Modification of the structure and activity of lipid A in Yersinia pestis lipopolysaccharide by growth temperature

被引:202
作者
Kawahara, K
Tsukano, H
Watanabe, H
Lindner, B
Matsuura, M
机构
[1] Kitasato Inst, Dept Bacteriol, Minato Ku, Tokyo 1088642, Japan
[2] Res Ctr Borstel, Div Biophys, D-23845 Borstel, Germany
[3] Jichi Med Sch, Dept Microbiol, Minami Kawachi, Tochigi 3290498, Japan
[4] Natl Inst Infect Dis, Dept Bacteriol, Tokyo 1628640, Japan
关键词
D O I
10.1128/IAI.70.8.4092-4098.2002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Yeisinia pestis strain Yreka was grown at 27 or 37degreesC, and the lipid A structures (lipid A-27degreesC and lipid A-37degreesC) of the respective lipopolysaccharides (LPS) were investigated by matrix-assisted laser desorption ionization-time-of-flight (MALDI-TOF) mass spectrometry. Lipid A-27degreesC consisted of a mixture of tri-acyl, tetra-acyl, penta-acyl, and hexa-acyl lipid A's, of which tetra-acyl lipid A was most abundant. Lipid A-37degreesC consisted predominantly of tri- and tetra-acylated molecules, with only small amounts of penta-acyl lipid A; no hexa.-acyl lipid A was detected. Furthermore, the amount of 4-amino-arabinose was substantially higher in lipid A-27degreesC than in lipid A-37degreesC. By use of mouse and human macrophage cell lines, the biological activities of the LPS and lipid A preparations were measured via their abilities to induce production of tumor necrosis factor alpha (TNF-alpha). In both cell lines the LPS and the lipid A from bacteria grown at 27degreesC were stronger inducers of TNF-a than those from bacteria grown at 37degreesC. However, the difference in activity was more prominent in human macrophage cells. These results suggest that in order to reduce the activation of human macrophages, it may be more advantageous for Y. pestis to produce less-acylated lipid A at 37degreesC.
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页码:4092 / 4098
页数:7
相关论文
共 42 条
[1]  
ALBIZO J M, 1970, Infection and Immunity, V2, P229
[2]   Novel variation of lipid A structures in strains of different Yersinia species [J].
Aussel, L ;
Thérisod, H ;
Karibian, D ;
Perry, MB ;
Bruneteau, M ;
Caroff, M .
FEBS LETTERS, 2000, 465 (01) :87-92
[3]   DIAGNOSIS OF PLAGUE - ANALYSIS OF YERSIN-KITASATO CONTROVERSY [J].
BIBEL, DJ ;
CHEN, TH .
BACTERIOLOGICAL REVIEWS, 1976, 40 (03) :633-651
[4]   LIPOPOLYSACCHARIDES FROM A SLIGHTLY VIRULENT-STRAIN OF YERSINIA-PESTIS [J].
BORDET, C ;
BRUNETEAU, M ;
MICHEL, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1977, 79 (02) :443-449
[5]   FACTORS PROMOTING ACUTE AND CHRONIC DISEASES CAUSED BY YERSINIAE [J].
BRUBAKER, RR .
CLINICAL MICROBIOLOGY REVIEWS, 1991, 4 (03) :309-324
[6]   Effect of cold shock on lipid A biosynthesis in Escherichia coli -: Induction at 12°C of an acyltransferase specific for palmitoleoyl-acyl carrier protein [J].
Carty, SM ;
Sreekumar, KR ;
Raetz, CRH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (14) :9677-9685
[7]   DIFFERENTIATION OF YERSINIA-PESTIS AND Y-PSEUDOTUBERCULOSIS BY SDS-PAGE ANALYSIS OF LIPOPOLYSACCHARIDE [J].
CHART, H ;
CHEASTY, T ;
ROWE, B .
LETTERS IN APPLIED MICROBIOLOGY, 1995, 20 (06) :369-370
[8]   LIPOPOLYSACCHARIDES FROM YERSINIA-PESTIS - STUDIES ON LIPID-A OF LIPOPOLYSACCHARIDES-I AND LIPOPOLYSACCHARIDE-II [J].
DALLAVENEZIA, N ;
MINKA, S ;
BRUNETEAU, M ;
MAYER, H ;
MICHEL, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1985, 151 (02) :399-404
[9]   EFFECTS OF GROWTH TEMPERATURE, 47-MEGADALTON PLASMID, AND CALCIUM DEFICIENCY ON THE OUTER-MEMBRANE PROTEIN PORIN AND LIPOPOLYSACCHARIDE COMPOSITION OF YERSINIA-PESTIS EV76 [J].
DARVEAU, RP ;
CHARNETZKY, WT ;
HURLBERT, RE ;
HANCOCK, REW .
INFECTION AND IMMUNITY, 1983, 42 (03) :1092-1101
[10]   Relationship of structure and biological activity of monosaccharide lipid A analogues to induction of nitric oxide production by murine macrophage RAW264.7 cells [J].
Funatogawa, K ;
Matsuura, M ;
Nakano, M ;
Kiso, M ;
Hasegawa, A .
INFECTION AND IMMUNITY, 1998, 66 (12) :5792-5798