Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain
Animals exhibit innate and learned preferences for temperature and humidity—conditions critical for their survival and reproduction. Leveraging a whole-brain electron microscopy volume, we studied the adult Drosophila melanogaster circuitry associated with antennal thermo- and hygrosensory neurons....
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creator | Marin, Elizabeth C. Büld, Laurin Theiss, Maria Sarkissian, Tatevik Roberts, Ruairí J.V. Turnbull, Robert Tamimi, Imaan F.M. Pleijzier, Markus W. Laursen, Willem J. Drummond, Nik Schlegel, Philipp Bates, Alexander S. Li, Feng Landgraf, Matthias Costa, Marta Bock, Davi D. Garrity, Paul A. Jefferis, Gregory S.X.E. |
description | Animals exhibit innate and learned preferences for temperature and humidity—conditions critical for their survival and reproduction. Leveraging a whole-brain electron microscopy volume, we studied the adult Drosophila melanogaster circuitry associated with antennal thermo- and hygrosensory neurons. We have identified two new target glomeruli in the antennal lobe, in addition to the five known ones, and the ventroposterior projection neurons (VP PNs) that relay thermo- and hygrosensory information to higher brain centers, including the mushroom body and lateral horn, seats of learned and innate behavior. We present the first connectome of a thermo- and hygrosensory neuropil, the lateral accessory calyx (lACA), by reconstructing neurons downstream of heating- and cooling-responsive VP PNs. A few mushroom body-intrinsic neurons solely receive thermosensory input from the lACA, while most receive additional olfactory and thermo- and/or hygrosensory PN inputs. Furthermore, several classes of lACA-associated neurons form a local network with outputs to other brain neuropils, suggesting that the lACA serves as a hub for thermo- and hygrosensory circuitry. For example, DN1a neurons link thermosensory PNs in the lACA to the circadian clock via the accessory medulla. Finally, we survey strongly connected downstream partners of VP PNs across the protocerebrum; these include a descending neuron targeted by dry-responsive VP PNs, meaning that just two synapses might separate hygrosensory inputs from motor circuits. These data provide a comprehensive first- and second-order layer analysis of Drosophila thermo- and hygrosensory systems and an initial survey of third-order neurons that could directly modulate behavior.
[Display omitted]
•Two novel thermo- and/or hygrosensory glomeruli in the fly antennal lobe•First complete set of thermosensory and hygrosensory projection neurons•First connectome for a thermo- and hygrosensory neuropil•Third-order thermo- and hygrosensory neurons, including link to circadian clock
Marin et al. use connectomics and genetics for comprehensive identification of temperature and humidity sensory neurons in the Drosophila brain. They reconstruct all projections to higher brain areas and select higher-order targets, including the mushroom body lateral accessory calyx, linking thermosensation to memory and the circadian clock. |
doi_str_mv | 10.1016/j.cub.2020.06.028 |
format | Article |
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[Display omitted]
•Two novel thermo- and/or hygrosensory glomeruli in the fly antennal lobe•First complete set of thermosensory and hygrosensory projection neurons•First connectome for a thermo- and hygrosensory neuropil•Third-order thermo- and hygrosensory neurons, including link to circadian clock
Marin et al. use connectomics and genetics for comprehensive identification of temperature and humidity sensory neurons in the Drosophila brain. They reconstruct all projections to higher brain areas and select higher-order targets, including the mushroom body lateral accessory calyx, linking thermosensation to memory and the circadian clock.</description><identifier>ISSN: 0960-9822</identifier><identifier>EISSN: 1879-0445</identifier><identifier>DOI: 10.1016/j.cub.2020.06.028</identifier><identifier>PMID: 32619476</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Animals ; antennal lobe ; circadian clock ; Connectome ; connectomics ; Drosophila ; Drosophila melanogaster - physiology ; Female ; hygrosensation ; lateral accessory calyx ; lateral horn ; mushroom body ; Neurons - cytology ; Neurons - metabolism ; Neuropil - metabolism ; Olfactory Pathways ; projection neuron ; Sensory Receptor Cells - metabolism ; Synapses - physiology ; Thermoreceptors - metabolism ; thermosensation</subject><ispartof>Current biology, 2020-08, Vol.30 (16), p.3167-3182.e4</ispartof><rights>2020 MRC Laboratory of Molecular Biology</rights><rights>Copyright © 2020 MRC Laboratory of Molecular Biology. Published by Elsevier Inc. All rights reserved.</rights><rights>2020 MRC Laboratory of Molecular Biology 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c565t-d65c76e97dd56a52c82940d4512ee9712775ed0664b9098bdf8624bffc19b1fa3</citedby><cites>FETCH-LOGICAL-c565t-d65c76e97dd56a52c82940d4512ee9712775ed0664b9098bdf8624bffc19b1fa3</cites><orcidid>0000-0002-5969-4778 ; 0000-0001-5948-3092 ; 0000-0002-8274-6564 ; 0000-0002-3630-057X ; 0000-0002-7843-2351 ; 0000-0001-5142-1997</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0960982220308447$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32619476$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marin, Elizabeth C.</creatorcontrib><creatorcontrib>Büld, Laurin</creatorcontrib><creatorcontrib>Theiss, Maria</creatorcontrib><creatorcontrib>Sarkissian, Tatevik</creatorcontrib><creatorcontrib>Roberts, Ruairí J.V.</creatorcontrib><creatorcontrib>Turnbull, Robert</creatorcontrib><creatorcontrib>Tamimi, Imaan F.M.</creatorcontrib><creatorcontrib>Pleijzier, Markus W.</creatorcontrib><creatorcontrib>Laursen, Willem J.</creatorcontrib><creatorcontrib>Drummond, Nik</creatorcontrib><creatorcontrib>Schlegel, Philipp</creatorcontrib><creatorcontrib>Bates, Alexander S.</creatorcontrib><creatorcontrib>Li, Feng</creatorcontrib><creatorcontrib>Landgraf, Matthias</creatorcontrib><creatorcontrib>Costa, Marta</creatorcontrib><creatorcontrib>Bock, Davi D.</creatorcontrib><creatorcontrib>Garrity, Paul A.</creatorcontrib><creatorcontrib>Jefferis, Gregory S.X.E.</creatorcontrib><title>Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain</title><title>Current biology</title><addtitle>Curr Biol</addtitle><description>Animals exhibit innate and learned preferences for temperature and humidity—conditions critical for their survival and reproduction. Leveraging a whole-brain electron microscopy volume, we studied the adult Drosophila melanogaster circuitry associated with antennal thermo- and hygrosensory neurons. We have identified two new target glomeruli in the antennal lobe, in addition to the five known ones, and the ventroposterior projection neurons (VP PNs) that relay thermo- and hygrosensory information to higher brain centers, including the mushroom body and lateral horn, seats of learned and innate behavior. We present the first connectome of a thermo- and hygrosensory neuropil, the lateral accessory calyx (lACA), by reconstructing neurons downstream of heating- and cooling-responsive VP PNs. A few mushroom body-intrinsic neurons solely receive thermosensory input from the lACA, while most receive additional olfactory and thermo- and/or hygrosensory PN inputs. Furthermore, several classes of lACA-associated neurons form a local network with outputs to other brain neuropils, suggesting that the lACA serves as a hub for thermo- and hygrosensory circuitry. For example, DN1a neurons link thermosensory PNs in the lACA to the circadian clock via the accessory medulla. Finally, we survey strongly connected downstream partners of VP PNs across the protocerebrum; these include a descending neuron targeted by dry-responsive VP PNs, meaning that just two synapses might separate hygrosensory inputs from motor circuits. These data provide a comprehensive first- and second-order layer analysis of Drosophila thermo- and hygrosensory systems and an initial survey of third-order neurons that could directly modulate behavior.
[Display omitted]
•Two novel thermo- and/or hygrosensory glomeruli in the fly antennal lobe•First complete set of thermosensory and hygrosensory projection neurons•First connectome for a thermo- and hygrosensory neuropil•Third-order thermo- and hygrosensory neurons, including link to circadian clock
Marin et al. use connectomics and genetics for comprehensive identification of temperature and humidity sensory neurons in the Drosophila brain. They reconstruct all projections to higher brain areas and select higher-order targets, including the mushroom body lateral accessory calyx, linking thermosensation to memory and the circadian clock.</description><subject>Animals</subject><subject>antennal lobe</subject><subject>circadian clock</subject><subject>Connectome</subject><subject>connectomics</subject><subject>Drosophila</subject><subject>Drosophila melanogaster - physiology</subject><subject>Female</subject><subject>hygrosensation</subject><subject>lateral accessory calyx</subject><subject>lateral horn</subject><subject>mushroom body</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>Neuropil - metabolism</subject><subject>Olfactory Pathways</subject><subject>projection neuron</subject><subject>Sensory Receptor Cells - metabolism</subject><subject>Synapses - physiology</subject><subject>Thermoreceptors - metabolism</subject><subject>thermosensation</subject><issn>0960-9822</issn><issn>1879-0445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9v1DAQxS0EokvhA3BBPnIgwXYcJxYS0rLQP1JFJShny7EnXa8Se2snK-2ZL47Ltiu49OTRvDdvbP8QektJSQkVHzelmbuSEUZKIkrC2mdoQdtGFoTz-jlaEClIIVvGTtCrlDaEUNZK8RKdVExQyRuxQL9XwXswUxidSXjp9bBPLuEfsAM9JHzmYpqKD_gnmOBtLrS3-Gbtoi2uo4WYa4hjSOBTiPu_6sX-Nh4b32GOwSfsPJ7WgJd2Hib8Nethu3aDxl-idv41etHnZfDm4TxFv86-3awuiqvr88vV8qowtainworaNAJkY20tdM1MyyQnlteUQe5S1jQ1WCIE7ySRbWf7VjDe9b2hsqO9rk7R50Pudu5GsAb8FPWgttGNOu5V0E79r3i3VrdhpxrOq4bwHPD-ISCGuxnSpEaXDAyD9hDmpBhnhPKKyipb6cFq8mNThP64hhJ1D09tVIan7uEpIlSGl2fe_Xu_48QjrWz4dDBA_qWdg6iSceANWBczQ2WDeyL-D3uSrPg</recordid><startdate>20200817</startdate><enddate>20200817</enddate><creator>Marin, Elizabeth C.</creator><creator>Büld, Laurin</creator><creator>Theiss, Maria</creator><creator>Sarkissian, Tatevik</creator><creator>Roberts, Ruairí J.V.</creator><creator>Turnbull, Robert</creator><creator>Tamimi, Imaan F.M.</creator><creator>Pleijzier, Markus W.</creator><creator>Laursen, Willem J.</creator><creator>Drummond, Nik</creator><creator>Schlegel, Philipp</creator><creator>Bates, Alexander S.</creator><creator>Li, Feng</creator><creator>Landgraf, Matthias</creator><creator>Costa, Marta</creator><creator>Bock, Davi D.</creator><creator>Garrity, Paul A.</creator><creator>Jefferis, Gregory S.X.E.</creator><general>Elsevier Inc</general><general>Cell Press</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5969-4778</orcidid><orcidid>https://orcid.org/0000-0001-5948-3092</orcidid><orcidid>https://orcid.org/0000-0002-8274-6564</orcidid><orcidid>https://orcid.org/0000-0002-3630-057X</orcidid><orcidid>https://orcid.org/0000-0002-7843-2351</orcidid><orcidid>https://orcid.org/0000-0001-5142-1997</orcidid></search><sort><creationdate>20200817</creationdate><title>Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain</title><author>Marin, Elizabeth C. ; Büld, Laurin ; Theiss, Maria ; Sarkissian, Tatevik ; Roberts, Ruairí J.V. ; Turnbull, Robert ; Tamimi, Imaan F.M. ; Pleijzier, Markus W. ; Laursen, Willem J. ; Drummond, Nik ; Schlegel, Philipp ; Bates, Alexander S. ; Li, Feng ; Landgraf, Matthias ; Costa, Marta ; Bock, Davi D. ; Garrity, Paul A. ; Jefferis, Gregory S.X.E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c565t-d65c76e97dd56a52c82940d4512ee9712775ed0664b9098bdf8624bffc19b1fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>antennal lobe</topic><topic>circadian clock</topic><topic>Connectome</topic><topic>connectomics</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - physiology</topic><topic>Female</topic><topic>hygrosensation</topic><topic>lateral accessory calyx</topic><topic>lateral horn</topic><topic>mushroom body</topic><topic>Neurons - cytology</topic><topic>Neurons - metabolism</topic><topic>Neuropil - metabolism</topic><topic>Olfactory Pathways</topic><topic>projection neuron</topic><topic>Sensory Receptor Cells - metabolism</topic><topic>Synapses - physiology</topic><topic>Thermoreceptors - metabolism</topic><topic>thermosensation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marin, Elizabeth C.</creatorcontrib><creatorcontrib>Büld, Laurin</creatorcontrib><creatorcontrib>Theiss, Maria</creatorcontrib><creatorcontrib>Sarkissian, Tatevik</creatorcontrib><creatorcontrib>Roberts, Ruairí J.V.</creatorcontrib><creatorcontrib>Turnbull, Robert</creatorcontrib><creatorcontrib>Tamimi, Imaan F.M.</creatorcontrib><creatorcontrib>Pleijzier, Markus W.</creatorcontrib><creatorcontrib>Laursen, Willem J.</creatorcontrib><creatorcontrib>Drummond, Nik</creatorcontrib><creatorcontrib>Schlegel, Philipp</creatorcontrib><creatorcontrib>Bates, Alexander S.</creatorcontrib><creatorcontrib>Li, Feng</creatorcontrib><creatorcontrib>Landgraf, Matthias</creatorcontrib><creatorcontrib>Costa, Marta</creatorcontrib><creatorcontrib>Bock, Davi D.</creatorcontrib><creatorcontrib>Garrity, Paul A.</creatorcontrib><creatorcontrib>Jefferis, Gregory S.X.E.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Current biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marin, Elizabeth C.</au><au>Büld, Laurin</au><au>Theiss, Maria</au><au>Sarkissian, Tatevik</au><au>Roberts, Ruairí J.V.</au><au>Turnbull, Robert</au><au>Tamimi, Imaan F.M.</au><au>Pleijzier, Markus W.</au><au>Laursen, Willem J.</au><au>Drummond, Nik</au><au>Schlegel, Philipp</au><au>Bates, Alexander S.</au><au>Li, Feng</au><au>Landgraf, Matthias</au><au>Costa, Marta</au><au>Bock, Davi D.</au><au>Garrity, Paul A.</au><au>Jefferis, Gregory S.X.E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain</atitle><jtitle>Current biology</jtitle><addtitle>Curr Biol</addtitle><date>2020-08-17</date><risdate>2020</risdate><volume>30</volume><issue>16</issue><spage>3167</spage><epage>3182.e4</epage><pages>3167-3182.e4</pages><issn>0960-9822</issn><eissn>1879-0445</eissn><abstract>Animals exhibit innate and learned preferences for temperature and humidity—conditions critical for their survival and reproduction. Leveraging a whole-brain electron microscopy volume, we studied the adult Drosophila melanogaster circuitry associated with antennal thermo- and hygrosensory neurons. We have identified two new target glomeruli in the antennal lobe, in addition to the five known ones, and the ventroposterior projection neurons (VP PNs) that relay thermo- and hygrosensory information to higher brain centers, including the mushroom body and lateral horn, seats of learned and innate behavior. We present the first connectome of a thermo- and hygrosensory neuropil, the lateral accessory calyx (lACA), by reconstructing neurons downstream of heating- and cooling-responsive VP PNs. A few mushroom body-intrinsic neurons solely receive thermosensory input from the lACA, while most receive additional olfactory and thermo- and/or hygrosensory PN inputs. Furthermore, several classes of lACA-associated neurons form a local network with outputs to other brain neuropils, suggesting that the lACA serves as a hub for thermo- and hygrosensory circuitry. For example, DN1a neurons link thermosensory PNs in the lACA to the circadian clock via the accessory medulla. Finally, we survey strongly connected downstream partners of VP PNs across the protocerebrum; these include a descending neuron targeted by dry-responsive VP PNs, meaning that just two synapses might separate hygrosensory inputs from motor circuits. These data provide a comprehensive first- and second-order layer analysis of Drosophila thermo- and hygrosensory systems and an initial survey of third-order neurons that could directly modulate behavior.
[Display omitted]
•Two novel thermo- and/or hygrosensory glomeruli in the fly antennal lobe•First complete set of thermosensory and hygrosensory projection neurons•First connectome for a thermo- and hygrosensory neuropil•Third-order thermo- and hygrosensory neurons, including link to circadian clock
Marin et al. use connectomics and genetics for comprehensive identification of temperature and humidity sensory neurons in the Drosophila brain. They reconstruct all projections to higher brain areas and select higher-order targets, including the mushroom body lateral accessory calyx, linking thermosensation to memory and the circadian clock.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>32619476</pmid><doi>10.1016/j.cub.2020.06.028</doi><orcidid>https://orcid.org/0000-0002-5969-4778</orcidid><orcidid>https://orcid.org/0000-0001-5948-3092</orcidid><orcidid>https://orcid.org/0000-0002-8274-6564</orcidid><orcidid>https://orcid.org/0000-0002-3630-057X</orcidid><orcidid>https://orcid.org/0000-0002-7843-2351</orcidid><orcidid>https://orcid.org/0000-0001-5142-1997</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals antennal lobe circadian clock Connectome connectomics Drosophila Drosophila melanogaster - physiology Female hygrosensation lateral accessory calyx lateral horn mushroom body Neurons - cytology Neurons - metabolism Neuropil - metabolism Olfactory Pathways projection neuron Sensory Receptor Cells - metabolism Synapses - physiology Thermoreceptors - metabolism thermosensation |
title | Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain |
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