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The Inactivated gE/TK Gene-Deleted Vaccine Against Pseudorabies Virus Type II Confers Effective Protection in Mice and Pigs

The highly virulent and antigenic variant of Pseudorabies virus (PRV) that emerged from classical Bartha-K61-vaccinated pig herds has caused substantial economic losses to the swine industry in China since 2011. A safe and more effective vaccine is most desirable. In this study, a gE/TK gene-deficie...

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Autores principales: Jin, Yu-Lan, Yin, Di, Xing, Gang, Huang, Yan-Ming, Fan, Chun-Mei, Fan, Cheng-Fei, Qiu, Xiao-Huo, Dong, Wei-Ren, Yan, Yan, Gu, Jin-Yan, Zhou, Ji-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389536/
https://www.ncbi.nlm.nih.gov/pubmed/35992698
http://dx.doi.org/10.3389/fmicb.2022.943707
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author Jin, Yu-Lan
Yin, Di
Xing, Gang
Huang, Yan-Ming
Fan, Chun-Mei
Fan, Cheng-Fei
Qiu, Xiao-Huo
Dong, Wei-Ren
Yan, Yan
Gu, Jin-Yan
Zhou, Ji-Yong
author_facet Jin, Yu-Lan
Yin, Di
Xing, Gang
Huang, Yan-Ming
Fan, Chun-Mei
Fan, Cheng-Fei
Qiu, Xiao-Huo
Dong, Wei-Ren
Yan, Yan
Gu, Jin-Yan
Zhou, Ji-Yong
author_sort Jin, Yu-Lan
collection PubMed
description The highly virulent and antigenic variant of Pseudorabies virus (PRV) that emerged from classical Bartha-K61-vaccinated pig herds has caused substantial economic losses to the swine industry in China since 2011. A safe and more effective vaccine is most desirable. In this study, a gE/TK gene-deficient PRV, namely, HD/c, was constructed based on a PRV type II DX strain isolated from a commercial vaccine-immunized farm and the HD/c-based inactivated vaccine was formulated and evaluated for its safety, immunogenicity, and protective efficacy in mice and piglets. The resulting PRV HD/c strain has a similar growth curve to the parental DX strain. After vaccination, the inactivated HD/c vaccine did not cause any visible gross pathological or histopathological changes in the tissues of mice and piglets and provided rapid and potent protection against the challenge of the classical and variant PRVs at day 21 post-vaccination in mice. A single immunization of 10(8.5)TCID(50) inactivated PRV HD/c strain-elicited robust immunity with high titer of neutralizing antibody and provided complete protection from the lethal challenge of PRV DX strain in piglets. These results indicated that the inactivated PRV HD/c vaccine with the deletion of gE/TK genes was a safe and effective PRV vaccine candidate for the control of PRV.
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spelling pubmed-93895362022-08-20 The Inactivated gE/TK Gene-Deleted Vaccine Against Pseudorabies Virus Type II Confers Effective Protection in Mice and Pigs Jin, Yu-Lan Yin, Di Xing, Gang Huang, Yan-Ming Fan, Chun-Mei Fan, Cheng-Fei Qiu, Xiao-Huo Dong, Wei-Ren Yan, Yan Gu, Jin-Yan Zhou, Ji-Yong Front Microbiol Microbiology The highly virulent and antigenic variant of Pseudorabies virus (PRV) that emerged from classical Bartha-K61-vaccinated pig herds has caused substantial economic losses to the swine industry in China since 2011. A safe and more effective vaccine is most desirable. In this study, a gE/TK gene-deficient PRV, namely, HD/c, was constructed based on a PRV type II DX strain isolated from a commercial vaccine-immunized farm and the HD/c-based inactivated vaccine was formulated and evaluated for its safety, immunogenicity, and protective efficacy in mice and piglets. The resulting PRV HD/c strain has a similar growth curve to the parental DX strain. After vaccination, the inactivated HD/c vaccine did not cause any visible gross pathological or histopathological changes in the tissues of mice and piglets and provided rapid and potent protection against the challenge of the classical and variant PRVs at day 21 post-vaccination in mice. A single immunization of 10(8.5)TCID(50) inactivated PRV HD/c strain-elicited robust immunity with high titer of neutralizing antibody and provided complete protection from the lethal challenge of PRV DX strain in piglets. These results indicated that the inactivated PRV HD/c vaccine with the deletion of gE/TK genes was a safe and effective PRV vaccine candidate for the control of PRV. Frontiers Media S.A. 2022-08-04 /pmc/articles/PMC9389536/ /pubmed/35992698 http://dx.doi.org/10.3389/fmicb.2022.943707 Text en Copyright © 2022 Jin, Yin, Xing, Huang, Fan, Fan, Qiu, Dong, Yan, Gu and Zhou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Jin, Yu-Lan
Yin, Di
Xing, Gang
Huang, Yan-Ming
Fan, Chun-Mei
Fan, Cheng-Fei
Qiu, Xiao-Huo
Dong, Wei-Ren
Yan, Yan
Gu, Jin-Yan
Zhou, Ji-Yong
The Inactivated gE/TK Gene-Deleted Vaccine Against Pseudorabies Virus Type II Confers Effective Protection in Mice and Pigs
title The Inactivated gE/TK Gene-Deleted Vaccine Against Pseudorabies Virus Type II Confers Effective Protection in Mice and Pigs
title_full The Inactivated gE/TK Gene-Deleted Vaccine Against Pseudorabies Virus Type II Confers Effective Protection in Mice and Pigs
title_fullStr The Inactivated gE/TK Gene-Deleted Vaccine Against Pseudorabies Virus Type II Confers Effective Protection in Mice and Pigs
title_full_unstemmed The Inactivated gE/TK Gene-Deleted Vaccine Against Pseudorabies Virus Type II Confers Effective Protection in Mice and Pigs
title_short The Inactivated gE/TK Gene-Deleted Vaccine Against Pseudorabies Virus Type II Confers Effective Protection in Mice and Pigs
title_sort inactivated ge/tk gene-deleted vaccine against pseudorabies virus type ii confers effective protection in mice and pigs
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389536/
https://www.ncbi.nlm.nih.gov/pubmed/35992698
http://dx.doi.org/10.3389/fmicb.2022.943707
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