IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-42864-5.html
   My bibliography  Save this article

Rapid threat assessment in the Drosophila thermosensory system

Author

Listed:
  • Genevieve C. Jouandet

    (Northwestern University)

  • Michael H. Alpert

    (Northwestern University)

  • José Miguel Simões

    (Northwestern University)

  • Richard Suhendra

    (Northwestern University)

  • Dominic D. Frank

    (Northwestern University
    The Rockefeller University)

  • Joshua I. Levy

    (Northwestern University
    The Scripps Research Institute)

  • Alessia Para

    (Northwestern University)

  • William L. Kath

    (Northwestern University
    Northwestern University
    National Institute for Theory and Mathematics in Biology, Northwestern University)

  • Marco Gallio

    (Northwestern University)

Abstract

Neurons that participate in sensory processing often display “ON” responses, i.e., fire transiently at the onset of a stimulus. ON transients are widespread, perhaps universal to sensory coding, yet their function is not always well-understood. Here, we show that ON responses in the Drosophila thermosensory system extrapolate the trajectory of temperature change, priming escape behavior if unsafe thermal conditions are imminent. First, we show that second-order thermosensory projection neurons (TPN-IIIs) and their Lateral Horn targets (TLHONs), display ON responses to thermal stimuli, independent of direction of change (heating or cooling) and of absolute temperature. Instead, they track the rate of temperature change, with TLHONs firing exclusively to rapid changes (>0.2 °C/s). Next, we use connectomics to track TLHONs’ output to descending neurons that control walking and escape, and modeling and genetic silencing to demonstrate how ON transients can flexibly amplify aversive responses to small thermal change. Our results suggest that, across sensory systems, ON transients may represent a general mechanism to systematically anticipate and respond to salient or dangerous conditions.

Suggested Citation

  • Genevieve C. Jouandet & Michael H. Alpert & José Miguel Simões & Richard Suhendra & Dominic D. Frank & Joshua I. Levy & Alessia Para & William L. Kath & Marco Gallio, 2023. "Rapid threat assessment in the Drosophila thermosensory system," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42864-5
    DOI: 10.1038/s41467-023-42864-5
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-42864-5
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-42864-5?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. Ricardo Zacarias & Shigehiro Namiki & Gwyneth M. Card & Maria Luisa Vasconcelos & Marta A. Moita, 2018. "Speed dependent descending control of freezing behavior in Drosophila melanogaster," Nature Communications, Nature, vol. 9(1), pages 1-11, December.
    2. Dominic D. Frank & Genevieve C. Jouandet & Patrick J. Kearney & Lindsey J. Macpherson & Marco Gallio, 2015. "Temperature representation in the Drosophila brain," Nature, Nature, vol. 519(7543), pages 358-361, March.
    3. Vanessa Ruta & Sandeep Robert Datta & Maria Luisa Vasconcelos & Jessica Freeland & Loren L. Looger & Richard Axel, 2010. "A dimorphic pheromone circuit in Drosophila from sensory input to descending output," Nature, Nature, vol. 468(7324), pages 686-690, December.
    4. Wendy W. Liu & Ofer Mazor & Rachel I. Wilson, 2015. "Thermosensory processing in the Drosophila brain," Nature, Nature, vol. 519(7543), pages 353-357, March.
    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. Pranjul Singh & Shefali Goyal & Smith Gupta & Sanket Garg & Abhinav Tiwari & Varad Rajput & Alexander Shakeel Bates & Arjit Kant Gupta & Nitin Gupta, 2023. "Combinatorial encoding of odors in the mosquito antennal lobe," Nature Communications, Nature, vol. 14(1), pages 1-19, December.
    2. Tyler R. Sizemore & Julius Jonaitis & Andrew M. Dacks, 2023. "Heterogeneous receptor expression underlies non-uniform peptidergic modulation of olfaction in Drosophila," Nature Communications, Nature, vol. 14(1), pages 1-22, December.
    3. Martin F Strube-Bloss & Austin Brown & Johannes Spaethe & Thomas Schmitt & Wolfgang Rössler, 2015. "Extracting the Behaviorally Relevant Stimulus: Unique Neural Representation of Farnesol, a Component of the Recruitment Pheromone of Bombus terrestris," PLOS ONE, Public Library of Science, vol. 10(9), pages 1-16, September.
    4. Maria E Yurgel & Priyanka Kakad & Meet Zandawala & Dick R Nässel & Tanja A Godenschwege & Alex C Keene, 2019. "A single pair of leucokinin neurons are modulated by feeding state and regulate sleep–metabolism interactions," PLOS Biology, Public Library of Science, vol. 17(2), pages 1-26, February.
    5. Shiu-Ling Chen & Bo-Ting Liu & Wang-Pao Lee & Sin-Bo Liao & Yao-Bang Deng & Chia-Lin Wu & Shuk-Man Ho & Bing-Xian Shen & Guan-Hock Khoo & Wei-Chiang Shiu & Chih-Hsuan Chang & Hui-Wen Shih & Jung-Kun W, 2022. "WAKE-mediated modulation of cVA perception via a hierarchical neuro-endocrine axis in Drosophila male-male courtship behaviour," Nature Communications, Nature, vol. 13(1), pages 1-18, 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:14:y:2023:i:1:d:10.1038_s41467-023-42864-5. 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.