Structure and Antigenicity of the Porcine Astrovirus 4 Capsid Spike

Porcine astrovirus 4 (PoAstV4) has been recently associated with respiratory disease in pigs. In order to understand the scope of PoAstV4 infections and to support the development of a vaccine to combat PoAstV4 disease in pigs, we designed and produced a recombinant PoAstV4 capsid spike protein for use as an antigen in serological assays and for potential future use as a vaccine antigen. Structural prediction of the full-length PoAstV4 capsid protein guided the design of the recombinant PoAstV4 capsid spike domain expression plasmid. The recombinant PoAstV4 capsid spike was expressed in <i>Escherichia coli</i>, purified by affinity and size-exclusion chromatography, and its crystal structure was determined at 1.85 Å resolution, enabling structural comparisons to other animal and human astrovirus capsid spike structures. The recombinant PoAstV4 capsid spike protein was also used as an antigen for the successful development of a serological assay to detect PoAstV4 antibodies, demonstrating that the recombinant PoAstV4 capsid spike retains antigenic epitopes found on the native PoAstV4 capsid. These studies lay a foundation for seroprevalence studies and the development of a PoAstV4 vaccine for swine.

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Publication Details

Journal
Viruses
Published
2024-10-11
DOI
https://doi.org/10.3390/v16101596
Primary Topic
Animal Virus Infections Studies
Type
article
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article

Structure and Antigenicity of the Porcine Astrovirus 4 Capsid Spike

Armen Mardirossian, Rebecca M. DuBois, Sarah Lanning, Michael P. Murtaugh et al.
1 links
Viruses
Animal Virus Infections Studies
article

Structure and Antigenicity of the Porcine Astrovirus 4 Capsid Spike

Armen Mardirossian, Rebecca M. DuBois, Sarah Lanning, Michael P. Murtaugh, Danielle J. Haley, Kyle E. Henricson, Iyan Cirillo
article en

Abstract

Porcine astrovirus 4 (PoAstV4) has been recently associated with respiratory disease in pigs. In order to understand the scope of PoAstV4 infections and to support the development of a vaccine to combat PoAstV4 disease in pigs, we designed and produced a recombinant PoAstV4 capsid spike protein for use as an antigen in serological assays and for potential future use as a vaccine antigen. Structural prediction of the full-length PoAstV4 capsid protein guided the design of the recombinant PoAstV4 capsid spike domain expression plasmid. The recombinant PoAstV4 capsid spike was expressed in <i>Escherichia coli</i>, purified by affinity and size-exclusion chromatography, and its crystal structure was determined at 1.85 Å resolution, enabling structural comparisons to other animal and human astrovirus capsid spike structures. The recombinant PoAstV4 capsid spike protein was also used as an antigen for the successful development of a serological assay to detect PoAstV4 antibodies, demonstrating that the recombinant PoAstV4 capsid spike retains antigenic epitopes found on the native PoAstV4 capsid. These studies lay a foundation for seroprevalence studies and the development of a PoAstV4 vaccine for swine.

VirusesVol. 16(10)
North Carolina State University (US), University of California, Santa Cruz (US)
Openalex Percentile: Top 80%
Animal Virus Infections Studies
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