水传播的亚致死暴露于全氟丁烷磺酸会导致小蝌蚪肠道生态失调

IF 5.1 Q1 ENVIRONMENTAL SCIENCES
Yilin Shu , Luting Wei , Huiling Jiang , Wenchao Wang , Huijuan Zhang , Lizhu Tang , Jun He , Kanghua Jiang , Hailong Wu , Lianguo Chen
{"title":"水传播的亚致死暴露于全氟丁烷磺酸会导致小蝌蚪肠道生态失调","authors":"Yilin Shu ,&nbsp;Luting Wei ,&nbsp;Huiling Jiang ,&nbsp;Wenchao Wang ,&nbsp;Huijuan Zhang ,&nbsp;Lizhu Tang ,&nbsp;Jun He ,&nbsp;Kanghua Jiang ,&nbsp;Hailong Wu ,&nbsp;Lianguo Chen","doi":"10.1016/j.watbs.2022.100075","DOIUrl":null,"url":null,"abstract":"<div><p>Perfluorobutanesulfonate (PFBS) is a ubiquitous pollutant in the aquatic environment, but its toxic effects and mechanisms on amphibian species remain largely unknown. In the present study, tadpoles (<em>Lithobates catesbeianus</em>) were exposed to various concentrations of PFBS (0, 1, 3, 10, and 30 ​μg/L) for 14 days, with the goal of unveiling the impairment of intestinal health. Histopathological examination showed that sub-lethal exposure of tadpoles to PFBS at concentrations as low as 3 ​μg/L could result in the injury of intestinal structures. In a clear concentration-dependent manner, the expressions of epithelial barrier components (i.e., <em>Claudin 1</em> gene and tight junction protein 2) were significantly decreased in PFBS-exposed intestines, while the intestinal content of lipopolysaccharide (LPS) and transcriptions of downstream responsive genes (e.g., <em>TLR4</em>, <em>MyD88</em>, and <em>NF-κB</em>) were concurrently significantly increased by exposure to 3, 10, and 30 ​μg/L of PFBS. As a consequence, the number of eosinophils and expression of pro-inflammatory cytokines (e.g., IL-1β and <em>TNF-α</em>) were increased therein. Furthermore, PFBS exposure induced oxidative stress in intestinal tissues by increasing the level of reactive oxygen species (ROS) and suppressing antioxidant capacity. The transcriptional levels of <em>CytoC</em> and <em>Bax</em> genes as well as activities of caspase 9 and caspase 3 enzymes were remarkably increased, while the transcript abundance of <em>Bcl-2</em> was down-regulated significantly after PFBS exposure, thereby favoring apoptosis in tadpole intestines. PFBS sub-lethal exposure also drove the composition of intestinal microbiota to a dysbiosis status. Correlation analysis further revealed that the relative abundance of members of the genus <em>Bosea</em> was positively related with the contents of LPS and IL-1β. Overall, the present study provides the first evidence for pronounced impacts of PFBS on amphibian intestinal ecology, highlighting the susceptibility of tadpoles to the environmental risks of PFBS.</p></div>","PeriodicalId":101277,"journal":{"name":"Water Biology and Security","volume":null,"pages":null},"PeriodicalIF":5.1000,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772735122000981/pdfft?md5=69d2ced274595adf9966217d153ed49b&pid=1-s2.0-S2772735122000981-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Waterborne sub-lethal exposure to perfluorobutanesulfonate causes intestinal dysbiosis in tadpoles of Lithobates catesbeianus\",\"authors\":\"Yilin Shu ,&nbsp;Luting Wei ,&nbsp;Huiling Jiang ,&nbsp;Wenchao Wang ,&nbsp;Huijuan Zhang ,&nbsp;Lizhu Tang ,&nbsp;Jun He ,&nbsp;Kanghua Jiang ,&nbsp;Hailong Wu ,&nbsp;Lianguo Chen\",\"doi\":\"10.1016/j.watbs.2022.100075\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Perfluorobutanesulfonate (PFBS) is a ubiquitous pollutant in the aquatic environment, but its toxic effects and mechanisms on amphibian species remain largely unknown. In the present study, tadpoles (<em>Lithobates catesbeianus</em>) were exposed to various concentrations of PFBS (0, 1, 3, 10, and 30 ​μg/L) for 14 days, with the goal of unveiling the impairment of intestinal health. Histopathological examination showed that sub-lethal exposure of tadpoles to PFBS at concentrations as low as 3 ​μg/L could result in the injury of intestinal structures. In a clear concentration-dependent manner, the expressions of epithelial barrier components (i.e., <em>Claudin 1</em> gene and tight junction protein 2) were significantly decreased in PFBS-exposed intestines, while the intestinal content of lipopolysaccharide (LPS) and transcriptions of downstream responsive genes (e.g., <em>TLR4</em>, <em>MyD88</em>, and <em>NF-κB</em>) were concurrently significantly increased by exposure to 3, 10, and 30 ​μg/L of PFBS. As a consequence, the number of eosinophils and expression of pro-inflammatory cytokines (e.g., IL-1β and <em>TNF-α</em>) were increased therein. Furthermore, PFBS exposure induced oxidative stress in intestinal tissues by increasing the level of reactive oxygen species (ROS) and suppressing antioxidant capacity. The transcriptional levels of <em>CytoC</em> and <em>Bax</em> genes as well as activities of caspase 9 and caspase 3 enzymes were remarkably increased, while the transcript abundance of <em>Bcl-2</em> was down-regulated significantly after PFBS exposure, thereby favoring apoptosis in tadpole intestines. PFBS sub-lethal exposure also drove the composition of intestinal microbiota to a dysbiosis status. Correlation analysis further revealed that the relative abundance of members of the genus <em>Bosea</em> was positively related with the contents of LPS and IL-1β. Overall, the present study provides the first evidence for pronounced impacts of PFBS on amphibian intestinal ecology, highlighting the susceptibility of tadpoles to the environmental risks of PFBS.</p></div>\",\"PeriodicalId\":101277,\"journal\":{\"name\":\"Water Biology and Security\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2022-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2772735122000981/pdfft?md5=69d2ced274595adf9966217d153ed49b&pid=1-s2.0-S2772735122000981-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Water Biology and Security\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2772735122000981\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Water Biology and Security","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772735122000981","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

全氟丁烷磺酸(PFBS)是水生环境中普遍存在的污染物,但其对两栖动物的毒性作用及其机制仍不清楚。本研究将蝌蚪(Lithobates catesbeianus)暴露于不同浓度的PFBS(0、1、3、10和30 μg/L)中14天,目的是揭示对肠道健康的损害。组织病理学检查显示,低至3 μg/L浓度的PFBS可导致蝌蚪肠道结构损伤。暴露于3、10、30 μg/L的PFBS后,肠道上皮屏障成分(Claudin 1基因和紧密连接蛋白2)的表达明显降低,而肠道脂多糖(LPS)含量和下游应答基因(TLR4、MyD88、NF-κB)的转录量同时显著升高,呈明显的浓度依赖性。结果,嗜酸性粒细胞的数量和促炎细胞因子(如IL-1β和TNF-α)的表达增加。此外,PFBS暴露通过增加活性氧(ROS)水平和抑制抗氧化能力诱导肠道组织氧化应激。PFBS暴露后,蝌蚪肠道细胞c和Bax基因的转录水平以及caspase 9和caspase 3酶的活性显著升高,而Bcl-2的转录丰度显著下调,有利于蝌蚪肠道细胞凋亡。PFBS亚致死暴露也使肠道微生物群的组成处于生态失调状态。相关分析进一步表明,该属成员的相对丰度与脂多糖和IL-1β含量呈正相关。总体而言,本研究首次证明了PFBS对两栖动物肠道生态的显著影响,突出了蝌蚪对PFBS环境风险的易感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Waterborne sub-lethal exposure to perfluorobutanesulfonate causes intestinal dysbiosis in tadpoles of Lithobates catesbeianus

Waterborne sub-lethal exposure to perfluorobutanesulfonate causes intestinal dysbiosis in tadpoles of Lithobates catesbeianus

Perfluorobutanesulfonate (PFBS) is a ubiquitous pollutant in the aquatic environment, but its toxic effects and mechanisms on amphibian species remain largely unknown. In the present study, tadpoles (Lithobates catesbeianus) were exposed to various concentrations of PFBS (0, 1, 3, 10, and 30 ​μg/L) for 14 days, with the goal of unveiling the impairment of intestinal health. Histopathological examination showed that sub-lethal exposure of tadpoles to PFBS at concentrations as low as 3 ​μg/L could result in the injury of intestinal structures. In a clear concentration-dependent manner, the expressions of epithelial barrier components (i.e., Claudin 1 gene and tight junction protein 2) were significantly decreased in PFBS-exposed intestines, while the intestinal content of lipopolysaccharide (LPS) and transcriptions of downstream responsive genes (e.g., TLR4, MyD88, and NF-κB) were concurrently significantly increased by exposure to 3, 10, and 30 ​μg/L of PFBS. As a consequence, the number of eosinophils and expression of pro-inflammatory cytokines (e.g., IL-1β and TNF-α) were increased therein. Furthermore, PFBS exposure induced oxidative stress in intestinal tissues by increasing the level of reactive oxygen species (ROS) and suppressing antioxidant capacity. The transcriptional levels of CytoC and Bax genes as well as activities of caspase 9 and caspase 3 enzymes were remarkably increased, while the transcript abundance of Bcl-2 was down-regulated significantly after PFBS exposure, thereby favoring apoptosis in tadpole intestines. PFBS sub-lethal exposure also drove the composition of intestinal microbiota to a dysbiosis status. Correlation analysis further revealed that the relative abundance of members of the genus Bosea was positively related with the contents of LPS and IL-1β. Overall, the present study provides the first evidence for pronounced impacts of PFBS on amphibian intestinal ecology, highlighting the susceptibility of tadpoles to the environmental risks of PFBS.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
4.10
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