFT073 strain.
45 d by the urinary tract mucosa in response to uropathogenic E. coli challenge and acts in innate immun
46  to urinary catheters and ability to prevent uropathogenic E. coli from colonizing urinary catheters
47                  In order to find additional uropathogenic E. coli genes, we used genomic subtraction
48              Rectal isolates were considered uropathogenic E. coli if genetically identical to the ur
49 monstrated by a defect in acute clearance of uropathogenic E. coli in IL-17A(-/-) mice.
50 e to the bladder wall and to detect and kill uropathogenic E. coli in the event of colonization.
51 as an important factor in the persistence of uropathogenic E. coli in vivo.
52 erric iron in the growth medium of wild-type uropathogenic E. coli induced the expression of qseBC in
53      The results show that pap expression in uropathogenic E. coli is initial-state-dependent, as pre
54 nst challenge with a broad range of clinical uropathogenic E. coli isolates and produced immunity tha
55  genes to a well-characterized collection of uropathogenic E. coli isolates to compare the discrimina
56 ne cluster was significantly associated with uropathogenic E. coli isolates.
57                                              Uropathogenic E. coli mutants in siderophore receptors f
58 ating that these are conserved properties of uropathogenic E. coli pili.
59  explants, we discovered that IBCs formed by uropathogenic E. coli progressed through four distinct d
60 , and dramatically increased colonization by uropathogenic E. coli strain 536.
61 ke inflammation suppressor genes A and B) of uropathogenic E. coli strain CFT073, homologs of the Shi
62  mutants of candidate genes were made in the uropathogenic E. coli strain CFT073.
63 as induced by intraurethral inoculation of a uropathogenic E. coli strain in mice.
64 R was also assessed in a clinically relevant uropathogenic E. coli strain.
65 antly less prevalent or functional among the uropathogenic E. coli strains (both in 6% of strains) th
66  fecal-commensal, intestinal pathogenic, and uropathogenic E. coli strains all displayed similar grow
67  linked next to the dsdCXA locus in 24 of 67 uropathogenic E. coli strains but are found in only 1 of
68                                              Uropathogenic E. coli strains express a number of virule
69  vat, fyuA, and chuA, highly associated with uropathogenic E. coli strains that can distinguish three
70 islands of CFT073 and two other well-studied uropathogenic E. coli strains, J96 and 536.
71  encompasses avian, neonatal meningitis, and uropathogenic E. coli strains.
72               By selecting and screening for uropathogenic E. coli transposon mutants that are unable
73      Together, these findings illustrate how uropathogenic E. coli use the multifunctional virulence
74                       A single gene from the uropathogenic E. coli UT189, which codes for a gmrS/gmrD
75 s for the subversion of TLR signaling by the uropathogenic E. coli virulence factor TcpC and furnish
76 repressor of sigma E, DegS, is essential for uropathogenic E. coli virulence.
77 d from the culture broths of S. enterica and uropathogenic E. coli, but MGE and TGE have not been rep
78 rhagic E. coli, enterotoxigenic E. coli, and uropathogenic E. coli, in dendritic cells or HeLa cells
79 r the generation of a protective response to uropathogenic E. coli, its importance in innate immunity
80 ture to FimH, the type 1 fimbrial adhesin of uropathogenic E. coli, which shows shear-dependent bindi
81                          Therefore, Auf is a uropathogenic E. coli-associated structure that plays an
82 and is essential in the infection process of uropathogenic E. coli.
83 cteristic contribute to systemic invasion by uropathogenic E. coli.
84 current urinary tract infection by caused by uropathogenic E. coli.
85 aling in global virulence gene regulation of uropathogenic E. coli.
86 n of the capsule assembly region 1 operon in uropathogenic E. coli.
87 hypothesis that Iha is a virulence factor in uropathogenic E. coli.
88 than that of PFGE for epidemiologic study of uropathogenic E. coli.
89 enabling assembly and secretion of P pili in uropathogenic E. coli.
90 a clinically important pathogenic bacterium--uropathogenic E. coli.
91 of the O antigen ligase gene, waaL, from the uropathogenic E. coliisolate NU14 results in a strain th
92 s the expression of pili genes necessary for uropathogenic E.coli cellular adhesion.
93 ladder epithelial cells were challenged with uropathogenic Escherichia coli (CFT073) and microbial PA
94 ession and attenuates enterohaemorrhagic and uropathogenic Escherichia coli (EHEC and UPEC), Salmonel
95                                              Uropathogenic Escherichia coli (UPEC) accounts for 80 to
96    Urinary tract infections (UTIs) caused by uropathogenic Escherichia coli (UPEC) affect 150 million
97    Urinary tract infections (UTIs) caused by uropathogenic Escherichia coli (UPEC) are a significant
98                                              Uropathogenic Escherichia coli (UPEC) are capable of for
99                                              Uropathogenic Escherichia coli (UPEC) are the chief caus
100                                              Uropathogenic Escherichia coli (UPEC) are the major caus
101                                   Strains of uropathogenic Escherichia coli (UPEC) are the primary ca
102                                Gram-negative uropathogenic Escherichia coli (UPEC) bacteria are a cau
103 ction of the prostate by clinically relevant uropathogenic Escherichia coli (UPEC) can initiate and e
104                                              Uropathogenic Escherichia coli (UPEC) cause most uncompl
105                                              Uropathogenic Escherichia coli (UPEC) causes most commun
106                                              Uropathogenic Escherichia coli (UPEC) causes most uncomp
107             We report that type 1 fimbriated uropathogenic Escherichia coli (UPEC) circumvents the bl
108                                              Uropathogenic Escherichia coli (UPEC) contain multiple h
109      Invasion of bladder epithelial cells by uropathogenic Escherichia coli (UPEC) contributes to ant
110                                        Acute uropathogenic Escherichia coli (UPEC) cystitis in C57BL/
111  describe the whole bladder transcriptome of uropathogenic Escherichia coli (UPEC) cystitis in mice u
112 e insights into the transcriptional state of uropathogenic Escherichia coli (UPEC) during infection.
113                                   Strains of uropathogenic Escherichia coli (UPEC) encode filamentous
114 The metV genomic island in the chromosome of uropathogenic Escherichia coli (UPEC) encodes a putative
115   While in transit within and between hosts, uropathogenic Escherichia coli (UPEC) encounters multipl
116  Here, we show in a murine model of UTI that uropathogenic Escherichia coli (UPEC) established quiesc
117 elial cells (BECs) that expels intracellular uropathogenic Escherichia coli (UPEC) from their intrace
118  binding, invasion, and biofilm formation of uropathogenic Escherichia coli (UPEC) in the host urothe
119 s bladder epithelial binding and invasion by uropathogenic Escherichia coli (UPEC) in the initial sta
120                       During acute cystitis, uropathogenic Escherichia coli (UPEC) induce bladder epi
121                                              Uropathogenic Escherichia coli (UPEC) induces a variety
122                                      We used uropathogenic Escherichia coli (UPEC) infection of wild-
123      Urinary tract infection (UTI) caused by uropathogenic Escherichia coli (UPEC) is a substantial e
124 The pathogenesis of pyelonephritis caused by uropathogenic Escherichia coli (UPEC) is not well unders
125                                              Uropathogenic Escherichia coli (UPEC) is responsible for
126                                              Uropathogenic Escherichia coli (UPEC) is responsible for
127                                              Uropathogenic Escherichia coli (UPEC) is the leading cau
128                                              Uropathogenic Escherichia coli (UPEC) is the leading cau
129                                              Uropathogenic Escherichia coli (UPEC) is the major causa
130                                              Uropathogenic Escherichia coli (UPEC) is the major cause
131                                              Uropathogenic Escherichia coli (UPEC) is the most common
132                                              Uropathogenic Escherichia coli (UPEC) is the most common
133                                              Uropathogenic Escherichia coli (UPEC) is the predominant
134                                              Uropathogenic Escherichia coli (UPEC) is the predominant
135                                              Uropathogenic Escherichia coli (UPEC) is the primary cau
136                        The invasive pathogen uropathogenic Escherichia coli (UPEC) is the primary cau
137 is isolate TOP52 was compared to that of the uropathogenic Escherichia coli (UPEC) isolate UTI89 in a
138   Here, we show that Hfq is critical for the uropathogenic Escherichia coli (UPEC) isolate UTI89 to e
139         Studies with mice have revealed that uropathogenic Escherichia coli (UPEC) isolates invade su
140                     In a test of 49 clinical uropathogenic Escherichia coli (UPEC) isolates, all were
141                                              Uropathogenic Escherichia coli (UPEC) modulates aspects
142  urinary tract infections (UTI), cystitis by uropathogenic Escherichia coli (UPEC) occurs through an
143                                              Uropathogenic Escherichia coli (UPEC) of sequence type 1
144 tandem mass spectrometry to characterize the uropathogenic Escherichia coli (UPEC) outer membrane sub
145           Urinary tract infections caused by uropathogenic Escherichia coli (UPEC) pathovars belong t
146           Urinary tract infections caused by uropathogenic Escherichia coli (UPEC) pathovars belong t
147                              Many strains of uropathogenic Escherichia coli (UPEC) produce cytotoxic
148 ated urinary tract infection (UTI) caused by uropathogenic Escherichia coli (UPEC) represents a preva
149                                              Uropathogenic Escherichia coli (UPEC) strain CFT073 cont
150 ified two chromosomal open reading frames in uropathogenic Escherichia coli (UPEC) strain CFT073 whic
151                                              Uropathogenic Escherichia coli (UPEC) strain CP9 coloniz
152                    Here, we demonstrate that uropathogenic Escherichia coli (UPEC) strain UTI89 incor
153 ed transurethrally with the cystitis-derived uropathogenic Escherichia coli (UPEC) strain UTI89.
154                                              Uropathogenic Escherichia coli (UPEC) strains are respon
155                                         Most uropathogenic Escherichia coli (UPEC) strains harbor gen
156                                         Many uropathogenic Escherichia coli (UPEC) strains produce bo
157                                              Uropathogenic Escherichia coli (UPEC) strains suppress t
158  overwhelming majority of UTIs are caused by uropathogenic Escherichia coli (UPEC) strains.
159 tions are caused by a heterogeneous group of uropathogenic Escherichia coli (UPEC) strains.
160                             During cystitis, uropathogenic Escherichia coli (UPEC) subvert innate def
161                 They prevent the adhesion of uropathogenic Escherichia coli (UPEC) to urothelial cell
162 own that 36% (5 of 14) of mice infected with uropathogenic Escherichia coli (UPEC) will have at least
163 usly shown to contribute to the virulence of uropathogenic Escherichia coli (UPEC) within the urinary
164                                              Uropathogenic Escherichia coli (UPEC), a leading cause o
165  (UTIs), the majority of which are caused by uropathogenic Escherichia coli (UPEC), afflict nearly 60
166 tract infections (UTIs), primarily caused by uropathogenic Escherichia coli (UPEC), annually affect o
167  tract infections (UTI), primarily caused by uropathogenic Escherichia coli (UPEC), are one of the le
168 t infections (UTIs), predominantly caused by uropathogenic Escherichia coli (UPEC), belong to the mos
169 re fundamental for keeping kidneys free from uropathogenic Escherichia coli (UPEC), but we have shown
170  (CNF1), a toxin produced by many strains of uropathogenic Escherichia coli (UPEC), constitutively ac
171            FimH, the type 1 pilus adhesin of uropathogenic Escherichia coli (UPEC), contains a recept
172                    Two surface organelles of uropathogenic Escherichia coli (UPEC), flagella and type
173                                              Uropathogenic Escherichia coli (UPEC), however, has been
174 cal for colonization of the urinary tract by uropathogenic Escherichia coli (UPEC), mediate opposing
175 nfections (UTIs) have complex dynamics, with uropathogenic Escherichia coli (UPEC), the major causati
176                                              Uropathogenic Escherichia coli (UPEC), the most common c
177                                              Uropathogenic Escherichia coli (UPEC), the most frequent
178                                              Uropathogenic Escherichia coli (UPEC), the predominant c
179                                              Uropathogenic Escherichia coli (UPEC), the predominant c
180 haracterize the adaptive immune responses to uropathogenic Escherichia coli (UPEC), the predominant u
181                                              Uropathogenic Escherichia coli (UPEC), the primary causa
182                                              Uropathogenic Escherichia coli (UPEC), the principal cau
183 ulator of stress resistance and virulence in uropathogenic Escherichia coli (UPEC), the principal cau
184                                              Uropathogenic Escherichia coli (UPEC), which accounts fo
185                                              Uropathogenic Escherichia coli (UPEC), which are the lea
186 1 pili (T1P) are major virulence factors for uropathogenic Escherichia coli (UPEC), which cause both
187 pe 1 pili are important virulence factors in uropathogenic Escherichia coli (UPEC), which cause the m
188  a key event in the pathogenesis mediated by uropathogenic Escherichia coli (UPEC), yet the mechanism
189 ract infection (UTI) is most often caused by uropathogenic Escherichia coli (UPEC).
190 nt disease in humans, is primarily caused by uropathogenic Escherichia coli (UPEC).
191 rinary tract infections (UTIs) are caused by uropathogenic Escherichia coli (UPEC).
192 infections (UTI) are caused most commonly by uropathogenic Escherichia coli (UPEC).
193 is caused predominantly by type 1-fimbriated uropathogenic Escherichia coli (UPEC).
194  have been proven important for virulence of uropathogenic Escherichia coli (UPEC).
195 cal for colonization of the urinary tract by uropathogenic Escherichia coli (UPEC).
196 hose of the urinary tract, caused chiefly by uropathogenic Escherichia coli (UPEC).
197 gnized globally dispersed clonal lineages of uropathogenic Escherichia coli (UPEC).
198 Cu) content is elevated during UTI caused by uropathogenic Escherichia coli (UPEC).
199 and hemolysin (HlyA1) are toxins produced by uropathogenic Escherichia coli (UPEC).
200                               UTIs caused by uropathogenic Escherichia coli (UTI89), Klebsiella pneum
201               The CdiA-CT(EC536) deployed by uropathogenic Escherichia coli 536 (EC536) is a bacteria
202                       The CdiA-CT toxin from uropathogenic Escherichia coli 536 is a latent tRNase th
203 e show that purified CdiA-CT(536) toxin from uropathogenic Escherichia coli 536 translocates into bac
204  ArdB encoded on a pathogenicity island from uropathogenic Escherichia coli and a KlcA from an IncP-1
205 o interfere with adhesive fiber formation in uropathogenic Escherichia coli and oligomerization of am
206  antivirulence strategies aimed at targeting uropathogenic Escherichia coli and potentially other Qse
207                                              Uropathogenic Escherichia coli are the leading cause of
208                                              Uropathogenic Escherichia coli assemble P and type 1 pil
209 nt communication pathway by which strains of uropathogenic Escherichia coli can inhibit the growth of
210                                              Uropathogenic Escherichia coli cause urinary tract infec
211 d hepcidin-knockout (Hepc-/-) mice using the uropathogenic Escherichia coli CFT073 strain.
212 we report the crystal structure of IroE from uropathogenic Escherichia coli CFT073.
213                                          The uropathogenic Escherichia coli colonize the host body by
214 iae are homopolymeric adhesive organelles of uropathogenic Escherichia coli composed of DraE subunits
215      Type 1 fimbrial phase-locked mutants of uropathogenic Escherichia coli cystitis isolate F11 were
216  The secreted autotransporter toxin (Sat) of uropathogenic Escherichia coli exhibits cytopathic activ
217 he otherwise healthy host is the movement of uropathogenic Escherichia coli from the intestinal tract
218                   However, recent studies of uropathogenic Escherichia coli have found that it can ca
219                   By observing the growth of uropathogenic Escherichia coli in gas permeable polymeri
220                         We demonstrated that uropathogenic Escherichia coli infection stimulates the
221                                              Uropathogenic Escherichia coli invade bladder epithelial
222 monas aeruginosa, Staphylococcus aureus, and uropathogenic Escherichia coli is assessed.
223 n of pyelonephritis-associated pili (Pap) in uropathogenic Escherichia coli is epigenetically control
224 ephritis-associated pili (Pap) expression in uropathogenic Escherichia coli is regulated by a complex
225                                              Uropathogenic Escherichia coli is the causative agent fo
226                                              Uropathogenic Escherichia coli is the most common etiolo
227 h this platform, we observed the growth of a uropathogenic Escherichia coli isolate, with an initial
228      During urinary tract infections (UTIs), uropathogenic Escherichia coli must maintain a delicate
229 he assembly of type 1 pili on the surface of uropathogenic Escherichia coli proceeds via the chaperon
230           Pilus biogenesis on the surface of uropathogenic Escherichia coli requires the chaperone/us
231          Here, we show that the CdiA-CT from uropathogenic Escherichia coli strain 536 (UPEC536) is a
232 s study was to determine whether OMVs from a uropathogenic Escherichia coli strain can induce cardiac
233        A D-serine deaminase (DsdA) mutant of uropathogenic Escherichia coli strain CFT073 has a hyper
234 e gene encoding d-serine deaminase, dsdA, in uropathogenic Escherichia coli strain CFT073 results in
235         Genomic DNA sequence analysis of the uropathogenic Escherichia coli strain CFT073 revealed th
236 ntly, we identified a fimbrial usher gene in uropathogenic Escherichia coli strain CFT073 that is abs
237                                            A uropathogenic Escherichia coli strain CFT073-specific DN
238 vic pain behavior elicited by infection with uropathogenic Escherichia coli strain NU14 and ASB strai
239 ide triggers rugose biofilm formation by the uropathogenic Escherichia coli strain UTI89 and by enter
240                                 For example, uropathogenic Escherichia coli strains, such as CFT073,
241  the P pilus, a key virulence factor used by uropathogenic Escherichia coli to adhere to the host uri
242 onserved chaperone/usher pathway and used by uropathogenic Escherichia coli to attach to bladder cell
243   Pyelonephritis-associated pili (pap) allow uropathogenic Escherichia coli to bind to epithelial cel
244          Type 1 fimbriae mediate adhesion of uropathogenic Escherichia coli to host cells.
245 mH, which would otherwise mediate binding of uropathogenic Escherichia coli to the host urothelium to
246  appendages responsible for the targeting of uropathogenic Escherichia coli to the kidney.
247 polymeric structures that mediate binding of uropathogenic Escherichia coli to the surface of the kid
248  copolymer nanoparticles are conjugated with uropathogenic Escherichia coli type 1 pilus adhesin FimH
249 in-containing protein C (TcpC) from virulent uropathogenic Escherichia coli, a common human pathogen.
250                     Type 1 pili, produced by uropathogenic Escherichia coli, are multisubunit fibres
251 nsporter toxin (Sat), found predominantly in uropathogenic Escherichia coli, is a member of the SPATE
252 t infections (UTIs), predominantly caused by uropathogenic Escherichia coli, is the adhesion of bacte
253                        Enteroaggregative and uropathogenic Escherichia coli, Shigella flexneri 2a, an
254 of fimbriae are the type 1 and P fimbriae of uropathogenic Escherichia coli, the major causative agen
255                                          For uropathogenic Escherichia coli, these interactions are m
256      Using the P and type 1 pilus systems of uropathogenic Escherichia coli, we show that a conserved
257          Recently, a siderophore produced by uropathogenic Escherichia coli, yersiniabactin, was foun
258  fimbria-mediated haemagglutination assay of uropathogenic Escherichia coli.
259 fter receiving intravesical inoculation with uropathogenic Escherichia coli.
260 1 fimbriae (FimH) are positively selected in uropathogenic Escherichia coli.
261 in two different pilus biogenesis systems in uropathogenic Escherichia coli.
262 flammatory markers typically associated with uropathogenic Escherichia coli.
263 mice, but not humans, and known to recognize uropathogenic Escherichia coli.
264 ired for assembly and secretion of P pili in uropathogenic Escherichia coli.
265  of P pili by the chaperone/usher pathway in uropathogenic Escherichia coli.
266  prototypic self-associating AT protein from uropathogenic Escherichia coli.
267 natonium), umami (monosodium glutamate), and uropathogenic Escherichia coli; and release acetylcholin
268 and Tap, were determined for a collection of uropathogenic, fecal-commensal, and diarrheagenic Escher
269                      We investigated whether uropathogenic GBS can bind to bladder uroepithelium to i
270 y infected mice revealed superior fitness of uropathogenic GBS for bladder colonization and potent ur
271                                              Uropathogenic GBS isolated from a patient with acute cys
272                             Thus, binding of uropathogenic GBS to uroepithelium and vigorous inductio
273 enic GBS for bladder colonization and potent uropathogenic GBS-specific up-regulation of interleukin
274                           The most prevalent uropathogenic gram negative bacteria are Escherichia col
275 ostatitis (category II) are characterized by uropathogenic infections of the prostate gland that resp
276                                One strain, a uropathogenic isolate, had a pathoadaptive variant of fi
277 t to the betABIT locus was found in 42 of 67 uropathogenic isolates and 8 of 15 of the commensal stra
278 equent catheter colonization by a variety of uropathogenic organisms.
279 as a critical bladder colonization factor of uropathogenic P. mirabilis and also suggested that the a
280 e presence of the predictors correlates with uropathogenic potential.
281                             MR/P fimbriae of uropathogenic Proteus mirabilis undergo invertible eleme
282 ase ZapA is an important virulence factor of uropathogenic Proteus mirabilis.
283 S. agalactiae (ABSA) that was not seen among uropathogenic S. agalactiae (UPSA) strains isolated from
284                         The Escherichia coli uropathogenic-specific protein gene, usp, and its linked
285 and marker], pap [P fimbriae] elements, usp [uropathogenic-specific protein], and fyuA [yersiniabacti
286 raction to identify DNA regions present in a uropathogenic strain of E. coli (1128-11).
287 egulator of motility in E. coli K12 and in a uropathogenic strain; surface attachment assays revealed
288 type 1 pili (adhesive organelles produced by uropathogenic strains of E. coli and assembled by the ch
289 uroepithelial adhesion are commonly found in uropathogenic strains of E. coli.
290 , is extremely susceptible to infection with uropathogenic strains of E. coli.
291 tract infections are most commonly caused by uropathogenic strains of Escherichia coli (UPEC), which
292                                              Uropathogenic strains of Escherichia coli assemble type
293                      We have found that many uropathogenic strains of Escherichia coli display far gr
294 s expressed by the majority of commensal and uropathogenic strains of Escherichia coli on the tips of
295 und that certain Escherichia coli, including uropathogenic strains, contained a bacterial growth-inhi
296  the B2 phylogroup, which contains primarily uropathogenic strains, suggesting that the E. coli/Shige
297 the SP mutations are relatively common among uropathogenic strains.
298 s observation of disease progression and the uropathogenic virulence cascade using a variety of micro
299                                      Several uropathogenic virulence factors have been identified, bu
300  electrophoresis analysis) with a profile of uropathogenic virulence genes similar to that of the tes

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