上海崇明岛人与动物接触区大肠杆菌和金黄色葡萄球菌的抗菌药耐药性:同一健康视角

IF 4.1 2区 医学 Q1 INFECTIOUS DISEASES
Chao Lv , Jun Leng , Minjian Qian , Bingqing Sun , HuiPing Ye , Min Li , Nan Zhou , Zile Cheng , Yiwen Chen , Xiaokui Guo , Jun Shang , Li Zhang , Yongzhang Zhu
{"title":"上海崇明岛人与动物接触区大肠杆菌和金黄色葡萄球菌的抗菌药耐药性:同一健康视角","authors":"Chao Lv ,&nbsp;Jun Leng ,&nbsp;Minjian Qian ,&nbsp;Bingqing Sun ,&nbsp;HuiPing Ye ,&nbsp;Min Li ,&nbsp;Nan Zhou ,&nbsp;Zile Cheng ,&nbsp;Yiwen Chen ,&nbsp;Xiaokui Guo ,&nbsp;Jun Shang ,&nbsp;Li Zhang ,&nbsp;Yongzhang Zhu","doi":"10.1016/j.onehlt.2024.100910","DOIUrl":null,"url":null,"abstract":"<div><div>Antimicrobial resistance (AMR) is a significant concern within the One Health framework due to its ability to spread across multiple interfaces. Phenotypic data remains the primary type for AMR surveillance, but exploring association across multiple interfaces poses certain challenges. In this study, AMR phenotypic data of clinical and food animal <em>E. coli</em> and <em>S. aureus</em> from Chongming Island over the past five years were analyzed to determine key characteristics of AMR and explore its association at the human-animal interface.</div><div>The clinical <em>E. coli</em> isolates showed significant resistance to penicillins (83.92 %), cephems (63.05 %), fluoroquinolones (62.21 %), and tetracyclines (57.77 %), while <em>S. aureus</em> exhibited high resistance to penicillinase-labile penicillins (90.89 %), macrolides (51.51 %), penicillinase-stable penicillins (43.96 %), and lincosamides (43.55 %). Extended-spectrum β-lactamase (ESBL)-producing <em>E. coli</em> isolates accounted for 53.26 % (1398/2526), while methicillin-resistant <em>Staphylococcus aureus</em> (MRSA) prevalence was 43.81 % (435/993). Notably, there has been an increase in the proportion of <em>E. coli</em> isolates resistant to 8 to 12 antimicrobial classes, and in the proportion of <em>S. aureus</em> isolates resistant to 5 to 9 classes. Certain multi-drug resistance (MDR) phenotypes were first identified in food animal isolates and later emerged in clinical settings. Meanwhile, several MDR phenotypes were shared between the two interfaces, with 44 identified in <em>E. coli</em> and 12 in <em>S. aureus</em>. Further co-occurrence analysis in <em>E. coli</em> and <em>S. aureus</em> identified several co-occurrence phenotypic pairs or clusters, potentially mediated by a single plasmid or multiple plasmids within a bacterium, indicating potential associations at the human-animal interface.</div><div>To summarize, a heightened prevalence of MDR in clinical <em>E. coli</em> and <em>S. aureus</em> has been observed, with some MDR profiles appearing in food animals before emerging in clinical settings. The co-occurrence of phenotypic pairs or clusters underscores the potential for AMR association and transmission between humans and food animals. Within the One Health framework, integrating genomic data into AMR monitoring is a crucial next step.</div></div>","PeriodicalId":19577,"journal":{"name":"One Health","volume":"19 ","pages":"Article 100910"},"PeriodicalIF":4.1000,"publicationDate":"2024-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Antimicrobial resistance in Escherichia coli and Staphylococcus aureus at human-animal interfaces on Chongming Island, Shanghai: A One Health perspective\",\"authors\":\"Chao Lv ,&nbsp;Jun Leng ,&nbsp;Minjian Qian ,&nbsp;Bingqing Sun ,&nbsp;HuiPing Ye ,&nbsp;Min Li ,&nbsp;Nan Zhou ,&nbsp;Zile Cheng ,&nbsp;Yiwen Chen ,&nbsp;Xiaokui Guo ,&nbsp;Jun Shang ,&nbsp;Li Zhang ,&nbsp;Yongzhang Zhu\",\"doi\":\"10.1016/j.onehlt.2024.100910\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Antimicrobial resistance (AMR) is a significant concern within the One Health framework due to its ability to spread across multiple interfaces. Phenotypic data remains the primary type for AMR surveillance, but exploring association across multiple interfaces poses certain challenges. In this study, AMR phenotypic data of clinical and food animal <em>E. coli</em> and <em>S. aureus</em> from Chongming Island over the past five years were analyzed to determine key characteristics of AMR and explore its association at the human-animal interface.</div><div>The clinical <em>E. coli</em> isolates showed significant resistance to penicillins (83.92 %), cephems (63.05 %), fluoroquinolones (62.21 %), and tetracyclines (57.77 %), while <em>S. aureus</em> exhibited high resistance to penicillinase-labile penicillins (90.89 %), macrolides (51.51 %), penicillinase-stable penicillins (43.96 %), and lincosamides (43.55 %). Extended-spectrum β-lactamase (ESBL)-producing <em>E. coli</em> isolates accounted for 53.26 % (1398/2526), while methicillin-resistant <em>Staphylococcus aureus</em> (MRSA) prevalence was 43.81 % (435/993). Notably, there has been an increase in the proportion of <em>E. coli</em> isolates resistant to 8 to 12 antimicrobial classes, and in the proportion of <em>S. aureus</em> isolates resistant to 5 to 9 classes. Certain multi-drug resistance (MDR) phenotypes were first identified in food animal isolates and later emerged in clinical settings. Meanwhile, several MDR phenotypes were shared between the two interfaces, with 44 identified in <em>E. coli</em> and 12 in <em>S. aureus</em>. Further co-occurrence analysis in <em>E. coli</em> and <em>S. aureus</em> identified several co-occurrence phenotypic pairs or clusters, potentially mediated by a single plasmid or multiple plasmids within a bacterium, indicating potential associations at the human-animal interface.</div><div>To summarize, a heightened prevalence of MDR in clinical <em>E. coli</em> and <em>S. aureus</em> has been observed, with some MDR profiles appearing in food animals before emerging in clinical settings. The co-occurrence of phenotypic pairs or clusters underscores the potential for AMR association and transmission between humans and food animals. Within the One Health framework, integrating genomic data into AMR monitoring is a crucial next step.</div></div>\",\"PeriodicalId\":19577,\"journal\":{\"name\":\"One Health\",\"volume\":\"19 \",\"pages\":\"Article 100910\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2024-10-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"One Health\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2352771424002362\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"One Health","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2352771424002362","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

摘要

抗菌素耐药性(AMR)是 "一个健康 "框架内的一个重大问题,因为它能够在多个界面上传播。表型数据仍是 AMR 监测的主要类型,但探索跨多个界面的关联性具有一定的挑战性。本研究分析了崇明岛过去五年中临床和食用动物大肠杆菌和金黄色葡萄球菌的AMR表型数据,以确定AMR的主要特征,并探索其在人与动物界面上的关联。92 %)、头孢菌素类(63.05 %)、氟喹诺酮类(62.21 %)和四环素类(57.77 %),而金黄色葡萄球菌对青霉素酶抑制型青霉素类(90.89 %)、大环内酯类(51.51 %)、青霉素酶稳定型青霉素类(43.96 %)和林可酰胺类(43.55 %)表现出较高的耐药性。产生广谱β-内酰胺酶(ESBL)的大肠杆菌分离物占 53.26 %(1398/2526),而耐甲氧西林金黄色葡萄球菌(MRSA)的流行率为 43.81 %(435/993)。值得注意的是,对 8 至 12 种抗菌药物产生耐药性的大肠杆菌分离株比例有所增加,对 5 至 9 种抗菌药物产生耐药性的金黄色葡萄球菌分离株比例有所增加。某些耐多药(MDR)表型首先在食用动物分离物中发现,随后在临床环境中出现。同时,两个界面之间有几种 MDR 表型是共享的,在大肠杆菌中发现了 44 种,在金黄色葡萄球菌中发现了 12 种。总之,在临床大肠杆菌和金黄色葡萄球菌中观察到 MDR 的高流行率,一些 MDR 表现型先出现在食用动物中,然后才出现在临床环境中。表型对或表型群的共同出现突出表明了人类与食用动物之间可能存在 AMR 关联和传播。在 "一个健康 "框架内,将基因组数据纳入 AMR 监测是至关重要的下一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antimicrobial resistance in Escherichia coli and Staphylococcus aureus at human-animal interfaces on Chongming Island, Shanghai: A One Health perspective
Antimicrobial resistance (AMR) is a significant concern within the One Health framework due to its ability to spread across multiple interfaces. Phenotypic data remains the primary type for AMR surveillance, but exploring association across multiple interfaces poses certain challenges. In this study, AMR phenotypic data of clinical and food animal E. coli and S. aureus from Chongming Island over the past five years were analyzed to determine key characteristics of AMR and explore its association at the human-animal interface.
The clinical E. coli isolates showed significant resistance to penicillins (83.92 %), cephems (63.05 %), fluoroquinolones (62.21 %), and tetracyclines (57.77 %), while S. aureus exhibited high resistance to penicillinase-labile penicillins (90.89 %), macrolides (51.51 %), penicillinase-stable penicillins (43.96 %), and lincosamides (43.55 %). Extended-spectrum β-lactamase (ESBL)-producing E. coli isolates accounted for 53.26 % (1398/2526), while methicillin-resistant Staphylococcus aureus (MRSA) prevalence was 43.81 % (435/993). Notably, there has been an increase in the proportion of E. coli isolates resistant to 8 to 12 antimicrobial classes, and in the proportion of S. aureus isolates resistant to 5 to 9 classes. Certain multi-drug resistance (MDR) phenotypes were first identified in food animal isolates and later emerged in clinical settings. Meanwhile, several MDR phenotypes were shared between the two interfaces, with 44 identified in E. coli and 12 in S. aureus. Further co-occurrence analysis in E. coli and S. aureus identified several co-occurrence phenotypic pairs or clusters, potentially mediated by a single plasmid or multiple plasmids within a bacterium, indicating potential associations at the human-animal interface.
To summarize, a heightened prevalence of MDR in clinical E. coli and S. aureus has been observed, with some MDR profiles appearing in food animals before emerging in clinical settings. The co-occurrence of phenotypic pairs or clusters underscores the potential for AMR association and transmission between humans and food animals. Within the One Health framework, integrating genomic data into AMR monitoring is a crucial next step.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
One Health
One Health Medicine-Infectious Diseases
CiteScore
8.10
自引率
4.00%
发文量
95
审稿时长
18 weeks
期刊介绍: One Health - a Gold Open Access journal. The mission of One Health is to provide a platform for rapid communication of high quality scientific knowledge on inter- and intra-species pathogen transmission, bringing together leading experts in virology, bacteriology, parasitology, mycology, vectors and vector-borne diseases, tropical health, veterinary sciences, pathology, immunology, food safety, mathematical modelling, epidemiology, public health research and emergency preparedness. As a Gold Open Access journal, a fee is payable on acceptance of the paper. Please see the Guide for Authors for more information. Submissions to the following categories are welcome: Virology, Bacteriology, Parasitology, Mycology, Vectors and vector-borne diseases, Co-infections and co-morbidities, Disease spatial surveillance, Modelling, Tropical Health, Discovery, Ecosystem Health, Public Health.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信