Construction and characterization of a full-length cDNA infectious clone of emerging porcine Senecavirus A

被引:47
作者
Chen, Zhenhai [1 ]
Yuan, Fangfeng [1 ,2 ]
Li, Yanhua [1 ]
Shang, Pengcheng [1 ]
Schroeder, Robin [3 ]
Lechtenberg, Kelly [3 ]
Henningson, Jamie [1 ,2 ]
Hause, Benjamin [1 ,2 ]
Bai, Jianfa [1 ,2 ]
Rowland, Raymond R. R. [1 ]
Clavijo, Alfonso [1 ,2 ]
Fang, Ying [1 ,2 ]
机构
[1] Kansas State Univ, Dept Diagnost Med & Pathobiol, Coll Vet Med, Manhattan, KS 66506 USA
[2] Kansas State Univ, Coll Vet Med, Kansas State Vet Diagnost Lab, Manhattan, KS 66506 USA
[3] Midwest Vet Serv Inc, Oakland, NE 68045 USA
关键词
Senecavirus A; Picornavirus infection; Infectious clone; Reverse genetics; EGFP reporter virus; Swine; Vesicular lesion; Vesicular disease; SVA pathogenesis; RESPIRATORY SYNDROME VIRUS; IDIOPATHIC VESICULAR DISEASE; ONCOLYTIC PICORNAVIRUS; VALLEY-VIRUS; NONSTRUCTURAL PROTEINS; MOLECULAR DETERMINANTS; COXSACKIEVIRUS B1; COMPLETE GENOME; VIRULENCE; REGION;
D O I
10.1016/j.virol.2016.07.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A full-length cDNA infectious clone, pKS15-01-Clone, was constructed from an emerging Senecavirus A (SVA; strain KS15-01). To explore the potential use as a viral backbone for expressing marker genes, the enhanced green fluorescent protein (EGFP)-tagged reporter virus (vKS15-01-EGFP) was generated using reverse genetics. Compared to the parental virus, the pKS15-01-Clone derived virus (vKS15-01-Clone) replicated efficiently in vitro and in vivo, and induced similar levels of neutralizing antibody and cytokine responses in infected animals. In contrast, the vKS15-01-EGFP virus showed impaired growth ability and induced lower level of immune response in infected animals. Lesions on the dorsal snout and coronary bands were observed in all pigs infected by parental virus KS15-01, but not in pigs infected with vKS15-01-Clone or vKS15-01-EGFP viruses. These results demonstrated that the infectious clone and EGFP reporter virus could be used as important tools in further elucidating the SVA pathogenesis and development of control measures. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:111 / 124
页数:14
相关论文
共 33 条
[1]   Ratification vote on taxonomic proposals to the International Committee on Taxonomy of Viruses (2015) [J].
Adams, M. J. ;
Lefkowitz, E. J. ;
King, A. M. Q. ;
Bamford, D. H. ;
Breitbart, M. ;
Davison, A. J. ;
Ghabrial, S. A. ;
Gorbalenya, A. E. ;
Knowles, N. J. ;
Krell, P. ;
Lavigne, R. ;
Prangishvili, D. ;
Sanfacon, H. ;
Siddell, S. G. ;
Simmonds, P. ;
Carstens, E. B. .
ARCHIVES OF VIROLOGY, 2015, 160 (07) :1837-1850
[2]  
[Anonymous], 2015, GENOME ANNOUNC
[3]   The substitution U475→C with Sabin3-like mutation within the IRES attenuate Coxsackievirus B3 cardiovirulence [J].
Ben M'hadheb-Gharbi, Manel ;
Paulous, Sylvie ;
Aouni, Mahjoub ;
Kean, Katherine M. ;
Gharbi, Jawhar .
MOLECULAR BIOTECHNOLOGY, 2007, 36 (01) :52-60
[4]   Antibody Response to Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) Nonstructural Proteins and Implications for Diagnostic Detection and Differentiation of PRRSV Types I and II [J].
Brown, Elizabeth ;
Lawson, Steven ;
Welbon, Craig ;
Gnanandarajah, Josephine ;
Li, Juan ;
Murtaugh, Michael P. ;
Nelson, Eric A. ;
Molina, Ramon M. ;
Zimmerman, Jeffery J. ;
Rowland, Raymond R. R. ;
Fang, Ying .
CLINICAL AND VACCINE IMMUNOLOGY, 2009, 16 (05) :628-635
[5]   Analysis of the aphthovirus 2A/2B polyprotein 'cleavage' mechanism indicates not a proteolytic reaction, but a novel translational effect: a putative ribosomal 'skip' [J].
Donnelly, MLL ;
Luke, G ;
Mehrotra, A ;
Li, XJ ;
Hughes, LE ;
Gani, D ;
Ryan, MD .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :1013-1025
[6]   Genomic determinants of cardiovirulence in coxsackievirus B3 clinical isolates:: Localization to the 5′ nontranslated region [J].
Dunn, JJ ;
Chapman, NM ;
Tracy, S ;
Romero, JR .
JOURNAL OF VIROLOGY, 2000, 74 (10) :4787-4794
[7]   Development of genetic markers in the non-structural protein 2 region of a US type 1 porcine reproductive and respiratory syndrome virus: implications for future recombinant marker vaccine development [J].
Fang, Ying ;
Christopher-Hennings, Jane ;
Brown, Elizabeth ;
Liu, Haixia ;
Chen, Zhenhai ;
Lawson, Steven R. ;
Breen, Rachael ;
Clement, Travis ;
Gao, Xiaofei ;
Bao, Jingjing ;
Knudsen, David ;
Daly, Russell ;
Nelson, Eric .
JOURNAL OF GENERAL VIROLOGY, 2008, 89 :3086-3096
[8]   A full-length cDNA infectious clone of North American type 1 porcine reproductive and respiratory syndrome virus: Expression of green fluorescent protein in the Nsp2 region [J].
Fang, Ying ;
Rowland, Raymond R. R. ;
Roof, Michael ;
Lunney, Joan K. ;
Christopher-Hennings, Jane ;
Nelson, Eric A. .
JOURNAL OF VIROLOGY, 2006, 80 (23) :11447-11455
[9]   Multi-spectral fluorescent reporter influenza viruses (Color-flu) as powerful tools for in vivo studies [J].
Fukuyama, Satoshi ;
Katsura, Hiroaki ;
Zhao, Dongming ;
Ozawa, Makoto ;
Ando, Tomomi ;
Shoemaker, Jason E. ;
Ishikawa, Izumi ;
Yamada, Shinya ;
Neumann, Gabriele ;
Watanabe, Shinji ;
Kitano, Hiroaki ;
Kawaoka, Yoshihiro .
NATURE COMMUNICATIONS, 2015, 6
[10]   Enhanced IRES activity by the 3′UTR element determines the virulence of FMDV isolates [J].
Garcia-Nunez, Soledad ;
Ines Gismondi, Maria ;
Koenig, Guido ;
Berinstein, Analia ;
Taboga, Oscar ;
Rieder, Elizabeth ;
Martinez-Salas, Encarnacion ;
Carrillo, Elisa .
VIROLOGY, 2014, 448 :303-313