Cargando…

Development of a Recombinant Pichinde Virus-Vectored Vaccine against Turkey Arthritis Reovirus and Its Immunological Response Characterization in Vaccinated Animals

Vaccination may be an effective way to reduce turkey arthritis reovirus (TARV)-induced lameness in turkey flocks. However, there are currently no commercial vaccines available against TARV infection. Here, we describe the use of reverse genetics technology to generate a recombinant Pichinde virus (P...

Descripción completa

Detalles Bibliográficos
Autores principales: Kumar, Pawan, Sharafeldin, Tamer A., Kumar, Rahul, Huang, Qinfeng, Liang, Yuying, Goyal, Sagar M., Porter, Robert E., Ly, Hinh, Mor, Sunil K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918942/
https://www.ncbi.nlm.nih.gov/pubmed/33668435
http://dx.doi.org/10.3390/pathogens10020197
_version_ 1783658037401092096
author Kumar, Pawan
Sharafeldin, Tamer A.
Kumar, Rahul
Huang, Qinfeng
Liang, Yuying
Goyal, Sagar M.
Porter, Robert E.
Ly, Hinh
Mor, Sunil K.
author_facet Kumar, Pawan
Sharafeldin, Tamer A.
Kumar, Rahul
Huang, Qinfeng
Liang, Yuying
Goyal, Sagar M.
Porter, Robert E.
Ly, Hinh
Mor, Sunil K.
author_sort Kumar, Pawan
collection PubMed
description Vaccination may be an effective way to reduce turkey arthritis reovirus (TARV)-induced lameness in turkey flocks. However, there are currently no commercial vaccines available against TARV infection. Here, we describe the use of reverse genetics technology to generate a recombinant Pichinde virus (PICV) that expresses the Sigma C and/or Sigma B proteins of TARV as antigens. Nine recombinant PICV-based TARV vaccines were developed carrying the wild-type S1 (Sigma C) and/or S3 (Sigma B) genes from three different TARV strains. In addition, three recombinant PICV-based TARV vaccines were produced carrying codon-optimized S1 and/or S3 genes of a TARV strain. The S1 and S3 genes and antigens were found to be expressed in virus-infected cells via reverse transcriptase polymerase chain reaction (RT-PCR) and the direct fluorescent antibody (DFA) technique, respectively. Turkey poults inoculated with the recombinant PICV-based TARV vaccine expressing the bivalent TARV S1 and S3 antigens developed high anti-TARV antibody titers, indicating the immunogenicity (and safety) of this vaccine. Future in vivo challenge studies using a turkey reovirus infection model will determine the optimum dose and protective efficacy of this recombinant virus-vectored candidate vaccine.
format Online
Article
Text
id pubmed-7918942
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-79189422021-03-02 Development of a Recombinant Pichinde Virus-Vectored Vaccine against Turkey Arthritis Reovirus and Its Immunological Response Characterization in Vaccinated Animals Kumar, Pawan Sharafeldin, Tamer A. Kumar, Rahul Huang, Qinfeng Liang, Yuying Goyal, Sagar M. Porter, Robert E. Ly, Hinh Mor, Sunil K. Pathogens Article Vaccination may be an effective way to reduce turkey arthritis reovirus (TARV)-induced lameness in turkey flocks. However, there are currently no commercial vaccines available against TARV infection. Here, we describe the use of reverse genetics technology to generate a recombinant Pichinde virus (PICV) that expresses the Sigma C and/or Sigma B proteins of TARV as antigens. Nine recombinant PICV-based TARV vaccines were developed carrying the wild-type S1 (Sigma C) and/or S3 (Sigma B) genes from three different TARV strains. In addition, three recombinant PICV-based TARV vaccines were produced carrying codon-optimized S1 and/or S3 genes of a TARV strain. The S1 and S3 genes and antigens were found to be expressed in virus-infected cells via reverse transcriptase polymerase chain reaction (RT-PCR) and the direct fluorescent antibody (DFA) technique, respectively. Turkey poults inoculated with the recombinant PICV-based TARV vaccine expressing the bivalent TARV S1 and S3 antigens developed high anti-TARV antibody titers, indicating the immunogenicity (and safety) of this vaccine. Future in vivo challenge studies using a turkey reovirus infection model will determine the optimum dose and protective efficacy of this recombinant virus-vectored candidate vaccine. MDPI 2021-02-13 /pmc/articles/PMC7918942/ /pubmed/33668435 http://dx.doi.org/10.3390/pathogens10020197 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kumar, Pawan
Sharafeldin, Tamer A.
Kumar, Rahul
Huang, Qinfeng
Liang, Yuying
Goyal, Sagar M.
Porter, Robert E.
Ly, Hinh
Mor, Sunil K.
Development of a Recombinant Pichinde Virus-Vectored Vaccine against Turkey Arthritis Reovirus and Its Immunological Response Characterization in Vaccinated Animals
title Development of a Recombinant Pichinde Virus-Vectored Vaccine against Turkey Arthritis Reovirus and Its Immunological Response Characterization in Vaccinated Animals
title_full Development of a Recombinant Pichinde Virus-Vectored Vaccine against Turkey Arthritis Reovirus and Its Immunological Response Characterization in Vaccinated Animals
title_fullStr Development of a Recombinant Pichinde Virus-Vectored Vaccine against Turkey Arthritis Reovirus and Its Immunological Response Characterization in Vaccinated Animals
title_full_unstemmed Development of a Recombinant Pichinde Virus-Vectored Vaccine against Turkey Arthritis Reovirus and Its Immunological Response Characterization in Vaccinated Animals
title_short Development of a Recombinant Pichinde Virus-Vectored Vaccine against Turkey Arthritis Reovirus and Its Immunological Response Characterization in Vaccinated Animals
title_sort development of a recombinant pichinde virus-vectored vaccine against turkey arthritis reovirus and its immunological response characterization in vaccinated animals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918942/
https://www.ncbi.nlm.nih.gov/pubmed/33668435
http://dx.doi.org/10.3390/pathogens10020197
work_keys_str_mv AT kumarpawan developmentofarecombinantpichindevirusvectoredvaccineagainstturkeyarthritisreovirusanditsimmunologicalresponsecharacterizationinvaccinatedanimals
AT sharafeldintamera developmentofarecombinantpichindevirusvectoredvaccineagainstturkeyarthritisreovirusanditsimmunologicalresponsecharacterizationinvaccinatedanimals
AT kumarrahul developmentofarecombinantpichindevirusvectoredvaccineagainstturkeyarthritisreovirusanditsimmunologicalresponsecharacterizationinvaccinatedanimals
AT huangqinfeng developmentofarecombinantpichindevirusvectoredvaccineagainstturkeyarthritisreovirusanditsimmunologicalresponsecharacterizationinvaccinatedanimals
AT liangyuying developmentofarecombinantpichindevirusvectoredvaccineagainstturkeyarthritisreovirusanditsimmunologicalresponsecharacterizationinvaccinatedanimals
AT goyalsagarm developmentofarecombinantpichindevirusvectoredvaccineagainstturkeyarthritisreovirusanditsimmunologicalresponsecharacterizationinvaccinatedanimals
AT porterroberte developmentofarecombinantpichindevirusvectoredvaccineagainstturkeyarthritisreovirusanditsimmunologicalresponsecharacterizationinvaccinatedanimals
AT lyhinh developmentofarecombinantpichindevirusvectoredvaccineagainstturkeyarthritisreovirusanditsimmunologicalresponsecharacterizationinvaccinatedanimals
AT morsunilk developmentofarecombinantpichindevirusvectoredvaccineagainstturkeyarthritisreovirusanditsimmunologicalresponsecharacterizationinvaccinatedanimals