4.6 Article

Stable Display of Artificially Long Foreign Antigens on Chimeric Bamboo mosaic virus Particles

Journal

VIRUSES-BASEL
Volume 13, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/v13040572

Keywords

Bamboo mosaic virus; longer antigens; chimeric virus particles (CVPs); flexible linker; peptide properties; virus accumulation

Categories

Funding

  1. National Science Council, Taiwan [NSC 98-2321-B-005-005-MY3]
  2. Advanced Plant Biotechnology Center from The Featured Areas Research Center Program within Ministry of Education (MOE) in Taiwan

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In this study, chimeric virus particles (CVPs) carrying heterologous peptides on the surface of coat protein subunits were generated by genetically modifying plant viruses. The properties of these chimeras were determined by factors such as the length and source of the inserted peptides. It was found that using plant virus-based chimeras to express foreign proteins can increase their length limitations and has potential for novel vaccine development.
Plant viruses can be genetically modified to generate chimeric virus particles (CVPs) carrying heterologous peptides fused on the surface of coat protein (CP) subunits as vaccine candidates. However, some factors may be especially significant in determining the properties of chimeras. In this study, peptides from various sources and of various lengths were inserted into the Bamboo mosaic virus-based (BaMV) vector CP N-terminus to examine the chimeras infecting and accumulating in plants. Interestingly, it was found that the two different strains Foot-and-mouth disease virus (FMDV) VP1 antigens with flexible linker peptides (77 or 82 amino acids) were directly expressed on the BaMV CP, and the chimeric particles self-assembled and continued to express FMDV antigens. The chimeric CP, when directly fused with a large foreign protein (117 amino acids), can self-fold into incomplete virus particles or disks. The physicochemical properties of heterologus peptides N-terminus, complex strand structures of heterologus peptides C-terminus and different flexible linker peptides, can affect the chimera accumulation. Based on these findings, using plant virus-based chimeras to express foreign proteins can increase their length limitations, and engineered plant-made CVP-based vaccines have increasing potential for further development as novel vaccines.

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