» Articles » PMID: 22638862

Bacterial Species-characteristic Profiles of Molecular Species, and the Antigenicity of Phospholipids and Glycolipids in Symbiotic Lactobacillus, Staphylococcus and Streptococcus Species

Overview
Journal Glycoconj J
Publisher Springer
Date 2012 May 29
PMID 22638862
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Human symbiotic bacteria, Lactobacillus reuteri (LR) in the intestines, Staphylococcus epidermidis (SE) in skin and Streptococcus salivalis (SS) in the oral cavity, contain dihexaosyl diglycerides (DH-DG) in concentrations equivalent to those of phosphatidyl glycerol (PG) and cardiolipin (CL), together with mono- to tetrahexaosyl DGs. The molecular species, as the combination of fatty acids in the DG moiety, were revealed to be bacterial species-characteristic, but to be similar between glycolipids and phospholipids in individual bacteria, the major ones being 16:0 and cy19:0 for LR, ai15:0 and ai17:0 for SE, and 16:0 and 18:1 for SS, respectively. The carbohydrate structures of DH-DGs were also bacterial species-characteristic, being Galα1-2Glcα for LR, Glcβ1-6Glcβ for SE, and Glcα1-2Glcα for SS, respectively. Also, bacterial glycolipids were revealed to provide antigenic determinants characteristic of bacterial species on immunization of rabbits with the respective bacteria. Anti-L. johnsonii antiserum intensely reacted with tri- and tetrahexaosyl DGs, in which Galα was bound to DH-DG through an α1-6 linkage, as well as with DH-DG from LR. Although anti-SE antiserum preferentially reacted with DH-DG from SE, anti-SS antiserum reacted with DH-DG from SS and, to a lesser extent, with DH-DGs from LR and SE. But, both anti-SE and anti-SS antiserum did not react at all with monohexaosyl DG or glycosphingolipids with the same carbohydrates at the nonreducing terminals. In addition, 75 % of human sera, irrespective of the ABO blood group, were found to contain IgM to tri- and tetrahexaosyl DGs from LR, but not to DH-DGs from LR, SE and SS.

Citing Articles

Enhanced fucosylation of GA1 in the digestive tracts of X-ray-irradiated mice.

Iwamori M, Tanaka K, Adachi S, Aoki D, Nomura T Glycoconj J. 2016; 34(2):163-169.

PMID: 27858203 DOI: 10.1007/s10719-016-9746-3.


Enhanced expression of unique gangliosides with GM2-determinant in human uterine cervical carcinoma-derived cell lines.

Tanaka K, Miyazawa M, Mikami M, Aoki D, Kiguchi K, Iwamori M Glycoconj J. 2016; 33(5):745-54.

PMID: 27270764 DOI: 10.1007/s10719-016-9668-0.


Changes in bacterial glycolipids as an index of intestinal lactobacilli and epithelial glycolipids in the digestive tracts of mice after administration of penicillin and streptomycin.

Iwamori M, Iwamori Y, Adachi S, Nomura T Glycoconj J. 2013; 30(9):889-97.

PMID: 23996013 DOI: 10.1007/s10719-013-9494-6.

References
1.
Xu Y, Condell M, Plesken H, Edelman-Novemsky I, Ma J, Ren M . A Drosophila model of Barth syndrome. Proc Natl Acad Sci U S A. 2006; 103(31):11584-8. PMC: 1544213. DOI: 10.1073/pnas.0603242103. View

2.
Sugiyama T, Smith P, Langworthy T, Mayberry W . Immunological analysis of glycolipids and lipopolysaccharides derived from various mycoplasmas. Infect Immun. 1974; 10(6):1273-9. PMC: 423099. DOI: 10.1128/iai.10.6.1273-1279.1974. View

3.
Koch H, Fischer W . Acyldiglucosyldiacylglycerol-containing lipoteichoic acid with a poly(3-O-galabiosyl-2-O-galactosyl-sn-glycero-1-phosphate) chain from Streptococcus lactis Kiel 42172. Biochemistry. 1978; 17(24):5275-81. DOI: 10.1021/bi00617a030. View

4.
Fullekrug J, Simons K . Lipid rafts and apical membrane traffic. Ann N Y Acad Sci. 2004; 1014:164-9. DOI: 10.1196/annals.1294.017. View

5.
Folch J, Lees M, SLOANE STANLEY G . A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957; 226(1):497-509. View