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Shigeo Nagashima

Researcher at Jichi Medical University

Publications -  98
Citations -  3548

Shigeo Nagashima is an academic researcher from Jichi Medical University. The author has contributed to research in topics: Hepatitis E virus & Hepatitis E. The author has an hindex of 34, co-authored 91 publications receiving 3079 citations. Previous affiliations of Shigeo Nagashima include Sapporo Medical University.

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Hepatitis E Virus (HEV) Strains in Serum Samples Can Replicate Efficiently in Cultured Cells Despite the Coexistence of HEV Antibodies: Characterization of HEV Virions in Blood Circulation

TL;DR: The results suggest that the in vitro cell culture system developed can be used for propagation of a wide variety of HEV strains in sera from various infected patients, allowing extended studies on viral replication specific to differentHEV strains.
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ORF3 protein of hepatitis E virus is essential for virion release from infected cells.

TL;DR: Results suggest that the ORF3 protein is responsible for virion egress from infected cells and is present on the surface of released HEV particles, which may be associated with lipids.
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Analysis of the full-length genome of a hepatitis E virus isolate obtained from a wild boar in Japan that is classifiable into a novel genotype.

TL;DR: In this paper, the authors performed a nationwide survey of hepatitis E virus (HEV) infection among 450 wild boars (Sus scrofa leucomystax) that had been captured in Japan between November 2005 and March 2010.

Short Communication Analysis of the full-length genome of a hepatitis E virus isolate obtained from a wild boar in Japan that is classifiable into a novel genotype

TL;DR: The wbJOY_06 isolate is proposed to be the first member of a previously unidentified genotype of hepatitis E virus, which is highly divergent from known genotype 1-4 HEV isolates derived from humans, swine, wild boars, deer, mongoose and rabbits.
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Hepatitis E virus egress depends on the exosomal pathway, with secretory exosomes derived from multivesicular bodies

TL;DR: Findings indicate that membrane-associated HEV particles are released together with internal vesicles through MVBs by the cellular exosomal pathway.