Abstract

Porcine epidemic diarrhea virus (PEDV), an enteric coronavirus, is the causative agent of porcine epidemic diarrhea (PED) that damages intestinal epithelial cells and results in severe diarrhea and dehydration in neonatal suckling pigs with up to 100% mortality. The oral vaccine route is reported as a promising approach for inducing protective immunity against PEDV invasion. Furthermore, dendritic cells (DCs), professional antigen-presenting cells, link humoral and cellular immune responses for homeostasis of the intestinal immune environment. In this study, in order to explore an efficient oral vaccine against PEDV infection, a mucosal DC-targeting oral vaccine was developed using Lactobacillus casei to deliver the DC-targeting peptide (DCpep) fused with the PEDV core neutralizing epitope (COE) antigen. This probiotic vaccine could efficiently elicit secretory immunoglobulin A (SIgA)-based mucosal and immunoglobulin G (IgG)-based humoral immune responses via oral vaccination in vivo. Significant differences (p < 0.05) in the immune response levels were observed between probiotics expressing the COE-DCpep fusion protein and COE antigen alone, suggesting better immune efficiency of the probiotics vaccine expressing the DC-targeting peptide fused with PEDV COE antigen. This mucosal DC-targeting oral vaccine delivery effectively enhances vaccine antigen delivery efficiency, providing a useful strategy to induce efficient immune responses against PEDV infection.

Highlights

  • Porcine epidemic diarrhea virus (PEDV) infection, causing an acute and highly contagious enteric disease in nursing pigs with up to 100% mortality, mainly results in intestinal-epithelial-cell damage [1].Currently, an RNA vaccine and an inactivated whole-virus vaccine of porcine epidemic diarrhea were developed at HarrisvaccinesTM and Zoetis (Florham Park, NJ, USA), respectively, widely used and considered to be effective [2]

  • To reach the mucosal immunity-related sites in sufficient amounts, oral mucosal vaccines need to withstand harsh digestive environments, which are proving to be a big challenge for mucosal vaccine development [3]; effective antigen delivery vehicles and the adjuvant limit the availability of oral mucosal vaccines for stimulation of immunity [4]

  • In order to enhance the deliver efficiency of vaccine antigens to mucosal immune tissues via oral administration, a dendritic cell (DC)-targeting mucosal vaccine was suggested as a realistic approach for oral vaccination to induce high mucosal immune responses against infection [10]

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Summary

Introduction

Porcine epidemic diarrhea virus (PEDV) infection, causing an acute and highly contagious enteric disease in nursing pigs with up to 100% mortality, mainly results in intestinal-epithelial-cell damage [1].Currently, an RNA vaccine and an inactivated whole-virus vaccine of porcine epidemic diarrhea were developed at HarrisvaccinesTM and Zoetis (Florham Park, NJ, USA), respectively, widely used and considered to be effective [2]. Porcine epidemic diarrhea virus (PEDV) infection, causing an acute and highly contagious enteric disease in nursing pigs with up to 100% mortality, mainly results in intestinal-epithelial-cell damage [1]. It is important to develop oral mucosa vaccines that can elicit effective mucosal. Viruses 2017, 9, 312 immune responses against PEDV infection. There is increasing interest in the development of lactic acid bacteria (LAB)-based oral vaccines against enteric viruses; this approach is crucial for the effective induction of a mucosal immune response. In order to enhance the deliver efficiency of vaccine antigens to mucosal immune tissues via oral administration, a dendritic cell (DC)-targeting mucosal vaccine was suggested as a realistic approach for oral vaccination to induce high mucosal immune responses against infection [10]

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