Immunochemical identification of Brucella abortus lipopolysaccharide epitopes.
about
The two-component system BvrR/BvrS essential for Brucella abortus virulence regulates the expression of outer membrane proteins with counterparts in members of the RhizobiaceaeVirulent Brucella abortus prevents lysosome fusion and is distributed within autophagosome-like compartments.O-Polysaccharide epitopic heterogeneity at the surface of Brucella spp. studied by enzyme-linked immunosorbent assay and flow cytometryInteraction of Brucella abortus lipopolysaccharide with major histocompatibility complex class II molecules in B lymphocytes.The outer membrane of Brucella ovis shows increased permeability to hydrophobic probes and is more susceptible to cationic peptides than are the outer membranes of mutant rough Brucella abortus strains.Characterization of Brucella abortus O-polysaccharide and core lipopolysaccharide mutants and demonstration that a complete core is required for rough vaccines to be efficient against Brucella abortus and Brucella ovis in the mouse model.Lipopolysaccharide-Deficient Brucella Variants Arise Spontaneously during Infection.Antibody and delayed-type hypersensitivity responses to Ochrobactrum anthropi cytosolic and outer membrane antigens in infections by smooth and rough Brucella spp.Brucella abortus Induces the Premature Death of Human Neutrophils through the Action of Its Lipopolysaccharide.Brucella-Salmonella lipopolysaccharide chimeras are less permeable to hydrophobic probes and more sensitive to cationic peptides and EDTA than are their native Brucella sp. counterparts.Brucella spp noncanonical LPS: structure, biosynthesis, and interaction with host immune system.Brucellosis vaccines: assessment of Brucella melitensis lipopolysaccharide rough mutants defective in core and O-polysaccharide synthesis and exportCharacterization of Brucella abortus and Brucella melitensis native haptens as outer membrane O-type polysaccharides independent from the smooth lipopolysaccharide.Neurobrucellosis in stranded dolphins, Costa Rica.Performance of competitive and indirect enzyme-linked immunosorbent assays, gel immunoprecipitation with native hapten polysaccharide, and standard serological tests in diagnosis of sheep brucellosis.Evaluation of lipopolysaccharides and polysaccharides of different epitopic structures in the indirect enzyme-linked immunosorbent assay for diagnosis of brucellosis in small ruminants and cattle.The outer membranes of Brucella spp. are resistant to bactericidal cationic peptides.Efficacy of several serological tests and antigens for diagnosis of bovine brucellosis in the presence of false-positive serological results due to Yersinia enterocolitica O:9.The lipopolysaccharide of Brucella abortus BvrS/BvrR mutants contains lipid A modifications and has higher affinity for bactericidal cationic peptides.WadD, a New Lipopolysaccharide Core Glycosyltransferase Identified by Genomic Search and Phenotypic Characterization
P2860
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P2860
Immunochemical identification of Brucella abortus lipopolysaccharide epitopes.
description
1994 nî lūn-bûn
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1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Immunochemical identification of Brucella abortus lipopolysaccharide epitopes.
@en
type
label
Immunochemical identification of Brucella abortus lipopolysaccharide epitopes.
@en
prefLabel
Immunochemical identification of Brucella abortus lipopolysaccharide epitopes.
@en
P2093
P2860
P1476
Immunochemical identification of Brucella abortus lipopolysaccharide epitopes.
@en
P2093
P2860
P304
P577
1994-03-01T00:00:00Z