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Compound- and context-dependent effects of antibiotics on greenhouse gas emissions from livestock

The use of antibiotics in livestock production may trigger ecosystem disservices, including increased emissions of greenhouse gases. To evaluate this, we conducted two separate animal experiments, administering two widely used antibiotic compounds (benzylpenicillin and tetracycline) to dairy cows ov...

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Autores principales: Danielsson, Rebecca, Lucas, Jane, Dahlberg, Josef, Ramin, Mohammad, Agenäs, Sigrid, Bayat, Ali-Reza, Tapio, Ilma, Hammer, Tobin, Roslin, Tomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837215/
https://www.ncbi.nlm.nih.gov/pubmed/31824677
http://dx.doi.org/10.1098/rsos.182049
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author Danielsson, Rebecca
Lucas, Jane
Dahlberg, Josef
Ramin, Mohammad
Agenäs, Sigrid
Bayat, Ali-Reza
Tapio, Ilma
Hammer, Tobin
Roslin, Tomas
author_facet Danielsson, Rebecca
Lucas, Jane
Dahlberg, Josef
Ramin, Mohammad
Agenäs, Sigrid
Bayat, Ali-Reza
Tapio, Ilma
Hammer, Tobin
Roslin, Tomas
author_sort Danielsson, Rebecca
collection PubMed
description The use of antibiotics in livestock production may trigger ecosystem disservices, including increased emissions of greenhouse gases. To evaluate this, we conducted two separate animal experiments, administering two widely used antibiotic compounds (benzylpenicillin and tetracycline) to dairy cows over a 4- or 5-day period locally and/or systemically. We then recorded enteric methane production, total gas production from dung decomposing under aerobic versus anaerobic conditions, prokaryotic community composition in rumen and dung, and accompanying changes in nutrient intake, rumen fermentation, and digestibility resulting from antibiotic administration. The focal antibiotics had no detectable effect on gas emissions from enteric fermentation or dung in aerobic conditions, while they decreased total gas production from anaerobic dung. Microbiome-level effects of benzylpenicillin proved markedly different from those previously recorded for tetracycline in dung, and did not differ by the mode of administration (local or systemic). Antibiotic effects on gas production differed substantially between dung maintained under aerobic versus anaerobic conditions and between compounds. These findings demonstrate compound- and context-dependent impacts of antibiotics on methane emissions and underlying processes, and highlight the need for a global synthesis of data on agricultural antibiotic use before understanding their climatic impacts.
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spelling pubmed-68372152019-12-10 Compound- and context-dependent effects of antibiotics on greenhouse gas emissions from livestock Danielsson, Rebecca Lucas, Jane Dahlberg, Josef Ramin, Mohammad Agenäs, Sigrid Bayat, Ali-Reza Tapio, Ilma Hammer, Tobin Roslin, Tomas R Soc Open Sci Biology (Whole Organism) The use of antibiotics in livestock production may trigger ecosystem disservices, including increased emissions of greenhouse gases. To evaluate this, we conducted two separate animal experiments, administering two widely used antibiotic compounds (benzylpenicillin and tetracycline) to dairy cows over a 4- or 5-day period locally and/or systemically. We then recorded enteric methane production, total gas production from dung decomposing under aerobic versus anaerobic conditions, prokaryotic community composition in rumen and dung, and accompanying changes in nutrient intake, rumen fermentation, and digestibility resulting from antibiotic administration. The focal antibiotics had no detectable effect on gas emissions from enteric fermentation or dung in aerobic conditions, while they decreased total gas production from anaerobic dung. Microbiome-level effects of benzylpenicillin proved markedly different from those previously recorded for tetracycline in dung, and did not differ by the mode of administration (local or systemic). Antibiotic effects on gas production differed substantially between dung maintained under aerobic versus anaerobic conditions and between compounds. These findings demonstrate compound- and context-dependent impacts of antibiotics on methane emissions and underlying processes, and highlight the need for a global synthesis of data on agricultural antibiotic use before understanding their climatic impacts. The Royal Society 2019-10-30 /pmc/articles/PMC6837215/ /pubmed/31824677 http://dx.doi.org/10.1098/rsos.182049 Text en © 2019 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Biology (Whole Organism)
Danielsson, Rebecca
Lucas, Jane
Dahlberg, Josef
Ramin, Mohammad
Agenäs, Sigrid
Bayat, Ali-Reza
Tapio, Ilma
Hammer, Tobin
Roslin, Tomas
Compound- and context-dependent effects of antibiotics on greenhouse gas emissions from livestock
title Compound- and context-dependent effects of antibiotics on greenhouse gas emissions from livestock
title_full Compound- and context-dependent effects of antibiotics on greenhouse gas emissions from livestock
title_fullStr Compound- and context-dependent effects of antibiotics on greenhouse gas emissions from livestock
title_full_unstemmed Compound- and context-dependent effects of antibiotics on greenhouse gas emissions from livestock
title_short Compound- and context-dependent effects of antibiotics on greenhouse gas emissions from livestock
title_sort compound- and context-dependent effects of antibiotics on greenhouse gas emissions from livestock
topic Biology (Whole Organism)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837215/
https://www.ncbi.nlm.nih.gov/pubmed/31824677
http://dx.doi.org/10.1098/rsos.182049
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