Journal article
Authors list: Lamp, B; Riedel, C; Roman-Sosa, G; Heimann, M; Jacobi, S; Becher, P; Thiel, HJ; Rümenapf, T
Publication year: 2011
Pages: 3607-3620
Journal: Journal of Virology
Volume number: 85
Issue number: 7
ISSN: 0022-538X
eISSN: 1098-5514
Open access status: Green
DOI Link: https://doi.org/10.1128/JVI.02206-10
Publisher: American Society for Microbiology
Abstract:
Proteolytic processing of polyproteins is considered a crucial step in the life cycle of most positive-strand RNA viruses. An enhancement of NS2-3 processing has been described as a major difference between the noncytopathogenic (non-CP) and the cytopathogenic (CP) biotypes of pestiviruses. The effects of accelerated versus delayed NS2-3 processing on the maturation of the other nonstructural proteins (NSP) have never been compared. In this study, we analyzed the proteolytic processing of NSP in Classical swine fever virus (CSFV). Key to the investigation was a panel of newly developed monoclonal antibodies (MAbs) that facilitated monitoring of all nonstructural proteins involved in virus replication (NS2, NS3, NS4A, NS5A, and NS5B). Applying these MAbs in Western blotting and radioimmunoprecipitation allowed an unambiguous identification of the mature proteins and precursors in non-CP CSFV-infected cells. Furthermore, the kinetics of processing were determined by pulse-chase analyses for non-CP CSFV, CP CSFV, and a CP CSFV replicon. A slow but constant processing of NS4A/B-5A/B occurred in non-CP CSFV-infected cells, leading to balanced low-level concentrations of mature NSP. In contrast, the turnover of the polyprotein precursors was three times faster in CP CSFV-infected cells and in cells transfected with a CP CSFV replicon, causing a substantial increase of mature NSP concentrations. We conclude that a delayed processing not only of NS3 but further of all NSP represents a hallmark of regulation in non-CP pestiviruses.
Citation Styles
Harvard Citation style: Lamp, B., Riedel, C., Roman-Sosa, G., Heimann, M., Jacobi, S., Becher, P., et al. (2011) Biosynthesis of Classical Swine Fever Virus Nonstructural Proteins, Journal of Virology, 85(7), pp. 3607-3620. https://doi.org/10.1128/JVI.02206-10
APA Citation style: Lamp, B., Riedel, C., Roman-Sosa, G., Heimann, M., Jacobi, S., Becher, P., Thiel, H., & Rümenapf, T. (2011). Biosynthesis of Classical Swine Fever Virus Nonstructural Proteins. Journal of Virology. 85(7), 3607-3620. https://doi.org/10.1128/JVI.02206-10