Characterization of BoHV-1 gG-/tk-/gE- Mutant in Differential Protein Expression, Virulence, and Immunity

Infectious bovine rhinotracheitis (IBR), caused by bovine alphaherpesvirus 1 (BoHV-1), is an important disease affecting cattle worldwide resulting in great economic losses. Marker vaccines are effective in controlling infectious diseases including IBR, because they allow the discrimination between...

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Main Authors: Marawan A. Marawan, Mingliang Deng, Chen Wang, Yingyu Chen, Changmin Hu, Jianguo Chen, Xi Chen, Huanchun Chen, Aizhen Guo
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Veterinary Sciences
Subjects:
Online Access:https://www.mdpi.com/2306-7381/8/11/253
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author Marawan A. Marawan
Mingliang Deng
Chen Wang
Yingyu Chen
Changmin Hu
Jianguo Chen
Xi Chen
Huanchun Chen
Aizhen Guo
author_facet Marawan A. Marawan
Mingliang Deng
Chen Wang
Yingyu Chen
Changmin Hu
Jianguo Chen
Xi Chen
Huanchun Chen
Aizhen Guo
author_sort Marawan A. Marawan
collection DOAJ
description Infectious bovine rhinotracheitis (IBR), caused by bovine alphaherpesvirus 1 (BoHV-1), is an important disease affecting cattle worldwide resulting in great economic losses. Marker vaccines are effective in controlling infectious diseases including IBR, because they allow the discrimination between the natural infection and the vaccination. Therefore, a triple gene deleted strain BoHV-1 gG-/tk-/gE- was developed and evaluated in vivo and in vitro as a marker vaccine. In cell culture, this triple mutant virus showed significantly slower growth kinetics and smaller plaques when compared to wild-type (wt) BoHV-1 and double mutant BoHV-1 gG-/tk- (<i>p</i> < 0.01). On proteomic level, it revealed downregulation of some virulence related proteins including thymidine kinase, glycoproteins G, E, I, and K when compared to the wt. In vitro, the triple mutant virus showed a significantly lower and shorter viral shedding period (<i>p</i> < 0.001) in calves compared to double mutant. Moreover, the immunized calves with triple mutant virus showed protection rates of 64.2% and 68.6% against wt BoHV-1 and wt BoHV-5 challenge, respectively, without reactivation of latency after dexamethasone injection. In conclusion, BoHV-1 gG-/tk-/gE- is a safer marker vaccine against IBR although its immunogenicity in calves was decreased when compared to double mutant virus.
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spelling doaj.art-702d3ae7020849d78c92a325c4fe0e4a2023-11-23T01:54:13ZengMDPI AGVeterinary Sciences2306-73812021-10-0181125310.3390/vetsci8110253Characterization of BoHV-1 gG-/tk-/gE- Mutant in Differential Protein Expression, Virulence, and ImmunityMarawan A. Marawan0Mingliang Deng1Chen Wang2Yingyu Chen3Changmin Hu4Jianguo Chen5Xi Chen6Huanchun Chen7Aizhen Guo8State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, ChinaState Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, ChinaState Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, ChinaCollege of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, ChinaCollege of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, ChinaCollege of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, ChinaCollege of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, ChinaState Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, ChinaState Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, ChinaInfectious bovine rhinotracheitis (IBR), caused by bovine alphaherpesvirus 1 (BoHV-1), is an important disease affecting cattle worldwide resulting in great economic losses. Marker vaccines are effective in controlling infectious diseases including IBR, because they allow the discrimination between the natural infection and the vaccination. Therefore, a triple gene deleted strain BoHV-1 gG-/tk-/gE- was developed and evaluated in vivo and in vitro as a marker vaccine. In cell culture, this triple mutant virus showed significantly slower growth kinetics and smaller plaques when compared to wild-type (wt) BoHV-1 and double mutant BoHV-1 gG-/tk- (<i>p</i> < 0.01). On proteomic level, it revealed downregulation of some virulence related proteins including thymidine kinase, glycoproteins G, E, I, and K when compared to the wt. In vitro, the triple mutant virus showed a significantly lower and shorter viral shedding period (<i>p</i> < 0.001) in calves compared to double mutant. Moreover, the immunized calves with triple mutant virus showed protection rates of 64.2% and 68.6% against wt BoHV-1 and wt BoHV-5 challenge, respectively, without reactivation of latency after dexamethasone injection. In conclusion, BoHV-1 gG-/tk-/gE- is a safer marker vaccine against IBR although its immunogenicity in calves was decreased when compared to double mutant virus.https://www.mdpi.com/2306-7381/8/11/253bovine herpesvirus 1,5proteomicsglycoproteinmarker vaccinesvirulenceimmunity
spellingShingle Marawan A. Marawan
Mingliang Deng
Chen Wang
Yingyu Chen
Changmin Hu
Jianguo Chen
Xi Chen
Huanchun Chen
Aizhen Guo
Characterization of BoHV-1 gG-/tk-/gE- Mutant in Differential Protein Expression, Virulence, and Immunity
Veterinary Sciences
bovine herpesvirus 1,5
proteomics
glycoprotein
marker vaccines
virulence
immunity
title Characterization of BoHV-1 gG-/tk-/gE- Mutant in Differential Protein Expression, Virulence, and Immunity
title_full Characterization of BoHV-1 gG-/tk-/gE- Mutant in Differential Protein Expression, Virulence, and Immunity
title_fullStr Characterization of BoHV-1 gG-/tk-/gE- Mutant in Differential Protein Expression, Virulence, and Immunity
title_full_unstemmed Characterization of BoHV-1 gG-/tk-/gE- Mutant in Differential Protein Expression, Virulence, and Immunity
title_short Characterization of BoHV-1 gG-/tk-/gE- Mutant in Differential Protein Expression, Virulence, and Immunity
title_sort characterization of bohv 1 gg tk ge mutant in differential protein expression virulence and immunity
topic bovine herpesvirus 1,5
proteomics
glycoprotein
marker vaccines
virulence
immunity
url https://www.mdpi.com/2306-7381/8/11/253
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