Lv. Hooper et Ji. Gordon, Glycans as legislators of host-microbial interactions: spanning the spectrum from symbiosis to pathogenicity, GLYCOBIOLOG, 11(2), 2001, pp. 1R-10R
The number of microbes associated with our gut likely exceeds our total num
ber of somatic and germ cells. Despite their numbers, almost nothing is kno
wn about the molecular mechanisms that determine whether the interaction be
tween a microbial species and its host will be beneficial. Recent results o
btained from in vivo models have revealed critical roles for glycoconjugate
s in helping define the outcome of two such host-microbial relationships. I
n one case, attachment of Helicobacter pylori to fucosylated or sialylated
glycans produced by various gastric epithelial lineages and their progenito
rs skews the destiny of colonization toward pathogenicity. In the second ca
se, a molecular dissection of how Bacteroides thetaiotaomicron, a normal in
habitant of the distal small intestine, is able to communicate with intesti
nal epithelial cells has revealed a novel role for host fucosylated glycans
in forging a mutually beneficial relationship. These observations lend sup
port to the hypothesis that the capacity to synthesize diverse carbohydrate
structures may have arisen in part from our need to both evade pathogenic
relationships and to coevolve symbiotic relationships with our nonpathogeni
c resident microbes.