Literature DB >> 15914838

Reduced expression of the rotavirus NSP5 gene has a pleiotropic effect on virus replication.

Tomás López1, Margarito Rojas1, Camilo Ayala-Bretón1, Susana López1, Carlos F Arias1.   

Abstract

Rotavirus RRV gene 11 encodes two non-structural proteins, NSP5 and NSP6. NSP5 is a phosphorylated non-structural protein that binds single- and double-stranded RNA in a non-specific manner. Transient expression of this protein in uninfected cells has provided evidence for its participation in the formation of electron-dense cytoplasmic structures, known as viroplasms, which are thought to be key structures for the replication of the virus. NSP6 is a protein of unknown function that seems not to be essential for virus replication in cell culture. To study the function of NSP5 in the context of a viral infection, the expression of RRV gene 11 was silenced by RNA interference. Reduction in the synthesis of NSP5, as shown by immunoblot and immunofluorescence assays, correlated with a reduction in the number and size of viroplasms and with an altered intracellular distribution of other viroplasm-associated proteins. Silencing of gene 11 also resulted in a reduced synthesis of viral RNA(+) and double-stranded RNA and of all viral proteins, as well as in a decreased production of infectious virus. A similar phenotype was observed when the NSP5 coding gene of the lapine rotavirus strain Alabama was silenced. The fact that the NSP5 gene of rotavirus Alabama lacks the AUG initiator codon for a complete NSP6 protein, suggests that the described phenotype in gene 11-silenced cells is mostly due to the absence of NSP5. The data presented in this work suggest that NSP5 is a key protein during the replication cycle of rotaviruses.

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Year:  2005        PMID: 15914838     DOI: 10.1099/vir.0.80827-0

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  42 in total

1.  Crystallographic analysis reveals octamerization of viroplasm matrix protein P9-1 of Rice black streaked dwarf virus.

Authors:  Fusamichi Akita; Akifumi Higashiura; Takumi Shimizu; Yingying Pu; Mamoru Suzuki; Tamaki Uehara-Ichiki; Takahide Sasaya; Shuji Kanamaru; Fumio Arisaka; Tomitake Tsukihara; Atsushi Nakagawa; Toshihiro Omura
Journal:  J Virol       Date:  2011-11-09       Impact factor: 5.103

2.  Gene-specific inhibition of reovirus replication by RNA interference.

Authors:  Takeshi Kobayashi; James D Chappell; Pranav Danthi; Terence S Dermody
Journal:  J Virol       Date:  2006-09       Impact factor: 5.103

3.  Rotavirus Nonstructural Protein NSP3 is not required for viral protein synthesis.

Authors:  Hilda Montero; Carlos F Arias; Susana Lopez
Journal:  J Virol       Date:  2006-09       Impact factor: 5.103

4.  Rotavirus glycoprotein NSP4 is a modulator of viral transcription in the infected cell.

Authors:  Lynn S Silvestri; M Alejandra Tortorici; Rodrigo Vasquez-Del Carpio; John T Patton
Journal:  J Virol       Date:  2005-12       Impact factor: 5.103

5.  Dissecting rotavirus particle-raft interaction with small interfering RNAs: insights into rotavirus transit through the secretory pathway.

Authors:  Mariela A Cuadras; Bruno B Bordier; Jose L Zambrano; Juan E Ludert; Harry B Greenberg
Journal:  J Virol       Date:  2006-04       Impact factor: 5.103

6.  Interaction of rotavirus polymerase VP1 with nonstructural protein NSP5 is stronger than that with NSP2.

Authors:  F Arnoldi; M Campagna; C Eichwald; U Desselberger; O R Burrone
Journal:  J Virol       Date:  2006-12-20       Impact factor: 5.103

7.  Hyperphosphorylation of the rotavirus NSP5 protein is independent of serine 67, [corrected] NSP2, or [corrected] the intrinsic insolubility of NSP5 is regulated by cellular phosphatases.

Authors:  Adrish Sen; Darin Agresti; Erich R Mackow
Journal:  J Virol       Date:  2006-02       Impact factor: 5.103

8.  The formation of viroplasm-like structures by the rotavirus NSP5 protein is calcium regulated and directed by a C-terminal helical domain.

Authors:  Adrish Sen; Nandini Sen; Erich R Mackow
Journal:  J Virol       Date:  2007-08-15       Impact factor: 5.103

9.  A novel form of rotavirus NSP2 and phosphorylation-dependent NSP2-NSP5 interactions are associated with viroplasm assembly.

Authors:  Jeanette M Criglar; Liya Hu; Sue E Crawford; Joseph M Hyser; James R Broughman; B V Venkataram Prasad; Mary K Estes
Journal:  J Virol       Date:  2013-11-06       Impact factor: 5.103

10.  A Genetically Engineered Rotavirus NSP2 Phosphorylation Mutant Impaired in Viroplasm Formation and Replication Shows an Early Interaction between vNSP2 and Cellular Lipid Droplets.

Authors:  Jeanette M Criglar; Sue E Crawford; Boyang Zhao; Hunter G Smith; Fabio Stossi; Mary K Estes
Journal:  J Virol       Date:  2020-07-16       Impact factor: 5.103

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