淡水湿地地下沉积物反硝化厌氧甲烷氧化(DAMO)过程对典型喹诺酮类抗生素的响应机制

IF 6.1 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES
Ecotoxicology and Environmental Safety Pub Date : 2025-09-01 Epub Date: 2025-07-09 DOI:10.1016/j.ecoenv.2025.118624
Yuewen Zhao, Xinbo Zhang, Qichen Hao, Wenzhi Cao, Yuanjing Zhang, Chunlei Liu, Shengwei Cao, Yaci Liu, Yasong Li
{"title":"淡水湿地地下沉积物反硝化厌氧甲烷氧化(DAMO)过程对典型喹诺酮类抗生素的响应机制","authors":"Yuewen Zhao, Xinbo Zhang, Qichen Hao, Wenzhi Cao, Yuanjing Zhang, Chunlei Liu, Shengwei Cao, Yaci Liu, Yasong Li","doi":"10.1016/j.ecoenv.2025.118624","DOIUrl":null,"url":null,"abstract":"<p><p>Sub-surface sediments in freshwater wetlands function as active habitats for microbial denitrifying anaerobic methane oxidation (DAMO) processes and as hotspots for antibiotic accumulation. Focusing on the Baiyangdian wetland, which is contaminated with quinolone antibiotics (QNs) and hosts active DAMO processes, this study employed <sup>13</sup>C-labeled microcosm incubation experiments, RT-qPCR, and gene sequencing to decipher the response mechanisms of DAMO processes to prevalent QNs in the sub-surface sediments (0.5 20 cm) of study area. Short-term exposure (24 h) to typical QNs at 200 ng·g<sup>-1</sup> reduced nitrite-DAMO activities by approximately 33 %, primarily through selective inhibition of antibiotic-sensitive species within NC10 bacteria. In contrast, exposure to the same concentration of QNs enhanced nitrate-DAMO activities by about 450 %, likely due to hormetic stimulation of antibiotic-resistant ANME-2d archaea, combined with the inhibition of substrate competitor. Long-term exposure (90 days) to typical QNs mitigated these effects as bacterial adaptation to antibiotics occurred, resulting in a time-dependent attenuation of their impacts. This study underscores the significance of DAMO processes as methane sinks in changing environments and broadens the understanding of the ecological risks posed by antibiotics.</p>","PeriodicalId":303,"journal":{"name":"Ecotoxicology and Environmental Safety","volume":"302 ","pages":"118624"},"PeriodicalIF":6.1000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Response mechanisms of denitrifying anaerobic methane oxidation (DAMO) processes to typical quinolone antibiotics in freshwater wetland sub-surface sediments.\",\"authors\":\"Yuewen Zhao, Xinbo Zhang, Qichen Hao, Wenzhi Cao, Yuanjing Zhang, Chunlei Liu, Shengwei Cao, Yaci Liu, Yasong Li\",\"doi\":\"10.1016/j.ecoenv.2025.118624\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Sub-surface sediments in freshwater wetlands function as active habitats for microbial denitrifying anaerobic methane oxidation (DAMO) processes and as hotspots for antibiotic accumulation. Focusing on the Baiyangdian wetland, which is contaminated with quinolone antibiotics (QNs) and hosts active DAMO processes, this study employed <sup>13</sup>C-labeled microcosm incubation experiments, RT-qPCR, and gene sequencing to decipher the response mechanisms of DAMO processes to prevalent QNs in the sub-surface sediments (0.5 20 cm) of study area. Short-term exposure (24 h) to typical QNs at 200 ng·g<sup>-1</sup> reduced nitrite-DAMO activities by approximately 33 %, primarily through selective inhibition of antibiotic-sensitive species within NC10 bacteria. In contrast, exposure to the same concentration of QNs enhanced nitrate-DAMO activities by about 450 %, likely due to hormetic stimulation of antibiotic-resistant ANME-2d archaea, combined with the inhibition of substrate competitor. Long-term exposure (90 days) to typical QNs mitigated these effects as bacterial adaptation to antibiotics occurred, resulting in a time-dependent attenuation of their impacts. This study underscores the significance of DAMO processes as methane sinks in changing environments and broadens the understanding of the ecological risks posed by antibiotics.</p>\",\"PeriodicalId\":303,\"journal\":{\"name\":\"Ecotoxicology and Environmental Safety\",\"volume\":\"302 \",\"pages\":\"118624\"},\"PeriodicalIF\":6.1000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ecotoxicology and Environmental Safety\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1016/j.ecoenv.2025.118624\",\"RegionNum\":2,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/7/9 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ecotoxicology and Environmental Safety","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1016/j.ecoenv.2025.118624","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/9 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

淡水湿地的地下沉积物是微生物反硝化厌氧甲烷氧化(DAMO)过程的活跃栖息地,也是抗生素积累的热点。本研究以白洋淀湿地为研究区,喹诺酮类抗生素(QNs)污染严重,DAMO过程活跃的湿地为研究区,采用13c标记的微观培养实验、RT-qPCR和基因测序等方法,分析了DAMO过程对研究区0.5 20 cm地下沉积物中常见QNs的响应机制。短期暴露于200 ng·g-1的典型QNs(24 h)可使亚硝酸盐- damo活性降低约33 %,主要是通过选择性抑制NC10细菌中抗生素敏感的物种。相比之下,暴露于相同浓度的QNs使硝酸盐- damo活性提高了约450 %,这可能是由于耐抗生素的ANME-2d古菌的激电刺激,以及对底物竞争对手的抑制。长期暴露于典型QNs(90天)会减轻这些影响,因为细菌对抗生素发生了适应,导致其影响随时间衰减。这项研究强调了DAMO过程在不断变化的环境中作为甲烷汇的重要性,并拓宽了对抗生素造成的生态风险的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Response mechanisms of denitrifying anaerobic methane oxidation (DAMO) processes to typical quinolone antibiotics in freshwater wetland sub-surface sediments.

Sub-surface sediments in freshwater wetlands function as active habitats for microbial denitrifying anaerobic methane oxidation (DAMO) processes and as hotspots for antibiotic accumulation. Focusing on the Baiyangdian wetland, which is contaminated with quinolone antibiotics (QNs) and hosts active DAMO processes, this study employed 13C-labeled microcosm incubation experiments, RT-qPCR, and gene sequencing to decipher the response mechanisms of DAMO processes to prevalent QNs in the sub-surface sediments (0.5 20 cm) of study area. Short-term exposure (24 h) to typical QNs at 200 ng·g-1 reduced nitrite-DAMO activities by approximately 33 %, primarily through selective inhibition of antibiotic-sensitive species within NC10 bacteria. In contrast, exposure to the same concentration of QNs enhanced nitrate-DAMO activities by about 450 %, likely due to hormetic stimulation of antibiotic-resistant ANME-2d archaea, combined with the inhibition of substrate competitor. Long-term exposure (90 days) to typical QNs mitigated these effects as bacterial adaptation to antibiotics occurred, resulting in a time-dependent attenuation of their impacts. This study underscores the significance of DAMO processes as methane sinks in changing environments and broadens the understanding of the ecological risks posed by antibiotics.

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
12.10
自引率
5.90%
发文量
1234
审稿时长
88 days
期刊介绍: Ecotoxicology and Environmental Safety is a multi-disciplinary journal that focuses on understanding the exposure and effects of environmental contamination on organisms including human health. The scope of the journal covers three main themes. The topics within these themes, indicated below, include (but are not limited to) the following: Ecotoxicology、Environmental Chemistry、Environmental Safety etc.
×
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