Competitive replication kinetics and pathogenicity in pigs co-infected with historical and newly invading classical swine fever viruses

被引:4
作者
Huang, Yu-Liang [1 ]
Deng, Ming-Chung [1 ]
Tsai, Kuo-Jung [1 ]
Liu, Hsin-Meng [1 ]
Huang, Chin-Cheng [2 ]
Wang, Fun-In [3 ]
Chang, Chia-Yi [1 ]
机构
[1] Council Agr, Anim Hlth Res Inst, 376 Chung Cheng Rd, New Taipei 25158, Taiwan
[2] Council Agr, 37 Nanhai Rd, Taipei 10014, Taiwan
[3] Natl Taiwan Univ, Sch Vet Med, 1,Sect 4,Roosevelt Rd, Taipei 10617, Taiwan
关键词
Classical swine fever virus; Genotype; Virus shift; Viral replication; Pathogenesis; PORCINE; TAIWAN;
D O I
10.1016/j.virusres.2016.11.022
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Classical swine fever (CSF), an economically important and highly contagious disease of pigs, is caused by classical swine fever virus (CSFV). In Taiwan, CSFVs from field outbreaks belong to two distinct genotypes. The historical genotype 3.4 dominated from the 1920s to 1996, and since 1996, the newly invading genotype 2.1 has dominated. To explain the phenomenon of this virus shift in the field, representative viruses belonging to genotypes 2.1 and 3.4 were either inoculated alone (single infection) or co-inoculated (co-infection), both in vivo and in vitro, to compare the virus replication and pathogenesis. In pigs co-infected with the genotype 2.1 TD/96/TWN strain and the genotype 3.4 94.4/IL/94/TWN strain, the newly invading genotype 2.1 was detected earlier in the blood, oral fluid, and feces, and the viral loads were consistently and significantly higher than that of the historical genotype 3.4. In cell cultures, the ratio of secreted virus to cell-associated virus of the genotype 2.1 strain was higher than that of the genotype 3.4 strain. This study is the first to demonstrate a possible explanation of virus shift in the field, wherein the newly invading genotype 2.1 replicates more efficiently than did genotype 3.4 and outcompetes the replication and pathogenicity of genotype 3.4 in pigs in the field. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 45
页数:7
相关论文
共 26 条
[1]  
[Anonymous], THESIS
[2]   Genetic variability and distribution of Classical swine fever virus [J].
Beer, Martin ;
Goller, Katja V. ;
Staubach, Christoph ;
Blome, Sandra .
ANIMAL HEALTH RESEARCH REVIEWS, 2015, 16 (01) :33-39
[3]   Phylogenetic characterization of classical swine fever viruses isolated in Korea between 1988 and 2003 [J].
Cha, Sang-Ho ;
Choi, Eun-Jin ;
Park, Jong-Hyun ;
Yoon, So-Ra ;
Kwon, Jun-Hun ;
Yoon, Kyoung-Jin ;
Song, Jae-Young .
VIRUS RESEARCH, 2007, 126 (1-2) :256-261
[4]  
Chen Z, 2002, THESIS
[5]   Phylogenetic analysis of classical swine fever virus isolated from Taiwan [J].
Deng, MC ;
Huang, CC ;
Huang, TS ;
Chang, CY ;
Lin, YJ ;
Chien, MS ;
Jong, MH .
VETERINARY MICROBIOLOGY, 2005, 106 (3-4) :187-193
[6]   Characterisation of experimental infections of domestic pigs with genotype 2.1 and 3.3 isolates of classical swine fever virus [J].
Everett, H. ;
Salguero, F. J. ;
Graham, S. P. ;
Haines, F. ;
Johns, H. ;
Clifford, D. ;
Nunez, A. ;
La Rocca, S. A. ;
Parchariyanon, S. ;
Steinbach, F. ;
Drew, T. ;
Crooke, H. .
VETERINARY MICROBIOLOGY, 2010, 142 (1-2) :26-33
[7]   Molecular epidemiology of a large classical swine fever epidemic in the European Union in 1997-1998 [J].
Greiser-Wilke, I ;
Fritzemeier, J ;
Koenen, F ;
Vanderhallen, H ;
Rutili, D ;
De Mia, GM ;
Romero, L ;
Rosell, R ;
Sanchez-Vizcaino, JM ;
San Gabriel, A .
VETERINARY MICROBIOLOGY, 2000, 77 (1-2) :17-27
[8]   The challenges of classical swine fever control: Modified live and E2 subunit vaccines [J].
Huang, Yu-Liang ;
Deng, Ming-Chung ;
Wang, Fun-In ;
Huang, Chin-Cheng ;
Chang, Chia-Yi .
VIRUS RESEARCH, 2014, 179 :1-11
[9]   Development of a reverse transcription multiplex real-time PCR for the detection and genotyping of classical swine fever virus [J].
Huang, Yu-Liang ;
Pang, Victor Fei ;
Pan, Chu-Hsiang ;
Chen, Tsu-Han ;
Jong, Ming-Hwa ;
Huang, Tien-Shine ;
Jeng, Chian-Ren .
JOURNAL OF VIROLOGICAL METHODS, 2009, 160 (1-2) :111-118
[10]   Studying classical swine fever virus: Making the best of a bad virus [J].
Ji, Wei ;
Guo, Zhen ;
Ding, Nai-zheng ;
He, Cheng-qiang .
VIRUS RESEARCH, 2015, 197 :35-47