コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
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
5 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
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.
15 y susceptible to infection of the kidneys by uropathogenic bacteria, indicating a potentially importa
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
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
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
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
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
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
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
52 erric iron in the growth medium of wild-type uropathogenic E. coli induced the expression of qseBC in
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
59 explants, we discovered that IBCs formed by uropathogenic E. coli progressed through four distinct d
61 ke inflammation suppressor genes A and B) of uropathogenic E. coli strain CFT073, homologs of the Shi
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
69 vat, fyuA, and chuA, highly associated with uropathogenic E. coli strains that can distinguish three
75 s for the subversion of TLR signaling by the uropathogenic E. coli virulence factor TcpC and furnish
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
91 of the O antigen ligase gene, waaL, from the uropathogenic E. coliisolate NU14 results in a strain th
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
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
103 ction of the prostate by clinically relevant uropathogenic Escherichia coli (UPEC) can initiate and e
109 Invasion of bladder epithelial cells by uropathogenic Escherichia coli (UPEC) contributes to ant
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.
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
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
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
142 urinary tract infections (UTI), cystitis by uropathogenic Escherichia coli (UPEC) occurs through an
144 tandem mass spectrometry to characterize the uropathogenic Escherichia coli (UPEC) outer membrane sub
148 ated urinary tract infection (UTI) caused by uropathogenic Escherichia coli (UPEC) represents a preva
150 ified two chromosomal open reading frames in uropathogenic Escherichia coli (UPEC) strain CFT073 whic
153 ed transurethrally with the cystitis-derived uropathogenic Escherichia coli (UPEC) strain UTI89.
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
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
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
180 haracterize the adaptive immune responses to uropathogenic Escherichia coli (UPEC), the predominant u
183 ulator of stress resistance and virulence in uropathogenic Escherichia coli (UPEC), the principal cau
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
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
209 nt communication pathway by which strains of uropathogenic Escherichia coli can inhibit the growth of
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
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
227 h this platform, we observed the growth of a uropathogenic Escherichia coli isolate, with an initial
229 he assembly of type 1 pili on the surface of uropathogenic Escherichia coli proceeds via the chaperon
232 s study was to determine whether OMVs from a uropathogenic Escherichia coli strain can induce cardiac
234 e gene encoding d-serine deaminase, dsdA, in uropathogenic Escherichia coli strain CFT073 results in
236 ntly, we identified a fimbrial usher gene in uropathogenic Escherichia coli strain CFT073 that is abs
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
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
245 mH, which would otherwise mediate binding of uropathogenic Escherichia coli to the host urothelium to
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.
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
254 of fimbriae are the type 1 and P fimbriae of uropathogenic Escherichia coli, the major causative agen
256 Using the P and type 1 pilus systems of uropathogenic Escherichia coli, we show that a conserved
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
270 y infected mice revealed superior fitness of uropathogenic GBS for bladder colonization and potent ur
273 enic GBS for bladder colonization and potent uropathogenic GBS-specific up-regulation of interleukin
275 ostatitis (category II) are characterized by uropathogenic infections of the prostate gland that resp
277 t to the betABIT locus was found in 42 of 67 uropathogenic isolates and 8 of 15 of the commensal stra
279 as a critical bladder colonization factor of uropathogenic P. mirabilis and also suggested that the a
283 S. agalactiae (ABSA) that was not seen among uropathogenic S. agalactiae (UPSA) strains isolated from
285 and marker], pap [P fimbriae] elements, usp [uropathogenic-specific protein], and fyuA [yersiniabacti
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
291 tract infections are most commonly caused by uropathogenic strains of Escherichia coli (UPEC), which
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
298 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
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。