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Combined effects of composting and antibiotic administration on cattle manure–borne antibiotic resistance genes
BACKGROUND: Research is needed to delineate the relative and combined effects of different antibiotic administration and manure management practices in either amplifying or attenuating the potential for antibiotic resistance to spread. Here, we carried out a comprehensive parallel examination of the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017830/ https://www.ncbi.nlm.nih.gov/pubmed/33795006 http://dx.doi.org/10.1186/s40168-021-01006-z |
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author | Keenum, Ishi Williams, Robert K. Ray, Partha Garner, Emily D. Knowlton, Katharine F. Pruden, Amy |
author_facet | Keenum, Ishi Williams, Robert K. Ray, Partha Garner, Emily D. Knowlton, Katharine F. Pruden, Amy |
author_sort | Keenum, Ishi |
collection | PubMed |
description | BACKGROUND: Research is needed to delineate the relative and combined effects of different antibiotic administration and manure management practices in either amplifying or attenuating the potential for antibiotic resistance to spread. Here, we carried out a comprehensive parallel examination of the effects of small-scale (> 55 °C × 3 days) static and turned composting of manures from dairy and beef cattle collected during standard antibiotic administration (cephapirin/pirlimycin or sulfamethazine/chlortetracycline/tylosin, respectively), versus from untreated cattle, on “resistomes” (total antibiotic resistance genes (ARGs) determined via shotgun metagenomic sequencing), bacterial microbiota, and indicator ARGs enumerated via quantitative polymerase chain reaction. To gain insight into the role of the thermophilic phase, compost was also externally heated to > 55 °C × 15 days. RESULTS: Progression of composting with time and succession of the corresponding bacterial microbiota was the overarching driver of the resistome composition (ANOSIM; R = 0.424, p = 0.001, respectively) in all composts at the small-scale. Reduction in relative abundance (16S rRNA gene normalized) of total ARGs in finished compost (day 42) versus day 0 was noted across all conditions (ANOSIM; R = 0.728, p = 0.001), except when externally heated. Sul1, intI1, beta-lactam ARGs, and plasmid-associated genes increased in all finished composts as compared with the initial condition. External heating more effectively reduced certain clinically relevant ARGs (bla(OXA), bla(CARB)), fecal coliforms, and resistome risk scores, which take into account putative pathogen annotations. When manure was collected during antibiotic administration, taxonomic composition of the compost was distinct according to nonmetric multidimensional analysis and tet(W) decayed faster in the dairy manure with antibiotic condition and slower in the beef manure with antibiotic condition. CONCLUSIONS: This comprehensive, integrated study revealed that composting had a dominant effect on corresponding resistome composition, while little difference was noted as a function of collecting manure during antibiotic administration. Reduction in total ARGs, tet(W), and resistome risk suggested that composting reduced some potential for antibiotic resistance to spread, but the increase and persistence of other indicators of antibiotic resistance were concerning. Results indicate that composting guidelines intended for pathogen reduction do not necessarily provide a comprehensive barrier to ARGs or their mobility prior to land application and additional mitigation measures should be considered. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01006-z. |
format | Online Article Text |
id | pubmed-8017830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80178302021-04-05 Combined effects of composting and antibiotic administration on cattle manure–borne antibiotic resistance genes Keenum, Ishi Williams, Robert K. Ray, Partha Garner, Emily D. Knowlton, Katharine F. Pruden, Amy Microbiome Research BACKGROUND: Research is needed to delineate the relative and combined effects of different antibiotic administration and manure management practices in either amplifying or attenuating the potential for antibiotic resistance to spread. Here, we carried out a comprehensive parallel examination of the effects of small-scale (> 55 °C × 3 days) static and turned composting of manures from dairy and beef cattle collected during standard antibiotic administration (cephapirin/pirlimycin or sulfamethazine/chlortetracycline/tylosin, respectively), versus from untreated cattle, on “resistomes” (total antibiotic resistance genes (ARGs) determined via shotgun metagenomic sequencing), bacterial microbiota, and indicator ARGs enumerated via quantitative polymerase chain reaction. To gain insight into the role of the thermophilic phase, compost was also externally heated to > 55 °C × 15 days. RESULTS: Progression of composting with time and succession of the corresponding bacterial microbiota was the overarching driver of the resistome composition (ANOSIM; R = 0.424, p = 0.001, respectively) in all composts at the small-scale. Reduction in relative abundance (16S rRNA gene normalized) of total ARGs in finished compost (day 42) versus day 0 was noted across all conditions (ANOSIM; R = 0.728, p = 0.001), except when externally heated. Sul1, intI1, beta-lactam ARGs, and plasmid-associated genes increased in all finished composts as compared with the initial condition. External heating more effectively reduced certain clinically relevant ARGs (bla(OXA), bla(CARB)), fecal coliforms, and resistome risk scores, which take into account putative pathogen annotations. When manure was collected during antibiotic administration, taxonomic composition of the compost was distinct according to nonmetric multidimensional analysis and tet(W) decayed faster in the dairy manure with antibiotic condition and slower in the beef manure with antibiotic condition. CONCLUSIONS: This comprehensive, integrated study revealed that composting had a dominant effect on corresponding resistome composition, while little difference was noted as a function of collecting manure during antibiotic administration. Reduction in total ARGs, tet(W), and resistome risk suggested that composting reduced some potential for antibiotic resistance to spread, but the increase and persistence of other indicators of antibiotic resistance were concerning. Results indicate that composting guidelines intended for pathogen reduction do not necessarily provide a comprehensive barrier to ARGs or their mobility prior to land application and additional mitigation measures should be considered. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01006-z. BioMed Central 2021-04-01 /pmc/articles/PMC8017830/ /pubmed/33795006 http://dx.doi.org/10.1186/s40168-021-01006-z Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Keenum, Ishi Williams, Robert K. Ray, Partha Garner, Emily D. Knowlton, Katharine F. Pruden, Amy Combined effects of composting and antibiotic administration on cattle manure–borne antibiotic resistance genes |
title | Combined effects of composting and antibiotic administration on cattle manure–borne antibiotic resistance genes |
title_full | Combined effects of composting and antibiotic administration on cattle manure–borne antibiotic resistance genes |
title_fullStr | Combined effects of composting and antibiotic administration on cattle manure–borne antibiotic resistance genes |
title_full_unstemmed | Combined effects of composting and antibiotic administration on cattle manure–borne antibiotic resistance genes |
title_short | Combined effects of composting and antibiotic administration on cattle manure–borne antibiotic resistance genes |
title_sort | combined effects of composting and antibiotic administration on cattle manure–borne antibiotic resistance genes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017830/ https://www.ncbi.nlm.nih.gov/pubmed/33795006 http://dx.doi.org/10.1186/s40168-021-01006-z |
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