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一种通过单分子荧光显微镜检测细菌质粒上抗菌药物耐药基因的简单切割和延伸检测方法。

A simple cut and stretch assay to detect antimicrobial resistance genes on bacterial plasmids by single-molecule fluorescence microscopy.

机构信息

Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.

Department of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.

出版信息

Sci Rep. 2022 Jun 3;12(1):9301. doi: 10.1038/s41598-022-13315-w.

DOI:10.1038/s41598-022-13315-w
PMID:35660772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9166776/
Abstract

Antimicrobial resistance (AMR) is a fast-growing threat to global health. The genes conferring AMR to bacteria are often located on plasmids, circular extrachromosomal DNA molecules that can be transferred between bacterial strains and species. Therefore, effective methods to characterize bacterial plasmids and detect the presence of resistance genes can assist in managing AMR, for example, during outbreaks in hospitals. However, existing methods for plasmid analysis either provide limited information or are expensive and challenging to implement in low-resource settings. Herein, we present a simple assay based on CRISPR/Cas9 excision and DNA combing to detect antimicrobial resistance genes on bacterial plasmids. Cas9 recognizes the gene of interest and makes a double-stranded DNA cut, causing the circular plasmid to linearize. The change in plasmid configuration from circular to linear, and hence the presence of the AMR gene, is detected by stretching the plasmids on a glass surface and visualizing by fluorescence microscopy. This single-molecule imaging based assay is inexpensive, fast, and in addition to detecting the presence of AMR genes, it provides detailed information on the number and size of plasmids in the sample. We demonstrate the detection of several β-lactamase-encoding genes on plasmids isolated from clinical samples. Furthermore, we demonstrate that the assay can be performed using standard microbiology and clinical laboratory equipment, making it suitable for low-resource settings.

摘要

抗微生物药物耐药性(AMR)是对全球健康的一个快速增长的威胁。赋予细菌抗微生物药物耐药性的基因通常位于质粒上,质粒是一种可在细菌菌株和物种之间转移的圆形染色体外 DNA 分子。因此,有效的方法来描述细菌质粒并检测耐药基因的存在可以协助管理 AMR,例如在医院爆发期间。然而,现有的质粒分析方法要么提供有限的信息,要么昂贵且难以在资源匮乏的环境中实施。在这里,我们提出了一种基于 CRISPR/Cas9 切割和 DNA 梳理的简单检测方法,用于检测细菌质粒上的抗微生物药物耐药基因。Cas9 识别感兴趣的基因并进行双链 DNA 切割,导致圆形质粒线性化。质粒构型从圆形到线性的变化,以及因此 AMR 基因的存在,通过在玻璃表面上拉伸质粒并通过荧光显微镜可视化来检测。这种基于单分子成像的检测方法成本低廉、快速,除了检测 AMR 基因的存在外,还提供了关于样品中质粒数量和大小的详细信息。我们展示了从临床样本中分离的质粒上几种β-内酰胺酶编码基因的检测。此外,我们证明该检测可以使用标准微生物学和临床实验室设备进行,使其适合资源匮乏的环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6178/9166776/7fef861e0ce6/41598_2022_13315_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6178/9166776/7b7448152f9a/41598_2022_13315_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6178/9166776/7f32196a623d/41598_2022_13315_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6178/9166776/b7a8785470b8/41598_2022_13315_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6178/9166776/60ed8a50388e/41598_2022_13315_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6178/9166776/7fef861e0ce6/41598_2022_13315_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6178/9166776/7b7448152f9a/41598_2022_13315_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6178/9166776/7f32196a623d/41598_2022_13315_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6178/9166776/b7a8785470b8/41598_2022_13315_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6178/9166776/60ed8a50388e/41598_2022_13315_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6178/9166776/7fef861e0ce6/41598_2022_13315_Fig5_HTML.jpg

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High diversity of bla-encoding plasmids in Klebsiella pneumoniae isolated from neonates in a Vietnamese hospital.越南医院新生儿分离的肺炎克雷伯菌中 bla 编码质粒的多样性很高。
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