Spread of antimicrobial resistance genes via pig manure from organic and conventional farms in the presence or absence of antibiotic use
- PMID: 35835564
- DOI: 10.1111/jam.15717
Spread of antimicrobial resistance genes via pig manure from organic and conventional farms in the presence or absence of antibiotic use
Abstract
Aims: Antibiotic-resistant bacteria affect human and animal health. Hence, their environmental spread represents a potential hazard for mankind. Livestock farming is suspected to be a key factor for spreading antibiotic resistance; consumers expect organic farming to imply less environmental health risk. This study aimed to assess the role of manure from organic and conventional farms for spreading antimicrobial resistance (AMR) genes.
Methods and results: AMR-genes-namely tet(A), tet(B), tet(M), sul2 and qacE/qacEΔ1 (potentially associated with multiresistance) were quantified by qPCR. Antimicrobial use during the study period was qualitatively assessed from official records in a binary mode (yes/no). Median concentrations were between 6.44 log copy-equivalents/g for tet(A) and 7.85 for tet(M) in organic liquid manure, and between 7.48 for tet(A) and 8.3 for sul2 in organic farmyard manure. In conventional manure, median concentrations were 6.67 log copy-equivalents/g for sul2, 6.89 for tet(A), 6.77 for tet(B) and 8.36 for tet(M). Integron-associated qac-genes reached median concentrations of 7.06 log copy-equivalents/g in organic liquid manure, 7.13 in conventional manure and 8.18 in organic farmyard manure. The use of tetracyclines or sulfonamides increased concentrations of tet(A) and tet(M), or of sul2, respectively. Comparing farms that did not apply tetracyclines during the study, the relative abundance of tet(A) and tet(M) was still higher for conventional piggeries than for organic ones.
Conclusions: Relative abundances of AMR genes were higher in conventional farms, compared to organic ones. Antibiotic use was linked to the relative abundance of AMR-genes. However, due to the bacterial load, absolute concentrations of AMR-genes were comparable between fertilizers of organic and conventional farms.
Significance and impact of study: To our knowledge, this is the first absolute quantification of AMR-genes in manure from organic farms. Our study underlines the importance of long-term reduction in the use of antimicrobial agents in order to minimize antibiotic resistance.
Keywords: antibiotic resistance; antimicrobial resistance genes; integrons; organic farming; pig manure; qPCR; sulfonamide; tetracycline.
© 2022 The Authors. Journal of Applied Microbiology published by John Wiley & Sons Ltd on behalf of Society for Applied Microbiology.
Similar articles
-
Phenotypic and genotypic bacterial antimicrobial resistance in liquid pig manure is variously associated with contents of tetracyclines and sulfonamides.J Appl Microbiol. 2010 May;108(5):1642-56. doi: 10.1111/j.1365-2672.2009.04570.x. Epub 2009 Sep 29. J Appl Microbiol. 2010. PMID: 19895649
-
A Comprehensive Analysis on Spread and Distribution Characteristic of Antibiotic Resistance Genes in Livestock Farms of Southeastern China.PLoS One. 2016 Jul 7;11(7):e0156889. doi: 10.1371/journal.pone.0156889. eCollection 2016. PLoS One. 2016. PMID: 27388166 Free PMC article.
-
Abundance and persistence of antibiotic resistance genes in livestock farms: a comprehensive investigation in eastern China.Environ Int. 2013 Nov;61:1-7. doi: 10.1016/j.envint.2013.08.023. Epub 2013 Oct 2. Environ Int. 2013. PMID: 24091253
-
Insights into the impact of manure on the environmental antibiotic residues and resistance pool.Front Microbiol. 2022 Sep 16;13:965132. doi: 10.3389/fmicb.2022.965132. eCollection 2022. Front Microbiol. 2022. PMID: 36187968 Free PMC article. Review.
-
Overcoming China's animal waste disposal challenge brought by elevated levels of veterinary antimicrobial residues and antimicrobial resistance.Environ Int. 2024 Sep;191:109009. doi: 10.1016/j.envint.2024.109009. Epub 2024 Sep 12. Environ Int. 2024. PMID: 39278046 Review.
Cited by
-
Improvements of weaned pigs barn hygiene to reduce the spread of antimicrobial resistance.Front Microbiol. 2024 May 14;15:1393923. doi: 10.3389/fmicb.2024.1393923. eCollection 2024. Front Microbiol. 2024. PMID: 38812683 Free PMC article.
-
The Development of the Bacterial Community of Brown Trout (Salmo trutta) during Ontogeny.Microorganisms. 2023 Jan 14;11(1):211. doi: 10.3390/microorganisms11010211. Microorganisms. 2023. PMID: 36677503 Free PMC article.
-
Invisible Engines of Resistance: How Global Inequities Drive Antimicrobial Failure.Antibiotics (Basel). 2025 Jun 30;14(7):659. doi: 10.3390/antibiotics14070659. Antibiotics (Basel). 2025. PMID: 40723962 Free PMC article. Review.
-
Cultivating antimicrobial resistance: how intensive agriculture ploughs the way for antibiotic resistance.Microbiology (Reading). 2023 Aug;169(8):001384. doi: 10.1099/mic.0.001384. Microbiology (Reading). 2023. PMID: 37606636 Free PMC article. Review.
-
Distribution Patterns of Antibiotic Resistance Genes and Their Bacterial Hosts in a Manure Lagoon of a Large-Scale Swine Finishing Facility.Microorganisms. 2022 Nov 20;10(11):2301. doi: 10.3390/microorganisms10112301. Microorganisms. 2022. PMID: 36422370 Free PMC article.
References
REFERENCES
-
- Alonso, A., Sánchez, P. & Martínez, J.L. (2001) Environmental selection of antibiotic resistance genes. Environmental Microbiology, 3(1), 1-9. Available from: https://doi.org/10.1046/j.1462-2920.2001.00161.x
-
- Aminov, R.I., Chee-Sanford, J.C., Garrigues, N., Teferedegne, B., Krapac, I.J., White, B.A. et al. (2002) Development, validation, and application of PCR primers for detection of tetracycline efflux genes of gram-negative bacteria. Applied and Environmental Microbiology, 68(4), 1786-1793. Available from: https://doi.org/10.1128/aem.68.4.1786-1793.2002
-
- Aminov, R.I., Garrigues-Jeanjean, N. & Mackie, R.I. (2001) Molecular ecology of tetracycline resistance: development and validation of primers for detection of tetracycline resistance genes encoding ribosomal protection proteins. Applied and Environmental Microbiology, 67(1), 22-32. Available from: https://doi.org/10.1128/AEM.67.1.22-32.2001
-
- Armalytė, J., Skerniškytė, J., Bakienė, E., Krasauskas, R., Šiugždinienė, R., Kareivienė, V. et al. (2019) Microbial diversity and antimicrobial resistance profile in microbiota from soils of conventional and organic farming systems. Frontiers in Microbiology, 10, 892. Available from: https://doi.org/10.3389/fmicb.2019.00892
-
- Baquero, F., Martínez, J.L. & Cantón, R. (2008) Antibiotics and antibiotic resistance in water environments. Current Opinion in Biotechnology, 19(3), 260-265. Available from: https://doi.org/10.1016/j.copbio.2008.05.006
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials
