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Nitrogen represses haustoria formation through abscisic acid in the parasitic plant Phtheirospermum japonicum

Author

Listed:
  • Anna Kokla

    (Linnean Center for Plant Biology, Swedish University of Agricultural Sciences)

  • Martina Leso

    (Linnean Center for Plant Biology, Swedish University of Agricultural Sciences)

  • Xiang Zhang

    (Nara Institute of Science and Technology, Grad. School. Sci. Tech., Ikoma)

  • Jan Simura

    (Swedish University of Agricultural Sciences)

  • Phanu T. Serivichyaswat

    (Linnean Center for Plant Biology, Swedish University of Agricultural Sciences)

  • Songkui Cui

    (Nara Institute of Science and Technology, Grad. School. Sci. Tech., Ikoma)

  • Karin Ljung

    (Swedish University of Agricultural Sciences)

  • Satoko Yoshida

    (Nara Institute of Science and Technology, Grad. School. Sci. Tech., Ikoma)

  • Charles W. Melnyk

    (Linnean Center for Plant Biology, Swedish University of Agricultural Sciences)

Abstract

Parasitic plants are globally prevalent pathogens that withdraw nutrients from their host plants using an organ known as the haustorium. The external environment including nutrient availability affects the extent of parasitism and to understand this phenomenon, we investigated the role of nutrients and found that nitrogen is sufficient to repress haustoria formation in the root parasite Phtheirospermum japonicum. Nitrogen increases levels of abscisic acid (ABA) in P. japonicum and prevents the activation of hundreds of genes including cell cycle and xylem development genes. Blocking ABA signaling overcomes nitrogen’s inhibitory effects indicating that nitrogen represses haustoria formation by increasing ABA. The effect of nitrogen appears more widespread since nitrogen also inhibits haustoria in the obligate root parasite Striga hermonthica. Together, our data show that nitrogen acts as a haustoria repressing factor and suggests a mechanism whereby parasitic plants use nitrogen availability in the external environment to regulate the extent of parasitism.

Suggested Citation

  • Anna Kokla & Martina Leso & Xiang Zhang & Jan Simura & Phanu T. Serivichyaswat & Songkui Cui & Karin Ljung & Satoko Yoshida & Charles W. Melnyk, 2022. "Nitrogen represses haustoria formation through abscisic acid in the parasitic plant Phtheirospermum japonicum," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-30550-x
    DOI: 10.1038/s41467-022-30550-x
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    References listed on IDEAS

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    1. Takema Sasaki & Takuya Suzaki & Takashi Soyano & Mikiko Kojima & Hitoshi Sakakibara & Masayoshi Kawaguchi, 2014. "Shoot-derived cytokinins systemically regulate root nodulation," Nature Communications, Nature, vol. 5(1), pages 1-9, December.
    2. Anuphon Laohavisit & Takanori Wakatake & Nobuaki Ishihama & Hugh Mulvey & Kaori Takizawa & Takamasa Suzuki & Ken Shirasu, 2020. "Quinone perception in plants via leucine-rich-repeat receptor-like kinases," Nature, Nature, vol. 587(7832), pages 92-97, November.
    3. Saima Shahid & Gunjune Kim & Nathan R. Johnson & Eric Wafula & Feng Wang & Ceyda Coruh & Vivian Bernal-Galeano & Tamia Phifer & Claude W. dePamphilis & James H. Westwood & Michael J. Axtell, 2018. "MicroRNAs from the parasitic plant Cuscuta campestris target host messenger RNAs," Nature, Nature, vol. 553(7686), pages 82-85, January.
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