Recovery of Recombinant Rotaviruses by Reverse Genetics

Chantal A. Agbemabiese, Asha A. Philip, John T. Patton

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

1 Citation (Scopus)

Abstract

Rotaviruses are the primary cause of severe gastroenteritis in infants and young children throughout the world. To combat rotavirus illness, several live oral vaccines have been developed, or are under development, that are formulated from attenuated human or human–animal reassortant strains of rotavirus. While the effectiveness of these vaccines is generally high in developed countries, the same vaccines are significantly less effective in many developing countries, where the need for rotavirus vaccines is greatest. Recently, reverse genetics systems have been developed that allow modification of the segmented double-stranded (ds)RNA genome of rotavirus, including reprogramming the genome to allow expression of additional proteins that may stimulate expanded neutralizing antibody responses in vaccinated children. The use of reverse genetics systems may not only lead to the development of more potent classes of vaccines but can be used to better explore the intricacies of rotavirus molecular biology and pathogenesis. In this article, we share protocols that can be used to generate recombinant rotaviruses, including modified strains that express foreign proteins.

Original languageEnglish
Title of host publicationMethods in Molecular Biology
PublisherHumana Press Inc.
Pages249-263
Number of pages15
DOIs
Publication statusPublished - 2024
Externally publishedYes

Publication series

NameMethods in Molecular Biology
Volume2733
ISSN (Print)1064-3745
ISSN (Electronic)1940-6029

Keywords

  • Double-stranded RNA
  • Gastroenteritis
  • Reverse genetics
  • Rotavirus
  • Segmented genome
  • dsRNA

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