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Conservation of molecular responses upon viral infection in the non-vascular plant Marchantia polymorpha

Author

Listed:
  • Eric Ros-Moner

    (Campus UAB-Edifci CRAG)

  • Tamara Jiménez-Góngora

    (Campus UAB-Edifci CRAG)

  • Luis Villar-Martín

    (Campus UAB-Edifci CRAG)

  • Lana Vogrinec

    (National Institute of Biology
    Jožef Stefan International Postgraduate School)

  • Víctor M. González-Miguel

    (Campus UAB-Edifci CRAG)

  • Denis Kutnjak

    (National Institute of Biology)

  • Ignacio Rubio-Somoza

    (Campus UAB-Edifci CRAG
    Consejo Superior de Investigaciones Científicas (CSIC))

Abstract

After plants transitioned from water to land around 450 million years ago, they faced novel pathogenic microbes. Their colonization of diverse habitats was driven by anatomical innovations like roots, stomata, and vascular tissue, which became central to plant-microbe interactions. However, the impact of these innovations on plant immunity and pathogen infection strategies remains poorly understood. Here, we explore plant-virus interactions in the bryophyte Marchantia polymorpha to gain insights into the evolution of these relationships. Virome analysis reveals that Marchantia is predominantly associated with RNA viruses. Comparative studies with tobacco mosaic virus (TMV) show that Marchantia shares core defense responses with vascular plants but also exhibits unique features, such as a sustained wound response preventing viral spread. Additionally, general defense responses in Marchantia are equivalent to those restricted to vascular tissues in Nicotiana, suggesting that evolutionary acquisition of developmental innovations results in re-routing of defense responses in vascular plants.

Suggested Citation

  • Eric Ros-Moner & Tamara Jiménez-Góngora & Luis Villar-Martín & Lana Vogrinec & Víctor M. González-Miguel & Denis Kutnjak & Ignacio Rubio-Somoza, 2024. "Conservation of molecular responses upon viral infection in the non-vascular plant Marchantia polymorpha," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-52610-0
    DOI: 10.1038/s41467-024-52610-0
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