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PMID: 9375006 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Ultrastructure and localization of E proteins in cultured neuron cells infected with Japanese encephalitis virus.

Virology ·Vol. 238 ·No. 1 ·1997-11-10 ·Pages 30-9

Wang JJ, Liao CL, Chiou YW, Chiou CT, Huang YL, Chen LK

Abstract

A unique structure and in situ localization of E proteins were demonstrated in cultured neurons infected with neurovirulent and aneurovirulent strains of local Japanese encephalitis virus (JEV). Dilated rough endoplasmic reticulum (rER) containing smooth membrane structures (SMS) was continuous with the outer membrane of the nuclear envelope. These membranes were found to be connected to unique dense bodies, membrane vesicle structures (MVS). The de novo formation of SMS, annulate lamellae, and the appearance of MVS indicated proliferation of the membranous system in response to JEV infection. E proteins were possibly assembled in the virions in the nuclear envelope or rER or on the plasma membrane. The interconnections between MVS, rER, and the nuclear envelope and immunogold labeling of E proteins on the MVS provided strong evidence that MVS serve as a reservoir of JEV components during virus assembly.

MeSH Terms
Animals Carcinoma, Embryonal Cell Differentiation/drug effects Cells, Cultured Encephalitis Virus, Japanese/physiology,ultrastructure Humans Mice Microscopy, Immunoelectron Neuroblastoma Neurons/cytology,virology Tretinoin/pharmacology Tumor Cells, Cultured Viral Envelope Proteins/analysis,ultrastructure Virus Replication
Chemicals
Viral Envelope Proteins Tretinoin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Wang J J
Institute of Biology and Anatomy, National Defense Medical Center, Taipei, Taiwan, Republic of China. jjw@ndmc1.ndmctsgh.edu.tw
Liao C L
Chiou Y W
Chiou C T
Huang Y L
Chen L K
Article Info
Journal
Virology
Abbr.
Virology
ISSN
0042-6822
Published
1997-11-10
Pages
30-9
Language
English
Region
United States
NLM ID
0110674
Subset
IM
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