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Characterization of a recombinant pseudorabies virus expressing porcine parvovirus VP2 protein and porcine IL-6

BACKGROUND: Porcine parvovirus (PPV) and pseudorabies virus (PRV) are the important etiological agents of swine infectious diseases, resulting in huge economic losses to the Chinese swine industry. Interleukin-6 (IL-6) has the roles to support host immune response to infections as a pleiotropic cyto...

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Autores principales: Zheng, Hui-Hua, Wang, Lin-Qing, Fu, Peng-Fei, Zheng, Lan-Lan, Chen, Hong-Ying, Liu, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6998180/
https://www.ncbi.nlm.nih.gov/pubmed/32014014
http://dx.doi.org/10.1186/s12985-020-1292-8
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author Zheng, Hui-Hua
Wang, Lin-Qing
Fu, Peng-Fei
Zheng, Lan-Lan
Chen, Hong-Ying
Liu, Fang
author_facet Zheng, Hui-Hua
Wang, Lin-Qing
Fu, Peng-Fei
Zheng, Lan-Lan
Chen, Hong-Ying
Liu, Fang
author_sort Zheng, Hui-Hua
collection PubMed
description BACKGROUND: Porcine parvovirus (PPV) and pseudorabies virus (PRV) are the important etiological agents of swine infectious diseases, resulting in huge economic losses to the Chinese swine industry. Interleukin-6 (IL-6) has the roles to support host immune response to infections as a pleiotropic cytokine. It is essential to construct a live attenuated vaccine-based recombinant PRV that expresses PPV VP2 protein and porcine IL-6 for prevention and control of PRV and PPV. METHODS: The recombinant plasmid, pGVP2-IL6, was constructed by porcine IL-6 gene substituting for EGFP gene of the PRV transfer plasmid pGVP2-EGFP containing VP2 gene of PPV. Plasmid pGVP2-IL6 was transfected into swine testicle cells pre-infected with the virus rPRV-VP2-EGFP strain through homologous recombination and plaque purification to generate a recombinant virus rPRV-VP2-IL6. The recombinant PRV was further identified by PCR and DNA sequencing, and the expression of the VP2 protein and porcine IL-6 was analyzed by reverse transcription-PCR (RT-PCR) and Western blot. The virus titer was calculated according to Reed and Muench method. The immunogenicity of the recombinant virus was preliminarily evaluated in mice by intramuscular administration twice with the rPRV-VP2-IL6 at 4-week intervals. RESULTS: A recombinant virus rPRV-VP2-IL6 was successfully constructed and confirmed in this study. The properties of rPRV-VP2-IL6 were similar to the parental virus HB98 in terms of growth curve, morphogenesis and virus plaque sizes, and rPRV-VP2-IL6 was proliferated in different cell types. It induced specific antibodies against PPV as well as a strong increase of PPV-specific lymphocyte proliferation responses in mice immunized with rPRV-VP2-IL6, and provided partial protection against the virulent PPV challenge. rPRV-VP2-IL6 also induced a high level of neutralizing antibodies against PRV, and significantly reduced the mortality rate of (1 of 10) following virulent PRV challenge compared with the control (10 of 10). CONCLUSIONS: The recombinant rPRV-VP2-IL6 might be a potential candidate vaccine against PRV and PPV infections in pigs.
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spelling pubmed-69981802020-02-05 Characterization of a recombinant pseudorabies virus expressing porcine parvovirus VP2 protein and porcine IL-6 Zheng, Hui-Hua Wang, Lin-Qing Fu, Peng-Fei Zheng, Lan-Lan Chen, Hong-Ying Liu, Fang Virol J Research BACKGROUND: Porcine parvovirus (PPV) and pseudorabies virus (PRV) are the important etiological agents of swine infectious diseases, resulting in huge economic losses to the Chinese swine industry. Interleukin-6 (IL-6) has the roles to support host immune response to infections as a pleiotropic cytokine. It is essential to construct a live attenuated vaccine-based recombinant PRV that expresses PPV VP2 protein and porcine IL-6 for prevention and control of PRV and PPV. METHODS: The recombinant plasmid, pGVP2-IL6, was constructed by porcine IL-6 gene substituting for EGFP gene of the PRV transfer plasmid pGVP2-EGFP containing VP2 gene of PPV. Plasmid pGVP2-IL6 was transfected into swine testicle cells pre-infected with the virus rPRV-VP2-EGFP strain through homologous recombination and plaque purification to generate a recombinant virus rPRV-VP2-IL6. The recombinant PRV was further identified by PCR and DNA sequencing, and the expression of the VP2 protein and porcine IL-6 was analyzed by reverse transcription-PCR (RT-PCR) and Western blot. The virus titer was calculated according to Reed and Muench method. The immunogenicity of the recombinant virus was preliminarily evaluated in mice by intramuscular administration twice with the rPRV-VP2-IL6 at 4-week intervals. RESULTS: A recombinant virus rPRV-VP2-IL6 was successfully constructed and confirmed in this study. The properties of rPRV-VP2-IL6 were similar to the parental virus HB98 in terms of growth curve, morphogenesis and virus plaque sizes, and rPRV-VP2-IL6 was proliferated in different cell types. It induced specific antibodies against PPV as well as a strong increase of PPV-specific lymphocyte proliferation responses in mice immunized with rPRV-VP2-IL6, and provided partial protection against the virulent PPV challenge. rPRV-VP2-IL6 also induced a high level of neutralizing antibodies against PRV, and significantly reduced the mortality rate of (1 of 10) following virulent PRV challenge compared with the control (10 of 10). CONCLUSIONS: The recombinant rPRV-VP2-IL6 might be a potential candidate vaccine against PRV and PPV infections in pigs. BioMed Central 2020-02-03 /pmc/articles/PMC6998180/ /pubmed/32014014 http://dx.doi.org/10.1186/s12985-020-1292-8 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zheng, Hui-Hua
Wang, Lin-Qing
Fu, Peng-Fei
Zheng, Lan-Lan
Chen, Hong-Ying
Liu, Fang
Characterization of a recombinant pseudorabies virus expressing porcine parvovirus VP2 protein and porcine IL-6
title Characterization of a recombinant pseudorabies virus expressing porcine parvovirus VP2 protein and porcine IL-6
title_full Characterization of a recombinant pseudorabies virus expressing porcine parvovirus VP2 protein and porcine IL-6
title_fullStr Characterization of a recombinant pseudorabies virus expressing porcine parvovirus VP2 protein and porcine IL-6
title_full_unstemmed Characterization of a recombinant pseudorabies virus expressing porcine parvovirus VP2 protein and porcine IL-6
title_short Characterization of a recombinant pseudorabies virus expressing porcine parvovirus VP2 protein and porcine IL-6
title_sort characterization of a recombinant pseudorabies virus expressing porcine parvovirus vp2 protein and porcine il-6
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6998180/
https://www.ncbi.nlm.nih.gov/pubmed/32014014
http://dx.doi.org/10.1186/s12985-020-1292-8
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