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Immune responses induced by DNA vaccines bearing Spike gene of PEDV combined with porcine IL-18

Porcine epidemic diarrhea virus (PEDV) is the causative agent of porcine epidemic diarrhea, a highly contagious enteric disease of swine. The Spike (S) protein is one of the main structural proteins of PEDV capable of inducing neutralizing antibodies in vivo. Herein, we generated three distinct DNA...

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Detalles Bibliográficos
Autores principales: Suo, Siqingaowa, Ren, Yudong, Li, Guangxing, Zarlenga, Dante, Bu, Ri-e, Su, Dingding, Li, Xunliang, Li, Pengchong, Meng, Fandan, Wang, Chao, Ren, Xiaofeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. Published by Elsevier B.V. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114480/
https://www.ncbi.nlm.nih.gov/pubmed/22643071
http://dx.doi.org/10.1016/j.virusres.2012.05.007
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author Suo, Siqingaowa
Ren, Yudong
Li, Guangxing
Zarlenga, Dante
Bu, Ri-e
Su, Dingding
Li, Xunliang
Li, Pengchong
Meng, Fandan
Wang, Chao
Ren, Xiaofeng
author_facet Suo, Siqingaowa
Ren, Yudong
Li, Guangxing
Zarlenga, Dante
Bu, Ri-e
Su, Dingding
Li, Xunliang
Li, Pengchong
Meng, Fandan
Wang, Chao
Ren, Xiaofeng
author_sort Suo, Siqingaowa
collection PubMed
description Porcine epidemic diarrhea virus (PEDV) is the causative agent of porcine epidemic diarrhea, a highly contagious enteric disease of swine. The Spike (S) protein is one of the main structural proteins of PEDV capable of inducing neutralizing antibodies in vivo. Herein, we generated three distinct DNA constructs in the eukaryotic expression plasmid pVAX1; one encoding the S protein [pVAX1-(PEDV-S)], the second encoding the N-terminal fragment (S1) [pVAX1-(PEDV-S1)] containing potent antigenic sites, and the third expressing the porcine interleukin-18 (pIL-18) [pVAX1-(IL-18)]. Immunofluorescence assays in BHK-21 cells demonstrated successful protein expression from all 3 constructs. Kunming mice were injected separately with each of these constructs or with a pVAX1-(PEDV-S1)/pVAX1-(IL-18) combination, an attenuated PEDV vaccine, or vector only control. Animals were examined for T lymphocyte proliferation, anti-PEDV antibodies, IFN-γ and IL-4 protein levels, and cytotoxic T cell function in mouse peripheral blood and spleen. In all cases, results showed that pVAX1-(PEDV-S) and the combination of pVAX1-(PEDV-S1) with pVAX1-(IL-18) induced the strongest responses; however, pIL-18 had no adjuvant effects when given in combination with pVAX1-(PEDV-S1).
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spelling pubmed-71144802020-04-02 Immune responses induced by DNA vaccines bearing Spike gene of PEDV combined with porcine IL-18 Suo, Siqingaowa Ren, Yudong Li, Guangxing Zarlenga, Dante Bu, Ri-e Su, Dingding Li, Xunliang Li, Pengchong Meng, Fandan Wang, Chao Ren, Xiaofeng Virus Res Article Porcine epidemic diarrhea virus (PEDV) is the causative agent of porcine epidemic diarrhea, a highly contagious enteric disease of swine. The Spike (S) protein is one of the main structural proteins of PEDV capable of inducing neutralizing antibodies in vivo. Herein, we generated three distinct DNA constructs in the eukaryotic expression plasmid pVAX1; one encoding the S protein [pVAX1-(PEDV-S)], the second encoding the N-terminal fragment (S1) [pVAX1-(PEDV-S1)] containing potent antigenic sites, and the third expressing the porcine interleukin-18 (pIL-18) [pVAX1-(IL-18)]. Immunofluorescence assays in BHK-21 cells demonstrated successful protein expression from all 3 constructs. Kunming mice were injected separately with each of these constructs or with a pVAX1-(PEDV-S1)/pVAX1-(IL-18) combination, an attenuated PEDV vaccine, or vector only control. Animals were examined for T lymphocyte proliferation, anti-PEDV antibodies, IFN-γ and IL-4 protein levels, and cytotoxic T cell function in mouse peripheral blood and spleen. In all cases, results showed that pVAX1-(PEDV-S) and the combination of pVAX1-(PEDV-S1) with pVAX1-(IL-18) induced the strongest responses; however, pIL-18 had no adjuvant effects when given in combination with pVAX1-(PEDV-S1). Elsevier B.V. Published by Elsevier B.V. 2012-08 2012-05-19 /pmc/articles/PMC7114480/ /pubmed/22643071 http://dx.doi.org/10.1016/j.virusres.2012.05.007 Text en Copyright © 2012 Elsevier B.V. Published by Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Suo, Siqingaowa
Ren, Yudong
Li, Guangxing
Zarlenga, Dante
Bu, Ri-e
Su, Dingding
Li, Xunliang
Li, Pengchong
Meng, Fandan
Wang, Chao
Ren, Xiaofeng
Immune responses induced by DNA vaccines bearing Spike gene of PEDV combined with porcine IL-18
title Immune responses induced by DNA vaccines bearing Spike gene of PEDV combined with porcine IL-18
title_full Immune responses induced by DNA vaccines bearing Spike gene of PEDV combined with porcine IL-18
title_fullStr Immune responses induced by DNA vaccines bearing Spike gene of PEDV combined with porcine IL-18
title_full_unstemmed Immune responses induced by DNA vaccines bearing Spike gene of PEDV combined with porcine IL-18
title_short Immune responses induced by DNA vaccines bearing Spike gene of PEDV combined with porcine IL-18
title_sort immune responses induced by dna vaccines bearing spike gene of pedv combined with porcine il-18
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114480/
https://www.ncbi.nlm.nih.gov/pubmed/22643071
http://dx.doi.org/10.1016/j.virusres.2012.05.007
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