Androgenic agricultural pollution suppresses immune function and alters reproductive allocation in eastern mosquitofish.

IF 2.5 3区 环境科学与生态学 Q2 BIODIVERSITY CONSERVATION
Conservation Physiology Pub Date : 2026-07-23 eCollection Date: 2026-01-01 DOI:10.1093/conphys/coag052
Upama Aich, Gabriel Melhado, Raiko Rafeeq, Morelia Camacho-Cervantes, Jack Manera, Bob B M Wong
{"title":"Androgenic agricultural pollution suppresses immune function and alters reproductive allocation in eastern mosquitofish.","authors":"Upama Aich, Gabriel Melhado, Raiko Rafeeq, Morelia Camacho-Cervantes, Jack Manera, Bob B M Wong","doi":"10.1093/conphys/coag052","DOIUrl":null,"url":null,"abstract":"<p><p>Anthropogenic pollution poses a serious threat to wildlife. Particularly concerning are endocrine-disrupting chemicals (EDCs) due to their ability to mimic or interfere with hormone signalling. Given the fundamental role of hormones in regulating immunity and reproduction, androgenic EDCs are predicted to impact immunocompetence and associated life-history trade-offs. Yet, despite their potency and environmental ubiquity, the effects of androgenic EDCs on immune function and reproductive allocation remain poorly understood. Here, we tested how exposure to the androgenic agricultural pollutant 17β-trenbolone affects immunity and reproductive investment in eastern mosquitofish (<i>Gambusia holbrooki</i>). Adult mosquitofish were exposed to environmentally relevant concentrations of trenbolone (control: 0 ng/l, low: 11 ± 2.9 ng/l, high: 101 ± 13.6 ng/l) for 45 days. Immune function was assessed using phytohaemagglutinin (PHA)-induced skin swelling, white blood cell (WBC) counts and neutrophil-lymphocyte ratio (NLR), while male reproductive investment was quantified by sperm production. Trenbolone exposure significantly impaired immunity, reducing PHA-induced swelling by ~25%, decreasing total WBC counts and increasing NLRs, a biomarker of inflammation and immune response. In contrast, trenbolone exposure increased sperm number, and we found an overall negative correlation between immune response and sperm production. Our findings highlight how androgenic pollutants can simultaneously compromise immunity and alter reproductive allocation, enforcing evolutionary trade-offs that could negatively affect individual fitness and population resilience in contaminated environments.</p>","PeriodicalId":54331,"journal":{"name":"Conservation Physiology","volume":"14 1","pages":"coag052"},"PeriodicalIF":2.5000,"publicationDate":"2026-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13397028/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Conservation Physiology","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1093/conphys/coag052","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"BIODIVERSITY CONSERVATION","Score":null,"Total":0}
引用次数: 0

Abstract

Anthropogenic pollution poses a serious threat to wildlife. Particularly concerning are endocrine-disrupting chemicals (EDCs) due to their ability to mimic or interfere with hormone signalling. Given the fundamental role of hormones in regulating immunity and reproduction, androgenic EDCs are predicted to impact immunocompetence and associated life-history trade-offs. Yet, despite their potency and environmental ubiquity, the effects of androgenic EDCs on immune function and reproductive allocation remain poorly understood. Here, we tested how exposure to the androgenic agricultural pollutant 17β-trenbolone affects immunity and reproductive investment in eastern mosquitofish (Gambusia holbrooki). Adult mosquitofish were exposed to environmentally relevant concentrations of trenbolone (control: 0 ng/l, low: 11 ± 2.9 ng/l, high: 101 ± 13.6 ng/l) for 45 days. Immune function was assessed using phytohaemagglutinin (PHA)-induced skin swelling, white blood cell (WBC) counts and neutrophil-lymphocyte ratio (NLR), while male reproductive investment was quantified by sperm production. Trenbolone exposure significantly impaired immunity, reducing PHA-induced swelling by ~25%, decreasing total WBC counts and increasing NLRs, a biomarker of inflammation and immune response. In contrast, trenbolone exposure increased sperm number, and we found an overall negative correlation between immune response and sperm production. Our findings highlight how androgenic pollutants can simultaneously compromise immunity and alter reproductive allocation, enforcing evolutionary trade-offs that could negatively affect individual fitness and population resilience in contaminated environments.

雄激素农业污染抑制东部食蚊鱼的免疫功能并改变其生殖分配。
人为污染对野生动物构成严重威胁。特别值得关注的是内分泌干扰化学物质(EDCs),因为它们能够模仿或干扰激素信号。鉴于激素在调节免疫和生殖方面的基本作用,预计雄激素EDCs会影响免疫能力和相关的生活史权衡。然而,尽管它们的效力和环境无处不在,雄激素EDCs对免疫功能和生殖分配的影响仍然知之甚少。在这里,我们测试了暴露于雄激素农业污染物17β-trenbolone如何影响东方蚊鱼(Gambusia holbrooki)的免疫和生殖投资。将成蚊鱼暴露于环境相关浓度的trenbolone(对照:0 ng/l,低:11±2.9 ng/l,高:101±13.6 ng/l)中45 d。通过植物血凝素(PHA)诱导的皮肤肿胀、白细胞(WBC)计数和中性粒细胞-淋巴细胞比率(NLR)评估免疫功能,通过精子数量量化男性生殖投资。Trenbolone暴露显著降低免疫力,使pha诱导的肿胀减少约25%,减少WBC总数,增加NLRs(炎症和免疫反应的生物标志物)。相反,trenbolone暴露增加了精子数量,我们发现免疫反应和精子产生之间总体呈负相关。我们的研究结果强调了雄激素污染物如何同时损害免疫力和改变生殖分配,强制进化权衡,这可能会对污染环境中的个体健康和种群恢复力产生负面影响。
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
Conservation Physiology
Conservation Physiology Environmental Science-Management, Monitoring, Policy and Law
CiteScore
5.10
自引率
3.70%
发文量
71
审稿时长
11 weeks
期刊介绍: Conservation Physiology is an online only, fully open access journal published on behalf of the Society for Experimental Biology. Biodiversity across the globe faces a growing number of threats associated with human activities. Conservation Physiology will publish research on all taxa (microbes, plants and animals) focused on understanding and predicting how organisms, populations, ecosystems and natural resources respond to environmental change and stressors. Physiology is considered in the broadest possible terms to include functional and mechanistic responses at all scales. We also welcome research towards developing and refining strategies to rebuild populations, restore ecosystems, inform conservation policy, and manage living resources. We define conservation physiology broadly and encourage potential authors to contact the editorial team if they have any questions regarding the remit of the journal.
×
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:604180095
Book学术官方微信
小红书