Norwalk virus binds to histo-blood group antigens present on gastroduodenal epithelial cells of secretor individuals

S Marionneau, N Ruvoën, B Le Moullac–Vaidye… - Gastroenterology, 2002 - Elsevier
S Marionneau, N Ruvoën, B Le Moullac–Vaidye, M Clement, A Cailleau–Thomas…
Gastroenterology, 2002Elsevier
Background & Aims: Norwalk Virus (NV) is a member of the Caliciviridae family, which
causes acute epidemic gastroenteritis in humans of all ages and its cellular receptors have
not yet been characterized. Another calicivirus, Rabbit Hemorrhagic Disease Virus, attaches
to H type 2 histo-blood group oligosaccharide present on rabbit epithelial cells. Our aim was
to test if, by analogy, recombinant NV-like particles (rNV VLPs) use carbohydrates present
on human gastroduodenal epithelial cells as ligands. Methods: Attachment of rNV VLPs was …
Background & Aims
Norwalk Virus (NV) is a member of the Caliciviridae family, which causes acute epidemic gastroenteritis in humans of all ages and its cellular receptors have not yet been characterized. Another calicivirus, Rabbit Hemorrhagic Disease Virus, attaches to H type 2 histo-blood group oligosaccharide present on rabbit epithelial cells. Our aim was to test if, by analogy, recombinant NV-like particles (rNV VLPs) use carbohydrates present on human gastroduodenal epithelial cells as ligands.
Methods
Attachment of rNV VLPs was tested on tissue sections of the gastroduodenal junction and on saliva from individuals of known ABO, Lewis, and secretor phenotypes. It was also tested on human Caco-2 cells and on animal cell lines transfected with glycosyltransferases complementary DNA (cDNA). Competition experiments were performed with synthetic oligosaccharides and anticarbohydrate antibodies. Internalization was monitored by confocal microscopy.
Results
Attachment of rNV VLPs to surface epithelial cells of the gastroduodenal junction as well as to saliva was detected, yet only from secretor donors. It was abolished by α1,2fucosidase treatment, and by competition with the H types 1 and 3 trisaccharides or with anti-H type 1 and anti-H types 3 4 antibodies. Transfection of CHO and TS/A cells with an α1,2fucosyltransferase cDNA allowed attachment of VLPs. These transfectants as well as differentiated Caco-2 cells expressing H type 1 structures internalized the bound particles.
Conclusions
rNV VLPs use H type 1 and/or H types 3 4 as ligands on gastroduodenal epithelial cells of secretor individuals.
Elsevier