Human intestinal organoids express histo-blood group antigens, bind norovirus VLPs, and support limited norovirus replication

• Published in: Scientific reports Vol. 7; no. 1; pp. 12621 - 12
• Main Authors: Zhang, Dongsheng, Tan, Ming, Zhong, Weiming, Xia, Ming, Huang, Pengwei, Jiang, Xi
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 03.10.2017; Nature Publishing Group
• Subjects: 13; 13/100; 13/106; 38; 631/326/596/2557; 64; 692/4020/2199; Antigens; Fetuses; Humanities and Social Sciences; Intestine; multidisciplinary; Organoids; Pluripotency; Polymerase chain reaction; Replication; Science; Science (multidisciplinary); Stem cells; Structure-function relationships
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-017-12736-2

Through pluripotent stem cell (PSC) technology, human intestinal organoids (HIOs) with remarkably similarity to the fetal intestine in cellular composition, architecture, and absorptive/secretory functions have been successfully developed, providing a useful in vitro model system to study the structure and function of human congenital gut and intestinally related diseases. We report here the usefulness of HIOs as a model system to study intestinal carbohydrate expression, virus-host interaction, and replication of human noroviruses (huNoVs). We found that fully developed HIOs express effectively various types 1 and 2 HBGAs, including Lewis, secretor, and nonsecretor antigens, distributing on the glycocalyx. Selected huNoV-like particles (VLPs) bound the glycocalyx of HIOs with matched HBGA phenotypes. Using GII.4 huNoV positive stool filtrates, we demonstrated limited huNoV replication in HIOs with corresponding HBGAs through detection of viral RNAs by RT-PCR and capsid antigens by immunostaining methods. Our data suggested that, after further improvements, HIOs can be a useful model to study intestinal glycan expression, huNoV-intestine interaction, and huNoV infection in the intestine.