Comparison of lipoteichoic acid from different serotypes of Streptococcus pneumoniae

被引:78
作者
Draing, Christian
Pfitzenmaier, Markus
Zummo, Sebastiana
Mancuso, Giuseppe
Geyer, Armin
Hartung, Thomas
von Aulock, Sonja
机构
[1] Univ Konstanz, Dept Biochem Pharmacol, D-78457 Constance, Germany
[2] Univ Marburg, Dept Organ Chem, D-35043 Marburg, Germany
[3] Univ Messina, Dept Pathol & Expt Microbiol, I-98125 Messina, Italy
[4] European Ctr Validat Alternat Methods, Joint Res Ctr, I-21020 Ispra, Italy
关键词
D O I
10.1074/jbc.M602676200
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
Pneumococcal lipoteichoic acid (LTA) is known to have a completely different chemical structure compared with that of Staphylococcus aureus: the polyglycerophosphate in the backbone is replaced in the pneumococcal LTA by a pentamer repeating unit consisting of one ribitol and a tetrasaccharide carrying the unusual substituents phosphocholine andN-acetyl-D-galactosamine. Neither D-alaninenor N-acetyl-D-glucosamine, which play central roles in the biological activity of the staphylococcal LTA, has been reported. The extraction using butanol is more gentle compared with the previously reported chloroform-methanol extraction and results in a higher yield of LTA. We characterized the LTA of two different strains of Streptococcus pneumoniae: R6 (serotype 2) and Fp23 (serotype 4). NMR analysis confirmed the structure of LTA from R6 but showed that its ribitol carries an N-acetyl-D-galactosamine substituent. The NMR data for the LTA from Fp23 indicate that this LTA additionally contains ribitol-bound D-alanine. Dose-response curves of the two pneumococcal LTAs in human whole blood revealed that LTA from Fp23 was significantly more potent than LTA from R6 with regard to the induction of all cytokines measured (tumor necrosis factor, interleukin-1 (IL-1), IL-8, IL-10, granulocyte colony-stimulating factor, and interferon gamma). However, other characteristics, such as lack of inhibition by endotoxin-specific LAL-F, Toll-like receptor 2 and not 4 dependence, and lack of stimulation of neutrophilic granulocytes, were shared by both LTAs. This is the first report of a difference in the structure of LTA between two pneumococcal serotypes resulting in different immunostimulatory potencies.
引用
收藏
页码:33849 / 33859
页数:11
相关论文
共 41 条
[1]   STREPTOCOCCUS-PNEUMONIAE - VIRULENCE FACTORS, PATHOGENESIS, AND VACCINES [J].
ALONSODEVELASCO, E ;
VERHEUL, AFM ;
VERHOEF, J ;
SNIPPE, H .
MICROBIOLOGICAL REVIEWS, 1995, 59 (04) :591-&
[2]   THE STRUCTURE OF PNEUMOCOCCAL LIPOTEICHOIC ACID - IMPROVED PREPARATION, CHEMICAL AND MASS-SPECTROMETRIC STUDIES [J].
BEHR, T ;
FISCHER, W ;
PETERKATALINIC, J ;
EGGE, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 207 (03) :1063-1075
[3]   Structures of two cell wall-associated polysaccharides of a Streptococcus mitis biovar 1 strain -: A unique teichoic acid-like polysaccharide and the group O antigen which is a C-polysaccharide in common with pneumococci [J].
Bergström, N ;
Jansson, PE ;
Kilian, M ;
Sorensen, UBS .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (24) :7147-7157
[4]   STIMULATION OF MONOKINE PRODUCTION BY LIPOTEICHOIC ACIDS [J].
BHAKDI, S ;
KLONISCH, T ;
NUBER, P ;
FISCHER, W .
INFECTION AND IMMUNITY, 1991, 59 (12) :4614-4620
[5]   Streptococcus pneumoniae:: Description of the pathogen, disease epidemiology, treatment, and prevention [J].
Bridy-Pappas, AE ;
Margolis, MB ;
Center, KJ ;
Isaacman, DJ .
PHARMACOTHERAPY, 2005, 25 (09) :1193-1212
[6]   INTERACTION OF THE PNEUMOCOCCAL AMIDASE WITH LIPOTEICHOIC ACID AND CHOLINE [J].
BRIESE, T ;
HAKENBECK, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1985, 146 (02) :417-427
[7]  
BRILES EB, 1973, J BIOL CHEM, V248, P6394
[8]   Worldwide incidence, molecular epidemiology and mutations implicated in fluoroquinolone-resistant Streptococcus pneumoniae:: data from the global PROTEKT surveillance programme [J].
Canton, R ;
Morosini, M ;
Enright, MC ;
Morrissey, I .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 52 (06) :944-952
[9]   Definition of structural prerequisites for lipoteichoic acid-inducible cytokine induction by synthetic derivatives [J].
Deininger, S ;
Stadelmaier, A ;
von Aulock, S ;
Morath, S ;
Schmidt, RR ;
Hartung, T .
JOURNAL OF IMMUNOLOGY, 2003, 170 (08) :4134-4138
[10]   Toll-like receptor 2-deficient mice are highly susceptible to Streptococcus pneumoniae meningitis because of reduced bacterial clearing and enhanced inflammation [J].
Echchannaoui, H ;
Frei, K ;
Schnell, C ;
Leib, SL ;
Zimmerli, W ;
Landmann, R .
JOURNAL OF INFECTIOUS DISEASES, 2002, 186 (06) :798-806