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Ebolaviruses

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Cover of 'Ebolaviruses'

Table of Contents

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    Book Overview
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    Chapter 1 Marburg- and Ebolaviruses: A Look Back and Lessons for the Future
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    Chapter 2 Forty Years of Ebolavirus Molecular Biology: Understanding a Novel Disease Agent Through the Development and Application of New Technologies
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    Chapter 3 Ebolavirus: An Overview of Molecular and Clinical Pathogenesis
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    Chapter 4 Production of Filovirus Glycoprotein-Pseudotyped Vesicular Stomatitis Virus for Study of Filovirus Entry Mechanisms
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    Chapter 5 Lentiviral Vectors Pseudotyped with Filoviral Glycoproteins
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    Chapter 6 Modeling Ebola Virus Genome Replication and Transcription with Minigenome Systems
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    Chapter 7 Quantification of RNA Content in Reconstituted Ebola Virus Nucleocapsids by Immunoprecipitation
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    Chapter 8 Modeling Ebolavirus Budding with Virus Like Particles
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    Chapter 9 Modeling the Ebolavirus Life Cycle with Transcription and Replication-Competent Viruslike Particle Assays
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    Chapter 10 Assays to Measure Suppression of Type I Interferon Responses by Filovirus VP35 Proteins
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    Chapter 11 Nonradioactive Northern Blot Analysis to Detect Ebola Virus Minigenomic mRNA
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    Chapter 12 A Semi-automated High-Throughput Microtitration Assay for Filoviruses
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    Chapter 13 Generation of Recombinant Ebola Viruses Using Reverse Genetics
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    Chapter 14 Luciferase-Expressing Ebolaviruses as Tools for Screening of Antivirals
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    Chapter 15 Live-Cell Imaging of Filoviruses
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    Chapter 16 Assessment of Inhibition of Ebola Virus Progeny Production by Antiviral Compounds
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    Chapter 17 Analysis of the Cellular Stress Response During Ebola Virus Infection by Immunofluorescence
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    Chapter 18 Analyzing Apoptosis Induction and Evasion in Ebola Virus-Infected Cells
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    Chapter 19 Electron Microscopy of Ebola Virus-Infected Cells
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    Chapter 20 Validating the Inactivation Effectiveness of Chemicals on Ebola Virus
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    Chapter 21 Visualizing Ebolavirus Particles Using Single-Particle Interferometric Reflectance Imaging Sensor (SP-IRIS)
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    Chapter 22 Assessing Antiviral Countermeasures Using Mouse Models of Ebolavirus Infection
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    Chapter 23 Evaluation of Ebola Virus Countermeasures in Guinea Pigs
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    Chapter 24 Evaluation of Medical Countermeasures Against Ebolaviruses in Nonhuman Primate Models
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    Chapter 25 Quantification of Filovirus Glycoprotein-Specific Antibodies
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    Chapter 26 Monitoring Innate Immune Gene Responses in the Hamster Model of Ebola Virus Disease by RT-PCR
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    Chapter 27 Real-Time and End-Point PCR Diagnostics for Ebola Virus
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    Chapter 28 Production of Antigens for ELISA
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    Chapter 29 ELISA Methods for the Detection of Ebolavirus Infection
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    Chapter 30 Ebola Virus Field Sample Collection
Attention for Chapter 4: Production of Filovirus Glycoprotein-Pseudotyped Vesicular Stomatitis Virus for Study of Filovirus Entry Mechanisms
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Chapter title
Production of Filovirus Glycoprotein-Pseudotyped Vesicular Stomatitis Virus for Study of Filovirus Entry Mechanisms
Chapter number 4
Book title
Ebolaviruses
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7116-9_4
Pubmed ID
Book ISBNs
978-1-4939-7115-2, 978-1-4939-7116-9
Authors

Rachel B. Brouillette, Wendy Maury

Editors

Thomas Hoenen, Allison Groseth

Abstract

Members of the family Filoviridae are filamentous, enveloped, and nonsegmented negative-stranded RNA viruses that can cause severe hemorrhagic disease in humans and nonhuman primates with high mortality rates. Current efforts to analyze the structure and biology of these viruses as well as the development of antivirals have been hindered by the necessity of biosafety level 4 containment (BSL4). Here, we outline how to produce and work with Ebola virus glycoprotein bearing vesicular stomatitis virus (VSV) pseudovirions. These pseudovirions can be safely used to evaluate early steps of the filovirus life cycle without need for BSL4 containment. Virus gene expression in the transduced cells is easy to assess since the pseudovirions encode a reporter gene in place of the VSV G glycoprotein gene. Adoption of VSV for use as a pseudovirion system for filovirus GP has significantly expanded access for researchers to study specific aspects of the viral life cycle outside of BSL4 containment and has allowed substantial growth of filovirus research.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 17 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 17 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 18%
Student > Doctoral Student 2 12%
Student > Master 2 12%
Student > Bachelor 1 6%
Researcher 1 6%
Other 1 6%
Unknown 7 41%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 18%
Immunology and Microbiology 3 18%
Nursing and Health Professions 1 6%
Pharmacology, Toxicology and Pharmaceutical Science 1 6%
Medicine and Dentistry 1 6%
Other 1 6%
Unknown 7 41%