面向反刍动物乳中金黄色葡萄球菌肠毒素基因即时检测的样品到应答微流控装置。

IF 6.1 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS
Lab on a Chip Pub Date : 2025-01-08 DOI:10.1039/d4lc00907j
Maha Shalaby, Valentina Busin, Xiaoxiang Yan, Seyda Cengiz, Mehmet Cemal Adiguzel, Jonathan M Cooper, Taya Forde, Julien Reboud
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引用次数: 0

摘要

牛奶通常既要进行动物疾病和健康指标的筛查,也要进行食源性危害的筛查。这些分析包括对金黄色葡萄球菌的检测,金黄色葡萄球菌可以产生一种肠毒素,引起葡萄球菌性食物中毒(SFP),这通常会导致人类突然出现严重的胃肠道症状。关于SFP的流行病学数据有限,特别是在低收入和中等收入国家。许多用于检测葡萄球菌肠道毒素的传统检测方法依赖于检测编码它们的基因,要么直接在食品样品中检测,要么在细菌培养后检测。目前,许多基于核酸的方法需要特定的专业知识和设备,而细菌培养需要24-48小时;这两种因素都限制了在食品安全紧急情况或常规筛查期间的努力。在这里,我们提出了一种“样品到答案”的等温核酸环介导扩增(LAMP)实验在微流控装置中检测反刍动物牛奶中的金黄色葡萄球菌肠毒素基因。针对两种最常见的金黄色葡萄球菌肠毒素编码基因(A和B)的多重LAMP检测被整合到一个微流控装置中,该装置结合了简单的1:10稀释样品制备和易于读取的横向流动检测。我们在加了添加剂的牛奶和羊奶样品中达到了每毫升104个菌落形成单位的检测限,比欧洲对原料奶中凝固酶阳性葡萄球菌最大允许存在的建议灵敏度高了一个数量级。该试验在检测其他非产肠毒素金黄色葡萄球菌菌株或相关食源性病原体时无交叉反应性。该检测将微流控装置的使用简单性与核酸检测的灵敏度、特异性和快速性相结合,并提供简单的侧流读数,为确保人类食用牛奶的安全性提供了合适的设备。为了说明其在需求点实际应用方面的潜力,在土耳其农村的农业环境中进行了有限的可行性测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sample-to-answer microfluidic device towards the point-of-need detection of Staphylococcus aureus enterotoxin genes in ruminant milk.

Milk is commonly screened both for indicators of animal disease and health, but also for foodborne hazards. Included in these analyses is the detection of Staphylococcus aureus, that can produce an enterotoxin, causing staphylococcal food poisoning (SFP), which often leads to sudden onset of significant gastrointestinal symptoms in humans. Epidemiological data on SFP are limited, particularly in low- and middle-income countries. Many conventional assays for the detection of staphylococcal enterotoxins rely on the detection of the genes coding for them, either directly in food samples or after bacterial culture. Currently, many of the nucleic acid-based methods used require specific expertise and equipment, whilst bacterial culture takes 24-48 hours; both are contributory factors that limit efforts either during food safety emergencies or routine screening. Here we present the development of a "sample-to-answer" isothermal nucleic acid loop-mediated amplification (LAMP) assay in a microfluidic device for the detection of Staphylococcus aureus enterotoxin genes in ruminant milk. A multiplex LAMP assay targeting two of the most prevalent S. aureus enterotoxin-encoding genes (A and B) was integrated into a microfluidic device combining simple 1 : 10 dilution for sample preparation and a lateral flow assay for easy readout. We achieved a limit of detection of 104 colony forming units per ml in spiked cow and goat milk samples, an order of magnitude more sensitive than the European recommendation for the maximum allowable presence of coagulase-positive staphylococci in raw milk. The assay showed no cross-reactivity in detecting other tested non-enterotoxigenic S. aureus strains or associated foodborne pathogens. The test integrated the simplicity of use of microfluidic devices with the sensitivity, specificity and rapidity of a nucleic acid-based assay, and a simple lateral flow readout to provide an appropriate device to ensure the safety of milk for human consumption. To illustrate its potential for point-of-need practical applications, the test was performed in agricultural settings in rural Turkey in a limited feasibility exercise.

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来源期刊
Lab on a Chip
Lab on a Chip 工程技术-化学综合
CiteScore
11.10
自引率
8.20%
发文量
434
审稿时长
2.6 months
期刊介绍: Lab on a Chip is the premiere journal that publishes cutting-edge research in the field of miniaturization. By their very nature, microfluidic/nanofluidic/miniaturized systems are at the intersection of disciplines, spanning fundamental research to high-end application, which is reflected by the broad readership of the journal. Lab on a Chip publishes two types of papers on original research: full-length research papers and communications. Papers should demonstrate innovations, which can come from technical advancements or applications addressing pressing needs in globally important areas. The journal also publishes Comments, Reviews, and Perspectives.
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