The reproductive status determines tolerance and resistance to Mycobacterium marinum in Drosophila melanogaster.

IF 3.3 3区 医学 Q2 EVOLUTIONARY BIOLOGY Evolution, Medicine, and Public Health Pub Date : 2023-09-06 eCollection Date: 2023-01-01 DOI:10.1093/emph/eoad029
Marta Arch, Maria Vidal, Esther Fuentes, Anmaw Shite Abat, Pere-Joan Cardona
{"title":"The reproductive status determines tolerance and resistance to <i>Mycobacterium marinum</i> in <i>Drosophila melanogaster</i>.","authors":"Marta Arch,&nbsp;Maria Vidal,&nbsp;Esther Fuentes,&nbsp;Anmaw Shite Abat,&nbsp;Pere-Joan Cardona","doi":"10.1093/emph/eoad029","DOIUrl":null,"url":null,"abstract":"<p><p>Sex and reproductive status of the host have a major impact on the immune response against infection. Our aim was to understand their impact on host tolerance or resistance in the systemic <i>Mycobacterium marinum</i> infection of <i>Drosophila melanogaster</i>. We measured host survival and bacillary load at time of death, as well as expression by quantitative real-time polymerase chain reaction of immune genes (diptericin and drosomycin). We also assessed the impact of metabolic and hormonal regulation in the protection against infection by measuring expression of upd3, impl2 and ecR. Our data showed increased resistance in actively mating flies and in mated females, while reducing their tolerance to infection. Data suggests that Toll and immune deficiency (Imd) pathways determine tolerance and resistance, respectively, while higher basal levels of ecR favours the stimulation of the Imd pathway. A dual role has been found for upd3 expression, linked to increased/decreased mycobacterial load at the beginning and later in infection, respectively. Finally, impl2 expression has been related to increased resistance in non-actively mating males. These results allow further assessment on the differences between sexes and highlights the role of the reproductive status in <i>D. melanogaster</i> to face infections, demonstrating their importance to determine resistance and tolerance against <i>M. marinum</i> infection.</p>","PeriodicalId":12156,"journal":{"name":"Evolution, Medicine, and Public Health","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2023-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590161/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evolution, Medicine, and Public Health","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/emph/eoad029","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Sex and reproductive status of the host have a major impact on the immune response against infection. Our aim was to understand their impact on host tolerance or resistance in the systemic Mycobacterium marinum infection of Drosophila melanogaster. We measured host survival and bacillary load at time of death, as well as expression by quantitative real-time polymerase chain reaction of immune genes (diptericin and drosomycin). We also assessed the impact of metabolic and hormonal regulation in the protection against infection by measuring expression of upd3, impl2 and ecR. Our data showed increased resistance in actively mating flies and in mated females, while reducing their tolerance to infection. Data suggests that Toll and immune deficiency (Imd) pathways determine tolerance and resistance, respectively, while higher basal levels of ecR favours the stimulation of the Imd pathway. A dual role has been found for upd3 expression, linked to increased/decreased mycobacterial load at the beginning and later in infection, respectively. Finally, impl2 expression has been related to increased resistance in non-actively mating males. These results allow further assessment on the differences between sexes and highlights the role of the reproductive status in D. melanogaster to face infections, demonstrating their importance to determine resistance and tolerance against M. marinum infection.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
繁殖状态决定了黑腹果蝇对海洋分枝杆菌的耐受性和抗性。
宿主的性别和生殖状况对抵抗感染的免疫反应有重大影响。我们的目的是了解它们对果蝇系统性海洋分枝杆菌感染中宿主耐受性或耐药性的影响。我们测量了宿主存活率和死亡时的细菌载量,以及免疫基因(双tericin和drosomycin)的定量实时聚合酶链反应表达。我们还通过测量upd3、impl2和ecR的表达来评估代谢和激素调节对预防感染的影响。我们的数据显示,主动交配的苍蝇和交配的雌性苍蝇的抵抗力增加,同时降低了它们对感染的耐受力。数据表明,Toll和免疫缺陷(Imd)途径分别决定耐受性和耐药性,而较高的ecR基础水平有利于刺激Imd途径。已发现upd3表达的双重作用,分别与感染初期和后期分枝杆菌载量的增加/减少有关。最后,impl2的表达与非主动交配雄性的抗性增加有关。这些结果使人们能够进一步评估性别差异,并强调了繁殖状态在黑腹果蝇面对感染时的作用,证明了它们对确定对M.marinum感染的耐药性和耐受性的重要性。
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 去求助
来源期刊
Evolution, Medicine, and Public Health
Evolution, Medicine, and Public Health Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
5.40
自引率
2.70%
发文量
37
审稿时长
8 weeks
期刊介绍: About the Journal Founded by Stephen Stearns in 2013, Evolution, Medicine, and Public Health is an open access journal that publishes original, rigorous applications of evolutionary science to issues in medicine and public health. It aims to connect evolutionary biology with the health sciences to produce insights that may reduce suffering and save lives. Because evolutionary biology is a basic science that reaches across many disciplines, this journal is open to contributions on a broad range of topics.
期刊最新文献
Birth and household exposures are associated with changes to skin bacterial communities during infancy Low haemoglobin in arduous seasons is associated with reduced chance of ovulation among women living in the Bolivian altiplano Diagnostic testing and the evolution of detection avoidance by pathogens The Elephant and the Spandrel Coping with extreme heat: current exposure and implications for the future
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1