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Porta, C., Kotecha, A., Burman, A., Jackson, T., Ren, J., Loureiro, S., et al. (2013) Rational engineering of recombinant picornavirus capsids to produce safe, protective vaccine antigen. Plos Pathogens, 9, e1003255.
http://dx.doi.org/10.1371/journal.ppat.1003255

has been cited by the following article:

• TITLE: Comparison of transient and stable expression of foot-and-mouth disease virus capsid proteins in mammalian cells

  AUTHORS: Ana Clara Mignaqui, Vanesa Ruiz, Andrés Wigdorovitz

  KEYWORDS: Empty Capsids; Foot and Mouth Disease Virus; Mammalian Cells; Stable Expression; Transient Ex-pression

  JOURNAL NAME: Advances in Bioscience and Biotechnology, Vol.4 No.12, December 23, 2013

  ABSTRACT: Foot-and-mouth disease is a highly contagious disease that produces severe economic losses in the livestock industry. This disease is being controlled by the use of an inactivated vaccine. However, the use of recombinant empty capsids as a subunit vaccine has been reported to be a promising candidate because it avoids the use of virus in the vaccine production. A plasmid containing the capsid precursor P12A and protease 3C sequences of foot-and-mouth disease virus (FMDV) was constructed and used to compare transient and stable expression in mammalian cells. When BHK-21 cells were transfected with the recombinant vector, protease 3C cleaved the capsid precursor P12A into the structural proteins VP0, VP1 and VP3. A sucrose gradient demonstrated that the structural proteins assembled into different subviral particles. Attempts to generate a stable cell line only allowed isolating low-level-expressing clones, probably due to the effect of protease 3C on the cells. Moreover, the recombinant protein yield achieved in transient expression assays was much higher than the one achieved in stable expression assays. Results indicate that mammalian cells are a good strategy to produce recombinant FMDV subviral particles. However, the alternative approach of transient gene expression in scalable systems should be used instead of the standard method that involves the generation of a stable cell line.