Assessing antimicrobial resistance in pasture-based dairy farms: a 15-month surveillance study in New Zealand.

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2024-11-20 Epub Date: 2024-10-23 DOI:10.1128/aem.01390-24
Rose M Collis, Patrick J Biggs, Sara A Burgess, Anne C Midwinter, Jinxin Liu, Gale Brightwell, Adrian L Cookson
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Abstract

Antimicrobial resistance is a global public and animal health concern. Antimicrobial resistance genes (ARGs) have been detected in dairy farm environments globally; however, few longitudinal studies have utilized shotgun metagenomics for ARG surveillance in pasture-based systems. This 15-month study aimed to undertake a baseline survey using shotgun metagenomics to assess the relative abundance and diversity of ARGs in two pasture-based dairy farm environments in New Zealand with different management practices. There was no statistically significant difference in overall ARG relative abundance between the two dairy farms (P = 0.321) during the study period. Compared with overseas data, the relative abundance of ARG copies per 16S rRNA gene in feces (0.08-0.17), effluent (0.03-0.37), soil (0.20-0.63), and bulk tank milk (0.0-0.12) samples was low. Models comparing the presence or absence of resistance classes found in >10% of all feces, effluent, and soil samples demonstrated no statistically significant associations (P > 0.05) with "season," and only multi-metal (P = 0.020) and tetracycline (P = 0.0003) resistance were significant at the "farm" level. Effluent samples harbored the most diverse ARGs, some with a recognized public health risk, whereas soil samples had the highest ARG relative abundance but without recognized health risks. This highlights the importance of considering the genomic context and risk of ARGs in metagenomic data sets. This study suggests that antimicrobial resistance on pasture-based dairy farms is low and provides essential baseline ARG surveillance data for such farming systems.IMPORTANCEAntimicrobial resistance is a global threat to human and animal health. Despite the detection of antimicrobial resistance genes (ARGs) in dairy farm environments globally, longitudinal surveillance in pasture-based systems remains limited. This study assessed the relative abundance and diversity of ARGs in two New Zealand dairy farms with different management practices and provided important baseline ARG surveillance data on pasture-based dairy farms. The overall ARG relative abundance on these two farms was low, which provides further evidence for consumers of the safety of New Zealand's export products. Effluent samples harbored the most diverse range of ARGs, some of which were classified with a recognized risk to public health, whereas soil samples had the highest ARG relative abundance; however, the soil ARGs were not classified with a recognized public health risk. This emphasizes the need to consider genomic context and risk as well as ARG relative abundance in resistome studies.

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评估牧场奶牛场的抗菌药耐药性:新西兰为期 15 个月的监测研究。
抗菌素耐药性是一个全球性的公共和动物健康问题。抗菌药耐药性基因(ARGs)已在全球范围内的奶牛场环境中被检测到;然而,很少有纵向研究利用霰弹枪元基因组学来监测牧场系统中的ARGs。这项为期 15 个月的研究旨在利用霰弹枪元基因组学进行基线调查,以评估新西兰两个牧场环境中不同管理方法下 ARGs 的相对丰度和多样性。在研究期间,两个奶牛场之间 ARG 相对丰度的总体差异无统计学意义(P = 0.321)。与国外数据相比,粪便(0.08-0.17)、污水(0.03-0.37)、土壤(0.20-0.63)和散装罐装牛奶(0.0-0.12)样本中每个 16S rRNA 基因的 ARG 相对丰度较低。比较所有粪便、污水和土壤样本中大于 10% 的抗药性类别的存在与否的模型表明,抗药性类别与 "季节 "无统计学意义(P > 0.05),只有多金属(P = 0.020)和四环素(P = 0.0003)的抗药性在 "农场 "水平上有显著意义。污水样本中的 ARGs 种类最多,其中一些具有公认的公共健康风险,而土壤样本中的 ARGs 相对丰度最高,但没有公认的健康风险。这凸显了在元基因组数据集中考虑基因组背景和 ARGs 风险的重要性。这项研究表明,以牧草为基础的奶牛场的抗菌药耐药性较低,并为此类养殖系统提供了重要的 ARG 监测基线数据。重要意义抗菌药耐药性是对人类和动物健康的全球性威胁。尽管在全球范围内发现了奶牛场环境中的抗菌药耐药性基因(ARGs),但对牧场系统的纵向监测仍然有限。本研究评估了新西兰两个采用不同管理方法的奶牛场中 ARGs 的相对丰度和多样性,为牧场提供了重要的 ARG 监测基线数据。这两个牧场的 ARG 相对丰度总体较低,为消费者提供了新西兰出口产品安全性的进一步证据。污水样本中的 ARGs 种类最多,其中一些已被归类为对公共健康具有公认风险,而土壤样本中的 ARGs 相对丰度最高;不过,土壤中的 ARGs 未被归类为对公共健康具有公认风险。这强调了在抗性基因组研究中考虑基因组背景和风险以及 ARG 相对丰度的必要性。
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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
期刊最新文献
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