Surface presentation of Shigella flexneri invasion plasmid antigens requires the products of the spa locus.
about
Diarrheagenic Escherichia coliType III protein secretion systems in bacterial pathogens of animals and plantsHrpI of Erwinia amylovora functions in secretion of harpin and is a member of a new protein familyThe non-flagellar type III secretion system evolved from the bacterial flagellum and diversified into host-cell adapted systemsThe virulence plasmid of Yersinia, an antihost genomeShigella flexneri effectors OspE1 and OspE2 mediate induced adherence to the colonic epithelium following bile salts exposure.Characterization of the Shigella flexneri ipgD and ipgF genes, which are located in the proximal part of the mxi locusCharacterization of B-cell epitopes on IpaB, an invasion-associated antigen of Shigella flexneri: identification of an immunodominant domain recognized during natural infection.Delivery of the non-membrane-permeative antibiotic gentamicin into mammalian cells by using Shigella flexneri membrane vesiclesIdentification of epitope and surface-exposed domains of Shigella flexneri invasion plasmid antigen D (IpaD)The tripartite type III secreton of Shigella flexneri inserts IpaB and IpaC into host membranesEnteropathogenic Escherichia coli contains a putative type III secretion system necessary for the export of proteins involved in attaching and effacing lesion formationThe LysR-type regulator QseA regulates both characterized and putative virulence genes in enterohaemorrhagic Escherichia coli O157:H7.Shigella flexneri surface protein IcsA is sufficient to direct actin-based motilityDisulfide oxidoreductase activity of Shigella flexneri is required for release of Ipa proteins and invasion of epithelial cells.Chromosomal and plasmid-encoded factors of Shigella flexneri induce secretogenic activity ex vivoRequirement for exported proteins in secretion through the invasion-associated type III system of Salmonella typhimurium.Characterization of Pseudomonas aeruginosa fliO, a gene involved in flagellar biosynthesis and adherence.Increased protein secretion and adherence to HeLa cells by Shigella spp. following growth in the presence of bile saltsRecognition of three epitopic regions on invasion plasmid antigen C by immune sera of rhesus monkeys infected with Shigella flexneri 2a.Contact with cultured epithelial cells stimulates secretion of Salmonella typhimurium invasion protein InvJ.Lack of cleavage of IcsA in Shigella flexneri causes aberrant movement and allows demonstration of a cross-reactive eukaryotic protein.Functional analysis of the Shigella flexneri IpaC invasin by insertional mutagenesis.Analysis of the Legionella pneumophila fliI gene: intracellular growth of a defined mutant defective for flagellum biosynthesisCaulobacter FliQ and FliR membrane proteins, required for flagellar biogenesis and cell division, belong to a family of virulence factor export proteinsRegulated underexpression and overexpression of the FliN protein of Escherichia coli and evidence for an interaction between FliN and FliM in the flagellar motor.Temporal and spatial regulation of fliP, an early flagellar gene of Caulobacter crescentus that is required for motility and normal cell division.Mutations in yscC, yscD, and yscG prevent high-level expression and secretion of V antigen and Yops in Yersinia pestisHomologs of the Shigella IpaB and IpaC invasins are required for Salmonella typhimurium entry into cultured epithelial cells.Identification of two targets of the type III protein secretion system encoded by the inv and spa loci of Salmonella typhimurium that have homology to the Shigella IpaD and IpaA proteins.Erwinia amylovora secretes harpin via a type III pathway and contains a homolog of yopN of Yersinia spp.Characterization of EspC, a 110-kilodalton protein secreted by enteropathogenic Escherichia coli which is homologous to members of the immunoglobulin A protease-like family of secreted proteinsSelf-chaperoning of the type III secretion system needle tip proteins IpaD and BipD.Host cell killing and bacterial conjugation require overlapping sets of genes within a 22-kb region of the Legionella pneumophila genome.Molecular and functional characterization of the Salmonella typhimurium invasion genes invB and invC: homology of InvC to the F0F1 ATPase family of proteins.YscU, a Yersinia enterocolitica inner membrane protein involved in Yop secretion.vacC, a virulence-associated chromosomal locus of Shigella flexneri, is homologous to tgt, a gene encoding tRNA-guanine transglycosylase (Tgt) of Escherichia coli K-12Characterization of virulence genes of enteroinvasive Escherichia coli by TnphoA mutagenesis: identification of invX, a gene required for entry into HEp-2 cells.A low-Ca2+ response (LCR) secretion (ysc) locus lies within the lcrB region of the LCR plasmid in Yersinia pestisYscN, the putative energizer of the Yersinia Yop secretion machinery.
P2860
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P2860
Surface presentation of Shigella flexneri invasion plasmid antigens requires the products of the spa locus.
description
1992 nî lūn-bûn
@nan
1992 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի մարտին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Surface presentation of Shigel ...... the products of the spa locus.
@ast
Surface presentation of Shigel ...... the products of the spa locus.
@en
type
label
Surface presentation of Shigel ...... the products of the spa locus.
@ast
Surface presentation of Shigel ...... the products of the spa locus.
@en
prefLabel
Surface presentation of Shigel ...... the products of the spa locus.
@ast
Surface presentation of Shigel ...... the products of the spa locus.
@en
P2093
P2860
P1476
Surface presentation of Shigel ...... the products of the spa locus.
@en
P2093
P2860
P304
P356
10.1128/JB.174.6.1990-2001.1992
P407
P577
1992-03-01T00:00:00Z