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基于CRISPR Cas系统的病原体快速检测。

Rapid detection of pathogenic based on CRISPR Cas system.

作者信息

Rathore Pallavi, Basnet Ashesh, Kilonzo-Nthenge Agnes, Dumenyo Korsi, Yadegari Zeinab, Taheri Ali

机构信息

Department of Agricultural Science and Engineering, College of Agriculture, Tennessee State University, Nashville, TN, United States.

Department of Food and Animal Sciences, College of Agriculture, Tennessee State University, Nashville, TN, United States.

出版信息

Front Microbiol. 2024 Jun 26;15:1423478. doi: 10.3389/fmicb.2024.1423478. eCollection 2024.

Abstract

Access to safe and nutritious food is critical for maintaining life and supporting good health. Eating food that is contaminated with pathogens leads to serious diseases ranging from diarrhea to cancer. Many foodborne infections can cause long-term impairment or even death. Hence, early detection of foodborne pathogens such as pathogenic strains is essential for public safety. Conventional methods for detecting these bacteria are based on culturing on selective media and following standard biochemical identification. Despite their accuracy, these methods are time-consuming. PCR-based detection of pathogens relies on sophisticated equipment and specialized technicians which are difficult to find in areas with limited resources. Whereas CRISPR technology is more specific and sensitive for identifying pathogenic bacteria because it employs programmable CRISPR-Cas systems that target particular DNA sequences, minimizing non-specific binding and cross-reactivity. In this project, a robust detection method based on CRISPR-Cas12a sensing was developed, which is rapid, sensitive and specific for detection of pathogenic isolates that were collected from the fecal samples from adult goats from 17 farms in Tennessee. Detection reaction contained amplified PCR products for the pathogenic regions, reporter probe, Cas12a enzyme, and crRNA specific to three pathogenic genes-stx1, stx2, and hlyA. The CRISPR reaction with the pathogenic bacteria emitted fluorescence when excited under UV light. To evaluate the detection sensitivity and specificity of this assay, its results were compared with PCR based detection assay. Both methods resulted in similar results for the same samples. This technique is very precise, highly sensitive, quick, cost effective, and easy to use, and can easily overcome the limitations of the present detection methods. This project can result in a versatile detection method that is easily adaptable for rapid response in the detection and surveillance of diseases that pose large-scale biosecurity threats to human health, and plant and animal production.

摘要

获取安全且营养丰富的食物对于维持生命和促进健康至关重要。食用被病原体污染的食物会导致从腹泻到癌症等严重疾病。许多食源性感染可导致长期损害甚至死亡。因此,早期检测食源性病原体(如致病菌株)对公共安全至关重要。检测这些细菌的传统方法基于在选择性培养基上培养并遵循标准生化鉴定。尽管这些方法准确,但耗时较长。基于PCR的病原体检测依赖于精密设备和专业技术人员,在资源有限的地区很难找到。而CRISPR技术在识别致病细菌方面更具特异性和敏感性,因为它采用了靶向特定DNA序列的可编程CRISPR-Cas系统,最大限度地减少了非特异性结合和交叉反应。在本项目中,开发了一种基于CRISPR-Cas12a传感的强大检测方法,该方法对从田纳西州17个农场成年山羊粪便样本中分离出的致病菌株进行检测时快速、灵敏且特异。检测反应包含致病区域的扩增PCR产物、报告探针、Cas12a酶以及针对三个致病基因stx1、stx2和hlyA的crRNA。与致病细菌的CRISPR反应在紫外光激发下发出荧光。为了评估该检测方法的灵敏度和特异性,将其结果与基于PCR的检测方法进行了比较。两种方法对相同样本的检测结果相似。该技术非常精确、高度灵敏、快速、经济高效且易于使用,能够轻松克服现有检测方法的局限性。本项目可产生一种通用的检测方法,易于适应对人类健康、动植物生产构成大规模生物安全威胁的疾病的检测和监测中的快速响应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fc/11233538/9b44c1d0882d/fmicb-15-1423478-g001.jpg

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