Cargando…
A Novel Quadruple Gene-Deleted BoHV-1-Vectored RVFV Subunit Vaccine Induces Humoral and Cell-Mediated Immune Response against Rift Valley Fever in Calves
Rift Valley fever virus (RVFV) is considered to be a high biodefense priority based on its threat to livestock and its ability to cause human hemorrhagic fever. RVFV-infected livestock are also a significant risk factor for human infection by direct contact with contaminated blood, tissues, and abor...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10674938/ https://www.ncbi.nlm.nih.gov/pubmed/38005861 http://dx.doi.org/10.3390/v15112183 |
_version_ | 1785140946211438592 |
---|---|
author | Pavulraj, Selvaraj Stout, Rhett W. Barras, Elise D. Paulsen, Daniel B. Chowdhury, Shafiqul I. |
author_facet | Pavulraj, Selvaraj Stout, Rhett W. Barras, Elise D. Paulsen, Daniel B. Chowdhury, Shafiqul I. |
author_sort | Pavulraj, Selvaraj |
collection | PubMed |
description | Rift Valley fever virus (RVFV) is considered to be a high biodefense priority based on its threat to livestock and its ability to cause human hemorrhagic fever. RVFV-infected livestock are also a significant risk factor for human infection by direct contact with contaminated blood, tissues, and aborted fetal materials. Therefore, livestock vaccination in the affected regions has the direct dual benefit and one-health approach of protecting the lives of millions of animals and eliminating the risk of severe and sometimes lethal human Rift Valley fever (RVF) disease. Recently, we have developed a bovine herpesvirus type 1 (BoHV-1) quadruple gene mutant virus (BoHV-1qmv) vector that lacks virulence and immunosuppressive properties due to the deletion of envelope proteins UL49.5, glycoprotein G (gG), gE cytoplasmic tail, and US9 coding sequences. In the current study, we engineered the BoHV-1qmv further by incorporating a chimeric gene sequence to express a proteolytically cleavable polyprotein: RVFV envelope proteins Gn ectodomain sequence fused with bovine granulocyte-macrophage colony-stimulating factor (GMCSF) and Gc, resulting in a live BoHV-1qmv-vectored subunit vaccine against RVFV for livestock. In vitro, the resulting recombinant virus, BoHV-1qmv Sub-RVFV, was replicated in cell culture with high titers. The chimeric Gn-GMCSF and Gc proteins expressed by the vaccine virus formed the Gn–Gc complex. In calves, the BoHV-1qmv Sub-RVFV vaccination was safe and induced moderate levels of the RVFV vaccine strain, MP12-specific neutralizing antibody titers. Additionally, the peripheral blood mononuclear cells from the vaccinated calves had six-fold increased levels of interferon-gamma transcription compared with that of the BoHV-1qmv (vector)-vaccinated calves when stimulated with heat-inactivated MP12 antigen in vitro. Based on these findings, we believe that a single dose of BoHV-1qmv Sub-RVFV vaccine generated a protective RVFV-MP12-specific humoral and cellular immune response. Therefore, the BoHV-1qmv sub-RVFV can potentially be a protective subunit vaccine for cattle against RVFV. |
format | Online Article Text |
id | pubmed-10674938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106749382023-10-30 A Novel Quadruple Gene-Deleted BoHV-1-Vectored RVFV Subunit Vaccine Induces Humoral and Cell-Mediated Immune Response against Rift Valley Fever in Calves Pavulraj, Selvaraj Stout, Rhett W. Barras, Elise D. Paulsen, Daniel B. Chowdhury, Shafiqul I. Viruses Article Rift Valley fever virus (RVFV) is considered to be a high biodefense priority based on its threat to livestock and its ability to cause human hemorrhagic fever. RVFV-infected livestock are also a significant risk factor for human infection by direct contact with contaminated blood, tissues, and aborted fetal materials. Therefore, livestock vaccination in the affected regions has the direct dual benefit and one-health approach of protecting the lives of millions of animals and eliminating the risk of severe and sometimes lethal human Rift Valley fever (RVF) disease. Recently, we have developed a bovine herpesvirus type 1 (BoHV-1) quadruple gene mutant virus (BoHV-1qmv) vector that lacks virulence and immunosuppressive properties due to the deletion of envelope proteins UL49.5, glycoprotein G (gG), gE cytoplasmic tail, and US9 coding sequences. In the current study, we engineered the BoHV-1qmv further by incorporating a chimeric gene sequence to express a proteolytically cleavable polyprotein: RVFV envelope proteins Gn ectodomain sequence fused with bovine granulocyte-macrophage colony-stimulating factor (GMCSF) and Gc, resulting in a live BoHV-1qmv-vectored subunit vaccine against RVFV for livestock. In vitro, the resulting recombinant virus, BoHV-1qmv Sub-RVFV, was replicated in cell culture with high titers. The chimeric Gn-GMCSF and Gc proteins expressed by the vaccine virus formed the Gn–Gc complex. In calves, the BoHV-1qmv Sub-RVFV vaccination was safe and induced moderate levels of the RVFV vaccine strain, MP12-specific neutralizing antibody titers. Additionally, the peripheral blood mononuclear cells from the vaccinated calves had six-fold increased levels of interferon-gamma transcription compared with that of the BoHV-1qmv (vector)-vaccinated calves when stimulated with heat-inactivated MP12 antigen in vitro. Based on these findings, we believe that a single dose of BoHV-1qmv Sub-RVFV vaccine generated a protective RVFV-MP12-specific humoral and cellular immune response. Therefore, the BoHV-1qmv sub-RVFV can potentially be a protective subunit vaccine for cattle against RVFV. MDPI 2023-10-30 /pmc/articles/PMC10674938/ /pubmed/38005861 http://dx.doi.org/10.3390/v15112183 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pavulraj, Selvaraj Stout, Rhett W. Barras, Elise D. Paulsen, Daniel B. Chowdhury, Shafiqul I. A Novel Quadruple Gene-Deleted BoHV-1-Vectored RVFV Subunit Vaccine Induces Humoral and Cell-Mediated Immune Response against Rift Valley Fever in Calves |
title | A Novel Quadruple Gene-Deleted BoHV-1-Vectored RVFV Subunit Vaccine Induces Humoral and Cell-Mediated Immune Response against Rift Valley Fever in Calves |
title_full | A Novel Quadruple Gene-Deleted BoHV-1-Vectored RVFV Subunit Vaccine Induces Humoral and Cell-Mediated Immune Response against Rift Valley Fever in Calves |
title_fullStr | A Novel Quadruple Gene-Deleted BoHV-1-Vectored RVFV Subunit Vaccine Induces Humoral and Cell-Mediated Immune Response against Rift Valley Fever in Calves |
title_full_unstemmed | A Novel Quadruple Gene-Deleted BoHV-1-Vectored RVFV Subunit Vaccine Induces Humoral and Cell-Mediated Immune Response against Rift Valley Fever in Calves |
title_short | A Novel Quadruple Gene-Deleted BoHV-1-Vectored RVFV Subunit Vaccine Induces Humoral and Cell-Mediated Immune Response against Rift Valley Fever in Calves |
title_sort | novel quadruple gene-deleted bohv-1-vectored rvfv subunit vaccine induces humoral and cell-mediated immune response against rift valley fever in calves |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10674938/ https://www.ncbi.nlm.nih.gov/pubmed/38005861 http://dx.doi.org/10.3390/v15112183 |
work_keys_str_mv | AT pavulrajselvaraj anovelquadruplegenedeletedbohv1vectoredrvfvsubunitvaccineinduceshumoralandcellmediatedimmuneresponseagainstriftvalleyfeverincalves AT stoutrhettw anovelquadruplegenedeletedbohv1vectoredrvfvsubunitvaccineinduceshumoralandcellmediatedimmuneresponseagainstriftvalleyfeverincalves AT barraselised anovelquadruplegenedeletedbohv1vectoredrvfvsubunitvaccineinduceshumoralandcellmediatedimmuneresponseagainstriftvalleyfeverincalves AT paulsendanielb anovelquadruplegenedeletedbohv1vectoredrvfvsubunitvaccineinduceshumoralandcellmediatedimmuneresponseagainstriftvalleyfeverincalves AT chowdhuryshafiquli anovelquadruplegenedeletedbohv1vectoredrvfvsubunitvaccineinduceshumoralandcellmediatedimmuneresponseagainstriftvalleyfeverincalves AT pavulrajselvaraj novelquadruplegenedeletedbohv1vectoredrvfvsubunitvaccineinduceshumoralandcellmediatedimmuneresponseagainstriftvalleyfeverincalves AT stoutrhettw novelquadruplegenedeletedbohv1vectoredrvfvsubunitvaccineinduceshumoralandcellmediatedimmuneresponseagainstriftvalleyfeverincalves AT barraselised novelquadruplegenedeletedbohv1vectoredrvfvsubunitvaccineinduceshumoralandcellmediatedimmuneresponseagainstriftvalleyfeverincalves AT paulsendanielb novelquadruplegenedeletedbohv1vectoredrvfvsubunitvaccineinduceshumoralandcellmediatedimmuneresponseagainstriftvalleyfeverincalves AT chowdhuryshafiquli novelquadruplegenedeletedbohv1vectoredrvfvsubunitvaccineinduceshumoralandcellmediatedimmuneresponseagainstriftvalleyfeverincalves |