Abstract

Human noroviruses (NoVs) are a major cause of non-bacterial gastroenteritis. Although histo-blood group antigens (HBGAs) have been implicated in the initial binding of NoV, the mechanism of that binding before internalization is not clear. To determine the involvement of NoVs and HBGAs in cell binding, we examined the localization of NoV virus-like particles (VLPs) and HBGAs in a human intestinal cell line and the human ileum biopsy specimens by immunofluorescence microscopy. The localizations of Ueno 7k VLPs (genogroup II.6) and each HBGA (type H1-, H2- and Leb-HBGAs) on the human intestinal cell line, Caco-2, were examined by confocal laser-scanning microscopy. To explore any interactions of NoVs and HBGAs in vivo, fresh biopsy specimens from human ileum were directly incubated with NoV VLPs and examined by immunofluorescence microscopy. We found that VLP binding depended on the state of cell differentiation, but not on the presence of HBGAs. In differentiated Caco-2 cells, we detected no type H1 HBGAs, but VLPs bound to the cells anyway. We incubated fresh biopsies of human ileum directly with VLPs, a model that better replicates the in vivo environment. VLPs mainly bound epithelial cells and goblet cells. Although the incubations were performed at 4°C to hinder internalization, VLPs were still detected inside cells. Our results suggest that VLPs utilize molecule(s) other than HBGAs during binding and internalization into cells.

Highlights

  • Human noroviruses (NoVs) are members of the family Caliciviridae and the major cause of non-bacterial gastroenteritis worldwide [1]

  • We investigated the co-localization of NoV virus-like particles (VLPs) and histo-blood group antigens (HBGAs) to determine if expression of HBGAs has an effect on the binding of VLPs to Caco-2 cells

  • We found that the NoV VLPs bind preferentially to differentiated Caco-2 cells and that this binding is irrespective of HBGA expression

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Summary

Introduction

Human noroviruses (NoVs) are members of the family Caliciviridae and the major cause of non-bacterial gastroenteritis worldwide [1]. Caco-2 cells were originally isolated from a human colorectal carcinoma [4,5,6,7] They retain the ability to spontaneously differentiate into polarized, columnar cells with the characteristics of small intestine after reaching confluency [8]. VLPs self-assemble when the genes for the capsid protein are expressed in insect cells infected with a recombinant baculovirus [9]. These particles are thought to be morphologically and antigenically similar to native virions, and have been useful tools for studying virus-cell interactions [9]. A monoclonal antibody against the C-terminal region blocked its binding to Caco-2 cells [7]

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