Treating cattle with antibiotics affects greenhouse gas emissions, and microbiota in dung and dung beetles

Author:

Hammer Tobin J.12ORCID,Fierer Noah12,Hardwick Bess3,Simojoki Asko4,Slade Eleanor356,Taponen Juhani7,Viljanen Heidi38,Roslin Tomas39

Affiliation:

1. Department of Ecology and Evolutionary Biology, University of Colorado at Boulder, Boulder, CO, USA

2. Cooperative Institute for Research in Environmental Sciences, University of Colorado at Boulder, Boulder, CO, USA

3. Spatial Foodweb Ecology Group, Department of Agricultural Sciences, University of Helsinki, Helsinki, Finland

4. Department of Food and Environmental Sciences, University of Helsinki, Helsinki, Finland

5. Department of Zoology, University of Oxford, South Parks Road, Oxford, UK

6. Lancaster Environment Centre, University of Lancaster, Lancaster, UK

7. Department of Production Animal Medicine, University of Helsinki, Saarentaus, Finland

8. Metapopulation Research Centre, Department of Biosciences, University of Helsinki, Helsinki, Finland

9. Department of Ecology, Swedish University of Agricultural Sciences, Uppsala, Sweden

Abstract

Antibiotics are routinely used to improve livestock health and growth. However, this practice may have unintended environmental impacts mediated by interactions among the wide range of micro- and macroorganisms found in agroecosystems. For example, antibiotics may alter microbial emissions of greenhouse gases by affecting livestock gut microbiota. Furthermore, antibiotics may affect the microbiota of non-target animals that rely on dung, such as dung beetles, and the ecosystem services they provide. To examine these interactions, we treated cattle with a commonly used broad-spectrum antibiotic and assessed downstream effects on microbiota in dung and dung beetles, greenhouse gas fluxes from dung, and beetle size, survival and reproduction. We found that antibiotic treatment restructured microbiota in dung beetles, which harboured a microbial community distinct from those in the dung they were consuming. The antibiotic effect on beetle microbiota was not associated with smaller size or lower numbers. Unexpectedly, antibiotic treatment raised methane fluxes from dung, possibly by altering the interactions between methanogenic archaea and bacteria in rumen and dung environments. Our findings that antibiotics restructure dung beetle microbiota and modify greenhouse gas emissions from dung indicate that antibiotic treatment may have unintended, cascading ecological effects that extend beyond the target animal.

Funder

National Science Foundation

Academy of Finland

Publisher

The Royal Society

Subject

General Agricultural and Biological Sciences,General Environmental Science,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference72 articles.

1. Antimicrobial Use and Resistance in Animals

2. A global perspective on the use, sales, exposure pathways, occurrence, fate and effects of veterinary antibiotics (VAs) in the environment

3. Global trends in antimicrobial use in food animals

4. U.S. Food and Drug Administration. 2015 Summary report on antimicrobials sold or distributed for use in food-producing animals. See http://www.fda.gov/downloads/ForIndustry/UserFees/AnimalDrugUserFeeActADUFA/UCM476258.pdf.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3