Comparative bioinformatics analysis of the mammalian and bacterial glycomes

被引:118
作者
Adibekian, Alexander [1 ]
Stallforth, Pierre [1 ]
Hecht, Marie-Lyn [1 ]
Werz, Daniel B. [3 ]
Gagneux, Pascal [4 ]
Seeberger, Peter H. [1 ,2 ]
机构
[1] Max Planck Inst Colloids & Interfaces, Dept Biomol Syst, D-14424 Potsdam, Germany
[2] Free Univ Berlin, Inst Chem & Biochem, D-14195 Berlin, Germany
[3] Univ Gottingen, Inst Organ & Biomol Chem, D-37077 Gottingen, Germany
[4] Univ Calif San Diego, Sch Med, Glycobiol Res Training Ctr, La Jolla, CA 92093 USA
关键词
MYCOBACTERIUM-TUBERCULOSIS; SIALIC-ACID; EVOLUTION; DIVERSITY; LIPOPOLYSACCHARIDE; OLIGOSACCHARIDES; GALACTOFURANOSE; GLYCOBIOLOGY; BIOSYNTHESIS; INDUCTION;
D O I
10.1039/c0sc00322k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A comparative analysis of bacterial and mammalian glycomes based on the statistical analysis of two major carbohydrate databases, Bacterial Carbohydrate Structure Data Base (BCSDB) and GLYCOSCIENCES.de (GS), is presented. An in-depth comparison of these two glycomes reveals both striking differences and unexpected similarities. Within the prokaryotic kingdom, we focus on the glycomes of seven classes of pathogenic bacteria with respect to (i) their most abundant monosaccharide units; (ii) disaccharide pairs; (iii) carbohydrate modifications; (iv) occurrence and use of sialic acids; and (v) class-specific monosaccharides. The aim of this work is to gain insights into unique carbohydrate patterns in bacteria. Data interpretation reveals significant trends in the composition of specific carbohydrate classes as result of evolution-driven structural adaptations of bacterial pathogens and symbionts to their mammalian hosts. The differences are discussed in light of their value for biomedical applications, such as the targeting of unique glycosyl transferases, vaccine development, and devising novel diagnostic tools.
引用
收藏
页码:337 / 344
页数:8
相关论文
共 49 条
  • [1] Chemical glycobiology
    Bertozzi, CR
    Kiessling, LL
    [J]. SCIENCE, 2001, 291 (5512) : 2357 - 2364
  • [2] Evolution of carbohydrate antigens - microbial forces shaping host glycomes?
    Bishop, Joseph R.
    Gagneux, Pascal
    [J]. GLYCOBIOLOGY, 2007, 17 (05) : 23R - 34R
  • [3] Chemical Synthesis of All Phosphatidylinositol Mannoside (PIM) Glycans from Mycobacterium tuberculosis
    Boonyarattanakalin, Siwarutt
    Liu, Xinyu
    Michieletti, Mario
    Lepenies, Bernd
    Seeberger, Peter H.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (49) : 16791 - 16799
  • [4] Borrell S, 2009, INT J TUBERC LUNG D, V13, P1456
  • [5] Chen Y, 2008, MOL CELLS, V26, P415
  • [6] BACTERIAL BIOFILMS IN NATURE AND DISEASE
    COSTERTON, JW
    CHENG, KJ
    GEESEY, GG
    LADD, TI
    NICKEL, JC
    DASGUPTA, M
    MARRIE, TJ
    [J]. ANNUAL REVIEW OF MICROBIOLOGY, 1987, 41 : 435 - 464
  • [7] Siglecs and their roles in the immune system
    Crocker, Paul R.
    Paulson, James C.
    Varki, Ajit
    [J]. NATURE REVIEWS IMMUNOLOGY, 2007, 7 (04) : 255 - 266
  • [8] CROSS AS, 1990, CURR TOP MICROBIOL, V150, P87
  • [9] The HIV-1 envelope glycoprotein gp120 features four heparan sulfate binding domains, including the co-receptor binding site
    Crublet, Elodie
    Andrieu, Jean-Pierre
    Vives, Romain R.
    Lortat-Jacob, Hugues
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (22) : 15193 - 15200
  • [10] The human complement factor H:: functional roles, genetic variations and disease associations
    de Córdoba, SR
    Esparza-Gordillo, J
    de Jorge, EG
    Lopez-Trascasa, M
    Sánchez-Corral, P
    [J]. MOLECULAR IMMUNOLOGY, 2004, 41 (04) : 355 - 367