The Genetic Characterization of a Novel Natural Recombinant Pseudorabies Virus in China

We sequenced the complete genome of the pseudorabies virus (PRV) FJ epidemic strain, and we studied the characteristics and the differences compared with the classical Chinese strain and that of other countries. Third-generation sequencing and second-generation sequencing technology were used to con...

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Main Authors: Jianbo Huang, Wenjie Tang, Xvetao Wang, Jun Zhao, Kenan Peng, Xiangang Sun, Shuwei Li, Shengyao Kuang, Ling Zhu, Yuancheng Zhou, Zhiwen Xu
Format: Article
Language:English
Published: MDPI AG 2022-05-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/14/5/978
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author Jianbo Huang
Wenjie Tang
Xvetao Wang
Jun Zhao
Kenan Peng
Xiangang Sun
Shuwei Li
Shengyao Kuang
Ling Zhu
Yuancheng Zhou
Zhiwen Xu
author_facet Jianbo Huang
Wenjie Tang
Xvetao Wang
Jun Zhao
Kenan Peng
Xiangang Sun
Shuwei Li
Shengyao Kuang
Ling Zhu
Yuancheng Zhou
Zhiwen Xu
author_sort Jianbo Huang
collection DOAJ
description We sequenced the complete genome of the pseudorabies virus (PRV) FJ epidemic strain, and we studied the characteristics and the differences compared with the classical Chinese strain and that of other countries. Third-generation sequencing and second-generation sequencing technology were used to construct, sequence, and annotate an efficient, accurate PRV library. The complete FJ genome was 143,703 bp, the G+C content was 73.67%, and it encoded a total of 70 genes. The genetic evolution of the complete genome and some key gene sequences of the FJ strain and PRV reference strains were analyzed by the maximum likelihood (ML) method of MEGA 7.0 software. According to the ML tree based on the full-length genome sequences, PRV FJ strain was assigned to the branch of genotype II, and it showed a close evolutionary relationship with PRV epidemic variants isolated in China after 2011. The gB, gC, gD, gH, gL, gM, gN, TK, gI, and PK genes of the FJ strain were assigned to the same branch with other Chinese epidemic mutants; its gG gene was assigned to the same branch with the classic Chinese Fa and Ea strains; and its gE gene was assigned to a relatively independent branch. Potential recombination events were predicted by the RDP4 software, which showed that the predicted recombination sites were between 1694 and 1936 bp, 101,113 and 102,660 bp, and 107,964 and 111,481 bp in the non-coding region. This result broke the previously reported general rule that pseudorabies virus recombination events occur in the gene coding region. The major backbone strain of the recombination event was HLJ8 and the minor backbone strain was Ea. Our results allowed us to track and to grasp the recent molecular epidemiological changes of PRV. They also provide background materials for the development of new PRV vaccines, and they lay a foundation for further study of PRV.
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spelling doaj.art-5c25c77f6fda4a6d838700597970e98f2023-11-23T13:31:16ZengMDPI AGViruses1999-49152022-05-0114597810.3390/v14050978The Genetic Characterization of a Novel Natural Recombinant Pseudorabies Virus in ChinaJianbo Huang0Wenjie Tang1Xvetao Wang2Jun Zhao3Kenan Peng4Xiangang Sun5Shuwei Li6Shengyao Kuang7Ling Zhu8Yuancheng Zhou9Zhiwen Xu10College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, ChinaLivestock and Poultry Biological Products Key Laboratory of Sichuan Province, Animtech Bioengineering Co., Ltd., Chengdu 610299, ChinaVeterinary Biologicals Engineering and Technology Research Center of Sichuan Province, Animtech Bioengineering Co., Ltd., Chengdu 610066, ChinaCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, ChinaCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, ChinaCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, ChinaLivestock and Poultry Biological Products Key Laboratory of Sichuan Province, Animtech Bioengineering Co., Ltd., Chengdu 610299, ChinaLivestock and Poultry Biological Products Key Laboratory of Sichuan Province, Animtech Bioengineering Co., Ltd., Chengdu 610299, ChinaCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, ChinaLivestock and Poultry Biological Products Key Laboratory of Sichuan Province, Animtech Bioengineering Co., Ltd., Chengdu 610299, ChinaCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, ChinaWe sequenced the complete genome of the pseudorabies virus (PRV) FJ epidemic strain, and we studied the characteristics and the differences compared with the classical Chinese strain and that of other countries. Third-generation sequencing and second-generation sequencing technology were used to construct, sequence, and annotate an efficient, accurate PRV library. The complete FJ genome was 143,703 bp, the G+C content was 73.67%, and it encoded a total of 70 genes. The genetic evolution of the complete genome and some key gene sequences of the FJ strain and PRV reference strains were analyzed by the maximum likelihood (ML) method of MEGA 7.0 software. According to the ML tree based on the full-length genome sequences, PRV FJ strain was assigned to the branch of genotype II, and it showed a close evolutionary relationship with PRV epidemic variants isolated in China after 2011. The gB, gC, gD, gH, gL, gM, gN, TK, gI, and PK genes of the FJ strain were assigned to the same branch with other Chinese epidemic mutants; its gG gene was assigned to the same branch with the classic Chinese Fa and Ea strains; and its gE gene was assigned to a relatively independent branch. Potential recombination events were predicted by the RDP4 software, which showed that the predicted recombination sites were between 1694 and 1936 bp, 101,113 and 102,660 bp, and 107,964 and 111,481 bp in the non-coding region. This result broke the previously reported general rule that pseudorabies virus recombination events occur in the gene coding region. The major backbone strain of the recombination event was HLJ8 and the minor backbone strain was Ea. Our results allowed us to track and to grasp the recent molecular epidemiological changes of PRV. They also provide background materials for the development of new PRV vaccines, and they lay a foundation for further study of PRV.https://www.mdpi.com/1999-4915/14/5/978pseudorabies viruscomplete genome sequencingphylogenetic analysisgene recombination
spellingShingle Jianbo Huang
Wenjie Tang
Xvetao Wang
Jun Zhao
Kenan Peng
Xiangang Sun
Shuwei Li
Shengyao Kuang
Ling Zhu
Yuancheng Zhou
Zhiwen Xu
The Genetic Characterization of a Novel Natural Recombinant Pseudorabies Virus in China
Viruses
pseudorabies virus
complete genome sequencing
phylogenetic analysis
gene recombination
title The Genetic Characterization of a Novel Natural Recombinant Pseudorabies Virus in China
title_full The Genetic Characterization of a Novel Natural Recombinant Pseudorabies Virus in China
title_fullStr The Genetic Characterization of a Novel Natural Recombinant Pseudorabies Virus in China
title_full_unstemmed The Genetic Characterization of a Novel Natural Recombinant Pseudorabies Virus in China
title_short The Genetic Characterization of a Novel Natural Recombinant Pseudorabies Virus in China
title_sort genetic characterization of a novel natural recombinant pseudorabies virus in china
topic pseudorabies virus
complete genome sequencing
phylogenetic analysis
gene recombination
url https://www.mdpi.com/1999-4915/14/5/978
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