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Global antimicrobial-resistance drivers: an ecological country-level study at the human-animal interface.

Allel, K; Day, L; Hamilton, A; Lin, L; Furuya-Kanamori, L; Moore, CE; Van Boeckel, T; Laxminarayan, R; Yakob, L (2023) Global antimicrobial-resistance drivers: an ecological country-level study at the human-animal interface. Lancet Planet Health, 7 (4). e291-e303. ISSN 2542-5196 https://doi.org/10.1016/S2542-5196(23)00026-8
SGUL Authors: Moore, Catrin Elisabeth

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Abstract

BACKGROUND: Antimicrobial resistance (AMR) is a pressing, holistic, and multisectoral challenge facing contemporary global health. In this study we assessed the associations between socioeconomic, anthropogenic, and environmental indicators and country-level rates of AMR in humans and food-producing animals. METHODS: In this modelling study, we obtained data on Carbapenem-resistant Acinetobacter baumanii and Pseudomonas aeruginosa, third generation cephalosporins-resistant Escherichia coli and Klebsiella pneumoniae, oxacillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus faecium AMR in humans and food-producing animals from publicly available sources, including WHO, World Bank, and Center for Disease Dynamics Economics and Policy. AMR in food-producing animals presented a combined prevalence of AMR exposure in cattle, pigs, and chickens. We used multivariable β regression models to determine the adjusted association between human and food-producing animal AMR rates and an array of ecological country-level indicators. Human AMR rates were classified according to the WHO priority pathogens list and antibiotic-bacterium pairs. FINDINGS: Significant associations were identified between animal antimicrobial consumption and AMR in food-producing animals (OR 1·05 [95% CI 1·01-1·10]; p=0·013), and between human antimicrobial consumption and AMR specifically in WHO critical priority (1·06 [1·00-1·12]; p=0·035) and high priority (1·22 [1·09-1·37]; p<0·0001) pathogens. Bidirectional associations were also found: animal antibiotic consumption was positively linked with resistance in critical priority human pathogens (1·07 [1·01-1·13]; p=0·020) and human antibiotic consumption was positively linked with animal AMR (1·05 [1·01-1·09]; p=0·010). Carbapenem-resistant Acinetobacter baumanii, third generation cephalosporins-resistant Escherichia coli, and oxacillin-resistant Staphylococcus aureus all had significant associations with animal antibiotic consumption. Analyses also suggested significant roles of socioeconomics, including governance on AMR rates in humans and animals. INTERPRETATION: Reduced rates of antibiotic consumption alone will not be sufficient to combat the rising worldwide prevalence of AMR. Control methods should focus on poverty reduction and aim to prevent AMR transmission across different One Health domains while accounting for domain-specific risk factors. The levelling up of livestock surveillance systems to better match those reporting on human AMR, and, strengthening all surveillance efforts, particularly in low-income and middle-income countries, are pressing priorities. FUNDING: None.

Item Type: Article
Additional Information: Copyright © 2023 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.
Keywords: Humans, Animals, Cattle, Swine, Methicillin-Resistant Staphylococcus aureus, Drug Resistance, Bacterial, Chickens, Anti-Bacterial Agents, Carbapenems, Escherichia coli, Cephalosporins, Oxacillin, Animals, Chickens, Cattle, Swine, Humans, Escherichia coli, Carbapenems, Cephalosporins, Oxacillin, Anti-Bacterial Agents, Drug Resistance, Bacterial, Methicillin-Resistant Staphylococcus aureus
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Lancet Planet Health
ISSN: 2542-5196
Language: eng
Dates:
DateEvent
3 April 2023Published
1 February 2023Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
73200098Asociación Nacional de Investigación y DesarrolloUNSPECIFIED
CCF1918628National Science Foundationhttp://dx.doi.org/10.13039/100000001
21IPA2113462Centers for Disease Control and Preventionhttp://dx.doi.org/10.13039/100000030
PubMed ID: 37019570
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/115341
Publisher's version: https://doi.org/10.1016/S2542-5196(23)00026-8

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