Youjing Wang, Di Tong, Haodan Yu, Yujie Zhou, Caixian Tang, Randy A. Dahlgren, Jianming Xu
{"title":"Viral involvement in microbial anaerobic methane oxidation-mediated arsenic mobilization in paddy soil","authors":"Youjing Wang, Di Tong, Haodan Yu, Yujie Zhou, Caixian Tang, Randy A. Dahlgren, Jianming Xu","doi":"10.1016/j.jhazmat.2024.136758","DOIUrl":null,"url":null,"abstract":"Anaerobic oxidation of methane (AOM) facilitates As mobilization, posing a significant environmental risk. Soil viruses potentially participate in the microbial AOM process, yet their roles in methane-mediated As mobilization of paddy soil remain elusive. Here, an anaerobic microcosm study was conducted by inoculating microbial suspension with extracellular free virus and mitomycin C (MC)-induced virus, along with <sup>13</sup>CH<sub>4</sub> injection. The results showed that extracellular free virus enhanced while MC-induced virus suppressed <sup>13</sup>CH<sub>4</sub>-mediated As mobilization. During the AOM process, both viruses inhibited <sup>13</sup>CH<sub>4</sub> oxidation to <sup>13</sup>CO<sub>2</sub>. However, the extracellular free virus suppressed whereas the MC-induced virus enhanced <sup>13</sup>CH<sub>4</sub> consumption, likely attributed to the viral influence on the ANME-2d abundance. The methane consumption differences were inferred to influence As reduction, as evidenced by a strong correlation between As(III) and <sup>13</sup>CH<sub>4</sub> consumption concentrations. Moreover, virus-mediated methane assimilation into microbial biomass carbon influenced the overall microbial population. An increased abundance of <em>Geobacter</em> in the extracellular free virus treatment elevated net As(III) concentrations (up to 260%) relative to treatment without virus in the presence of <sup>13</sup>CH<sub>4</sub>. In contrast, MC-induced virus led to a net 122% reduction in As(III) concentration due to decreased <em>Geobacter</em> abundance. These findings provide new insights into soil viruses in microbial AOM-driven As mobilization, highlighting their crucial functions in soil ecosystems.","PeriodicalId":361,"journal":{"name":"Journal of Hazardous Materials","volume":"122 1","pages":""},"PeriodicalIF":12.2000,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Hazardous Materials","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1016/j.jhazmat.2024.136758","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
Anaerobic oxidation of methane (AOM) facilitates As mobilization, posing a significant environmental risk. Soil viruses potentially participate in the microbial AOM process, yet their roles in methane-mediated As mobilization of paddy soil remain elusive. Here, an anaerobic microcosm study was conducted by inoculating microbial suspension with extracellular free virus and mitomycin C (MC)-induced virus, along with 13CH4 injection. The results showed that extracellular free virus enhanced while MC-induced virus suppressed 13CH4-mediated As mobilization. During the AOM process, both viruses inhibited 13CH4 oxidation to 13CO2. However, the extracellular free virus suppressed whereas the MC-induced virus enhanced 13CH4 consumption, likely attributed to the viral influence on the ANME-2d abundance. The methane consumption differences were inferred to influence As reduction, as evidenced by a strong correlation between As(III) and 13CH4 consumption concentrations. Moreover, virus-mediated methane assimilation into microbial biomass carbon influenced the overall microbial population. An increased abundance of Geobacter in the extracellular free virus treatment elevated net As(III) concentrations (up to 260%) relative to treatment without virus in the presence of 13CH4. In contrast, MC-induced virus led to a net 122% reduction in As(III) concentration due to decreased Geobacter abundance. These findings provide new insights into soil viruses in microbial AOM-driven As mobilization, highlighting their crucial functions in soil ecosystems.
期刊介绍:
The Journal of Hazardous Materials serves as a global platform for promoting cutting-edge research in the field of Environmental Science and Engineering. Our publication features a wide range of articles, including full-length research papers, review articles, and perspectives, with the aim of enhancing our understanding of the dangers and risks associated with various materials concerning public health and the environment. It is important to note that the term "environmental contaminants" refers specifically to substances that pose hazardous effects through contamination, while excluding those that do not have such impacts on the environment or human health. Moreover, we emphasize the distinction between wastes and hazardous materials in order to provide further clarity on the scope of the journal. We have a keen interest in exploring specific compounds and microbial agents that have adverse effects on the environment.