Skip Navigation
Skip to contents

Journal of Microbiology : Journal of Microbiology

OPEN ACCESS
SEARCH
Search

Author index

Page Path
HOME > Browse Articles > Author index
Search
Han-Saem Jang 1 Article
Packaging of Porcine Reproductive and Respiratory Syndrome Virus Replicon RNA by a Stable Cell Line Expressing Its Nucleocapsid Protein
Byung-Hak Song , Jeong-Min Kim , Jin-Kyoung Kim , Han-Saem Jang , Gil-Nam Yun , Eun-Jin Choi , Jae-Young Song , Sang-Im Yun , Young-Min Lee
J. Microbiol. 2011;49(3):516-523.   Published online June 30, 2011
DOI: https://doi.org/10.1007/s12275-011-1280-1
  • 787 View
  • 2 Download
  • 5 Crossref
AbstractAbstract PDF
Porcine reproductive and respiratory syndrome virus (PRRSV), a member of the Arteriviridae family, is one of the most common and economically important swine pathogens. Although both live-attenuated and killed-inactivated vaccines against the virus have been available for a decade, PRRSV is still a major problem in the swine industry worldwide. To explore the possibility of producing single-round infectious PRRSV replicon particles as a potential vaccine strategy, we have now generated two necessary components: 1) a stable cell line (BHK/Sinrep19/PRRSV-N) that constitutively expresses the viral nucleocapsid (N) protein localized to the cytoplasm and the nucleolus and 2) a PRRSV replicon vector (pBAC/PRRSV/Replicon-ΔN) with a 177-nucleotide deletion, removing the 3′-half portion of ORF7 in the viral genome, from which the self-replicating propagation-defective replicon RNAs were synthesized in vitro by SP6 polymerase run-off transcription. Transfection of this replicon RNA into N protein-expressing BHK-21 cells led to the secretion of infectious particles that packaged the replicon RNA, albeit with a low production efficiency of 0.4×102 to 1.1×102 infectious units/ml; the produced particles had only single-round infectivity with no cell-to-cell spread. This trans-complementation system for PRRSV provides a useful platform for studies to define the packaging signals and motifs present within the viral genome and N protein, respectively, and to develop viral replicon-based antiviral vaccines that will stop the infection and spread of this pathogen.

Citations

Citations to this article as recorded by  
  • Research progress on the N protein of porcine reproductive and respiratory syndrome virus
    Yajie Zheng, Gan Li, Qin Luo, Huiyang Sha, Hang Zhang, Ruining Wang, Weili Kong, Jiedan Liao, Mengmeng Zhao
    Frontiers in Microbiology.2024;[Epub]     CrossRef
  • Glycosylated protein 4-deficient PRRSV in complementing cell line shows low virus titer
    Hao Guo, Wudong Gaowa, Hongzhe Zhao, Chunyu Liu, Lina Hou, Yongjun Wen, Fengxue Wang
    Research in Veterinary Science.2023; 158: 84.     CrossRef
  • Porcine Reproductive and Respiratory Syndrome Virus Reverse Genetics and the Major Applications
    Jayeshbhai Chaudhari, Hiep L. X. Vu
    Viruses.2020; 12(11): 1245.     CrossRef
  • Veterinary Replicon Vaccines
    Mia C. Hikke, Gorben P. Pijlman
    Annual Review of Animal Biosciences.2017; 5(1): 89.     CrossRef
  • Resolution of the cellular proteome of the nucleocapsid protein from a highly pathogenic isolate of porcine reproductive and respiratory syndrome virus identifies PARP-1 as a cellular target whose interaction is critical for virus biology
    Long Liu, Zoe Lear, David J. Hughes, Weining Wu, En-min Zhou, Adrian Whitehouse, Hongying Chen, Julian A. Hiscox
    Veterinary Microbiology.2015; 176(1-2): 109.     CrossRef

Journal of Microbiology : Journal of Microbiology
TOP