4.6 Article

Minimum Requirements for Bluetongue Virus Primary Replication In Vivo

Journal

JOURNAL OF VIROLOGY
Volume 87, Issue 2, Pages 882-889

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.02363-12

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Funding

  1. Biotechnology and Biological Sciences Research Council (United Kingdom)
  2. National Institute of Allergy and Infectious Diseases (United States)
  3. Grants-in-Aid for Scientific Research [24780285] Funding Source: KAKEN
  4. Biotechnology and Biological Sciences Research Council [BB/F021771/1] Funding Source: researchfish
  5. BBSRC [BB/F021771/1] Funding Source: UKRI

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The replication mechanism of bluetongue virus (BTV) has been studied by an in vivo reverse genetics (RG) system identifying the importance of certain BTV proteins for primary replication of the virus. However, a unique in vitro cell-free virus assembly system was subsequently developed, showing that it did not require the same set of viral components, which is indicative of differences in these two systems. Here, we studied the in vivo primary replicase complex more in-depth to determine the minimum components of the complex. We showed that while NS2 is an essential component of the primary replication stage during BTV infection, NS1 is not an essential component but may play a role in enhancing BTV protein synthesis. Furthermore, we demonstrated that VP7, a major structural protein of the inner core, is not required for primary replication but appears to stabilize the replicase complex. In contrast, VP3, the other major structural core protein, is an essential component of the complex, together with the three minor enzymatic proteins (VP1, VP4, and VP6) of the core. In addition, our data have demonstrated that the smallest minor protein, VP6, which is known to possess an RNA-dependent helicase activity, may also act as an RNA translocator during assembly of the primary replicase complex.

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