斯里兰卡南部畜牧农民、牲畜和畜牧产品中耐甲氧西林金黄色葡萄球菌的患病率和分子流行病学:一种健康方法。

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES Infection Genetics and Evolution Pub Date : 2024-12-01 Epub Date: 2024-11-29 DOI:10.1016/j.meegid.2024.105693
M R P Kurukulasooriya, L G Tillekeratne, W M D G B Wijayaratne, C K Bodinayake, U H B Y Dilshan, A D De Silva, B P Nicholson, T Østbye, C W Woods, A De S Nagahawatte
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引用次数: 0

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)定植可导致随后的严重感染。与社区和医院相关类型不同,家畜相关MRSA (LA-MRSA)通过直接接触牲畜和受污染的牲畜产品传播给人类。本研究旨在利用One Health方法调查斯里兰卡南部畜牧农民、牲畜和畜牧产品中MRSA的患病率和分子流行病学,包括人类和动物鼻腔微生物组中LA-MRSA的存在和MRSA的丰度。收集了50个农场(2020年11月至2021年12月)的农民和牲畜的鼻拭子和牲畜产品。采用标准微生物学技术分离和确认MRSA。进行葡萄球菌染色体盒式mec分型、spa分型和多位点序列分型。鉴定的克隆与医院分离株进行了比较。选取样本进行宏基因组学分析。MRSA在农场的流行率为24.0 %(12/50),农民为7.9% %(12/152),牲畜为2.1 %(5/240),产品为1.9 %(3/157)。372年 年代。临床培养金黄色葡萄球菌,59.4 %为MRSA。在农场人员(CC5/ST5/t002、CC1/ST1/t127和ST45/CC45/t026)、牲畜(CC5/ST5/t002)和临床培养物(CC5/ST5/t002和CC5/ST6/t304)中发现了MRSA克隆,其中斯里兰卡首次报道了ST45/CC45/t026和CC5/ST6/t304。未检出LA-MRSA克隆(ST389/ST9)。动物的鼻腔微生物组更多样化,MRSA丰度更低(82.3 %)。MRSA在斯里兰卡南部的定殖流行率相对较低。2个新克隆和未发现LA-MRSA克隆。本研究强调了在“同一个健康”框架下持续监测MRSA的重要性,以确定MRSA在人、动物和环境之间的传播。
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Prevalence and molecular epidemiology of methicillin-resistant Staphylococcus aureus in livestock farmers, livestock, and livestock products in southern Sri Lanka: A one health approach.

Methicillin-resistant Staphylococcus aureus (MRSA) colonization can lead to subsequent severe infections. Unlike community and hospital-associated types, Livestock-associated MRSA (LA-MRSA) transmits to humans through direct contact with livestock and contaminated livestock products. This study aimed to investigate MRSA prevalence and molecular epidemiology in livestock farmers, livestock, and livestock products, including LA-MRSA presence and MRSA abundance in human and animal nasal microbiome, in southern Sri Lanka using a One Health approach. Nasal swabs from farmers and livestock on 50 farms (Nov 2020 - Dec 2021) and livestock products were collected. MRSA was isolated and confirmed using standard microbiological techniques. Staphylococcal chromosomal cassette mec typing, spa typing, and multilocus sequence typing were performed. Identified clones were compared with hospital isolates. Metagenomics analysis was performed on selected samples. MRSA prevalence was 24.0 % (12/50) in farms, 7.9 % (12/152) in farmers, 2.1 % (5/240) in livestock, and 1.9 % (3/157) in products. Of 372 S. aureus collected from clinical cultures, 59.4 % were MRSA. MRSA clones were identified in farm personnel (CC5/ST5/t002, CC1/ST1/t127, and ST45/CC45/t026), livestock (CC5/ST5/t002), and clinical cultures (CC5/ST5/t002 and CC5/ST6/t304), with ST45/CC45/t026 and CC5/ST6/t304 reported for the first time in Sri Lanka. LA-MRSA clones (ST389/ST9) were not detected. Animals had more diverse nasal microbiomes and lower MRSA abundance (<1.4 %) compared to humans (>82.3 %). MRSA colonization prevalence in southern Sri Lanka was relatively low. Two new clones and no LA-MRSA clones were identified. This study highlights the importance of continuing MRSA surveillance under the One Health framework to identify MRSA transmission between humans, animals, and the environment.

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来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
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