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Query: UNIPROT:P43026 (lipopolysaccharide)
 62,215 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A method based on the inhibition of agglutination is described that may be used for the differential serological diagnosis between B. abortus and Y. enterocolitica serotype O:9. An antigen with high immunological capacity was isolated from Brucella. This antigen inhibited both homologous and heterologous agglutination by Brucella antiserum, but only the heterologous agglutination by Yersinia antiserum. It proved to be constitued of a polysaccharide (N-acetylglucosamine, glucose, mannose and 2-keto-3-deoxyoctonic acid), a protein and a phosphoglycerid moiety. Lipid A was absent from the Brucella antigen. Incomplete polysaccharide synthesis of the Brucella antigen, with concomitant loss of serological specificity by the rough mutant has been described. Oligosaccharides containing N-acetylgalactosamine, glucose and galactose were isolated from the specific side chain of Yersinia lipopolysaccharide. Lipid A constituents were also identified in the latter.
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PMID:Biochemical basis of the serological cross-reactions between Brucella abortus and Yersinia enterocolitica serotype O:9. 5 66

One the cell surface of smooth of Yersinia enterocolitica 75 (Ye 75 S), and electron-lucent layer was identified in thin sections after incubation with Ye 75 S-antiserum. It is adjacent to the "double track" of the outer membrane. This layer does not appear on the analogously treated rough mutant (Ye 75 R), whose lipopolysaccharide (LPS) does not contain O-specific polysaccharides. It could be shown that this layer is formed by the O-specific side chains of LPS, which are unstained by routine methods. As the side chains of LPS obviosly make it difficult to visualize the LPS-strands in the outer membrane of rough strands was investigated. On Ye 75 R, the LPS-strands could be demonstrated only after treatment of cells with polymyxin B. After short time of exposure, the LPS appeared as contigous strand-like structures (diameter roughly 60 A) on the cell surface of cells which were negatively stained or dried by the critical-point-method. After prolonging polymyxin B treatment, "blebs" or "protrusions" appeared on the surface of Ye 75 cells, which were in negatively stained preparations and in thin sections identified as partly loosened LPS. The demonstration of LPS-strands in untreated cells was possible only on a "deep rough" mutant (Ye 161-45 a R), whose LPS contains only glucosamine and KDO besides lipid A. It is suggested that the LPS form a layer of contiguous strands (mid-to-distance 62 +/- 3 A) on the surface of negatively stained cells. According to this view, on the Ye 75 S, the O-specific side chains extend from this layer into the medium.
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PMID:The arrangement of lipopolysaccharides on the outer membrane of Yersinia enterocolitica: an electron microscopic study. 6 41

Lipid A isolated from lipopolysaccharide of Yersinia pseudotuberculosis was used for immunization of rabbits to afford antisera to lipid A with titers of 1:640 in the passive hemolysis test. Exhaustion of immune serume with sheep erythrocytes decreased antibody titers up to 1:160. Authentic samples of 2-(DL-3-hydroxytetradecanoyl)amino-2-deoxy-D-glucose 6-phosphate, 2-tetradecanoylamino-2-deoxy-D-glucose 6-phosphate and 2-acetamido-2-deoxy-D-glucose 6-phosphate have been synthesized in order to carry out a comparative study of inhibitory activity of these compounds and lipid A using a system of lipid A and antiserum to lipid A. As a result, the immunodominant moiety of the lipid A of Y. pseudotuberculosis proved to contain a D-glucosamine residue acylated with 3-hydroxytetradecanoic acid at the amino group. The nature of the fatty acid acylating the amino group of glucosamine does not play an important role in the structure of immunodominant moiety of lipid A.
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PMID:Structural studies on the immunodominant group of lipid A from lipopolysaccharide of Yersinia pseudotuberculosis. 8 32

The presence of two distinct lipopolysaccharides in Yersinia enterocolitica O:9 is described: one isolated from the aqueous phase and one from the phenol phase (Westphal system). The sugar moiety of the phenol phase lipopolysaccharide has been identified as being responsible for the serologic cross-reaction of Y. enterocolitica O:9, Brucella abortus and Vibrio cholerae. The phenol phase antigen consists of glucose, galactose, glucosamine, 2-keto-3-deoxyoctonic acid, heptose, lipid A and a protein moiety. Haemagglutination experiments revealed two different structures: one that readily coats erythrocytes and another that requires alkali treatment. The former may be separated by repeated adsorptions on erythrocytes. Serologically, the two structures behave like a single antigen. The action of normal rabbit serum on the erythrocyte-containg capacity of the two structures was studied.
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PMID:Immunochemical studies on a Yersinia enterocolitica O:9 lipopolysaccharide cross-reacting with Brucella abortus and Vibrio cholerae extracts. 10 56

Vaccination with killed cells of Brucella abortus, Yersinia enterocolitica 0:9 and Salmonella neusdorf evoked cross-reacting antibodies in guinea pigs but only the homologous antigen effectively produced protective immunity to Br. abortus. None of these preparations induced protective immunity to Y. enterocolitica in gerbils but all stimulated protective immunity to S. landau in Balb/c mice. The antigenic determinants responsible for protective immunity to salmonella infection were located on the cross-reacting lipopolysaccharide-peptide agglutinogens of the brucella, yersinia and salmonella organisms. The protective effect could be passively transferred by serum and was probably mediated by IgM antibodies.
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PMID:The relationship between the protective and cross-reacting antigens of Brucella spp., Yersinia enterocolitica 0:9 and Salmonella serotypes of Kauffmann-White group N. 11 12

The rabbits infected intravenously with viable Yersinia enterocolitica (Y.e.) produced the precipitating antibodies against a protein component as well as lipopolysaccharide of the organism. The production of the precipitins against protein antigen persisted for a long period of time even after the O-agglutinins had disappeared. The rabbits infected orally with the organism produced only the precipitins against protein antigen, and the amount of the antibody was equal to or greater than that of intravenous infection. The same precipitins that rabbits produced were detected even in human patients with yersiniosis showing O-agglutinin titers as low as less than or equal to 1:20. The antibody titers of mice infected with Y.e. were markedly lower than those of rabbits.
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PMID:Antigenicity of protein and lipopolysaccharide from Yersinia enterocolitica. 11 13

Present laboratory tests for human typhoid vaccines use an intraperitoneal route of challenge given 7 days after injection of increasing doses of standard and test vaccines by the same route. In studies reported here, groups of B6D2 mice were vaccinated intraperitoneally with 2 x 10(8) acetone-killed Salmonella typhi Ty2, with the Vi antigen-free variant O-901, or with Yersinia enterocolitica and Serratia marcescens suspensions. Other groups of mice received 200 mug of purified S. typhi or S. marcescens endotoxin, or their corresponding purified lipid A components. All of the vaccinated mice (except for saline- or thioglycolate-injected controls) exhibited increased protection against the lethal intraperitoneal challenge with S. typhi Ty2. Serial quantitative bacterial counts carried out on peritoneal washouts and on homogenates of the draining mediastinal lymph nodes indicated the development of an antibacterial response by the vaccinated host which was not observed in the control animals. Mice receiving purified endotoxin (lipopolysaccharide) exhibited varying degrees of protection, both in terms of increased host survival and the amount of inactivation of the challenge population in vivo. The response seen when the antigenically unrelated S. marcescens lipopolysaccharide was injected was little different from that seen when the acetone-killed S. typhi Ty2 whole-cell vaccine was used. This suggests that nonspecific inactivation of the intraperitoneal challenge contributes substantially to the immune response seen in mice vaccinated intraperitoneally with specific typhoid antigens.
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PMID:Assessment of typhoid vaccines by using the intraperitoneal route of challenge. 33 27

Antibodies against Yersinia enterocolitica serotype O:3 lipopolysaccharide present in sera from patients with Yersinia infection were studied by using an enzyme-linked immunosorbent assay. Of the sera with significant bacterial agglutination titers against Y. enterocolitica type O:3, 86% contained anti-lipopolysaccharide antibodies of the immunoglobulin G class. With the sera of some patients, we demonstrated increasing anti-lipopolysaccharide antibody levels of immunoglobulin G class in spite of decreasing bacterial agglutination titers. The assay was specific for lipopolysaccharide from Y. enterocolitica type O:3, and in inhibition experiments lipopolysaccharide could be detected in amounts of greater than or equal to 0.5 micrograms/ml.
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PMID:Demonstration of antibodies against Yersinia enterocolitica lipopolysaccharide in human sera by enzyme-linked immunosorbent assay. 48 21

A comparative study of various procedures of a lipopolysaccharide-protein complex (LPPC) from Yersinia pseudotuberculosis was carried out. The materials obtained were fractionated by molecular-sieve chromatography on Sepharose 2B resulting in highly aggregated complexes with antigen activity. LPPC aggregates dissociated in the presence of sodium dodecylsulphate (SDS) and urea. The chemical composition and serologic properties of fractions obtained are under consideration. The protein component of the complex consists of two major polypeptides (molecular weights--45,000 and 20,000) and some minor ones. The LPS component appeared to give 2--3 narrow bands in gel under conditions of SDS-polyacrylamide gel electrophoresis. It is suggested that such fractionation is caused by LPS association-dissociation in the course of electrophoresis.
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PMID:Studies on a lipopolysaccharide-protein complex from Yersinia pseudotuberculosis. 1 isolation and characterization. 54

Lipid A was isolated from lipopolysaccharide of Yersinia pseudotuberculosis S form (strain 341, subtype IB) using mild hydrolysis with acetic acid. The purified material (yield about 25%, molecular weight about 2900) contained D-glucosamine (11%), fatty acids (54%), protein concomitant (9.7%) and phosphorus (approximately 2%). Dodecanoic and 3-hydroxy-tetradecanoic acids in a molar ratio of 1 : 3.6 were detected as major fatty acid constituents. The hydroxyl groups of D-glucosamine were acylated with the residues of both fatty acids, while the amino groups were substituted with the residue of 3-hydroxy-tetradecanoic acid. Such a simple fatty acid composition is reminiscent of that found in lipid A in Y. pestis.
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PMID:Studies on lipid A from Yersinia pseudotuberculosis lipopolysaccharide. Isolation and general characterization. 69 14


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