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PMID: 8661418 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Intracellular synthesis, processing, and transport of proteins encoded by ORFs 5 to 7 of porcine reproductive and respiratory syndrome virus.

Virology ·Vol. 221 ·No. 1 ·1996-07-01 ·Pages 98-112

Mardassi H, Massie B, Dea S

Abstract

Porcine Reproductive and Respiratory Syndrome Virus (PRRSV), a small enveloped virus containing a positive-strand RNA genome, possesses at least three major structural proteins designated N, M, and E. The N protein is considered as the major component of the nucleocapsid, whereas M and E are membrane-associated. Previous studies using peptide-specific antibodies assigned these proteins to ORFs 7, 6, and 5, respectively. In the present report, monospecific antisera raised against Escherichia coli-expressed ORFs 5, 6, and 7 products were used to study the synthesis and processing of PRRSV structural proteins in the highly permissive MARC-145 cell line. Treatment of viral proteins with various glycosidases showed that only E was modified by N-linked glycans. Pulse-chase experiments revealed that intracellular transport of the major envelope glycoprotein was delayed in the premedial Golgi compartment. During the first 30 min of chase, E undergoes a gradual downward shift of its apparent molecular weight, thought to result from trimming of the mannose-rich glycan structures. Once E is transported to the medial Golgi or proximal elements, some molecules undergo complete processing of all their high-mannose N-linked oligosaccharides to complex type, while in other molecules only a fraction of N-linked glycans are terminally glycosylated. These two differentially glycosylated forms of E were found to be incorporated into extracellular virions. In cells and virions, both M and E were shown to occur in heterodimeric complexes linked by disulfide bonds. The oligomerization process, as analyzed from pulse-chase experiments, showed that M and E are incorporated into M-E complexes with different kinetics and efficiencies, in a fashion similar to their counterparts in equine arteritis virus. Apparently, all steps of E protein N-glycans processing proceed after its association with M which occurs in the endoplasmic reticulum (ER). In the infected cells, E and M appear highly membrane-associated, while N is predominantly cytosolic.

MeSH Terms
Animals Arterivirus/genetics,metabolism,physiology Base Sequence Biological Transport Cell Line DNA, Viral Glycosylation Kinetics Mannose/metabolism Molecular Sequence Data Oligosaccharides/metabolism Open Reading Frames Protein Processing, Post-Translational Rabbits Viral Envelope Proteins Viral Proteins/metabolism Viral Structural Proteins/genetics,metabolism Virion/metabolism Virus Assembly
Chemicals
DNA, Viral Oligosaccharides Viral Envelope Proteins Viral Proteins Viral Structural Proteins glycoprotein 5, PRRSV Mannose
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Mardassi H
Centre de recherche en virologie, Institut Armand-Frappier, Université du Québec, Laval, Canada.
Massie B
Dea S
Article Info
Journal
Virology
Abbr.
Virology
ISSN
0042-6822
Published
1996-07-01
Pages
98-112
Language
English
Region
United States
NLM ID
0110674
Subset
IM
Databases
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