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Two PDZ binding motifs within NS5 have roles in Tick-borne encephalitis virus replication
Södertörns högskola, Institutionen för livsvetenskaper, Molekylärbiologi. Södertörns högskola, Institutionen för livsvetenskaper, Kemi.
Södertörns högskola, Institutionen för livsvetenskaper.
Södertörns högskola, Institutionen för livsvetenskaper, Molekylärbiologi. Södertörns högskola, Institutionen för livsvetenskaper, Kemi.
Södertörns högskola, Institutionen för livsvetenskaper, Molekylärbiologi.
Vise andre og tillknytning
2012 (engelsk)Inngår i: Virus Research, ISSN 0168-1702, E-ISSN 1872-7492, Vol. 169, nr 1, s. 54-62Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The flavivirus genus includes important human pathogens like Tick-borne encephalitis virus (TBEV), Dengue virus (DV) and West-Nile virus (WNV), that can cause severe disease e.g. encephalitis or hemorrhagic fever. The NS5 protein is a multifunctional RNA dependent RNA polymerase indispensable for the flavivirus replication. We have previously shown that TBEVNS5 contains a unique internal PDZ binding motif (YS223) for specific targeting of the PDZ protein Scribble. This interaction has impact on both viral down regulation of host cellular defense systems and neurite outgrowth. Putative C-terminal PDZ binding motifs present in TBEVNS5 (-SII903) and WNVNS5 (-TVL905) have also previously been highlighted.

To determine whether the PDZ binding motifs of TBEVNS5 has an effect on virus replication we constructed a DNA based sub-genomic TBEV replicon expressing firefly luciferase. The motifs within NS5 were mutated individually and in concert and the replicons were assayed in cell culture. Our results show that the replication rate was impaired in all mutants, which indicates that PDZ dependent host interactions influence flavivirus replication.We also find that the C-terminal PDZ binding motif present in TBEVNS5 and WNVNS5 are targeting various human PDZ domain proteins. TBEVNS5 has high affinity to Zonulaoccludens-2 (ZO-2),GIAP C-terminus interacting protein (GIPC), Calcium/calmodulin-dependent serine protein kinase (CASK) and Interleukin 16 (IL-16).A different pattern was observed for WNVNS5 as it associated with IL-16, and several other putative interaction partners.

sted, utgiver, år, opplag, sider
2012. Vol. 169, nr 1, s. 54-62
HSV kategori
Forskningsprogram
molekylärgenetik
Identifikatorer
URN: urn:nbn:se:sh:diva-14831DOI: 10.1016/j.virusres.2012.07.001ISI: 000311133800008PubMedID: 22796133Scopus ID: 2-s2.0-84867223730OAI: oai:DiVA.org:sh-14831DiVA, id: diva2:480491
Forskningsfinansiär
The Foundation for Baltic and East European StudiesKnowledge Foundation
Merknad

Som manuskript i avhandling. As manuscript in dissertation.

Tilgjengelig fra: 2011-12-22 Laget: 2012-01-19 Sist oppdatert: 2017-12-08bibliografisk kontrollert
Inngår i avhandling
1. Molecular characterization of the Tick-borne encephalitis virus: Environments and replication
Åpne denne publikasjonen i ny fane eller vindu >>Molecular characterization of the Tick-borne encephalitis virus: Environments and replication
2012 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

The flavivirus genus is of major concern for world morbidity and mortality and includes viruses causing both encephalitic as well as hemorrhagic diseases. The incidence of Tick-borne encephalitis is increasing in many European countries and several reports have emphasized the expansion of the main vector, Ixodes ricinus. The pattern of vector distribution is also changing in Sweden, which makes it important to set up solid and successful strategies for detection and genetic characterization of novel Swedish TBEV strains.

In this study we have generated strategies for detection of broad types of tick-borne flaviviruses in pools of I. ricinus sampled in Sweden.

The positive collection on the island of Torö was used to generate a sequence of a complete TBEV genome straight from the arthropod reservoir. This cloned virus was used to construct a self-replicating DNA based sub-genomic TBEV replicon capable of expressing reporter genes. The replicon was used to study the effect of TBEV on neurite outgrowth, which revealed that the MTase domain of NS5 block the formation of the Scribble/Rac1/βPIX protein complex, impairing neurite outgrowth in neuronal growth factor induced PC12 cells.

We also demonstrate that TBEV replication is affected by two PDZ binding motifs within NS5 and reveal putative PDZ binding proteins. These interactions might affect cellular pathways and might have a role in flavivirus replication.

We also characterize the variable 3´ non-coding region (V3’-NCR) by in silico studies on TBEV. Analysis brings new evidence that V3’-NCR region carries an enhancer element important for different replication/translation dynamics during the viral lifecycle in mammalian and tick cells. We also propose a temperature-sensitive trans-acting riboswitch mechanism; altering the secondary RNA structures of a closed form at lower temperatures and a form open for translation at higher temperatures. This mechanism may explain the low TBEV level observed in sampled ticks.

sted, utgiver, år, opplag, sider
Stockholm: Department of Genetics, Microbiology and Toxicology, Stockholm University, 2012. s. 71
Serie
Södertörn Doctoral Dissertations, ISSN 1652-7399 ; 63
Emneord
Tick-borne encephalitis virus
HSV kategori
Forskningsprogram
molekylärgenetik
Identifikatorer
urn:nbn:se:sh:diva-14829 (URN)978-91-7447-409-1 (ISBN)978-91-86069-42-1 (ISBN)
Disputas
2012-01-27, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 16 B, 10:00 (engelsk)
Opponent
Veileder
Merknad

At the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 4: Manuscript.

Tilgjengelig fra: 2012-01-19 Laget: 2012-01-19 Sist oppdatert: 2012-10-30bibliografisk kontrollert

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