Experimental virus evolution reveals a role of plant microtubule dynamics and TORTIFOLIA1/SPIRAL2 in RNA trafficking

PLoS One. 2014 Aug 18;9(8):e105364. doi: 10.1371/journal.pone.0105364. eCollection 2014.

Abstract

The cytoskeleton is a dynamic network composed of filamentous polymers and regulatory proteins that provide a flexible structural scaffold to the cell and plays a fundamental role in developmental processes. Mutations that alter the spatial orientation of the cortical microtubule (MT) array of plants are known to cause important changes in the pattern of cell wall synthesis and developmental phenotypes; however, the consequences of such alterations on other MT-network-associated functions in the cytoplasm are not known. In vivo observations suggested a role of cortical MTs in the formation and movement of Tobacco mosaic virus (TMV) RNA complexes along the endoplasmic reticulum (ER). Thus, to probe the significance of dynamic MT behavior in the coordination of MT-network-associated functions related to TMV infection and, thus, in the formation and transport of RNA complexes in the cytoplasm, we performed an evolution experiment with TMV in Arabidopsis thaliana tor1/spr2 and tor2 mutants with specific defects in MT dynamics and asked whether TMV is sensitive to these changes. We show that the altered cytoskeleton induced genetic changes in TMV that were correlated with efficient spread of infection in the mutant hosts. These observations demonstrate a role of dynamic MT rearrangements and of the MT-associated protein TORTIFOLIA1/SPIRAL2 in cellular functions related to virus spread and indicate that MT dynamics and MT-associated proteins represent constraints for virus evolution and adaptation. The results highlight the importance of the dynamic plasticity of the MT network in directing cytoplasmic functions in macromolecular assembly and trafficking and illustrate the value of experimental virus evolution for addressing the cellular functions of dynamic, long-range order systems in multicellular organisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / genetics
  • Arabidopsis / metabolism
  • Arabidopsis / virology*
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism*
  • Biological Evolution
  • Host-Pathogen Interactions
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism*
  • Microtubules / genetics
  • Microtubules / metabolism*
  • Mutation
  • Plant Diseases / genetics
  • Plant Diseases / virology*
  • RNA / genetics
  • RNA / metabolism
  • RNA Transport*
  • Tobacco Mosaic Virus / genetics
  • Tobacco Mosaic Virus / physiology*

Substances

  • Arabidopsis Proteins
  • Microtubule-Associated Proteins
  • SPIRAL2 protein, Arabidopsis
  • RNA

Grants and funding

Work of E.P. and of A.N. was supported by grants from the Agence National de la Recherche (ANR, grant ANR-08-BLAN-244) and the Swiss National Science Foundation (SNF, grant 310031A_140694) to M.H. We also acknowledge the funding of an EMBO short-term fellowship to H.B. I.F. was supported by a pre-doctoral fellowship from the Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA) from Spain. L.R. was supported by grant AGL2005-07754 from the Spanish Ministry of Science and Education and S.F.E. by grant BFU2012-30805 from the Spanish Secretaría de Estado de Investigación, Desarrollo e Innovación. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.