Literature DB >> 28701392

Partially Uncleaved Alphavirus Replicase Forms Spherule Structures in the Presence and Absence of RNA Template.

Kirsi Hellström1, Katri Kallio1, Age Utt2, Tania Quirin1, Eija Jokitalo3, Andres Merits2, Tero Ahola4.   

Abstract

Alphaviruses are positive-strand RNA viruses expressing their replicase as a polyprotein, P1234, which is cleaved to four final products, nonstructural proteins nsP1 to nsP4. The replicase proteins together with viral RNA and host factors form membrane invaginations termed spherules, which act as the replication complexes producing progeny RNAs. We have previously shown that the wild-type alphavirus replicase requires a functional RNA template and active polymerase to generate spherule structures. However, we now find that specific partially processed forms of the replicase proteins alone can give rise to membrane invaginations in the absence of RNA or replication. The minimal requirement for spherule formation was the expression of properly cleaved nsP4, together with either uncleaved P123 or with the combination of nsP1 and uncleaved P23. These inactive spherules were morphologically less regular than replication-induced spherules. In the presence of template, nsP1 plus uncleaved P23 plus nsP4 could efficiently assemble active replication spherules producing both negative-sense and positive-sense RNA strands. P23 alone did not have membrane affinity, but could be recruited to membrane sites in the presence of nsP1 and nsP4. These results define the set of viral components required for alphavirus replication complex assembly and suggest the possibility that it could be reconstituted from separately expressed nonstructural proteins.IMPORTANCE All positive-strand RNA viruses extensively modify host cell membranes to serve as efficient platforms for viral RNA replication. Alphaviruses and several other groups induce protective membrane invaginations (spherules) as their genome factories. Most positive-strand viruses produce their replicase as a polyprotein precursor, which is further processed through precise and regulated cleavages. We show here that specific cleavage intermediates of the alphavirus replicase can give rise to spherule structures in the absence of viral RNA. In the presence of template RNA, the same intermediates yield active replication complexes. Thus, partially cleaved replicase proteins play key roles that connect replication complex assembly, membrane deformation, and the different stages of RNA synthesis.
Copyright © 2017 American Society for Microbiology.

Entities:  

Keywords:  Semliki Forest virus; Sindbis virus; membrane; polyprotein processing; replication complex

Mesh:

Substances:

Year:  2017        PMID: 28701392      PMCID: PMC5571266          DOI: 10.1128/JVI.00787-17

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  42 in total

1.  Regulation of the sequential processing of Semliki Forest virus replicase polyprotein.

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Journal:  J Biol Chem       Date:  2003-08-12       Impact factor: 5.157

2.  Functional Sindbis virus replicative complexes are formed at the plasma membrane.

Authors:  Elena I Frolova; Rodion Gorchakov; Larisa Pereboeva; Svetlana Atasheva; Ilya Frolov
Journal:  J Virol       Date:  2010-09-08       Impact factor: 5.103

3.  mRNA Capping by Venezuelan Equine Encephalitis Virus nsP1: Functional Characterization and Implications for Antiviral Research.

Authors:  Changqing Li; Jaime Guillén; Nadia Rabah; Alexandre Blanjoie; Françoise Debart; Jean-Jacques Vasseur; Bruno Canard; Etienne Decroly; Bruno Coutard
Journal:  J Virol       Date:  2015-06-03       Impact factor: 5.103

4.  Assembly of alphavirus replication complexes from RNA and protein components in a novel trans-replication system in mammalian cells.

Authors:  Pirjo Spuul; Giuseppe Balistreri; Kirsi Hellström; Andrey V Golubtsov; Eija Jokitalo; Tero Ahola
Journal:  J Virol       Date:  2011-03-09       Impact factor: 5.103

5.  A positive-strand RNA virus replication complex parallels form and function of retrovirus capsids.

Authors:  Michael Schwartz; Jianbo Chen; Michael Janda; Michael Sullivan; Johan den Boon; Paul Ahlquist
Journal:  Mol Cell       Date:  2002-03       Impact factor: 17.970

6.  Brome mosaic virus 1a nucleoside triphosphatase/helicase domain plays crucial roles in recruiting RNA replication templates.

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7.  Correlative light and electron microscopy enables viral replication studies at the ultrastructural level.

Authors:  Kirsi Hellström; Helena Vihinen; Katri Kallio; Eija Jokitalo; Tero Ahola
Journal:  Methods       Date:  2015-04-24       Impact factor: 3.608

8.  Role of Viral RNA and Co-opted Cellular ESCRT-I and ESCRT-III Factors in Formation of Tombusvirus Spherules Harboring the Tombusvirus Replicase.

Authors:  Nikolay Kovalev; Isabel Fernández de Castro Martín; Judit Pogany; Daniel Barajas; Kunj Pathak; Cristina Risco; Peter D Nagy
Journal:  J Virol       Date:  2016-01-20       Impact factor: 5.103

Review 9.  Viral RNA replication in association with cellular membranes.

Authors:  A Salonen; T Ahola; L Kääriäinen
Journal:  Curr Top Microbiol Immunol       Date:  2005       Impact factor: 4.291

10.  Sequestration of G3BP coupled with efficient translation inhibits stress granules in Semliki Forest virus infection.

Authors:  Marc D Panas; Margus Varjak; Aleksei Lulla; Kai Er Eng; Andres Merits; Gunilla B Karlsson Hedestam; Gerald M McInerney
Journal:  Mol Biol Cell       Date:  2012-10-19       Impact factor: 4.138

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  21 in total

1.  Timeliness of Proteolytic Events Is Prerequisite for Efficient Functioning of the Alphaviral Replicase.

Authors:  Valeria Lulla; Liis Karo-Astover; Kai Rausalu; Sirle Saul; Andres Merits; Aleksei Lulla
Journal:  J Virol       Date:  2018-06-29       Impact factor: 5.103

2.  Crystal structures of alphavirus nonstructural protein 4 (nsP4) reveal an intrinsically dynamic RNA-dependent RNA polymerase fold.

Authors:  Yaw Bia Tan; Laura Sandra Lello; Xin Liu; Yee-Song Law; Congbao Kang; Julien Lescar; Jie Zheng; Andres Merits; Dahai Luo
Journal:  Nucleic Acids Res       Date:  2022-01-25       Impact factor: 16.971

Review 3.  mRNA-based therapeutics: powerful and versatile tools to combat diseases.

Authors:  Shugang Qin; Xiaoshan Tang; Yuting Chen; Kepan Chen; Na Fan; Wen Xiao; Qian Zheng; Guohong Li; Yuqing Teng; Min Wu; Xiangrong Song
Journal:  Signal Transduct Target Ther       Date:  2022-05-21

4.  Expression of Alphavirus Nonstructural Protein 2 (nsP2) in Mosquito Cells Inhibits Viral RNA Replication in Both a Protease Activity-Dependent and -Independent Manner.

Authors:  Liubov Cherkashchenko; Kai Rausalu; Sanjay Basu; Luke Alphey; Andres Merits
Journal:  Viruses       Date:  2022-06-17       Impact factor: 5.818

5.  Membrane binding and rearrangement by chikungunya virus capping enzyme nsP1.

Authors:  Keerthi Gottipati; Michael Woodson; Kyung H Choi
Journal:  Virology       Date:  2020-02-24       Impact factor: 3.616

6.  A Chikungunya Virus trans-Replicase System Reveals the Importance of Delayed Nonstructural Polyprotein Processing for Efficient Replication Complex Formation in Mosquito Cells.

Authors:  Koen Bartholomeeusen; Age Utt; Sandra Coppens; Kai Rausalu; Katleen Vereecken; Kevin K Ariën; Andres Merits
Journal:  J Virol       Date:  2018-06-29       Impact factor: 5.103

7.  Design and Use of Chikungunya Virus Replication Templates Utilizing Mammalian and Mosquito RNA Polymerase I-Mediated Transcription.

Authors:  Age Utt; Kai Rausalu; Madis Jakobson; Andres Männik; Luke Alphey; Rennos Fragkoudis; Andres Merits
Journal:  J Virol       Date:  2019-08-28       Impact factor: 5.103

8.  Corticosteroids and cellulose purification improve, respectively, the in vivo translation and vaccination efficacy of sa-mRNAs.

Authors:  Zifu Zhong; Séan McCafferty; Lisa Opsomer; Haixiu Wang; Hanne Huysmans; Joyca De Temmerman; Stefan Lienenklaus; João Paulo Portela Catani; Francis Combes; Niek N Sanders
Journal:  Mol Ther       Date:  2021-01-21       Impact factor: 11.454

9.  Semliki Forest Virus Chimeras with Functional Replicase Modules from Related Alphaviruses Survive by Adaptive Mutations in Functionally Important Hot Spots.

Authors:  Mona Teppor; Eva Žusinaite; Liis Karo-Astover; Ailar Omler; Kai Rausalu; Valeria Lulla; Aleksei Lulla; Andres Merits
Journal:  J Virol       Date:  2021-07-28       Impact factor: 5.103

10.  Sensitivity of Alphaviruses to G3BP Deletion Correlates with Efficiency of Replicase Polyprotein Processing.

Authors:  Benjamin Götte; Age Utt; Andres Merits; Gerald M McInerney; Rennos Fragkoudis
Journal:  J Virol       Date:  2020-03-17       Impact factor: 5.103

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