IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v15y2024i1d10.1038_s41467-024-48366-2.html
   My bibliography  Save this article

Coordinated wound responses in a regenerative animal-algal holobiont

Author

Listed:
  • Dania Nanes Sarfati

    (Stanford University)

  • Yuan Xue

    (Stanford University)

  • Eun Sun Song

    (Stanford University)

  • Ashley Byrne

    (Chan Zuckerberg Biohub)

  • Daniel Le

    (Chan Zuckerberg Biohub)

  • Spyros Darmanis

    (Chan Zuckerberg Biohub)

  • Stephen R. Quake

    (Stanford University
    Stanford University)

  • Adrien Burlacot

    (Stanford University
    Carnegie Institution for Science)

  • James Sikes

    (University of San Francisco)

  • Bo Wang

    (Stanford University
    Stanford University School of Medicine)

Abstract

Animal regeneration involves coordinated responses across cell types throughout the animal body. In endosymbiotic animals, whether and how symbionts react to host injury and how cellular responses are integrated across species remain unexplored. Here, we study the acoel Convolutriloba longifissura, which hosts symbiotic Tetraselmis sp. green algae and can regenerate entire bodies from tissue fragments. We show that animal injury causes a decline in the photosynthetic efficiency of the symbiotic algae, alongside two distinct, sequential waves of transcriptional responses in acoel and algal cells. The initial algal response is characterized by the upregulation of a cohort of photosynthesis-related genes, though photosynthesis is not necessary for regeneration. A conserved animal transcription factor, runt, is induced after injury and required for acoel regeneration. Knockdown of Cl-runt dampens transcriptional responses in both species and further reduces algal photosynthetic efficiency post-injury. Our results suggest that the holobiont functions as an integrated unit of biological organization by coordinating molecular networks across species through the runt-dependent animal regeneration program.

Suggested Citation

  • Dania Nanes Sarfati & Yuan Xue & Eun Sun Song & Ashley Byrne & Daniel Le & Spyros Darmanis & Stephen R. Quake & Adrien Burlacot & James Sikes & Bo Wang, 2024. "Coordinated wound responses in a regenerative animal-algal holobiont," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48366-2
    DOI: 10.1038/s41467-024-48366-2
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-024-48366-2
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-024-48366-2?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Ab. Matteen Rafiqi & Arjuna Rajakumar & Ehab Abouheif, 2020. "Origin and elaboration of a major evolutionary transition in individuality," Nature, Nature, vol. 585(7824), pages 239-244, September.
    2. Jörg Wiedenmann & Cecilia D’Angelo & M. Loreto Mardones & Shona Moore & Cassandra E. Benkwitt & Nicholas A. J. Graham & Bastian Hambach & Paul A. Wilson & James Vanstone & Gal Eyal & Or Ben-Zvi & Yoss, 2023. "Reef-building corals farm and feed on their photosynthetic symbionts," Nature, Nature, vol. 620(7976), pages 1018-1024, August.
    3. Graham Peers & Thuy B. Truong & Elisabeth Ostendorf & Andreas Busch & Dafna Elrad & Arthur R. Grossman & Michael Hippler & Krishna K. Niyogi, 2009. "An ancient light-harvesting protein is critical for the regulation of algal photosynthesis," Nature, Nature, vol. 462(7272), pages 518-521, November.
    4. Tingting Xiang & Erik Lehnert & Robert E. Jinkerson & Sophie Clowez & Rick G. Kim & Jan C. DeNofrio & John R. Pringle & Arthur R. Grossman, 2020. "Symbiont population control by host-symbiont metabolic interaction in Symbiodiniaceae-cnidarian associations," Nature Communications, Nature, vol. 11(1), pages 1-9, December.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Huan Zhang & Xiaofeng Xiong & Kangning Guo & Mengyuan Zheng & Tianjun Cao & Yuqing Yang & Jiaojiao Song & Jie Cen & Jiahuan Zhang & Yanyou Jiang & Shan Feng & Lijin Tian & Xiaobo Li, 2024. "A rapid aureochrome opto-switch enables diatom acclimation to dynamic light," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
    2. Marius Arend & Yizhong Yuan & M. Águila Ruiz-Sola & Nooshin Omranian & Zoran Nikoloski & Dimitris Petroutsos, 2023. "Widening the landscape of transcriptional regulation of green algal photoprotection," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    3. M. Águila Ruiz-Sola & Serena Flori & Yizhong Yuan & Gaelle Villain & Emanuel Sanz-Luque & Petra Redekop & Ryutaro Tokutsu & Anika Küken & Angeliki Tsichla & Georgios Kepesidis & Guillaume Allorent & M, 2023. "Light-independent regulation of algal photoprotection by CO2 availability," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    4. Nils Rädecker & Stéphane Escrig & Jorge E. Spangenberg & Christian R. Voolstra & Anders Meibom, 2023. "Coupled carbon and nitrogen cycling regulates the cnidarian–algal symbiosis," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
    5. Guoxin Cui & Jianing Mi & Alessandro Moret & Jessica Menzies & Huawen Zhong & Angus Li & Shiou-Han Hung & Salim Al-Babili & Manuel Aranda, 2023. "A carbon-nitrogen negative feedback loop underlies the repeated evolution of cnidarian–Symbiodiniaceae symbioses," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    6. Xiaojie Pang & Wojciech J. Nawrocki & Pierre Cardol & Mengyuan Zheng & Jingjing Jiang & Yuan Fang & Wenqiang Yang & Roberta Croce & Lijin Tian, 2023. "Weak acids produced during anaerobic respiration suppress both photosynthesis and aerobic respiration," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    7. Kaare-Rasmussen, Jakob O. & Moeller, Holly V. & Pfab, Ferdinand, 2023. "Modeling food dependent symbiosis in Exaiptasia pallida," Ecological Modelling, Elsevier, vol. 481(C).
    8. Mengyuan Zheng & Xiaojie Pang & Ming Chen & Lijin Tian, 2024. "Ultrafast energy quenching mechanism of LHCSR3-dependent photoprotection in Chlamydomonas," Nature Communications, Nature, vol. 15(1), pages 1-10, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48366-2. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.