White-nose syndrome increases torpid metabolic rate and evaporative water loss in hibernating bats
Fungal diseases of wildlife typically manifest as superficial skin infections but can have devastating consequences for host physiology and survival. White-nose syndrome (WNS) is a fungal skin disease that has killed millions of hibernating bats in North America since 2007. Infection with the fungus...
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Veröffentlicht in: | American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2017-12, Vol.313 (6), p.R680-R686 |
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creator | McGuire, Liam P Mayberry, Heather W Willis, Craig K R |
description | Fungal diseases of wildlife typically manifest as superficial skin infections but can have devastating consequences for host physiology and survival. White-nose syndrome (WNS) is a fungal skin disease that has killed millions of hibernating bats in North America since 2007. Infection with the fungus
causes bats to rewarm too often during hibernation, but the cause of increased arousal rates remains unknown. On the basis of data from studies of captive and free-living bats, two mechanistic models have been proposed to explain disease processes in WNS. Key predictions of both models are that WNS-affected bats will show
) higher metabolic rates during torpor (TMR) and
) higher rates of evaporative water loss (EWL). We collected bats from a WNS-negative hibernaculum, inoculated one group with
, and sham-inoculated a second group as controls. After 4 mo of hibernation, TMR and EWL were measured using respirometry. Both predictions were supported, and our data suggest that infected bats were more affected by variation in ambient humidity than controls. Furthermore, disease severity, as indicated by the area of the wing with UV fluorescence, was positively correlated with EWL, but not TMR. Our results provide the first direct evidence that heightened energy expenditure during torpor and higher EWL independently contribute to WNS pathophysiology, with implications for the design of potential treatments for the disease. |
doi_str_mv | 10.1152/ajpregu.00058.2017 |
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causes bats to rewarm too often during hibernation, but the cause of increased arousal rates remains unknown. On the basis of data from studies of captive and free-living bats, two mechanistic models have been proposed to explain disease processes in WNS. Key predictions of both models are that WNS-affected bats will show
) higher metabolic rates during torpor (TMR) and
) higher rates of evaporative water loss (EWL). We collected bats from a WNS-negative hibernaculum, inoculated one group with
, and sham-inoculated a second group as controls. After 4 mo of hibernation, TMR and EWL were measured using respirometry. Both predictions were supported, and our data suggest that infected bats were more affected by variation in ambient humidity than controls. Furthermore, disease severity, as indicated by the area of the wing with UV fluorescence, was positively correlated with EWL, but not TMR. Our results provide the first direct evidence that heightened energy expenditure during torpor and higher EWL independently contribute to WNS pathophysiology, with implications for the design of potential treatments for the disease.</description><identifier>ISSN: 0363-6119</identifier><identifier>EISSN: 1522-1490</identifier><identifier>DOI: 10.1152/ajpregu.00058.2017</identifier><identifier>PMID: 28835446</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animal diseases ; Animals ; Arousal ; Ascomycota - classification ; Ascomycota - pathogenicity ; Bats ; Body Temperature Regulation ; Chiroptera ; Chiroptera - metabolism ; Chiroptera - microbiology ; Correlation analysis ; Dermatomycoses - metabolism ; Dermatomycoses - microbiology ; Dermatomycoses - physiopathology ; Dermatomycoses - veterinary ; Disease control ; Energy expenditure ; Energy Metabolism ; Environment ; Fluorescence ; Fungal diseases ; Fungi ; Hibernation ; Humidity ; Infections ; Male ; Mathematical models ; Medical treatment ; Metabolic rate ; Nose ; Respirometry ; Severity of Illness Index ; Skin diseases ; Therapeutic applications ; Time Factors ; Torpor ; Up-Regulation ; Water loss ; Water Loss, Insensible ; White-nose syndrome ; Wildlife</subject><ispartof>American journal of physiology. Regulatory, integrative and comparative physiology, 2017-12, Vol.313 (6), p.R680-R686</ispartof><rights>Copyright © 2017 the American Physiological Society.</rights><rights>Copyright American Physiological Society Dec 2017</rights><rights>Copyright © 2017 the American Physiological Society 2017 American Physiological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-ff5ab070081a089f284e0de8fd0d5f4e9b77aa12b82be891b746013c8a2a52133</citedby><cites>FETCH-LOGICAL-c430t-ff5ab070081a089f284e0de8fd0d5f4e9b77aa12b82be891b746013c8a2a52133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,3037,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28835446$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McGuire, Liam P</creatorcontrib><creatorcontrib>Mayberry, Heather W</creatorcontrib><creatorcontrib>Willis, Craig K R</creatorcontrib><title>White-nose syndrome increases torpid metabolic rate and evaporative water loss in hibernating bats</title><title>American journal of physiology. Regulatory, integrative and comparative physiology</title><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><description>Fungal diseases of wildlife typically manifest as superficial skin infections but can have devastating consequences for host physiology and survival. White-nose syndrome (WNS) is a fungal skin disease that has killed millions of hibernating bats in North America since 2007. Infection with the fungus
causes bats to rewarm too often during hibernation, but the cause of increased arousal rates remains unknown. On the basis of data from studies of captive and free-living bats, two mechanistic models have been proposed to explain disease processes in WNS. Key predictions of both models are that WNS-affected bats will show
) higher metabolic rates during torpor (TMR) and
) higher rates of evaporative water loss (EWL). We collected bats from a WNS-negative hibernaculum, inoculated one group with
, and sham-inoculated a second group as controls. After 4 mo of hibernation, TMR and EWL were measured using respirometry. Both predictions were supported, and our data suggest that infected bats were more affected by variation in ambient humidity than controls. Furthermore, disease severity, as indicated by the area of the wing with UV fluorescence, was positively correlated with EWL, but not TMR. Our results provide the first direct evidence that heightened energy expenditure during torpor and higher EWL independently contribute to WNS pathophysiology, with implications for the design of potential treatments for the disease.</description><subject>Animal diseases</subject><subject>Animals</subject><subject>Arousal</subject><subject>Ascomycota - classification</subject><subject>Ascomycota - pathogenicity</subject><subject>Bats</subject><subject>Body Temperature Regulation</subject><subject>Chiroptera</subject><subject>Chiroptera - metabolism</subject><subject>Chiroptera - microbiology</subject><subject>Correlation analysis</subject><subject>Dermatomycoses - metabolism</subject><subject>Dermatomycoses - microbiology</subject><subject>Dermatomycoses - physiopathology</subject><subject>Dermatomycoses - veterinary</subject><subject>Disease control</subject><subject>Energy expenditure</subject><subject>Energy Metabolism</subject><subject>Environment</subject><subject>Fluorescence</subject><subject>Fungal diseases</subject><subject>Fungi</subject><subject>Hibernation</subject><subject>Humidity</subject><subject>Infections</subject><subject>Male</subject><subject>Mathematical models</subject><subject>Medical treatment</subject><subject>Metabolic rate</subject><subject>Nose</subject><subject>Respirometry</subject><subject>Severity of Illness Index</subject><subject>Skin diseases</subject><subject>Therapeutic applications</subject><subject>Time Factors</subject><subject>Torpor</subject><subject>Up-Regulation</subject><subject>Water loss</subject><subject>Water Loss, Insensible</subject><subject>White-nose syndrome</subject><subject>Wildlife</subject><issn>0363-6119</issn><issn>1522-1490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc1u1DAUhS0EotPCC7BAltiwyeDfxNkgoQoKUiU2IJbWdXIz41FiBzuZqm-Phw4VsLLs852je30IecXZlnMt3sFhTrhbt4wxbbaC8eYJ2RRBVFy17CnZMFnLqua8vSCXOR8Kp6SSz8mFMEZqpeoNcT_2fsEqxIw034c-xQmpD11CyJjpEtPsezrhAi6OvqMJFqQQeopHmGO5-SPSu_KY6BhzLla69w5TKErYUQdLfkGeDTBmfHk-r8j3Tx-_XX-ubr_efLn-cFt1SrKlGgYNjjWMGQ7MtIMwClmPZuhZrweFrWsaAC6cEQ5Ny12jasZlZ0CAFlzKK_L-IXde3YR9h2FJMNo5-QnSvY3g7b9K8Hu7i0erDVd1a0rA23NAij9XzIudfO5wHCFgXLPlrRS81oY1BX3zH3qIa1l6PFFG8EYb0xZKPFBdKn-TcHgchjN7qtCeK7S_K7SnCovp9d9rPFr-dCZ_Aagjm1w</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>McGuire, Liam P</creator><creator>Mayberry, Heather W</creator><creator>Willis, Craig K R</creator><general>American Physiological Society</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>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171201</creationdate><title>White-nose syndrome increases torpid metabolic rate and evaporative water loss in hibernating bats</title><author>McGuire, Liam P ; Mayberry, Heather W ; Willis, Craig K R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-ff5ab070081a089f284e0de8fd0d5f4e9b77aa12b82be891b746013c8a2a52133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animal diseases</topic><topic>Animals</topic><topic>Arousal</topic><topic>Ascomycota - classification</topic><topic>Ascomycota - pathogenicity</topic><topic>Bats</topic><topic>Body Temperature Regulation</topic><topic>Chiroptera</topic><topic>Chiroptera - metabolism</topic><topic>Chiroptera - microbiology</topic><topic>Correlation analysis</topic><topic>Dermatomycoses - metabolism</topic><topic>Dermatomycoses - microbiology</topic><topic>Dermatomycoses - physiopathology</topic><topic>Dermatomycoses - veterinary</topic><topic>Disease control</topic><topic>Energy expenditure</topic><topic>Energy Metabolism</topic><topic>Environment</topic><topic>Fluorescence</topic><topic>Fungal diseases</topic><topic>Fungi</topic><topic>Hibernation</topic><topic>Humidity</topic><topic>Infections</topic><topic>Male</topic><topic>Mathematical models</topic><topic>Medical treatment</topic><topic>Metabolic rate</topic><topic>Nose</topic><topic>Respirometry</topic><topic>Severity of Illness Index</topic><topic>Skin diseases</topic><topic>Therapeutic applications</topic><topic>Time Factors</topic><topic>Torpor</topic><topic>Up-Regulation</topic><topic>Water loss</topic><topic>Water Loss, Insensible</topic><topic>White-nose syndrome</topic><topic>Wildlife</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McGuire, Liam P</creatorcontrib><creatorcontrib>Mayberry, Heather W</creatorcontrib><creatorcontrib>Willis, Craig K R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McGuire, Liam P</au><au>Mayberry, Heather W</au><au>Willis, Craig K R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>White-nose syndrome increases torpid metabolic rate and evaporative water loss in hibernating bats</atitle><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>313</volume><issue>6</issue><spage>R680</spage><epage>R686</epage><pages>R680-R686</pages><issn>0363-6119</issn><eissn>1522-1490</eissn><abstract>Fungal diseases of wildlife typically manifest as superficial skin infections but can have devastating consequences for host physiology and survival. White-nose syndrome (WNS) is a fungal skin disease that has killed millions of hibernating bats in North America since 2007. Infection with the fungus
causes bats to rewarm too often during hibernation, but the cause of increased arousal rates remains unknown. On the basis of data from studies of captive and free-living bats, two mechanistic models have been proposed to explain disease processes in WNS. Key predictions of both models are that WNS-affected bats will show
) higher metabolic rates during torpor (TMR) and
) higher rates of evaporative water loss (EWL). We collected bats from a WNS-negative hibernaculum, inoculated one group with
, and sham-inoculated a second group as controls. After 4 mo of hibernation, TMR and EWL were measured using respirometry. Both predictions were supported, and our data suggest that infected bats were more affected by variation in ambient humidity than controls. Furthermore, disease severity, as indicated by the area of the wing with UV fluorescence, was positively correlated with EWL, but not TMR. Our results provide the first direct evidence that heightened energy expenditure during torpor and higher EWL independently contribute to WNS pathophysiology, with implications for the design of potential treatments for the disease.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>28835446</pmid><doi>10.1152/ajpregu.00058.2017</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animal diseases Animals Arousal Ascomycota - classification Ascomycota - pathogenicity Bats Body Temperature Regulation Chiroptera Chiroptera - metabolism Chiroptera - microbiology Correlation analysis Dermatomycoses - metabolism Dermatomycoses - microbiology Dermatomycoses - physiopathology Dermatomycoses - veterinary Disease control Energy expenditure Energy Metabolism Environment Fluorescence Fungal diseases Fungi Hibernation Humidity Infections Male Mathematical models Medical treatment Metabolic rate Nose Respirometry Severity of Illness Index Skin diseases Therapeutic applications Time Factors Torpor Up-Regulation Water loss Water Loss, Insensible White-nose syndrome Wildlife |
title | White-nose syndrome increases torpid metabolic rate and evaporative water loss in hibernating bats |
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