Comparative Molecular Biology Approaches for the Production of Poliovirus Virus-Like Particles Using Pichia pastoris

Author:

Sherry Lee1ORCID,Grehan Keith1ORCID,Snowden Joseph S.1ORCID,Knight Michael L.2ORCID,Adeyemi Oluwapelumi O.3ORCID,Rowlands David J.1ORCID,Stonehouse Nicola J.1ORCID

Affiliation:

1. School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds, United Kingdom

2. Sir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom

3. Department of Medical Microbiology and Parasitology, Faculty of Basic Medical Sciences, College of Health Sciences, University of Ilorin, Ilorin, Nigeria

Abstract

Although the current poliovirus immunization program has been extremely successful in reducing the number of cases of paralytic polio worldwide, now more cases are caused by vaccine-derived polioviruses than by wild poliovirus. Switching to inactivated poliovirus vaccines will reduce this over time; however, their production requires the growth of large amounts of virus. This biosafety concern can be addressed by producing just the virus capsid. The capsid serves to protect the genetic material, which causes disease when introduced into a cell. Therefore, empty capsids (virus-like particles [VLPs]), which lack the viral RNA genome, are safe both to make and to use. We exploit yeast as a versatile model expression system to produce VLPs, and here we specifically highlight the potential of this system to supply next-generation poliovirus vaccines to secure a polio-free world for the future.

Funder

World Health Organization

Wellcome Trust

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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