Inhibition of Helicobacter pylori and Helicobacter mustelae. Bonding to lipid receptors by bovine colostrum
Summary: Helicobacter pylori, an etiological factor of chronic, active gastritis and duodenal ulcers in humans, and Helicobacter mustelae - a gastric pathogen in ferrets binds to phosphatidylethanolamine (PE), a component of the host's gastric mucosa cells and gangliotetraosylceramide (Gg4) as well as gangliotriaosylceramide (Gg4) and gangliotriaosylceramide (Gg4).The effect of bovine colostrum concentrate (BCC) in interaction with H. pylori and H. mustelae on their lipid receptors has been studied. BCC blocked bonding from both species to Gg4, Gg3, and PE. Partial bonding inhibition has been noted with native bovine and human Colostrum. BCC lacked detectable antibodies (by immunobloting) to the surface of H. Pylori (adhesin) proteins. However, bovine lipid extracts contained PE and lyso-PE, which bond H. pylori in vitro. These results indicate that Colostrum may block the bonding of Helicobacter species to selected lipids and this bonding inhibition is entrusted, in part, by colostral phosphatidylethanolamines (PE) or their derivatives. Colostral lipids can modulate the interaction of H. pylori and other adhesin-expressing pathogens with their target tissues.