Change search
ReferencesLink to record
Permanent link

Direct link
Convergent evolution of argonaute-2 slicer antagonism in two distinct insect RNA viruses
Umeå University, Faculty of Medicine, Department of Molecular Biology (Faculty of Medicine). (Hultmark)
Show others and affiliations
2012 (English)In: PLoS Pathogens, ISSN 1553-7366, E-ISSN 1553-7374, Vol. 8, no 8, e1002872Article in journal (Refereed) Published
Abstract [en]

RNA interference (RNAi) is a major antiviral pathway that shapes evolution of RNA viruses. We show here that Nora virus, a natural Drosophila pathogen, is both a target and suppressor of RNAi. We detected viral small RNAs with a signature of Dicer-2 dependent small interfering RNAs in Nora virus infected Drosophila. Furthermore, we demonstrate that the Nora virus VP1 protein contains RNAi suppressive activity in vitro and in vivo that enhances pathogenicity of recombinant Sindbis virus in an RNAi dependent manner. Nora virus VP1 and the viral suppressor of RNAi of Cricket paralysis virus (1A) antagonized Argonaute-2 (AGO2) Slicer activity of RNA induced silencing complexes pre-loaded with a methylated single-stranded guide strand. The convergent evolution of AGO2 suppression in two unrelated insect RNA viruses highlights the importance of AGO2 in antiviral defense.

Place, publisher, year, edition, pages
2012. Vol. 8, no 8, e1002872
National Category
Cell and Molecular Biology
URN: urn:nbn:se:umu:diva-61306DOI: 10.1371/journal.ppat.1002872ISI: 000308558000047PubMedID: 22916019OAI: diva2:565801
Available from: 2012-11-08 Created: 2012-11-08 Last updated: 2016-11-10Bibliographically approved
In thesis
1. Biology of a small RNA virus that infects Drosophila melanogaster
Open this publication in new window or tab >>Biology of a small RNA virus that infects Drosophila melanogaster
2016 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Drosophila melanogaster has been extensively used as a model organism to study diverse facets of biology, including host-pathogen interactions and the basic biology of its pathogens. I have used the fruit fly as a model to study elementary aspects of Nora virus biology, such as the role of the different proteins encoded by the virus genome. Nora virus, an enteric virus transmitted via the feca-oral route, does not cause any obvious pathology in the fly, although the infection is persistent. Nora virus genome consists of a positive strand RNA that is translated in four open reading frames (ORF).  Since sequence homology studies did not yield much information about the different Nora virus proteins, I have used the cDNA clone of the virus to construct mutants to identify the specific function of each protein. My results have shown that,

1) The protein(s) encoded by ORF 1 are crucial for the replication of the virus genome.

2) The C-terminus of the ORF 1-encoded protein (VP1), is an inhibitor to the RNAi pathway.

3) The transmembrane domain in the N-terminus of the ORF2-encoded protein (VP2) is important for the formation of Nora virus virions.

4) The ORF 3-encoded protein (VP3) forms α-helical trimers and this protein is essential for the stability of Nora virus capsid.                                                    

I have also performed RNA sequencing to investigate the transcriptional response of D. melanogaster in response to Nora virus infection and my results indicate that,                       

5) The upregulation of genes related to cellular stress and protein synthesis and the downregulation of basal digestive machinery, together with the induction of upd3, implies major gut epithelium damage and subsequent regeneration.

Place, publisher, year, edition, pages
Umeå: Umeå University, 2016. 52 p.
Nora virus, Drosophila melanogaster, virus biology, host-pathogen interaction
National Category
Cell and Molecular Biology
Research subject
Molecular Biology
urn:nbn:se:umu:diva-127352 (URN)978-91-7601-593-3 (ISBN)
Public defence
2016-12-01, Hörsal 135, Byggnad 9A, Norrlands Universitetssjukhus, Umeå, 14:00 (English)
Available from: 2016-11-10 Created: 2016-11-09 Last updated: 2016-11-24Bibliographically approved

Open Access in DiVA

fulltext(4116 kB)8 downloads
File information
File name FULLTEXT01.pdfFile size 4116 kBChecksum SHA-512
Type fulltextMimetype application/pdf

Other links

Publisher's full textPubMed

Search in DiVA

By author/editor
Sadanandan, Sajna AEkström, Jens-OlaHultmark, Dan
By organisation
Department of Molecular Biology (Faculty of Medicine)
In the same journal
PLoS Pathogens
Cell and Molecular Biology

Search outside of DiVA

GoogleGoogle Scholar
Total: 8 downloads
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

Altmetric score

Total: 226 hits
ReferencesLink to record
Permanent link

Direct link