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A quantitative feeding assay in adult Drosophila reveals rapid modulation of food ingestion by its nutritional value
Food intake of the adult fruit fly Drosophila melanogaster, an intermittent feeder, is attributed to several behavioral elements including foraging, feeding initiation and termination, and food ingestion. Despite the development of various feeding assays in fruit flies, how each of these behavioral...
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Published in: | Molecular brain 2015-12, Vol.8 (87), p.87-87, Article 87 |
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description | Food intake of the adult fruit fly Drosophila melanogaster, an intermittent feeder, is attributed to several behavioral elements including foraging, feeding initiation and termination, and food ingestion. Despite the development of various feeding assays in fruit flies, how each of these behavioral elements, particularly food ingestion, is regulated remains largely uncharacterized.
To this end, we have developed a manual feeding (MAFE) assay that specifically measures food ingestion of an individual fly completely independent of the other behavioral elements. This assay reliably recapitulates the effects of known feeding modulators, and offers temporal resolution in the scale of seconds. Using this assay, we find that fruit flies can rapidly assess the nutritional value of sugars within 20-30 s, and increase the ingestion of nutritive sugars after prolonged periods of starvation. Two candidate nutrient sensors, SLC5A11 and Gr43a, are required for discriminating the nutritive sugars, D-glucose and D-fructose, from their non-nutritive enantiomers, respectively. This suggests that differential sensing mechanisms play a key role in determining food nutritional value.
Taken together, our MAFE assay offers a platform to specifically examine the regulation of food ingestion with excellent temporal resolution, and identifies a fast-acting neural mechanism that assesses food nutritional value and modulates food intake. |
doi_str_mv | 10.1186/s13041-015-0179-x |
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To this end, we have developed a manual feeding (MAFE) assay that specifically measures food ingestion of an individual fly completely independent of the other behavioral elements. This assay reliably recapitulates the effects of known feeding modulators, and offers temporal resolution in the scale of seconds. Using this assay, we find that fruit flies can rapidly assess the nutritional value of sugars within 20-30 s, and increase the ingestion of nutritive sugars after prolonged periods of starvation. Two candidate nutrient sensors, SLC5A11 and Gr43a, are required for discriminating the nutritive sugars, D-glucose and D-fructose, from their non-nutritive enantiomers, respectively. This suggests that differential sensing mechanisms play a key role in determining food nutritional value.
Taken together, our MAFE assay offers a platform to specifically examine the regulation of food ingestion with excellent temporal resolution, and identifies a fast-acting neural mechanism that assesses food nutritional value and modulates food intake.</description><identifier>ISSN: 1756-6606</identifier><identifier>EISSN: 1756-6606</identifier><identifier>DOI: 10.1186/s13041-015-0179-x</identifier><identifier>PMID: 26692189</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Animal Feed ; Animals ; Appetite Regulation - physiology ; Dextrose ; Drosophila melanogaster - genetics ; Drosophila melanogaster - physiology ; Drosophila Proteins - genetics ; Drosophila Proteins - physiology ; Dynamins - physiology ; Enantiomers ; Entomology - instrumentation ; Entomology - methods ; Feeding Behavior - physiology ; Food Deprivation ; Fructose ; Fructose - chemistry ; Fruit-flies ; Glucose ; Glucose - chemistry ; Health aspects ; Intestines - physiopathology ; Methodology ; Nutritive Value ; Receptors, Cell Surface - physiology ; Sodium-Glucose Transport Proteins - genetics ; Sodium-Glucose Transport Proteins - physiology ; Species Specificity ; Stereoisomerism ; TRPA1 Cation Channel ; TRPC Cation Channels - physiology</subject><ispartof>Molecular brain, 2015-12, Vol.8 (87), p.87-87, Article 87</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2015</rights><rights>Qi et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c630t-2246dd4260570555c47a537683db2dc9c4d42b2c19a497ce1ee25d84a68c84f13</citedby><cites>FETCH-LOGICAL-c630t-2246dd4260570555c47a537683db2dc9c4d42b2c19a497ce1ee25d84a68c84f13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687088/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1779608724?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26692189$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qi, Wei</creatorcontrib><creatorcontrib>Yang, Zhe</creatorcontrib><creatorcontrib>Lin, Ziao</creatorcontrib><creatorcontrib>Park, Jin-Yong</creatorcontrib><creatorcontrib>Suh, Greg S B</creatorcontrib><creatorcontrib>Wang, Liming</creatorcontrib><title>A quantitative feeding assay in adult Drosophila reveals rapid modulation of food ingestion by its nutritional value</title><title>Molecular brain</title><addtitle>Mol Brain</addtitle><description>Food intake of the adult fruit fly Drosophila melanogaster, an intermittent feeder, is attributed to several behavioral elements including foraging, feeding initiation and termination, and food ingestion. Despite the development of various feeding assays in fruit flies, how each of these behavioral elements, particularly food ingestion, is regulated remains largely uncharacterized.
To this end, we have developed a manual feeding (MAFE) assay that specifically measures food ingestion of an individual fly completely independent of the other behavioral elements. This assay reliably recapitulates the effects of known feeding modulators, and offers temporal resolution in the scale of seconds. Using this assay, we find that fruit flies can rapidly assess the nutritional value of sugars within 20-30 s, and increase the ingestion of nutritive sugars after prolonged periods of starvation. Two candidate nutrient sensors, SLC5A11 and Gr43a, are required for discriminating the nutritive sugars, D-glucose and D-fructose, from their non-nutritive enantiomers, respectively. This suggests that differential sensing mechanisms play a key role in determining food nutritional value.
Taken together, our MAFE assay offers a platform to specifically examine the regulation of food ingestion with excellent temporal resolution, and identifies a fast-acting neural mechanism that assesses food nutritional value and modulates food intake.</description><subject>Animal Feed</subject><subject>Animals</subject><subject>Appetite Regulation - physiology</subject><subject>Dextrose</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila melanogaster - physiology</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - physiology</subject><subject>Dynamins - physiology</subject><subject>Enantiomers</subject><subject>Entomology - instrumentation</subject><subject>Entomology - methods</subject><subject>Feeding Behavior - physiology</subject><subject>Food Deprivation</subject><subject>Fructose</subject><subject>Fructose - chemistry</subject><subject>Fruit-flies</subject><subject>Glucose</subject><subject>Glucose - chemistry</subject><subject>Health aspects</subject><subject>Intestines - physiopathology</subject><subject>Methodology</subject><subject>Nutritive Value</subject><subject>Receptors, Cell Surface - physiology</subject><subject>Sodium-Glucose Transport Proteins - genetics</subject><subject>Sodium-Glucose Transport Proteins - physiology</subject><subject>Species Specificity</subject><subject>Stereoisomerism</subject><subject>TRPA1 Cation Channel</subject><subject>TRPC Cation Channels - physiology</subject><issn>1756-6606</issn><issn>1756-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptUk1v1DAQjRCIlsIP4IIsceGSYjv-ygVpVSggVeICZ8trT7ausvbWTlbtv2fSLaVFyLI8mnnvWTPzmuYto6eMGfWxso4K1lIm8eq-vXnWHDMtVasUVc8fxUfNq1qvKFVcMfmyOeJK9ZyZ_riZVuR6dmmKk5viHsgAEGLaEFeruyUxERfmcSKfS655dxlHRwrswY2VFLeLgWwz1pGaE8kDGXIOSNpAvcusUWGqJM1TiUvCjWTvxhleNy8GlIA39-9J8-v8y8-zb-3Fj6_fz1YXrVcdnVrOhQpBcEWlplJKL7STnVamC2sefO8FFtfcs96JXntgAFwGI5wy3oiBdSfNp4Publ5vIXhIU3Gj3ZW4deXWZhft00qKl3aT91Yoo6kxKPDhXqDk6xm7sttYPYyjS5DnanHATBjV9Rqh7_-BXuW5YMsLSveKGs3FX9TGjWBjGjL-6xdRuxKS4Vp6umid_geFJ8A2-pxgiJh_QmAHgsc91QLDQ4-M2sUq9mAVi1axi1XsDXLePR7OA-OPN7rf1366wA</recordid><startdate>20151221</startdate><enddate>20151221</enddate><creator>Qi, Wei</creator><creator>Yang, Zhe</creator><creator>Lin, Ziao</creator><creator>Park, Jin-Yong</creator><creator>Suh, Greg S B</creator><creator>Wang, Liming</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><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>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151221</creationdate><title>A quantitative feeding assay in adult Drosophila reveals rapid modulation of food ingestion by its nutritional value</title><author>Qi, Wei ; Yang, Zhe ; Lin, Ziao ; Park, Jin-Yong ; Suh, Greg S B ; Wang, Liming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c630t-2246dd4260570555c47a537683db2dc9c4d42b2c19a497ce1ee25d84a68c84f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animal Feed</topic><topic>Animals</topic><topic>Appetite Regulation - physiology</topic><topic>Dextrose</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - physiology</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - physiology</topic><topic>Dynamins - physiology</topic><topic>Enantiomers</topic><topic>Entomology - instrumentation</topic><topic>Entomology - methods</topic><topic>Feeding Behavior - physiology</topic><topic>Food Deprivation</topic><topic>Fructose</topic><topic>Fructose - chemistry</topic><topic>Fruit-flies</topic><topic>Glucose</topic><topic>Glucose - chemistry</topic><topic>Health aspects</topic><topic>Intestines - physiopathology</topic><topic>Methodology</topic><topic>Nutritive Value</topic><topic>Receptors, Cell Surface - physiology</topic><topic>Sodium-Glucose Transport Proteins - genetics</topic><topic>Sodium-Glucose Transport Proteins - physiology</topic><topic>Species Specificity</topic><topic>Stereoisomerism</topic><topic>TRPA1 Cation Channel</topic><topic>TRPC Cation Channels - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qi, Wei</creatorcontrib><creatorcontrib>Yang, Zhe</creatorcontrib><creatorcontrib>Lin, Ziao</creatorcontrib><creatorcontrib>Park, Jin-Yong</creatorcontrib><creatorcontrib>Suh, Greg S B</creatorcontrib><creatorcontrib>Wang, Liming</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Biological Science Journals</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular brain</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qi, Wei</au><au>Yang, Zhe</au><au>Lin, Ziao</au><au>Park, Jin-Yong</au><au>Suh, Greg S B</au><au>Wang, Liming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A quantitative feeding assay in adult Drosophila reveals rapid modulation of food ingestion by its nutritional value</atitle><jtitle>Molecular brain</jtitle><addtitle>Mol Brain</addtitle><date>2015-12-21</date><risdate>2015</risdate><volume>8</volume><issue>87</issue><spage>87</spage><epage>87</epage><pages>87-87</pages><artnum>87</artnum><issn>1756-6606</issn><eissn>1756-6606</eissn><abstract>Food intake of the adult fruit fly Drosophila melanogaster, an intermittent feeder, is attributed to several behavioral elements including foraging, feeding initiation and termination, and food ingestion. Despite the development of various feeding assays in fruit flies, how each of these behavioral elements, particularly food ingestion, is regulated remains largely uncharacterized.
To this end, we have developed a manual feeding (MAFE) assay that specifically measures food ingestion of an individual fly completely independent of the other behavioral elements. This assay reliably recapitulates the effects of known feeding modulators, and offers temporal resolution in the scale of seconds. Using this assay, we find that fruit flies can rapidly assess the nutritional value of sugars within 20-30 s, and increase the ingestion of nutritive sugars after prolonged periods of starvation. Two candidate nutrient sensors, SLC5A11 and Gr43a, are required for discriminating the nutritive sugars, D-glucose and D-fructose, from their non-nutritive enantiomers, respectively. This suggests that differential sensing mechanisms play a key role in determining food nutritional value.
Taken together, our MAFE assay offers a platform to specifically examine the regulation of food ingestion with excellent temporal resolution, and identifies a fast-acting neural mechanism that assesses food nutritional value and modulates food intake.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26692189</pmid><doi>10.1186/s13041-015-0179-x</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal Feed Animals Appetite Regulation - physiology Dextrose Drosophila melanogaster - genetics Drosophila melanogaster - physiology Drosophila Proteins - genetics Drosophila Proteins - physiology Dynamins - physiology Enantiomers Entomology - instrumentation Entomology - methods Feeding Behavior - physiology Food Deprivation Fructose Fructose - chemistry Fruit-flies Glucose Glucose - chemistry Health aspects Intestines - physiopathology Methodology Nutritive Value Receptors, Cell Surface - physiology Sodium-Glucose Transport Proteins - genetics Sodium-Glucose Transport Proteins - physiology Species Specificity Stereoisomerism TRPA1 Cation Channel TRPC Cation Channels - physiology |
title | A quantitative feeding assay in adult Drosophila reveals rapid modulation of food ingestion by its nutritional value |
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