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Related Concept Videos

What are Viruses?00:50

What are Viruses?

Overview
Receptor-mediated Endocytosis01:20

Receptor-mediated Endocytosis

Receptor-mediated endocytosis is when bulk amounts of specific molecules are imported into a cell after binding to cell surface receptors. The molecules bound to these receptors are taken into the cell through inward folding of the cell surface membrane, which is eventually pinched off into a vesicle within the cell. Structural proteins, such as clathrin, coat the budding vesicle.
Clathrin-Mediated Endocytosis of LDL
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Receptor-mediated Endocytosis01:38

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Introduction to Virus01:28

Introduction to Virus

Viruses are unique biological entities that blur the boundary between living and non-living systems. Although they lack cellular structure and metabolic processes, they can exhibit characteristics of life when infecting a host. Their defining feature is a nucleic acid core, composed of either DNA or RNA, encapsulated within a protein coat called a capsid. This simple structure allows them to invade host cells and use their machinery for replication efficiently.Viral Structure and...
Retrovirus Life Cycles01:10

Retrovirus Life Cycles

Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the retrovirus to...
Retroviruses02:33

Retroviruses

Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...

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Related Experiment Video

Updated: May 15, 2026

Generation and Assembly of Virus-Specific Nucleocapsids of the Respiratory Syncytial Virus
09:08

Generation and Assembly of Virus-Specific Nucleocapsids of the Respiratory Syncytial Virus

Published on: July 27, 2021

How viruses use the endoplasmic reticulum for entry, replication, and assembly.

Takamasa Inoue1, Billy Tsai

  • 1Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48103, USA.

Cold Spring Harbor Perspectives in Biology
|January 4, 2013
PubMed
Summary

This review explores how viruses use the endoplasmic reticulum (ER) to support their infection cycle. The ER is a key organelle in cells that viruses manipulate for entry, replication, and assembly. The authors summarize current evidence showing that the ER provides a suitable environment for these processes. They highlight the importance of understanding how viruses interact with the ER to develop new antiviral strategies. The study uses a combination of biochemical and cell biology methods to analyze these interactions. The findings suggest that the ER is a central site for viral replication and assembly. The authors emphasize the need for further research to clarify the molecular mechanisms involved. This review provides a foundation for future studies on virus-ER dynamics.

Keywords:
virus infectionendoplasmic reticulumviral replicationhost-pathogen interactions

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Published on: March 27, 2016

Area of Science:

  • Virology
  • Cell biology
  • Molecular biology

Background:

The endoplasmic reticulum (ER) is a central organelle in eukaryotic cells, involved in protein synthesis and lipid metabolism. It has long been recognized as a site of interaction for various pathogens. However, the precise role of the ER in viral infection remains unclear. While some studies have suggested the ER supports viral replication, the mechanisms are not fully understood. This uncertainty drives the need for more detailed investigations. The ER's structure and functions make it a likely candidate for viral manipulation. Prior research has shown that the ER can be a target for bacterial toxins as well. Understanding how the ER is used during infection could reveal new insights into host-pathogen interactions. This gap motivated researchers to review the current evidence on virus-ER interactions.

Purpose Of The Study:

This review aims to summarize the current understanding of how viruses exploit the ER during infection. The study addresses the lack of clarity on the molecular mechanisms involved in virus-ER interactions. By compiling evidence from recent studies, the authors hope to clarify the role of the ER in viral entry, replication, and assembly. The purpose is to highlight the importance of the ER in supporting these key infection steps. The study also considers the broader implications for understanding host-pathogen interactions. The authors focus on the dynamic and coordinated nature of these processes. They emphasize the need for interdisciplinary approaches to study these interactions. This review serves as a foundation for future research on virus-ER dynamics.

Main Methods:

The authors employed a systematic review approach to analyze the literature on virus-ER interactions. They focused on molecular mechanisms and host-virus interactions. The review included biochemical and cell biological assays. Advanced microscopy techniques were also considered. The authors evaluated studies that examined viral entry, replication, and assembly. They compared findings across different viral families. The interdisciplinary nature of the methods allowed for a comprehensive analysis. The review approach emphasized the importance of rigorous experimental validation.

Main Results:

The review highlights that the ER supports viral entry, replication, and assembly. Viruses manipulate the ER to facilitate these processes. The ER's structure and functions are exploited for viral replication. Certain viral proteins interact with ER components. These interactions are crucial for viral replication and assembly. The study found that the ER can be a site for viral RNA replication. Viral assembly also occurs at the ER membrane. The findings suggest that the ER is a central hub for viral infection steps.

Conclusions:

The authors conclude that the ER plays a central role in supporting viral infection. The evidence suggests that the ER is co-opted by viruses for entry, replication, and assembly. These findings emphasize the need for further research into virus-ER interactions. The authors propose that understanding these interactions could lead to new therapeutic strategies. The study highlights the importance of interdisciplinary approaches. The conclusions are based on the synthesis of current evidence. The authors suggest that future studies should focus on the molecular details of these interactions. The findings may inform new approaches to antiviral therapies.

The ER supports viral entry, replication, and assembly by providing a site for these processes.

Viruses interact with ER components to facilitate RNA replication and viral assembly.

The ER's structure and functions make it a suitable environment for viral replication and assembly.

Biochemical assays, cell biology techniques, and advanced microscopy are used to study these interactions.

RNA replication in the ER is crucial for the production of new viral particles.

Understanding virus-ER interactions may lead to new therapeutic approaches for viral infections.