Characterisation of the core part of the lipopolysaccharide O-antigen of Francisella novicida (U112)

被引:16
作者
Vinogradov, E [1 ]
Perry, MB [1 ]
机构
[1] Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada
关键词
Francisella; Francisella novicida; LPS; core structure;
D O I
10.1016/j.carres.2004.04.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fransicella novicida (U112), a close relative of the highly virulent bacterium F tularensis, is known to produce a lipopolysaccharide that is significantly different in biological properties from the LPS of F tularensis. Here we present the results of the structural analysis of the F novicida LPS core part, which is found to be similar to that of F tularensis, differing only by one additional alpha-Glc residue: [GRAPHICS] where R is an beta-chain, linked via a beta-bacillosamine (2,4-diamino-2,4,6-trideoxyglucose) residue. The lipid part of F novicida LPS contains no phosphate substituent and apparently has a free reducing end, a feature also noted in F tularensis LPS. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1643 / 1648
页数:6
相关论文
共 13 条
[1]   Characterization of two unusual clinically significant Francisella strains [J].
Clarridge, JE ;
Raich, TJ ;
Sjosted, A ;
Sandstrom, G ;
Darouiche, RO ;
Shawar, RM ;
Georghiou, PR ;
Osting, C ;
Vo, L .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (08) :1995-2000
[2]   Mice vaccinated with the O-antigen of Francisella tularensis LVS lipopolysaccharide conjugated to bovine serum albumin develop varying degrees of protective immunity against systemic or aerosol challenge with virulent type A and type B strains of the pathogen [J].
Conlan, JW ;
Shen, H ;
Webb, A ;
Perry, MB .
VACCINE, 2002, 20 (29-30) :3465-3471
[3]   Phase variation in Francisella tularensis affecting intracellular growth, lipopolysaccharide antigenicity and nitric oxide production [J].
Cowley, SC ;
Myltseva, SV ;
Nano, FE .
MOLECULAR MICROBIOLOGY, 1996, 20 (04) :867-874
[4]  
ESCUDERO R, 2003, 4 INT TUL C BATH UK, P20
[5]   Detection of Francisella tularensis in biological specimens using a capture enzyme-linked immunosorbent assay, an immunochromatographic handheld assay, and a PCR [J].
Grunow, R ;
Splettstoesser, W ;
McDonald, S ;
Otterbein, C ;
O'Brien, T ;
Morgan, C ;
Aldrich, J ;
Hofer, E ;
Finke, EJ ;
Meyer, H .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2000, 7 (01) :86-90
[6]   FRANCISELLA-PHILOMIRAGIA COMB NOV (FORMERLY YERSINIA-PHILOMIRAGIA) AND FRANCISELLA-TULARENSIS BIOGROUP NOVICIDA (FORMERLY FRANCISELLA-NOVICIDA) ASSOCIATED WITH HUMAN-DISEASE [J].
HOLLIS, DG ;
WEAVER, RE ;
STEIGERWALT, AG ;
WENGER, JD ;
MOSS, CW ;
BRENNER, DJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (07) :1601-1608
[7]   Francisella novicida LPS has greater immunobiological activity in mice than F-tularensis LPS, and contributes to F-novicida murine pathogenesis [J].
Kieffer, TL ;
Cowley, S ;
Nano, FE ;
Elkins, KL .
MICROBES AND INFECTION, 2003, 5 (05) :397-403
[8]   The aqueous solution structure of a lipoteichoic acid from Streptococcus pneumoniae strain R6 containing 2,4-diamino-2,4,6-trideoxy-galactose: Evidence for conformational mobility of the galactopyranose ring [J].
Klein, RA ;
Hartmann, R ;
Egge, H ;
Behr, T ;
Fischer, W .
CARBOHYDRATE RESEARCH, 1996, 281 (01) :79-98
[9]   Histologic and molecular diagnosis of tularemia: a potential bioterrorism agent endemic to North America [J].
Lamps, LW ;
Havens, JM ;
Sjostedt, A ;
Page, DL ;
Scott, MA .
MODERN PATHOLOGY, 2004, 17 (05) :489-495
[10]  
TARNVIK A, 1989, REV INFECT DIS, V11, P440