• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

无细胞铜绿微囊藻培养基影响大型溞的生存和应激反应。

Cell free Microcystis aeruginosa spent medium affects Daphnia magna survival and stress response.

作者信息

Bojadzija Savic Gorenka, Colinet Hervé, Bormans Myriam, Edwards Christine, Lawton Linda A, Briand Enora, Wiegand Claudia

机构信息

UMR ECOBIO, 6553 CNRS, Université de Rennes 1, Campus de Beaulieu, Rennes, France.

School of Pharmacy and Life Sciences, Robert Gordon University, Aberdeen, AB10 7GJ, United Kingdom.

出版信息

Toxicon. 2021 May;195:37-47. doi: 10.1016/j.toxicon.2021.03.009. Epub 2021 Mar 11.

DOI:10.1016/j.toxicon.2021.03.009
PMID:33716069
Abstract

Primary consumers in freshwater ecosystems, such as the zooplankton organism Daphnia magna, are highly affected by cyanobacteria, both as they may use it as a food source but also by cyanobacterial metabolites present in the water. Here, we investigate the impacts of cyanobacterial metabolites focussing on the environmental realistic scenario of the naturally released mixture without crushing cyanobacterial cells or their uptake as food. Therefore, D. magna were exposed to two concentrations of cell free cyanobacterial spent medium from Microcystis aeruginosa PCC 7806 to represent higher and lower ecologically-relevant concentrations of cyanobacterial metabolites. Including microcystin-LR, 11 metabolites have been detected of which 5 were quantified. Hypothesising concentration and time dependent negative impact, survival, gene expression marking digestion and metabolism, oxidative stress response, cell cycle and molting as well as activities of detoxification and antioxidant enzymes were followed for 7 days. D. magna suffered from oxidative stress as both catalase and glutathione S-transferase enzyme activities significantly decreased, suggesting enzyme exhaustibility after 3 and 7 days. Moreover, gene-expressions of the 4 stress markers (glutathione S-transferase, glutathione peroxidase, catalase and thioredoxin) were merely downregulated after 7 days of exposure. Energy allocation (expression of glyceraldehyde-3-phosphate dehydrogenase) was increased after 3 days but decreased as well after 7 days exposure. Cell cycle was impacted time dependently but differently by the two concentrations, along with an increasing downregulation of myosin heavy chain responsible for cell arrangement and muscular movements. Deregulation of nuclear hormone receptor genes indicate that D. magna hormonal steering including molting seemed impaired despite no detection of microviridin J in the extracts. As a consequence of all those responses and presumably of more than investigated molecular and physiological changes, D. magna survival was impaired over time, in a concentration dependent manner. Our results confirm that besides microcystin-LR, other secondary metabolites contribute to negative impact on D. magna survival and stress response.

摘要

淡水生态系统中的初级消费者,如浮游动物大型溞,会受到蓝藻的严重影响,这既体现在它们可能将蓝藻作为食物来源,也体现在水中存在的蓝藻代谢产物上。在此,我们聚焦于自然释放的混合物这一环境现实情景,研究蓝藻代谢产物的影响,该情景不涉及破碎蓝藻细胞或其作为食物被摄取。因此,大型溞暴露于两种浓度的来自铜绿微囊藻PCC 7806的无细胞蓝藻用过的培养基中,以代表蓝藻代谢产物在生态上相关的较高和较低浓度。包括微囊藻毒素-LR在内,已检测到11种代谢产物,其中5种被定量。假设存在浓度和时间依赖性的负面影响,对大型溞的生存、标记消化和代谢的基因表达、氧化应激反应、细胞周期和蜕皮以及解毒和抗氧化酶的活性进行了7天的跟踪研究。大型溞遭受氧化应激,因为过氧化氢酶和谷胱甘肽S-转移酶的酶活性均显著降低,这表明在3天和7天后酶已耗尽。此外,在暴露7天后,4种应激标记物(谷胱甘肽S-转移酶、谷胱甘肽过氧化物酶、过氧化氢酶和硫氧还蛋白)的基因表达仅被下调。能量分配(3-磷酸甘油醛脱氢酶的表达)在3天后增加,但在暴露7天后也下降。细胞周期受到时间依赖性影响,但两种浓度的影响不同,同时负责细胞排列和肌肉运动的肌球蛋白重链的下调也在增加。核激素受体基因失调表明,尽管提取物中未检测到微病毒素J,但大型溞的激素调控(包括蜕皮)似乎受到了损害。由于所有这些反应以及可能还有更多未研究的分子和生理变化,大型溞的生存随着时间的推移受到损害,且呈浓度依赖性。我们的结果证实,除了微囊藻毒素-LR外,其他次生代谢产物也会对大型溞的生存和应激反应产生负面影响。

相似文献

1
Cell free Microcystis aeruginosa spent medium affects Daphnia magna survival and stress response.无细胞铜绿微囊藻培养基影响大型溞的生存和应激反应。
Toxicon. 2021 May;195:37-47. doi: 10.1016/j.toxicon.2021.03.009. Epub 2021 Mar 11.
2
Cross talk: Two way allelopathic interactions between toxic Microcystis and Daphnia.交流:产毒微囊藻与水蚤之间的双向化感相互作用。
Harmful Algae. 2020 Apr;94:101803. doi: 10.1016/j.hal.2020.101803. Epub 2020 Apr 25.
3
Exudates Impact Physiological and Metabolic Changes in .渗出物影响生理和代谢变化。
Toxins (Basel). 2019 Jul 19;11(7):421. doi: 10.3390/toxins11070421.
4
Stress-responsive expression of a glutathione S-transferase (delta) gene in waterflea Daphnia magna challenged by microcystin-producing and microcystin-free Microcystis aeruginosa.胁迫应答型谷胱甘肽 S-转移酶(δ)基因在受产微囊藻和非产微囊藻铜绿微囊藻胁迫的水蚤中的表达。
Harmful Algae. 2016 Jun;56:1-8. doi: 10.1016/j.hal.2016.04.009. Epub 2016 May 16.
5
Target gene approaches: Gene expression in Daphnia magna exposed to predator-borne kairomones or to microcystin-producing and microcystin-free Microcystis aeruginosa.靶标基因方法:溞属大型溞在接触到捕食者释放的信息素或产生和不产生微囊藻毒素的铜绿微囊藻时的基因表达。
BMC Genomics. 2009 Nov 16;10:527. doi: 10.1186/1471-2164-10-527.
6
Chronic effects of cyanobacterial toxins on Daphnia magna and their offspring.淡水蓝藻毒素对大型溞及其后代的慢性效应。
Toxicon. 2010 Jun 15;55(7):1244-54. doi: 10.1016/j.toxicon.2010.01.014. Epub 2010 Feb 2.
7
Physiological interaction of Daphnia and Microcystis with regard to cyanobacterial secondary metabolites.关于蓝藻次生代谢物的溞类和微囊藻的生理相互作用。
Aquat Toxicol. 2014 Nov;156:96-105. doi: 10.1016/j.aquatox.2014.08.003. Epub 2014 Aug 17.
8
Age related acute effects of microcystin-LR on Daphnia magna biotransformation and oxidative stress.微囊藻毒素-LR 对大型溞生物转化和氧化应激的年龄相关急性效应。
Toxicon. 2010 Dec;56(8):1342-9. doi: 10.1016/j.toxicon.2010.07.020. Epub 2010 Aug 6.
9
Response of Daphnia's antioxidant system to spatial heterogeneity in Cyanobacteria concentrations in a lowland reservoir.低地水库中大型溞抗氧化系统对蓝藻浓度空间异质性的响应
PLoS One. 2014 Nov 7;9(11):e112597. doi: 10.1371/journal.pone.0112597. eCollection 2014.
10
Dietary exposure of Daphnia to microcystins: no in vivo relevance of biotransformation.摄食微囊藻毒素的水蚤:生物转化无体内相关性。
Aquat Toxicol. 2014 May;150:73-82. doi: 10.1016/j.aquatox.2014.02.017. Epub 2014 Mar 4.