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Recombinant Virus Vaccines

Overview of attention for book
Cover of 'Recombinant Virus Vaccines'

Table of Contents

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    Book Overview
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    Chapter 1 Development of Novel Vaccines Against Infectious Diseases Based on Chimpanzee Adenoviral Vector
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    Chapter 2 Development of Recombinant Canarypox Viruses Expressing Immunogens
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    Chapter 3 Fowl Adenovirus-Based Vaccine Platform
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    Chapter 4 Development of Recombinant HSV-Based Vaccine Vectors
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    Chapter 5 Generating Recombinant Pseudorabies Virus for Use as a Vaccine Platform
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    Chapter 6 Generation and Production of Modified Vaccinia Virus Ankara (MVA) as a Vaccine Vector
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    Chapter 7 Poxvirus Safety Analysis in the Pregnant Mouse Model, Vaccinia, and Raccoonpox Viruses
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    Chapter 8 Development of Recombinant Arenavirus-Based Vaccines
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    Chapter 9 Development of Recombinant Measles Virus-Based Vaccines
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    Chapter 10 Recombinant Tri-Segmented Pichinde Virus as a Novel Live Viral Vaccine Platform
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    Chapter 11 Human Rhinovirus-A1 as an Expression Vector
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    Chapter 12 Generating Recombinant Vesicular Stomatitis Viruses for Use as Vaccine Platforms
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    Chapter 13 Alphavirus-Based Vaccines
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    Chapter 14 Display of HIV-1 Envelope Protein on Lambda Phage Scaffold as a Vaccine Platform
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    Chapter 15 Bacteriophage T4 as a Nanoparticle Platform to Display and Deliver Pathogen Antigens: Construction of an Effective Anthrax Vaccine
Attention for Chapter 3: Fowl Adenovirus-Based Vaccine Platform
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Citations

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Chapter title
Fowl Adenovirus-Based Vaccine Platform
Chapter number 3
Book title
Recombinant Virus Vaccines
Published in
Methods in molecular biology, April 2017
DOI 10.1007/978-1-4939-6869-5_3
Pubmed ID
28374242
Book ISBNs
978-1-4939-6867-1, 978-1-4939-6869-5
Authors

Juan C. Corredor, Yanlong Pei, Éva Nagy

Editors

Maureen C. Ferran, Gary R. Skuse

Abstract

Nonpathogenic fowl adenoviruses (FAdVs) are amenable for engineering multivalent vaccine platforms due to large stretches of nonessential DNA sequences in their genomes. We describe the generation of FAdV-9-based vaccine platforms by targeted homologous recombination in an infectious clone (pPacFAdV-9 or wild type FAdmid) containing the entire viral genome in a cosmid vector. The viral DNA is subsequently released from the cosmid by restriction enzyme digestion followed by transfection in a chicken hepatoma cell line (CH-SAH). Virus is harvested, propagated, and verified for foreign gene expression.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 4 27%
Researcher 4 27%
Student > Ph. D. Student 2 13%
Student > Bachelor 1 7%
Student > Postgraduate 1 7%
Other 0 0%
Unknown 3 20%
Readers by discipline Count As %
Veterinary Science and Veterinary Medicine 2 13%
Agricultural and Biological Sciences 2 13%
Unspecified 1 7%
Biochemistry, Genetics and Molecular Biology 1 7%
Computer Science 1 7%
Other 3 20%
Unknown 5 33%

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