The Lipooligosaccharides of Pathogenic Gram-Negative Bacteria

References

• Abu McLaughlin K. Y., Apicella R. E.M.A., Spinola S. M. Analysis of Haemophilus influenzae type b lipooligo-saccharide-synthesis genes that assemble or expose a 2-keto-3-deoxyoctulosonic acid epitope. Mol. Microbiol. 1991; 5: 2475
   PubMed Web of Science ®Google Scholar
• Adhya S. The galactose operon, in Escherichia coliSalmonella typhimurium. Cellular and Molecular Biology, F. C. Neidhard. American Society for Microbiology, Washington, D.C. 1987; Vol. 2: 1503
   Google Scholar
• Allen A., Maskell D. J. Identification, cloning and mutagenesis of a genetic locus required for lipopolysaccharide biosynthesis in. Bordetella pertussis, Mol. Microbiol. 1995; 19: 37
   Web of Science ®Google Scholar
• Anderson Bulawa M. S.C.E., Raetz C. R. The biosynthesis of Gram-negative endotoxin. Formation of lipid A precursors from UDP-GlcNAc in extracts of. Escherichia coli, J. Biol. Chem. 1985; 260: 15536
   PubMed Web of Science ®Google Scholar
• Anderson M. S., Raetz C. R. Biosynthesis of lipid A precursors in Escherichia coli. A cytoplasmic acyltransferase that converts UDP-N-acetylglucosamine to UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylgluco-samine. J. Biol. Chem 1987; 262: 5159
   PubMed Web of Science ®Google Scholar
• Anderson Robertson M. S., Macher A. D.I., Raetz C. R. Biosynthesis of lipid A in Escherichia coli: identification of UDP-3-O-[(R)-3-hydroxymyristoyl]-alpha-D-glucosamine as a precursor of UDP-N2,O3-bis[(R)-3-hydroxymyristoyl]-alpha-D-glucosamine. Biochemistry 1988; 27: 1908
   PubMed Web of Science ®Google Scholar
• Apicella M. A. Identification of two anti-genically distinct populations of gonococci: isolation and characterization of the responsible determinants. J. Infect. Dis. 1974; 130: 169
   PubMed Web of Science ®Google Scholar
• Apicella M. A. Serogroup classification of gonococci. J. Infect. Dis. 1976; 134: 377
   PubMed Web of Science ®Google Scholar
• Apicella Bennett M. A., Hermerath K. M.C.A., Roberts D. E. Monoclonal antibody analysis of lipopolysaccharide from Neisseria gonorrhoeae and. Neisseria meningitidis, Infect. Immun. 1981; 34: 751
   PubMed Web of Science ®Google Scholar
• Apicella Ketterer M. A., Lee M., Zhou F. K., Rice D.P.A., Blake M. S. The pathogenesis of gonococcal urethritis in men: confocal and immunoelectron microscopic analysis of urethral exudates from men infected with. Neisseria, J. Infect. Dis. 1996; 173: 636
   PubMed Web of Science ®Google Scholar
• Apicella Mandrell M. A., Shero R. E., Wilson M., Griffiss M., Brooks J. M., Fenner G. F., Breen C.J.F., Rice P. A. Modification of sialic acid of Neisseria gonorrhoeae lipooligosaccharide epitope expression in human urethral exudates: an immunoelectron microscopic analysis. J. Infect. Dis. 1990; 162: 506
   PubMed Web of Science ®Google Scholar
• Apicella Shero M. A., Jarvis M., Griffiss G. A., Mandrell J. M.R.E., Schneider H. Phenorypic variation in epitope expression of the Neisseria gonorrhoeae lipooligosaccharide. Infect. Immun. 1987; 55: 1755
   PubMed Web of Science ®Google Scholar
• Aspinall Fujimoto G. O., McDonald S., Pang A. G., Kurjanczyk H.L.A., Penner J. L. Lipopolysaccharides from Campylobacter jejuni associated with Guillain-Barré syndrome patients mimic human gangliosides in structure. Infect. Immun. 1994; 62: 2122
   PubMed Web of Science ®Google Scholar
• Aspinall Lynch G. O., Pang C. M., Shaver H.R.T., Moran A. P. Chemical structures of the core region of Campylobacter jejuni O: 3 lipopolysaccharide and an associated polysaccharide. Eur. J. Biochem. 1995; 231: 570
   PubMedGoogle Scholar
• Aspinall McDonald G. O., Pang A. G., Kurjanczyk H.L.A., Penner J. L. Lipopolysaccharide of Campylobacter coli serotype O: 30. Fractionation and structure of liberated core oligosaccharide. J. Biol. Chem. 1993; 268: 6263
   PubMed Web of Science ®Google Scholar
• Aspinall McDonald G. O., Pang A. G., Kurjanczyk H.L.A., Penner J. L. Lipopolysaccharides of Campylobacter jejuni serotype O: 19: structures of core oligosaccharide regions from the serostrain and two bacterial isolates from patients with the Guillain-Barré syndrome. Biochemistry. 1994; 33: 241
   PubMed Web of Science ®Google Scholar
• Aspinall McDonald G. O., Raju A. G., Pang T. S., Kurjanczyk H., Penner L. A.J.L., Moran A. P. Chemical structure of the core region of Campylobacter jejuni serotype O: 2 lipopolysaccharide. Eur. J. Biochem. 1993; 213: 1029
   PubMedGoogle Scholar
• Aspinall McDonald G. O., Raju A. G., Pang T. S., Mills H., Kurjanczyk S. D.L.A., Penner J. L. Serological diversity and chemical structures of Campylobacter jejuni low-molecular-weight lipopolysaccharides. J. Bacteriol. 1992; 174: 1324
   PubMed Web of Science ®Google Scholar
• Aspinall McDonald G. O., Raju A. G., Pang T. S., Moran H.A.P., Penner J. L. Chemical structures of the core regions of Campylobacter jejuni serotypes O: 1, O: 4, O: 23, and O: 36 lipopolysaccharides. Eur. J. Biochem 1993; 213: 1017, [published erratum appears in Eur. J. Biochem. 216, 880, 1993]
   PubMedGoogle Scholar
• Bachmann B. J. Linkage map of Escherichia coli K-12, edition 8 [published erratum appears in Microbiol. Rev. 55, 191, 1991]. Microbiol. Rev 1990; 54: 130
   PubMedGoogle Scholar
• Blake Blake M. S., Apicella C. M.M.A., Mandrell R. E. Gonococcal opacity: lectin-like interactions between Opa proteins and lipooligosaccharide. Infect. Immun. 1995; 63: 1434
   PubMed Web of Science ®Google Scholar
• Boons G., Overhand J. P. H.M., Vander Marel G. A., VanBoon J. H. Application of the dimethyl(phenyl)silyl groups as a masked form of hydroxy group in the synthesis of L-glycero-α-D-manno-hepto-pranoside-containing trisaccharide from the dephosphorylated inner core of. Neisseria meningitidis, Agnew. Chem. 1989; 28: 1504
   Google Scholar
• Brandtzaeg Mollnes P.T.E., Kierulf P. Complement activation and endotoxin levels in systemic meningococcal disease. J. Infect. Dis. 1989; 160: 58
   PubMed Web of Science ®Google Scholar
• Brooke J. S., Valvano M. A. Biosynthesis of inner core lipopolysaccharide in Enteric bacteria. Identification and characterization of a conserved phosphoheptose isomerase. J. Biol. Chem. 1996; 271: 3608
   PubMed Web of Science ®Google Scholar
• Campagnari Gupta A. A., Dudas M. R., Murphy K. C.T.F., Apicella M. A. Antigenic diversity of lipooligosaccharides of nontypeable. Haemophilus influenzae, Infect. Immun. 1987; 55: 882
   PubMed Web of Science ®Google Scholar
• Campagnari Karalus A. A., Apicella R., Melaugh M. A., Lesse W.A.J., Gibson B. W. Use of pyocin to select a Haemophilus ducreyi variant defective in lipooligosaccharide biosynthesis. Infect. Immun. 1994; 62: 2379
   PubMed Web of Science ®Google Scholar
• Campagnari Spinola A. A., Lesse S. M., Abu Kwaik Mandrell A. J. Y.R.E., Apicella M. A. Lipooligosaccharide epitopes shared among Gram-negative non-enteric mucosal pamogens. Microb. Pathog. 1990; 8: 353
   PubMed Web of Science ®Google Scholar
• Caroff Chaby M., Karibian R., Perry D., Deprun J.C., Szabo L. Variations in the carbohydrate regions of Bordetella pertussis lipopolysaccharides: electrophoretic, serological, and structural features. J. Bacteriol. 1990; 172: 1121
   PubMed Web of Science ®Google Scholar
• Clementz Bednarski T.J., Raetz C. R. H. Escherichia coli genes encoding KDO-dependent acyltransferases that incorporate laurate and myristate into lipid A. FASEB J. 1995; 9: 1311, (Abstr.)
   PubMed Web of Science ®Google Scholar
• Conrad R. S., Galano C. Characterization of Campylobacter jejuni lipopolysaccharide. Curr. Microbiol. 1990; 21: 377
   Web of Science ®Google Scholar
• Cope Yogev L. D., Mertsola R., Latimer J., Hanson J. L., McCracken M. S.G.J., Hansen E. J. Molecular cloning of a gene involved in lipooligosaccharide biosynthesis and virulence expression by Haemophilus influenzae type B. Mol. Microbiol. 1991; 5: 1113
   PubMed Web of Science ®Google Scholar
• de la Paz Cooke H.S.J., Heckels J. E. Effect of sialylation of lipopolysaccharide of Neisseria gonorrhoeae on recognition and complement-mediated killing by monoclonal antibodies directed against different outer-membrane antigens. Microbiology 1995; 141: 913
   PubMed Web of Science ®Google Scholar
• Demarco De Hormaeche Thornley R.M.J., Holmes A. Surface antigens of gonococci: correlation with virulence and serum resistance. J. Gen. Microbiol. 1983; 129: 1559
   PubMedGoogle Scholar
• Demarco de Hormaeche VanCrevel R.R., Hormaeche C. E. Neisseria gonorrhoeae LPS variation, serum-resistance and its induction by cytidine 5′-monophospho-N-acetylneuraminic acid. Microb. Pathog 1991; 10: 323
   PubMed Web of Science ®Google Scholar
• Denny F. W. Effect of a toxin produced by Haemophilus influenzae on ciliated respiratory epithelium. J. Immunol. 1974; 129: 93
   Google Scholar
• DiFabio Michon J. L., Brisson F.J.-R., Jennings H. J. Structure of the L1 and L6 core oligosaccharide epitopes of. Neisseria meningitidis. Can. J. Chem. 1990; 68: 1029
   Web of Science ®Google Scholar
• Drazek Stein E. S.D.C., Deal C. D. A mutation in the Neisseria gonorrhoeae rfaD homolog results in altered lipooligosaccharide expression. J. Bacteriol. 1995; 177: 2321
   PubMed Web of Science ®Google Scholar
• Dudas K. C., Apicella M. A. Selection and immunochemical analysis of lipooligosaccharide mutants of. Neisseria gonorrhoeae, Infect. Immun. 1988; 56: 499
   PubMed Web of Science ®Google Scholar
• Dziejman M., Mekalanos J. J. Two-component signal transduction and its role in the expression of bacterial virulence factors. Two-Component Signal Transduction, J. A. Hoch, T. J. Silhary. American Society for Microbiology, Washington, D. C. 1995; 305
   Google Scholar
• Elkins Carbonetti C., Varela N. H., Stirewalt V. A., Klapper D.D.G., Sparling P. F. Antibodies to N-terminal peptides of gonococcal porin are bactericidal when gonococcal lipopolysaccharide is not sialylated. Mol. Microbiol. 1992; 6: 2617
   PubMed Web of Science ®Google Scholar
• Estabrook Christopher M. M., Griffis N. N., Baker J. M.C.J., Mandrell R. E. Sialylation and human neutrophil killing of group C. Neisseria meningitidis, J. Infect. Dis. 1992; 166: 1079
   PubMed Web of Science ®Google Scholar
• Estabrook Mandrell M. M., Apicella R. E.M.A., Griffiss J. M. Measurement of the human immune response to meningococcal lipooligosaccharide antigens by using serum to inhibit monoclonal antibody binding to purified lipooligosaccharide. Infect. Immun. 1990; 58: 2204
   PubMed Web of Science ®Google Scholar
• Fleischmann Adams R. D., White M. D., Clayton O., Kirkness R. A., Kerlavage E. F., Bult A. R., Tomb C. J., Dougherty J. F., Merrick B. A., McKenney J. M., Sutton K., FitzHugh G., Fields W., Gocayne C., Scott J. D., Shirley J., Liu R., Glodek L. L., Kelley A., Weidman J. M., Phillips J. F., Spriggs C. A.T., Hedblom E. Whole-genome random sequencing and assembly of Haemophilus influenzae Rd. Science 1995; 269: 496
   PubMed Web of Science ®Google Scholar
• Flesher A. R., Insel R. A. Characterization of lipopolysaccharide of. H. influenzae, J. Infect. Dis. 1978; 138: 719
   PubMed Web of Science ®Google Scholar
• Fomsgaard Fomsgaard J. S., Hoiby A., Bruun B.B., Galanos C. Comparative immunochemistry of lipopolysaccharides from Branhamella catarrhalis strains. Infect. Immun. 1991; 59: 3346
   PubMed Web of Science ®Google Scholar
• Fox Jones A. J., Scotland D. M., Rowe S. M., Smith B., Brown A., Fitzgeorge M. R., Baskerville R. G., Parsons A.N.J., Cole J. A. Serum killing of meningococci and several other Gram-negative bacterial species is not decreased by incubating them with cytidine 5′-monophospho-N-acetyl neuraminic acid. Microb. Pathog. 1989; 7: 317
   PubMed Web of Science ®Google Scholar
• Frangipane J. V., Rest R. F. Anaerobic growth and cytidine 5′-monophospho-N-acetylneuraminic acid act synergistically to induce high-level serum resistance in. Neisseria gonorrhoeae. Infect. Immun. 1993; 61: 1657
   PubMed Web of Science ®Google Scholar
• Galloway S. M., Raetz C. R. A mutant of Escherichia coli defective in the first step of endotoxin biosynthesis. J. Biol. Chem. 1990; 265: 6394
   PubMed Web of Science ®Google Scholar
• Gamian Beurret A., Michon M., Brisson F.J.-R., Jennings H. J. Structure of the L2 lipopolysaccharide core oligaccharides of. Neisseria meningitidis, J. Biol. Chem. 1992; 267: 922
   PubMed Web of Science ®Google Scholar
• Gibson Melaugh B. W., Phillips W., Apicella N. J., Campagnari M. A.A.A., Griffiss J. M. Investigation of the structural heterogeneity of lipooligosaccharides from pathogenic Haemophilus, Neisseria species and of R-type lipopolysaccharides from Salmonella typhimurium by electrospray mass spectrometry. J. Bacteriol 1993; 175: 2702
   PubMed Web of Science ®Google Scholar
• Gibson Webb B. W., Yamasaki J. W., Fisher R., Burlingame S. J., Mandrell A. L., Schneider R. E.H., Griffiss J. M. Structure and heterogeneity of the oligosaccharides from the lipopolysaccharides of a pyocin-resistant. Neisseria gonorrhoeae, Proc. Natl. Acad. Set, U.S.A. 1989; 86: 17
   PubMed Web of Science ®Google Scholar
• Gotschlich E. C. Genetic locus for the biosynthesis of the variable portion of Neisseria gonorrhoeae lipooligosaccharide. J. Exp. Med. 1994; 180: 2181
   PubMed Web of Science ®Google Scholar
• Griffiss J. M. Mechanisms of host immunity. Meningococcal Disease, K. Cartwright. John Wiley and Sons, Chichester 1995; 35
   Google Scholar
• Griffiss Schneider J. M., Mandrell H., Yamasaki R. E., Jarvis R., Kim G. A., Gibson J. J., Hamadeh B. W.R., Apicella M. A. Lipooligosaccharides: the principal glycolipids of the neisserial outer membrane. Rev. Infect. Dis. 1988; 10: S287
   Google Scholar
• Haas R., Meyer T. F. The repertoire of silent pilus genes in Neisseria gonorrhoeae: evidence for gene conversion. Cell 1986; 44: 107
   PubMed Web of Science ®Google Scholar
• Hakamori S. Blood groups ABH and li antigens of human erythrocytes: chemistry, polymorphism, and their developmental change. Semin. Hematol. 1981; 18: 39
   PubMed Web of Science ®Google Scholar
• Hammerschmidt Birkholz S., Zah-Ringer C., Robertson U., VanPutten B. D., Ebeling J.O., Frosch M. Contribution of genes from the capsule gene complex (cps) to lipooligosaccharide biosynthesis and serum resistance in. Neisseria meningitidis, Mol. Microbiol. 1994; 11: 885
   PubMed Web of Science ®Google Scholar
• Hammerschmidt Hilse S., VanPutten R., Gerardy-Schahn J. P. M., Unkmeir R.A., Frosch M. Modulation of cell surface sialic acid expression in Neisseria meningitidis via a transposable genetic element. EMBO J. 1996; 15: 192
   PubMed Web of Science ®Google Scholar
• Helander Kilpelainen I. M.I., Vaara M. Increased substitution of phosphate groups in lipopoly saccharides and lipid A of the poly-myxin-resistant pmrA mutants of Salmonella typhimurium: a 31P-NMR study. Mol. Microbiol 1994; 11: 481
   PubMed Web of Science ®Google Scholar
• Helander Lindner I. M., Brade B., Altmann H., Lindberg K., Rietschel A. A.E.T., Zahringer U. Chemical structure of the lipopolysaccharide of Haemophilus influenzae strain 1–69 Rd-/b+. Description of a novel deep-rough chemotype. Eur. J. Biochem. 1988; 177: 483
   PubMedGoogle Scholar
• High Deadman N. J.M.E., Moxon E. R. The role of a repeteti ve DNA motif (5′-CAAT-3′) in the variable expression of the Haemophilus influenzae lipopolysaccharide epitope αGal(1–4)βGal. Mol. Microbiol. 1993; 9: 1275
   PubMed Web of Science ®Google Scholar
• Jarosik G. P., Hansen E. J. Identification of a new locus involved in expression of Haemophilus influenzae type b lipooligosaccharide. Infect. Immun. 1994; 62: 4861
   PubMed Web of Science ®Google Scholar
• Jennings H. J., Johnson H. G. The structure of an r-type oligosaccharide core obtained from some lipopolysaccharides of. Neisseria meningitidis, Carbohydr. Res. 1983; 121: 233
   PubMed Web of Science ®Google Scholar
• Jennings M. P., in preparation
   Google Scholar
• Jennings Hood M. P., Peak D. W., Virji I. R. A.M., Moxon E. R. Molecular analysis of a locus for the biosynthesis and phase-variable expression of the lacto-N-neotetraose terminal lipopolysaccharide structure in. Neisseria meningitidis, Mol. Microbiol. 1995; 18: 729
   PubMed Web of Science ®Google Scholar
• Jennings M. P., Vander Ley Wilks P., Maskeil K. E., Poolman D. J.J.T., Moxon E. R. Cloning and molecular analysis of the galE gene of Neisseria meningitidis and its role in lipopolysaccharide biosynthesis. Mol. Microbiol 1993; 10: 361
   Web of Science ®Google Scholar
• John Griffiss C. M., Apicella J., Mandrell M. A.R.E., Gibson B. W. The structural basis for pyocin resistance in Neisseria gonorrhoeae lipooligosaccharides. J. Biol. Chem. 1991; 266: 19303
   PubMed Web of Science ®Google Scholar
• Johnson A. P., Inzana T. J. Loss of ciliary activity in organ cultures of rat trachea treated with lipo-oligosaccharide from. Haemophilus influenzae, J. Med. Microbiol. 1986; 22: 265
   PubMed Web of Science ®Google Scholar
• Jones Borrow D. M., Fox R., Gray A. J., Cartwright S.K.A., Poolman J. T. The lipooligosaccharide immunotype as a virulence determinant in. Neisseria meningitidis, Microb. Pathog. 1992; 13: 219
   PubMed Web of Science ®Google Scholar
• Kaplan Hawkins S. L., Inzana E. P., Patrick T. J.C.C., Mason E. J. Contribution of Haemophilus influenzae type b lipopolysaccharide to pathogenesis of infection. Microb. Pathog. 1988; 5: 55
   PubMed Web of Science ®Google Scholar
• Karow Fayet M.O., Georgopoulos C. The lethal phenotype caused by null mutations in the Escherichia coli htrB gene is suppressed by mutations in the accBC operon, encoding two subunits of acetyl coenzyme A carboxylase. J. Bacteriol 1992; 174: 7407
   PubMed Web of Science ®Google Scholar
• Karow M., Georgopoulos C. Sequencing, mutational analysis, and transcriptional regulation of the Escherichia coli htrB gene. Mol. Microbiol. 1991; 5: 285
   Web of Science ®Google Scholar
• Karow M., Georgopoulos C. Isolation and characterization of the Escherichia coli msbB gene, a multicopy suppressor of null mutations in the high-temperataaure requirement gene. htrB, J. Bacteriol. 1992; 174: 702
   PubMed Web of Science ®Google Scholar
• Karow M., Georgopoulos C. The essential Escherichia coli msbA gene, a multicopy suppressor of null mutations in the htrB gene, is related to the universally conserved family of ATP-dependent translocators. Mol. Microbiol 1993; 7: 69
   PubMed Web of Science ®Google Scholar
• Kelly Thibault J. F., Massoud P., Perry H.M.B., Richards J. C. Presented at the Abs. 41st Conf. Mass Spectrom. 1993
   Google Scholar
• Kerwood Schneider D. E.H., Yamasaki R. Structural analysis of lipooligosaccharide produced by Neisseria gonorrhoeae strain MS1 1mk (variant A): a precursor for a gonococcal lipooligosaccharide associated with virulence. Biochemistry 1992; 31: 12760
   PubMed Web of Science ®Google Scholar
• Kim Mandrell J. J.R.E., Griffiss J. M. Neisseria lactamica, Neisseria meningitidis share lipooligosaccharide epitopes but lack common capsular and class 1, 2 and 3 protein epitopes. Infect. Immun 1989; 57: 602
   PubMed Web of Science ®Google Scholar
• Kim Zhou J. J., Mandrell D.R.E., Griffiss J. M. Effects of endogenous sialylation of the lipooligosaccharide of Neisseria gonorrhoeae on opsonophagocytosis. Infect. Immun. 1992; 60: 989
   PubMed Web of Science ®Google Scholar
• Kimura A., Hansen E. J. Antigenic and phenotypic variations of Haemophilus influenzae type b lipopolysaccharide and their relationship to virulence. Infect. Immun. 1986; 51: 69
   PubMed Web of Science ®Google Scholar
• Kimura Patrick A., Miller C. C., Cope E. E., McCracken L. D.G.J., Hansen E. J. Haemophilus influenzae type b lipooligosaccharide: stability of expression and association with virulence. Infect. Immun. 1987; 55: 1979
   PubMed Web of Science ®Google Scholar
• Klein Ison N. J., Peakman C. A., Levin M., Hammerschmidt M., Frosch S.M., Heyderman R. S. The influence of capsulation and lipooligosaccharide structure on neutrophil adhesion molecule expression and endothelial injury by. Neisseria meningitidis, J. Infect. Dis. 1996; 173: 172
   PubMed Web of Science ®Google Scholar
• Klemm P. Two regulatory fim genes, fimB, fimE control the phase variation of type 1 fimbriae in. Escherichia coli, EMBO J 1986; 5: 1389
   PubMed Web of Science ®Google Scholar
• Langford P. R., Moxon E. R. Growth of Haemophilus influenzae type b in continuous culture: effect of dilution rate on outer-membrane protein and lipopolysaccharide expression. FEMS Microbiol. Lett. 1992; 72: 43
   PubMed Web of Science ®Google Scholar
• Langford P. R., Moxon E. R. The dilution rate affects the outer membrane protein and lipopolysaccharide composition of Haemophilus influenzae type b grown under iron limitation. J. Bacteriol. 1993; 175: 2462
   PubMed Web of Science ®Google Scholar
• Langford Szabo P. R.M., Moxon E. R. In vitro cytotoxicity of Haemophilus influenzae lipopolysaccharides for bovine aortal endothelial cells. FEMS Microbiol. Lett 1991; 65: 161
   PubMed Web of Science ®Google Scholar
• Lasfargues Caroff A.M., Chaby R. Structural features involved in the mitogenic activity of Bordetella pertussis lipopolysaccharides for spleen cells of C3H/HeJ mice. FEMS Immun. Med. Microbiol. 1993; 7: 119
   PubMedGoogle Scholar
• Lebbar Caroff S., Szabo M., Merienne L.C., Szilogyi L. Structure of a hexasaccharide proximal to the hydrophobic region of lipopolysaccharides present in Bordetella pertussis endotoxin preparations. Carbohydr. Res. 1994; 259: 257
   PubMed Web of Science ®Google Scholar
• Lee Stephens F. K. N., Gibson D. S., Engstrom B. W., Zhou J. J.D., Apicella M. A. Microheterogeneity of Neisseria lipooligosaccharide: analysis of a UDP-glucose 4-epimerase mutant of Neisseria meningitidis NMB. Infect. Immun 1995; 63: 2805
   PubMed Web of Science ®Google Scholar
• Lee N.-Sunshine G.M.G., Apicella M. A. Molecular cloning and characterization of the nontypeable Haemophilus influenzae 2019 rfaE gene required for lipopolysaccharide biosynthesis. Infect. Immun 1995; 63: 818
   PubMed Web of Science ®Google Scholar
• Lee Sunshine N.-G., Engstrom M. G., Gibson J. J.B.W., Apicella M. A. Mutation of the htrB locus of Haemophilus influenzae nontypeable strain 2019 is associated with modifications of lipid A and phosphorylation of the lipooligosaccharide. J. Biol. Chem 1995; 270: 27151
   PubMed Web of Science ®Google Scholar
• Levinson G., Gutman G. A. Slipped-strand mispairing: a major mechanism for DNA sequence evolution. Mol. Biol. Evol. 1987; 4: 203
   PubMed Web of Science ®Google Scholar
• Luderitz Galanos O., Lehmann C., Nurminen V., Rietschel J., Rosenfelder E. T., Simon G.M., Westphal O. Lipid A: chemical structure and biological activity. J. Infect. Dis. 1973; 128: S17
   Web of Science ®Google Scholar
• Luderitz Galanos O., Risse C., Ruschmann H. J., Schlecht E., Schmidt S., Shulte-Hoithausen G., Wheat H.R., Westphal O. Structural relationships of Salmonella O and R antigens. Ann. N. Y. Acad. Sci. 1966; 133: 349
   PubMed Web of Science ®Google Scholar
• Mackinnon Borrow F. G., Gorringe R., Fox A. R., Jones A. J.D.M., Robinson A. Demonstration of lipooligosaccharide immunotype and capsule as virulence factors for Neisseria meningitidis using an infant mouse intranasal infection model. Microb. Pathog. 1993; 15: 359
   PubMed Web of Science ®Google Scholar
• Maeland J. A. Antigenic properties of various preparations of Neisseria gonorrhoeae endotoxin. Acta. Pathol. Microbiol. Scand. 1968; 73: 413
   PubMedGoogle Scholar
• Maeland J. A. Serological cross-reactions of aqueous ether extracted endotoxin from Neisseria gonorrhoeae strains. Acta Pathol. Microbiol. Scand. 1969; 77: 505
   PubMedGoogle Scholar
• Maeland Kristoffersen J. A.T., Hofstad T. Immunochemical investigations of Neisseria gonorrhoeae endotoxin. Acta Pathol. Microbiol. Scand. 1971; 79: 233
   Google Scholar
• Mandrell Schneider R., Apicella H., Zolliinger M. A., Rice W.P.A., Griffiss J. M. Antigenic and physical diversity of Neisseria gonorrhoeae lipooligosaccharides. Infect. Immun. 1986; 54: 63
   PubMed Web of Science ®Google Scholar
• Mandrell R. E. Further antigenic similarities of Neisseria gonorrhoeae lipooligosaccharides and human glycosphingolipids. Infect. Immun. 1992; 60: 3017
   Google Scholar
• Mandrell Griffiss R. E.J.M., Macher B. A. Lipooligosaccharides (LOS) of Neisseria gonorrhoeae, Neisseria meningitidis have components that are immunochemically similar to precursors of human blood group antigens. J. Exp. Med 1988; 168: 107
   PubMed Web of Science ®Google Scholar
• Mandrell Griffiss R. E., Smith J. M.H., Cole J. A. Distribution of a lipooligosaccharide-specific sialyltransferase in pathogenic and non-pathogenic. Neisseria, Microb. Pathog. 1993; 14: 315
   PubMed Web of Science ®Google Scholar
• Mandrell Kim R. E., John J. J., Gibson C. M., Sugai B. W., Apicella J. V., Griffiss M. A.J.M., Yamasaki R. Endogenous sialylation of the lipooligosaccharides of. Neisseria meningitidis, J. Bacteriol. 1991; 173: 2823
   PubMed Web of Science ®Google Scholar
• Mandrell Lesse R. E., Sugai A. J., Shero J. V., Griffiss M., Cole J. M., Parsons J. A., Smith N. J., Morse H.S.A., Apicella M. A. In vitro, in vivo modification of Neisseria gonorrhoeae lipooligosaccharide epitope structure by sialylation. J. Exp. Med 1990; 171: 1649
   PubMed Web of Science ®Google Scholar
• Mandrell McLaughlin R. E., Aba Kwaik Lesse R.Y., Yamasaki A., Gibson R., Spinola B.S.M., Apicella M. A. Lipooligosaccharides (LOS) of some Haemophilus species mimic human glycosphingolipids, and some LOS are sialylated. Infect. Immun. 1992; 60: 1322
   PubMed Web of Science ®Google Scholar
• Mandrell Smith R. E., Jarvis H., Griffiss G. A.J.M., Cole J. A. Detection and some properties of the sialyltransferase implicated in the sialylation of lipopolysaccharide of. Neisseria gonorrhoeae, Microb. Pathog. 1993; 14: 307
   Google Scholar
• Mandrell R. E., Zollinger W. D. Lipopolysaccharide serotyping of Neisseria meningitidis by hemagglutination inhibition. Infect. Immun. 1977; 16: 471
   PubMed Web of Science ®Google Scholar
• Martin Patel P. M. V., Parsons P. V.N.J., Smith H. Induction of serum resistance in recent isolates of Neisseria gonorrhoeae by a low-molecular-weight fraction of guinea pig serum. J. Infect. Dis. 1983; 148: 334
   PubMed Web of Science ®Google Scholar
• Maskell Szabo D. J., Butler M. J., Williams P. D.A.E., Moxon E. R. Molecular analysis of a complex locus from Haemophilus influenzae involved in phase-variable lipopolysaccharide biosynthesis. Mol. Microbiol. 1991; 5: 1013
   PubMed Web of Science ®Google Scholar
• Maskell Szabo D. J., Deadman M. J.M.E., Moxon E. R. The gal locus from Haemophilus influenzae: cloning, sequencing and the use of gal mutants to study lipopolysaccharide. Mol. Microbiol 1992; 6: 3051
   PubMed Web of Science ®Google Scholar
• McLaughlin Spinola R.S.M., Apicella M. A. Generation of lipooligosaccharide mutants of Haemophilus influenzae type b. J. Bacteriol. 1992; 174: 6455
   PubMed Web of Science ®Google Scholar
• Melaugh Gibson W.B.W., Campagnari A. A. The lipooligosaccharides of Haemophilus ducreyi are highly sialylated. J. Bacteriol. 1996; 178: 564
   PubMed Web of Science ®Google Scholar
• Melaugh Phillips W., Campagnari N., Karalus A. A.R., Gibson B. A. Partial characterization of the major lipooligoasccharide from a strain of Haemophilus ducreyi, z. genital ulcer disease. J. Biol. Chem. 1992; 267: 13434
   PubMed Web of Science ®Google Scholar
• Melaugh Phillips W., Campagnari N. J., Tullius A. A.M.V., Gibson B. W. Structure of the major oligosaccharide from the lipooligosaccharide of Haemophilus ducreyi strain 35000 and evidence for additional glycoforms. Biochemistry 1994; 33: 13070
   PubMed Web of Science ®Google Scholar
• Michon Beurret F., Gamian M., Brisson A.J.R., Jennings H. J. Structure of the L5 lipopolysaccharide core oligosaccharides of. Neisseria meningitidis, J. Biol. Chem. 1990; 265: 7243
   PubMed Web of Science ®Google Scholar
• Morse S. A., Apicella M. A. Isolation of a lipopolysaccharide mutant of Neisseria gonorrhoeae: an analysis of the antigenic and biologic differences. J. Infect. Dis. 1982; 145: 206
   PubMed Web of Science ®Google Scholar
• Morse Mintz S. A., Sarafian C. S., Bartenstein S. K., Bertram L.M., Apicella M. A. Effect of dilution rate on lipopolysaccharide and serum resistance of Neisseria gonorrhoeae grown in continuous culture. Infect. Immun. 1983; 41: 74
   PubMed Web of Science ®Google Scholar
• Murphy Connell G. L., Barritt T. D., Koomey D. S.M., Cannon J. G. Phase variation of gonococcal protein. II. Regulation of gene expression by slipped-strand mispairing of a repetitive DNA sequence. Cell 1989; 56: 539
   PubMed Web of Science ®Google Scholar
• Nagasawa Ishige S.K., Mizuno T. Novel members of the two-component signal transduction genes in. Escherichia col, J. Biochem. (Tokyo) 1993; 114: 350
   PubMed Web of Science ®Google Scholar
• Nairn Cole C. A., Patel J. A., Parsons P. V., Fox N. J.J.E., Smith H. Cytidine 5′-monophospho-N-acetylneuraminic acid or a related compound is the low Mr factor from human red blood cells that induces gonococcal resistance to killing by human serum. J. Gen. Microbiol 1988; 134: 3295
   PubMedGoogle Scholar
• Nichols Lee W. A.N., Sunshine G.M.G., Apicella M. A. Identification of the ADP-L-glycero-D-mannoheptose-6-epimerase (rfaD) and heptosyltransferase II (rfaF) biosynthesis genes from nontypeable. Haemophilus influenzae 1995, strain 2019, submitted
   Google Scholar
• Nummila Kilpelaeinen K., Zaehringer I., Vaara U.M., Helander I. M. Lipopolysaccharides of polymyxin B-resistant mutants of Escherichia coli are extensively substituted by 2-aminoethyl pyrophosphate and contain aminoarabinose in lipid A. Mol. Microbiol. 1995; 16: 271
   PubMed Web of Science ®Google Scholar
• Parsons Cole N. J.J.A., Smith H. Resistance to human serum of gonococci in urethral exudates is reduced by neuraminidase. Proc. R. Soc. Lond. B 1990; 241: 3
   PubMed Web of Science ®Google Scholar
• Parsons Patel N. J., Tan P. V., Andrade E. L., Nairn J. R., Goldner C. A., Cole M.J.A., Smith H. Cytidine 5′-monophospho-N-acetyl neuraminic acid and a low molecular weight factor from human blood cells induce lipopolysaccharide alteration in gonococci when conferring resistance to killing by human serum. Microb. Pathog. 1988; 5: 303
   PubMed Web of Science ®Google Scholar
• Patel Martin P. V., Tan P. M., Nairn E. L., Parsons C. A., Goldner N. J.M., Smith H. Protein changes associated with induced resistance of Neisseria gonorrhoeae to killing by human serum are relatively minor. J. Gen. Microbiol. 1988; 134: 499
   PubMedGoogle Scholar
• Patel Martin P. V., Goldner P. M. V., Parsons M.N.J., Smith H. Red blood cells, a source of factors that induce gonococci to resistance to complement mediated killing by human serum. J. Gen. Microbiol. 1984; 130: 2768
   Google Scholar
• Patel Parsons P. V., Andrade N. J., Nairn J. R. C., Tan C. A., Goldner E. L., Cole M.J.A., Smith H. White blood cells including polymorphonuclear phagocytes contain a factor that induces gonococcal resistance to complement-mediated serum killing. FEMS Microbiol. Lett. 1988; 50: 173
   Web of Science ®Google Scholar
• Patel Veale P. V., Fox R., Martin J. E., Parson V.N.J., Smith H. Fractionation of guinea pig serum for an inducer of gonococcal resistance to killing by human serum: active fractions containing glucopeptides similar to those from human red blood cells. J. Gen. Microbiol. 1984; 130: 2757
   PubMedGoogle Scholar
• Patrick Betts D., Frey J., Prameya E. A., Dorovini R.Z.K., Finlay B. B. Haemophilus influenzae lipopolysaccharide disrupts confluent monolayers of bovine brain endothelial cells via a serum-dependent cytotoxic pathway. J. Infect. Dis. 1992; 165: 865
   PubMed Web of Science ®Google Scholar
• Peppier M. S. Two physically and serologically distinct lipopolysaccharide profiles in strains of Bordetella pertussis and their phenotype variants. Infect. Immun. 1984; 43: 224
   PubMed Web of Science ®Google Scholar
• Perry M. B., Daoust V. The lipopolysaccharide of Neisseria gonorrhoeae colony type 1 and 4. Can. J. Biochem. 1975; 53: 623
   PubMedGoogle Scholar
• Pettit K. R., Wagner M. E. S.S.M., Bertolino V. J. Phenotypic modulation of gonococcal lipooligosaccharide in acidic and alkaline culture. Infect. Immun. 1995; 63: 2773
   PubMed Web of Science ®Google Scholar
• Phillips Apicella N. J., Griffiss M. A.J., Gibson B. W. Structural studies of the lipooligosaccharides from Haemophilus influenzae type b strain A2. Biochemistry 1993; 32: 2003
   PubMed Web of Science ®Google Scholar
• Phillips Apicella N. J.M.A., McLeod Griffiss J., Gibson B. W. Structural characterization of the cell surface lipooligosaccharides from a nontypeable strain of. Haemophilus influenzae, Biochemistry 1992; 31: 4515
   PubMed Web of Science ®Google Scholar
• Phillips John N. J., Reinders C. M., Gibson L. G., Apicella B. W.M.A., Griffiss J. M. Structural models for the cell surface lipooligosaccharides of Neisseria gonorrhoeae and. Haemophilus influenzae, Biomed. Environ. Mass Spectrom. 1990; 19: 731
   PubMed Web of Science ®Google Scholar
• Phillips McLaughlin N. J., Miller R., Apicella T. J.M.A., Gibson B. W. Characterization of two transposon mutants from Haemophilus influenzae type b with altered lipooligosaccharide biosynthesis. Biochemistry 1996, in press
   PubMed Web of Science ®Google Scholar
• Porat Apicella N.M.A., Blake M. S. A lipooligosaccharide binding site on HepG2 cells similar to the gonococcal opacity-associated surface protein opa. Infect. Immun. 1995; 63: 2164
   PubMed Web of Science ®Google Scholar
• Porat Apicella N.M.A., Blake M. S. Neisseria gonorrhoeae utilizes and enhances the biosynthesis of the asialoglycoprotein receptor expressed on the surface of the hepatic HepG2 cell line. Infect. Immun. 1995; 63: 1498
   PubMed Web of Science ®Google Scholar
• Preston Maskell A., Johnson D. J.A.P., Moxon E. R. Altered lipopolysaccharide characteristic of the 169 phenotype in Haemophilus influenzae results from mutations in a novel gene. isn, J. Bacteriol. 1996; 178: 396
   PubMed Web of Science ®Google Scholar
• Rest R. F., Frangipane J. V. Growth of Neisseria gonorrhoeae in CMP-N-acetylneuraminic acid inhibits nonopsonic (opacity-associated outer membrane protein-mediated) interactions with human neutrophils. Infect. Immun 1992; 60: 989
   PubMed Web of Science ®Google Scholar
• Rice Blake P. A.M.S., Joiner K. A. Mechanisms of stable serum resistance of. Neisseria gonorrhoeae, Antonie VanLeeuwenhoek 1987; 53: 565
   PubMed Web of Science ®Google Scholar
• Rice P. A., Kasper D. Natural serum bactericidal activity against Neisseria gonorrhoeae isolates from disseminated, locally invasive and uncomplicated disease. J. Immunol. 1977; 124: 2105
   Google Scholar
• Rick P. D. Lipopolysaccharide biosynthesis. Escherichia coli and Salmonella typhimurium. Cellular and Molecular Biology, F. C. Neidhardt. American Society for Microbiology, Washington, D. C. 1987; Vol. 1: 648
   Google Scholar
• Robertson Frosch B. D.M., VanPutten J. P. The identification of cryptic rhamnose biosynthesis genes in Neisseria gonorrhoeae and their relationship to lipopolysaccharide biosynthesis. J. Bacteriol. 1994; 176: 6915
   PubMed Web of Science ®Google Scholar
• Robertson Frosch B. D.M., VanPutten J. P. The role of galE in the biosynthesis and function of gonococcal lipopolysaccharide. Mol. Microbiol. 1993; 8: 891
   PubMed Web of Science ®Google Scholar
• Roland Martin K. L., Esther L. E.C.R., Spitznagel J. K. Spontaneous pmrA mutants of Salmonella typhimurium LT2 define a new two-component regulatory system with a possible role in virulence. J. Bacteriol 1993; 175: 4154
   PubMed Web of Science ®Google Scholar
• Sandlin R. C., Stein D. C. Role of phosphoglucomutase in lipooligosaccharide biosynthesis in. Neisseria gonorrhoeae, J. Bacteriol. 1994; 176: 2930
   PubMed Web of Science ®Google Scholar
• Schauer R. Sialic acids and their role as biological masks. TIBS 1985; 10: 357
   Web of Science ®Google Scholar
• Schnaitman C. A., Klena J. D. Genetics of lipopolysaccharide biosynthesis in enteric bacteria. Microbiol. Rev. 1993; 57: 655
   PubMedGoogle Scholar
• Schneider Griffiss H., Boslego J. M., Hitchcock J. W., Zahos P. J.K.M., Apicella M. A. Expression of paragloboside like lipooligosaccharides may be a necessary component of gonococcal pathogenesis in men. J. Exp. Med. 1991; 174: 1601
   PubMed Web of Science ®Google Scholar
• Schneider Hale H., Zollinger T. L., Seid W. D., Hammack R. C.C.A., Griffiss J. M. Heterogeneity of molecular size and antigenic expression within lipooligosaccharides of individual strains of Neisseria gonorrhoeae and. Neisseria meningitidis, Infect. Immun. 1984; 45: 544
   PubMed Web of Science ®Google Scholar
• Schneider Hammack H., Apicella C. A.M.A., Griffiss J. M. Instability of expression of lipooligosaccharides and their epitopes in. Neisseria gonorrhoeae, Infect. Immun. 1988; 56: 942
   PubMed Web of Science ®Google Scholar
• Schoolnik Buchanan G. K.T.M., Holmes K. K. Gonococci causing disseminated gonococcal infection are resistant to the bactericidal action of normal human sera. J. Clin. Invest. 1976; 58: 1163
   PubMed Web of Science ®Google Scholar
• Schwan Robertson E. T., Brade B. D.H., VanPutten J. P. Gonococcal rfaF mutants express Rd2 chemotype LPS and do not enter epithelial host cells. Mol. Microbiol. 1995; 15: 267
   PubMed Web of Science ®Google Scholar
• Schweda Jonasson E. K.J.A., Jansson P. E. Structural studies of lipooligosaccharides from Haemophilus ducreyi ITM 5535, ITM 3147, and a fresh clinical isolate, ACY1: evidence for intrastrain heterogeneity with the production of mutually exclusive sialylated or elongated glycoforms. J. Bacteriol. 1995; 177: 5316
   PubMed Web of Science ®Google Scholar
• Schweda Sundstrom E. K., Eriksson A. C., Jonasson L. M.J.A., Lindberg A. A. Structural studies of the cell envelope lipopolysaccharides from Haemophilus ducreyi strains ITM 2665 and ITM 4747. J. Biol. Chem. 1994; 269: 12040
   PubMed Web of Science ®Google Scholar
• Smith Cole H.J.A., Parsons N. J. The sialylation of gonococcal lipopolysaccharide by host factors: a major impact on pathogenicity. FEMS Microbiol Lett. 1992; 100: 287
   PubMed Web of Science ®Google Scholar
• Stephens D. S. Gonococcal and meningococcal pathogenesis as defined by human cell, cell culture and organ culture assays. Clin. Microbiol Rev. 1989; 2: S104
   PubMed Web of Science ®Google Scholar
• Stinavage Martin P.L.E., Spitznagel J. K. O-antigen and lipid A phosphoryl groups in resistance of Salmonellae typhimurium LT-2 to nonoxidative killing in human polymorphonuclear neutrophils. Infect. Immun. 1989; 57: 3894
   PubMed Web of Science ®Google Scholar
• Swanson Bergstrom J., Boslego S.J., Koomey M. Gene conversion accounts for pilin structural changes and for reversible piliation “phase” changes in gonococci. Gonococci and Meningococci. Epidemiology, Genetics, Immunochemistry, and Pathogenesis, J. T. Poolman Zanen, H. C. Meyer, T. F. Heckles, J. E. Makela, P. R. H. H. Smith, E. C. Beuvery. Kluwer Academic Publishers, Dordrecht 1988; 335
   Google Scholar
• Syrogiannopoulos Hansen G. A., Erwin E. J., Munford A. L., Rutledge A. S., Reisch J.J.S., McCracken G. J. Haemophilus influenzae type b lipooligosaccharide induces meningeal inflammation. J. Infect. Dis. 1988; 157: 237
   PubMed Web of Science ®Google Scholar
• Szabo Maskell M., Butler D., Love P.J., Moxon R. Use of chromosomal gene fusions to investigate the role of repetitive DNA in regulation of genes involved in lipopolysaccharide biosynthesis in. Haemophilus influenzae, J. Bacteriol. 1992; 174: 7245
   PubMed Web of Science ®Google Scholar
• Tan Patel E. L., Parsons P. V., Martin N. J.P.M., Smith H. Lipopolysaccharide alteration is associated with induced resistance of Neisseria gonorrhoeae to killing by human serum. J. Gen. Microbiol. 1986; 132: 1407
   PubMedGoogle Scholar
• Tsai Boykins C. M.R., Frasch C. E. Heterogeneity and variation among Neisseria meningitidis lipopolysaccharides. J. Bacteriol. 1983; 155: 498
   PubMed Web of Science ®Google Scholar
• Tullius M., Gibson B. W. Presented at the Abstracts of the 95th General Meeting of the American Society for Microbiology. Washington, D. C. May 21–25, 1995
   Google Scholar
• Ullrich J., VanPutten J. P. M. Identification of the gonococcal glmU gene encoding the enzyme N-acetylglucosamine 1-phosphate uridyltransferase involved in the synthesis of UDP-GlcNAc. J. Bacteriol 1995; 177: 6902
   PubMed Web of Science ®Google Scholar
• VanHam VanAlphen S. M., Mooi L.F.R., VanPutten J. P. Phase variation of H. influenzae fimbriae: transcriptional control of two divergent genes through a variable combined promoter region. Cell 1993; 73: 1187
   PubMed Web of Science ®Google Scholar
• Verheul Snippe A. F.H., Poolman J. T. Meningococcal lipopolysaccharides: virulence factor and potential vaccine component. [Review]. Microbiol. Rev. 1993; 57: 34
   PubMedGoogle Scholar
• Verheul Braat A. F. M., Leenhouts A. K., Hoogerhout J. M., Poolman P., Snippe J. T.H., Verhoef J. Preparation, characterization, and immunogenicity of meningococcal immunotype L2 and L3,7,9 phosphoethanolamine group containing oligosaccharide-protein conjugates. Infect. Immun. 1991; 59: 843
   PubMed Web of Science ®Google Scholar
• Virji Weiser M., Lindberg J. N.A.A., Moxon E. R. Antigenic similarities in lipopolysaccharides of Haemophilus, Neisseria and expression of a diagalacatoside structure also present on human cells. Microb. Pathog 1990; 9: 441
   PubMed Web of Science ®Google Scholar
• von Wulffen Hartard H.C., Scharein E. Seroreactivity to Campylobacter jejuni and gangliosides in patients with Guillain-Barré syndrome [see comments]. J. Infect. Dis. 1994; 170: 828
   PubMed Web of Science ®Google Scholar
• Ward Watt M. E.P.J., Glynn A. A. Gonococci in urethral exudates possess a virulence factor lost on subculture. Nature 1970; 227: 382
   PubMed Web of Science ®Google Scholar
• Weiser Lindberg J. N., Manning A. A., Hansen E. J.E.J., Moxon E. R. Identification of a chromosomal locus for expression of lipopolysaccharide epitopes in. Haemophilus influenzae, Infect. Immun. 1989; 57: 3045
   PubMed Web of Science ®Google Scholar
• Weiser Love J. N.J.M., Moxon E. R. The molecular mechanism of phase variation of Haemophilus influenzae lipopolysaccharide. Cell 1989; 59: 657
   PubMed Web of Science ®Google Scholar
• Weiser Maskell J. N., Butler D. J., Lindberg P. D.A.A., Moxon E. R. Characterization of repetitive sequences controlling phase variation of Haemophilus influenzae lipopolysaccharide. J. Bacteriol. 1990; 172: 3304
   PubMed Web of Science ®Google Scholar
• Weiser Williams J. N.A., Moxon E. R. Phase-variable lipopolysaccharide structures enhance the invasive capacity of. Haemophilus influenzae, Infect. Immun. 1990; 58: 3455
   PubMed Web of Science ®Google Scholar
• Westphal Jann O.K., Himmelspach K. Chemistry and immunochemistry of bacterial lipopolysaccharides as cell wall antigens and endotoxins. Prog. Allergy 1983; 33: 9
   PubMedGoogle Scholar
• Wetzler Barry L. M., Blake K.M.S., Gotschlich E. C. Gonococcal lipo-oligosaccharide sialylation prevents complement-dependent killing by immune sera. Infect. Immun. 1992; 60: 39
   PubMed Web of Science ®Google Scholar
• Willems Paul R.A., Vander Heide H. G.J., ter Avest A. R., Mooi F. R. Fimbrial phase variation in Bordetella pertussis: a novel mechanism for transcriptional regulation. EMBO J. 1990; 9: 2803
   PubMed Web of Science ®Google Scholar
• Winstanley Blackwell F. P., Tan C. C., Patel E. L., Parsons P. V., Martin N. J.P.M.V., Smith H. Alteration of pyocin-sensitivity pattern of Neisseria gonorrhoeae is associated with induced resistance to killing by human serum. J. Gen. Microbiol. 1984; 130: 1303
   PubMedGoogle Scholar
• Yamasaki Bacon R., Nasholds B. E., Schneider W.H., Griffiss J. M. Structural determination of oligosaccharides derived from lipooligosaccharide of Neisseria gonorrhoeae F62 by chemical, enzymatic, and two-dimensional NMR methods. Biochemistry 1991; 30: 10566
   PubMed Web of Science ®Google Scholar
• Yamasaki Griffiss R., Quinn J. M.K.P., Mandrell R. E. Neuraminic acid is alpha 2→3 linked in the lipooligosaccharide of Neisseria meningitidis serogroup B strain 6275. J. Bacteriol. 1993; 175: 4565
   PubMed Web of Science ®Google Scholar
• Yamasaki Kerwood R., Schneider D. E., Quinn H., Griffiss K. P.J.M., Mandrell R. E. The structure of lipooligosaccharide produced by Neisseria gonorrhoeae strain 15253, isolated from a patient with disseminated infection. Evidence for a new glycosylation pathway of the gonococcal lipooligosaccharide. J. Biol. Chem. 1994; 269: 30345
   PubMed Web of Science ®Google Scholar
• Yamasaki Nasholds R., Schneider W.H., Apicella M. A. Epitope expression and partial structural characterization of F62 lipooligosaccharide (LOS) of Neisseria gonorrhoeae: IgM monoclonal antibodies (3F11 and 1–1-M) recognize non-reducing termini of the LOS components. Mol. Immunol. 1991; 28: 1233
   PubMed Web of Science ®Google Scholar
• Yamasaki Schneider R., Griffiss H.J.M., Mandrell R. Epitope expression of gonococcal lipooligosaccharide (LOS). Importance of the lipoidal moiety for expression of an epitope that exists in the oligosaccharide moiety of LOS. Mol. Immunol. 1988; 25: 799
   PubMed Web of Science ®Google Scholar
• Yuki Taki N., Inagaki T., Kasama F., Takahashi T., Saito M., Handa K.S., Miyatake T. A bacterium lipopolysaccharide that elicits Guillain-Barré syndrome has a GM1 ganglioside-like structure. J. Exp. Med 1993; 178: 1771
   PubMed Web of Science ®Google Scholar
• Yuki Taki N., Takahashi T., Saito M., Tai K., Miyatake T.T., Handa S. Penner's serotype 4 of Campylobacter jejuni has a lipopolysaccharide that bears a GM1 ganglioside epitope as well as one that bears a GD1 epitope. Infect. Immun 1994; 62: 2101
   PubMed Web of Science ®Google Scholar
• Zhou Lee D.N.G., Apicella M. A. Lipooligosaccharide biosynthesis in Neisseria gonorrhoeae: cloning, identification and characterization of the alpha 1,5 heptosyltransferase I gene. (rfaC), Mol. Microbiol. 1994; 14: 609
   PubMed Web of Science ®Google Scholar
• Zhou Stephens D., Gibson D. S., Engstrom B. W., McAllister J. J., Lee C. F.F.K., Apicella M. A. Lipooligosaccharide biosynthesis in pathogenic Neisseria. Cloning, identification, and characterization of the phosphoglucomutase gene. J. Biol Chem. 1994; 269: 11162
   PubMed Web of Science ®Google Scholar
• Zieg Silverman J., Hilmen M.M., Simon M. Recombinational switch for gene expression. Science 1977; 196: 170
   PubMed Web of Science ®Google Scholar
• Zollinger Moran W., Ray D. E.J., McClain B. Presented at the International Symposium, Hanasaari, Espoo, Finland. 1991
   Google Scholar
• Zollinger W. D., Mandrell R. E. Type-specific antigens of group A Neisseria meningitidis: lipopolysaccharide and heat-modifiable outer membrane proteins. Infect. Immun. 1980; 28: 451
   PubMed Web of Science ®Google Scholar
• Zwahlen Rubin A., Connelly L. G., Inzana C. J.T.J., Moxon E. R. Alteration of the cell wall of Haemophilus influenzae type b by transformation with cloned DNA: association with attenuated virulence. J. Infect. Dis. 1985; 152: 485
   PubMed Web of Science ®Google Scholar