Flying on empty: Reduced mitochondrial function and flight capacity in food-deprived monarch butterflies.

K. Niitepõld, Hailey A. Parry, Natalie R. Harris, A. Appel, J. D. de Roode, A. Kavazis, W. Hood
{"title":"Flying on empty: Reduced mitochondrial function and flight capacity in food-deprived monarch butterflies.","authors":"K. Niitepõld, Hailey A. Parry, Natalie R. Harris, A. Appel, J. D. de Roode, A. Kavazis, W. Hood","doi":"10.1242/jeb.244431","DOIUrl":null,"url":null,"abstract":"Mitochondrial function is fundamental to organismal performance, health, and fitness - especially during energetically challenging events, such as migration. With this investigation, we evaluated mitochondrial sensitivity to ecologically relevant stressors. We focused on an iconic migrant, the North American monarch butterfly (Danaus plexippus), and examined the effects of two stressors: seven days of food deprivation, and infection by the protozoan parasite Ophryocystis elektroscirrha (known to reduce survival and flight performance). We measured whole-animal resting (RMR) and peak flight metabolic rate, and mitochondrial respiration of isolated mitochondria from the flight muscles. Food deprivation reduced mass-independent RMR and peak flight metabolic rate, whereas infection did not. Fed monarchs used mainly lipids in flight (respiratory quotient 0.73), but the respiratory quotient dropped in food-deprived individuals, possibly indicating switching to alternative energy sources, such as ketone bodies. Food deprivation decreased mitochondrial maximum oxygen consumption but not basal respiration, resulting in lower respiratory control ratio (RCR). Furthermore, food deprivation decreased mitochondrial complex III activity, but increased complex IV activity. Infection did not result in any changes in these mitochondrial variables. Mitochondrial maximum respiration rate correlated positively with mass-independent RMR and flight metabolic rate, suggesting a link between mitochondria and whole-animal performance. In conclusion, low food availability negatively affects mitochondrial function and flight performance, with potential implications on migration, fitness, and population dynamics. Although previous studies have reported poor flight performance in infected monarchs, we found no differences in physiological performance, suggesting that reduced flight capacity may be due to structural differences or low energy stores.","PeriodicalId":22458,"journal":{"name":"THE EGYPTIAN JOURNAL OF EXPERIMENTAL BIOLOGY","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"THE EGYPTIAN JOURNAL OF EXPERIMENTAL BIOLOGY","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1242/jeb.244431","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Mitochondrial function is fundamental to organismal performance, health, and fitness - especially during energetically challenging events, such as migration. With this investigation, we evaluated mitochondrial sensitivity to ecologically relevant stressors. We focused on an iconic migrant, the North American monarch butterfly (Danaus plexippus), and examined the effects of two stressors: seven days of food deprivation, and infection by the protozoan parasite Ophryocystis elektroscirrha (known to reduce survival and flight performance). We measured whole-animal resting (RMR) and peak flight metabolic rate, and mitochondrial respiration of isolated mitochondria from the flight muscles. Food deprivation reduced mass-independent RMR and peak flight metabolic rate, whereas infection did not. Fed monarchs used mainly lipids in flight (respiratory quotient 0.73), but the respiratory quotient dropped in food-deprived individuals, possibly indicating switching to alternative energy sources, such as ketone bodies. Food deprivation decreased mitochondrial maximum oxygen consumption but not basal respiration, resulting in lower respiratory control ratio (RCR). Furthermore, food deprivation decreased mitochondrial complex III activity, but increased complex IV activity. Infection did not result in any changes in these mitochondrial variables. Mitochondrial maximum respiration rate correlated positively with mass-independent RMR and flight metabolic rate, suggesting a link between mitochondria and whole-animal performance. In conclusion, low food availability negatively affects mitochondrial function and flight performance, with potential implications on migration, fitness, and population dynamics. Although previous studies have reported poor flight performance in infected monarchs, we found no differences in physiological performance, suggesting that reduced flight capacity may be due to structural differences or low energy stores.
空飞:缺乏食物的帝王蝶线粒体功能和飞行能力降低。
线粒体功能是机体性能、健康和适应性的基础,尤其是在具有能量挑战性的事件中,如迁徙。通过这项研究,我们评估了线粒体对生态相关应激源的敏感性。我们以一种标志性的迁徙动物——北美帝王蝶(Danaus plexippus)为研究对象,研究了两种压力源的影响:七天的食物剥夺,以及被原生动物寄生虫电斑蝶(Ophryocystis elektroscirrha)感染(已知会降低生存和飞行性能)。我们测量了全动物静息(RMR)和峰值飞行代谢率,以及从飞行肌肉中分离的线粒体的线粒体呼吸。食物剥夺降低了与质量无关的RMR和峰值飞行代谢率,而感染没有。进食的黑脉金斑蝶在飞行中主要使用脂质(呼吸商0.73),但缺乏食物的黑脉金斑蝶的呼吸商下降,这可能表明它们转向了替代能源,比如酮体。食物剥夺降低了线粒体最大耗氧量,但没有降低基础呼吸,导致呼吸控制比(RCR)降低。此外,食物剥夺降低了线粒体复合体III的活性,但增加了复合体IV的活性。感染没有导致这些线粒体变量的任何变化。线粒体最大呼吸速率与质量无关的RMR和飞行代谢率呈正相关,表明线粒体与全动物生产性能之间存在联系。总之,低食物供应会对线粒体功能和飞行性能产生负面影响,对迁徙、适应性和种群动态有潜在影响。虽然以前的研究报道了受感染的黑脉金斑蝶的飞行表现不佳,但我们发现生理表现没有差异,这表明飞行能力下降可能是由于结构差异或能量储存不足。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信