Immunogenicity and antigenic relationships among spike proteins of porcine epidemic diarrhea virus subtypes G1 and G2

• DOI: 10.1007/s00705-015-2694-6
• Publication Date: 2015-11-26T04:26:01Z
• Authors: Xiaobo Wang; Jianfei Chen; Da Shi; Hongyan Shi; Xin Zhang; Jing Yuan; Shibo Jiang; Li Feng
• Keywords: 0301 basic medicine; China; 0303 health sciences; Genotype; Porcine epidemic diarrhea virus; Enzyme-Linked Immunosorbent Assay; Antibodies, Viral; 3. Good health; Mice; 03 medical and health sciences; Neutralization Tests; Immunoglobulin G; Spike Glycoprotein, Coronavirus; Animals; Original Article; Immunization; Fluorescent Antibody Technique, Indirect; Antigens, Viral

Porcine epidemic diarrhea virus (PEDV) is a coronavirus that infects cells lining the small intestine of swine, resulting in vomiting, diarrhea, and dehydration. The amino acid sequence of the spike (S) protein, which is the principal target recognized by host immune cells, has multiple mutations that distinguish the two PEDV genotypes, G1 and G2. To determine whether these mutations lead to changes in antigenicity, as suggested by the failure of PEDV vaccines in China, we first optimized the codons of typical S genes of the CV777 vaccine strain (G1 subtype) and LNCT2 strain (G2 subtype) and expressed the recombinant full-length sequence of the S protein in a eukaryotic expression system. The IgG antibody levels of serum from mice immunized with purified S protein were markedly high. Antigenicity was compared by detection of polyclonal antibodies (PAbs) against the virus and S protein using an enzyme-linked immunosorbent assay (ELISA), an indirect immunofluorescence assay (IFA), and a serum cross-neutralization (SN) assay. Reactivity with the PAbs revealed significant cross-reactivity between the two PEDV subtypes, although there was a twofold difference in the antigenic responses based on PAb titers in the ELISA and IFA. Consistent with the variation in the S gene sequences, the SN titer suggested differences in the neutralization activity of the S protein between the two subtypes, which could explain the antigenic variation between the PEDV subtypes G1 and G2.