Previous Article | Next Article ![]()
Infect. Immun., 01 1998, 70-76, Vol 66, No. 1
BJ Appelmelk, B Shiberu, C Trinks, N Tapsi, PY Zheng, T Verboom, J Maaskant, CH Hokke, WE Schiphorst, D Blanchard, IM Simoons-Smit, DH van den Eijnden and CM Vandenbroucke-Grauls
Helicobacter pylori NCTC 11637 lipopolysaccharide (LPS) expresses the human
blood group antigen Lewis x (Le(x)) in a polymeric form. Le(x) is
beta-D-galactose-(1-4)-[alpha-L-fucose-(1-3)]-beta-D-acetylglucosamine.
Schematically the LPS structure is (Le(x))n-core-lipid A. In this report,
we show that Le(x) expression is not a stable trait but that LPS displays a
high frequency (0.2 to 0.5%) of phase variation, resulting in the presence
of several LPS variants in one bacterial cell population. One type of phase
variation implied the loss of alpha1,3- linked fucose, resulting in
variants that expressed nonsubstituted polylactosamines (also called the i
antigen), i.e., Le(x) minus fucose; LPS: (lactosamine)n-core-lipid A. The
switch of Le(x) to i antigen was reversible. A second group of variants
arose by loss of polymeric main chain which resulted in expression of
monomeric Le(y); LPS: (Le(y))- core-lipid A. A third group of variants
arose by acquisition of alpha1,2-linked fucose which hence expressed Le(x)
plus Le(y); LPS: (Le(y))(Le(x))n-core-lipid A. The second and third group
of variants switched back to the parental phenotype [(Le(x))-core-lipid A]
in lower frequencies. Part of the variation can be ascribed to altered
expression levels of glycosyltransferase levels as assessed by assaying the
activities of galactosyl-, fucosyl-, and N- acetylglucosaminyltransferases.
Clearly phase variation increases the heterogeneity of H. pylori, and this
process may be involved in generating the very closely related yet
genetically slightly different strains that have been isolated from one
patient.
Copyright © 1998, American Society for Microbiology
Phase variation in Helicobacter pylori lipopolysaccharide
Department of Medical Microbiology, Vrije Universiteit, Medical School, Amsterdam, The Netherlands. BJ.Appelmelk.mm@med.vu.nl
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»