Kurukulasooriya M R P, Tillekeratne L G, Wijayaratne W M D G B, Bodinayake C K, Dilshan U H B Y, De Silva A D, Nicholson B P, Østbye T, Woods C W, Nagahawatte A De S
Duke-Ruhuna Collaborative Research Centre, Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka.
Duke-Ruhuna Collaborative Research Centre, Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka; Duke Global Health Institute, Durham, NC, USA; Department of Medicine, Duke University, Durham, NC, USA; Department of Medicine, Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka.
Infect Genet Evol. 2024 Dec;126:105693. doi: 10.1016/j.meegid.2024.105693. Epub 2024 Nov 29.
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.
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。与社区型和医院型不同,家畜相关MRSA(LA-MRSA)通过与家畜及受污染的畜产品直接接触传播给人类。本研究旨在采用“同一健康”方法调查斯里兰卡南部家畜养殖者、家畜及畜产品中的MRSA流行情况和分子流行病学,包括人类和动物鼻腔微生物群中LA-MRSA的存在情况及MRSA丰度。收集了50个农场(2020年11月至2021年12月)养殖者和家畜的鼻拭子以及畜产品。使用标准微生物学技术分离并确认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。将鉴定出的克隆与医院分离株进行比较。对选定样本进行宏基因组学分析。农场中MRSA流行率为24.0%(12/50),养殖者中为7.9%(12/152),家畜中为2.1%(5/240),产品中为1.9%(3/157)。从临床培养物中收集的372株金黄色葡萄球菌中,59.4%为MRSA。在农场人员(CC5/ST5/t002、CC1/ST1/t127和ST45/CC45/t026)、家畜(CC5/ST5/t002)和临床培养物(CC5/ST5/t002和CC5/ST6/t304)中鉴定出MRSA克隆,其中ST45/CC45/t026和CC5/ST6/t304在斯里兰卡首次报道。未检测到LA-MRSA克隆。与人类(>82.3%)相比,动物的鼻腔微生物群更多样化,MRSA丰度更低(<1.4%)。斯里兰卡南部的MRSA定植流行率相对较低。鉴定出两个新克隆,未发现LA-MRSA克隆。本研究强调了在“同一健康”框架下持续进行MRSA监测以确定MRSA在人类、动物和环境之间传播的重要性。