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      Analysis of T omato spotted wilt virus  NSs protein indicates the importance of the N‐terminal domain for avirulence and RNA silencing suppression

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          Summary

          Recently, Tomato spotted wilt virus ( TSWV) nonstructural protein NSs has been identified unambiguously as an avirulence ( Avr) determinant for Tomato spotted wilt ( Tsw )‐based resistance. The observation that NSs from two natural resistance‐breaking isolates had lost RNA silencing suppressor ( RSS) activity and Avr suggested a link between the two functions. To test this, a large set of NSs mutants was generated by alanine substitutions in NSs from resistance‐inducing wild‐type strains ( NSs RI ), amino acid reversions in NSs from resistance‐breaking strains ( NSs RB ), domain deletions and swapping. Testing these mutants for their ability to suppress green fluorescent protein ( GFP) silencing and to trigger a Tsw ‐mediated hypersensitive response ( HR) revealed that the two functions can be separated. Changes in the N‐terminal domain were found to be detrimental for both activities and indicated the importance of this domain, additionally supported by domain swapping between NSs RI and NSs RB . Swapping domains between the closely related Tospovirus Groundnut ringspot virus ( GRSV) NSs and TSWV NSs RI showed that Avr functionality could not simply be transferred between species. Although deletion of the C‐terminal domain rendered NSs completely dysfunctional, only a few single‐amino‐acid mutations in the C‐terminus affected both functions. Mutation of a GW/ WG motif (position 17/18) rendered NSs completely dysfunctional for RSS and Avr activity, and indicated a putative interaction between NSs and Argonaute 1 ( AGO1), and its importance in TSWV virulence and viral counter defence against RNA interference.

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          Author and article information

          Journal
          Mol Plant Pathol
          Mol. Plant Pathol
          10.1111/(ISSN)1364-3703
          MPP
          Molecular Plant Pathology
          John Wiley and Sons Inc. (Hoboken )
          1464-6722
          1364-3703
          05 December 2013
          February 2014
          : 15
          : 2 ( doiID: 10.1111/mpp.2014.15.issue-2 )
          : 185-195
          Affiliations
          [ 1 ] Laboratory of Virology Department of Plant Sciences Wageningen University Droevendaalsesteeg 1 6708 PB Wageningen the Netherlands
          Author notes
          [*] [* ] Correspondence: Email: richard.kormelink@ 123456wur.nl
          Article
          PMC6638762 PMC6638762 6638762 MPP12082
          10.1111/mpp.12082
          6638762
          24103150
          a98dd4b2-d856-4a5e-8005-6525b9264535
          © 2013 BSPP AND JOHN WILEY & SONS LTD
          History
          Page count
          Pages: 11
          Funding
          Funded by: Dutch Technology Foundation (STW: Stichting Technische Wetenschappen) (Dryas de Ronde)
          Funded by: Applied Science Division of NWO (Nederlandse organisatie voor Wetenschappelijk Onderzoek)
          Categories
          Original Articles
          Original Article
          Custom metadata
          2.0
          mpp12082
          February 2014
          Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.4 mode:remove_FC converted:10.06.2019

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