Yersinia high-pathogenicity island contributes to virulence in Escherichia coli causing extraintestinal infections.
about
Genomic avenue to avian colisepticemiaDegS is necessary for virulence and is among extraintestinal Escherichia coli genes induced in murine peritonitis.Role of intraspecies recombination in the spread of pathogenicity islands within the Escherichia coli species.Yersiniabactin reduces the respiratory oxidative stress response of innate immune cellsEvolution in quantum leaps: multiple combinatorial transfers of HPI and other genetic modules in EnterobacteriaceaeIdentification of protective and broadly conserved vaccine antigens from the genome of extraintestinal pathogenic Escherichia coliFrom grazing resistance to pathogenesis: the coincidental evolution of virulence factors.Shiga toxin 2e-producing Escherichia coli isolates from humans and pigs differ in their virulence profiles and interactions with intestinal epithelial cells.Pathogenicity islands in bacterial pathogenesisDissemination and systemic colonization of uropathogenic Escherichia coli in a murine model of bacteremia.Yersiniabactin production by Pseudomonas syringae and Escherichia coli, and description of a second yersiniabactin locus evolutionary group.Redundancy and specificity of Escherichia coli iron acquisition systems during urinary tract infection.Interplay between siderophores and colibactin genotoxin biosynthetic pathways in Escherichia coliGenomic characterisation of an endometrial pathogenic Escherichia coli strain reveals the acquisition of genetic elements associated with extra-intestinal pathogenicity.Characterization of an iroBCDEN gene cluster on a transmissible plasmid of uropathogenic Escherichia coli: evidence for horizontal transfer of a chromosomal virulence factor.Comparative genomic analysis shows that avian pathogenic Escherichia coli isolate IMT5155 (O2:K1:H5; ST complex 95, ST140) shares close relationship with ST95 APEC O1:K1 and human ExPEC O18:K1 strains.The siderophore receptor IroN, but not the high-pathogenicity island or the hemin receptor ChuA, contributes to the bacteremic step of Escherichia coli neonatal meningitis.Contribution of siderophore systems to growth and urinary tract colonization of asymptomatic bacteriuria Escherichia coliIdentification of candidates for a subunit vaccine against extraintestinal pathogenic Escherichia coliImpact of pathogenicity islands in bacterial diagnostics.Crystallization and X-ray diffraction analysis of salicylate synthase, a chorismate-utilizing enyme involved in siderophore biosynthesisSpecific roles of the iroBCDEN genes in virulence of an avian pathogenic Escherichia coli O78 strain and in production of salmochelins.Characterization of Shiga Toxin Subtypes and Virulence Genes in Porcine Shiga Toxin-Producing Escherichia coliComparison of extraintestinal pathogenic Escherichia coli strains from human and avian sources reveals a mixed subset representing potential zoonotic pathogens.Fitness, stress resistance, and extraintestinal virulence in Escherichia coli.Immunization with the yersiniabactin receptor, FyuA, protects against pyelonephritis in a murine model of urinary tract infection.Genomic islands of uropathogenic Escherichia coli contribute to virulence.Colibacillosis in poultry: unravelling the molecular basis of virulence of avian pathogenic Escherichia coli in their natural hosts.Pathotype and antibiotic resistance gene distributions of Escherichia coli isolates from broiler chickens raised on antimicrobial-supplemented diets.Regulation of iron transport systems in Enterobacteriaceae in response to oxygen and iron availability.A structural and functional analysis of type III periplasmic and substrate binding proteins: their role in bacterial siderophore and heme transport.Interplay between siderophores and colibactin genotoxin in Escherichia coli.YeeJ is an inverse autotransporter from Escherichia coli that binds to peptidoglycan and promotes biofilm formation.Molecular epidemiology of the iron utilization genes of enteroaggregative Escherichia coli.Horizontal transfer of the high-pathogenicity island of Yersinia pseudotuberculosis.The Yersinia HPI is present in Serratia liquefaciens isolated from meat.Phylogenetic groups and pathogenicity island markers in fecal Escherichia coli isolates from asymptomatic humans in China.The salmochelin siderophore receptor IroN contributes to invasion of urothelial cells by extraintestinal pathogenic Escherichia coli in vitro.The high-pathogenicity island (HPI) promotes flagellum-mediated motility in extraintestinal pathogenic Escherichia coliIdentification of forces shaping the commensal Escherichia coli genetic structure by comparing animal and human isolates.
P2860
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P2860
Yersinia high-pathogenicity island contributes to virulence in Escherichia coli causing extraintestinal infections.
description
2002 nî lūn-bûn
@nan
2002 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Yersinia high-pathogenicity is ...... ng extraintestinal infections.
@ast
Yersinia high-pathogenicity is ...... ng extraintestinal infections.
@en
Yersinia high-pathogenicity is ...... ng extraintestinal infections.
@nl
type
label
Yersinia high-pathogenicity is ...... ng extraintestinal infections.
@ast
Yersinia high-pathogenicity is ...... ng extraintestinal infections.
@en
Yersinia high-pathogenicity is ...... ng extraintestinal infections.
@nl
prefLabel
Yersinia high-pathogenicity is ...... ng extraintestinal infections.
@ast
Yersinia high-pathogenicity is ...... ng extraintestinal infections.
@en
Yersinia high-pathogenicity is ...... ng extraintestinal infections.
@nl
P2093
P2860
P1476
Yersinia high-pathogenicity is ...... ng extraintestinal infections.
@en
P2093
Bertrand Picard
Erick Denamur
Jürgen Heesemann
Stéphanie Gouriou
Sören Schubert
P2860
P304
P356
10.1128/IAI.70.9.5335-5337.2002
P407
P577
2002-09-01T00:00:00Z