Replication of Human Sapovirus in Human-Induced Pluripotent Stem Cell-Derived Intestinal Epithelial Cells

Author:

Matsumoto Naomi1,Kurokawa Shiho2,Tamiya Shigeyuki3,Nakamura Yutaka3,Sakon Naomi4,Okitsu Shoko5ORCID,Ushijima Hiroshi5,Yuki Yoshikazu2,Kiyono Hiroshi267,Sato Shintaro13ORCID

Affiliation:

1. Department of Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan

2. Department of Human Mucosal Vaccinology, Chiba University Hospital, Chiba 260-8670, Japan

3. Department of Microbiology and Immunology, School of Pharmaceutical Sciences, Wakayama Medical University, Wakayama 640-8156, Japan

4. Department of Microbiology, Osaka Institute of Public Health, Osaka 537-0025, Japan

5. Division of Microbiology, Department of Pathology and Microbiology, Nihon University School of Medicine, Tokyo 173-8610, Japan

6. Future Medicine Education and Research Organization, Chiba University, Chiba 263-8522, Japan

7. CU-UCSD Center for Mucosal Immunology, Allergy, and Vaccines (cMAV), Departments of Medicine and Pathology, University of California, San Diego, CA 92093-0956, USA

Abstract

Sapoviruses, like noroviruses, are single-stranded positive-sense RNA viruses classified in the family Caliciviridae and are recognized as a causative pathogen of diarrhea in infants and the elderly. Like human norovirus, human sapovirus (HuSaV) has long been difficult to replicate in vitro. Recently, it has been reported that HuSaV can be replicated in vitro by using intestinal epithelial cells (IECs) derived from human tissues and cell lines derived from testicular and duodenal cancers. In this study, we report that multiple genotypes of HuSaV can sufficiently infect and replicate in human-induced pluripotent stem cell-derived IECs. We also show that this HuSaV replication system can be used to investigate the conditions for inactivation of HuSaV by heat and alcohol, and the effects of virus neutralization of antisera obtained by immunization with vaccine antigens, under conditions closer to the living environment. The results of this study confirm that HuSaV can also infect and replicate in human normal IECs regardless of their origin and are expected to contribute to future virological studies.

Funder

JSPS KAKENHI

AMED

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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