Oral Immunization against PEDV with Recombinant Lactobacillus casei Expressing Dendritic Cell-Targeting Peptide Fusing COE Protein of PEDV in Piglets
Porcine epidemic diarrhea (PED) is a highly contagious disease in newborn piglets. In our previous study, a genetically engineered oral vaccine ( ) expressing a dendritic cell (DC)-targeting peptide fused with porcine epidemic diarrhea virus (PEDV) COE antigen was developed. This vaccine induced sig...
Saved in:
Published in | Viruses Vol. 10; no. 3; p. 106 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
01.03.2018
MDPI |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Porcine epidemic diarrhea (PED) is a highly contagious disease in newborn piglets. In our previous study, a genetically engineered
oral vaccine (
) expressing a dendritic cell (DC)-targeting peptide fused with porcine epidemic diarrhea virus (PEDV) COE antigen was developed. This vaccine induced significant levels of anti-PEDV specific IgG and IgA antibody responses in mice, indicating a potential strategy against PEDV infection. In this study,
was used for oral vaccination of newborn piglets against PEDV. We then assessed the immune responses and protection efficacy of
. An indirect enzyme-linked immunosorbent assay (ELISA) showed that the recombinant
vaccine elicits a specific systemic and mucosal immune response. The T-helper cells mediated by
and PEDV infection display a Th1 phenotype. The histopathological results showed that
promotes lymphocyte proliferation and effectively protects piglets against PEDV infection. The transforming growth factor-β level indicated that the recombinant
vaccine plays a role in anti-inflammatory responses in mesenteric lymph nodes during PEDV infection. These results show that
is a potential vaccine against PEDV infection. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These author contributed equally to this work. |
ISSN: | 1999-4915 1999-4915 |
DOI: | 10.3390/v10030106 |