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Cas12a/Guide RNA 为基础的平台用于快速准确鉴定主要物种。

Cas12a/Guide RNA-Based Platform for Rapid and Accurate Identification of Major Species.

机构信息

National Clinical Research Center for Infectious Diseases, Guangdong Key Laboratory of Emerging Infectious Diseases, Shenzhen Third People's Hospital, Southern University of Science and Technology, Shenzhen, China.

State Key Laboratory of Respiratory Disease, Guangzhou Institutes of Biomedicine and Health (GIBH), Chinese Academy of Sciences (CAS), Guangzhou, China.

出版信息

J Clin Microbiol. 2020 Jan 28;58(2). doi: 10.1128/JCM.01368-19.

DOI:10.1128/JCM.01368-19
PMID:31723010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6989083/
Abstract

infection and nontuberculous mycobacteria (NTM) infections exhibit similar clinical symptoms; however, the therapies for these two types of infections are different. Therefore, the rapid and accurate identification of and NTM species is very important for the control of tuberculosis and NTM infections. In the present study, a Cas12a/guide RNA (gRNA)-based platform was developed to identify and most NTM species. By designing species-specific gRNA probes targeting the sequence, a Cas12a/gRNA-based platform successfully identified and six major NTM species (, , , , , and ) without cross-reactivity. In a blind assessment, a total of 72 out of 73 clinical isolates were correctly identified, which is consistent with previous sequencing results. These results suggest that the Cas12a/gRNA-based platform is a promising tool for the rapid, accurate, and cost-effective identification of both and NTM species.

摘要

感染和非结核分枝杆菌(NTM)感染表现出相似的临床症状;然而,这两种类型的感染的治疗方法是不同的。因此,快速准确地鉴定结核分枝杆菌和 NTM 物种对于控制结核病和 NTM 感染非常重要。在本研究中,开发了一种 Cas12a/guide RNA(gRNA)为基础的平台来鉴定结核分枝杆菌和大多数 NTM 物种。通过设计针对 序列的物种特异性 gRNA 探针,Cas12a/gRNA 为基础的平台成功地鉴定了结核分枝杆菌和六种主要的 NTM 物种(结核分枝杆菌、牛分枝杆菌、非洲分枝杆菌、堪萨斯分枝杆菌、海分枝杆菌和龟分枝杆菌),没有交叉反应。在一项盲法评估中,总共 73 株临床分离株中有 72 株得到了正确鉴定,这与之前的 测序结果一致。这些结果表明,Cas12a/gRNA 为基础的平台是一种快速、准确和具有成本效益的鉴定结核分枝杆菌和 NTM 物种的有前途的工具。

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本文引用的文献

1
Evaluation of the performance of two real-time PCR assays for detecting Mycobacterium species.两种用于检测分枝杆菌属的实时荧光定量PCR检测方法的性能评估。
J Clin Lab Anal. 2019 Jan;33(1):e22645. doi: 10.1002/jcla.22645. Epub 2018 Aug 13.
2
CRISPR-Cas12a-assisted nucleic acid detection.CRISPR-Cas12a辅助的核酸检测
Cell Discov. 2018 Apr 24;4:20. doi: 10.1038/s41421-018-0028-z. eCollection 2018.
3
Increasing nontuberculous mycobacteria reporting rates and species diversity identified in clinical laboratory reports.提高临床实验室报告中报告的非结核分枝杆菌的检出率和物种多样性。
BMC Infect Dis. 2018 Apr 10;18(1):163. doi: 10.1186/s12879-018-3043-7.
4
Paradigm for diagnosing mycobacterial disease: direct detection and differentiation of complex and non-tuberculous mycobacteria in clinical specimens using multiplex real-time PCR.用于诊断分枝杆菌病的模式:使用多重实时 PCR 直接检测和区分临床标本中的复杂和非结核分枝杆菌。
J Clin Pathol. 2018 Sep;71(9):774-780. doi: 10.1136/jclinpath-2017-204945. Epub 2018 Mar 20.
5
CRISPR-Cas12a has both cis- and trans-cleavage activities on single-stranded DNA.CRISPR-Cas12a对单链DNA具有顺式切割和反式切割活性。
Cell Res. 2018 Apr;28(4):491-493. doi: 10.1038/s41422-018-0022-x. Epub 2018 Mar 12.
6
CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity.CRISPR-Cas12a 靶向结合可释放非特异性单链 DNA 酶活性。
Science. 2018 Apr 27;360(6387):436-439. doi: 10.1126/science.aar6245. Epub 2018 Feb 15.
7
Genotyping Multidrug-Resistant Mycobacterium tuberculosis from Primary Sputum and Decontaminated Sediment with an Integrated Microfluidic Amplification Microarray Test.利用集成微流控扩增微阵列检测法对原发性痰液和去污染沉淀物中的耐多药结核分枝杆菌进行基因分型。
J Clin Microbiol. 2018 Feb 22;56(3). doi: 10.1128/JCM.01652-17. Print 2018 Mar.
8
Distribution of non-tuberculosis mycobacteria strains from suspected tuberculosis patients by heat shock protein 65 PCR-RFLP.采用热休克蛋白65聚合酶链反应-限制性片段长度多态性分析对疑似结核病患者的非结核分枝杆菌菌株进行分型
Saudi J Biol Sci. 2017 Sep;24(6):1380-1386. doi: 10.1016/j.sjbs.2016.02.001. Epub 2016 Feb 6.
9
Development of a One-Step Multiplex PCR Assay for Differential Detection of Major Mycobacterium Species.一种用于主要分枝杆菌菌种鉴别检测的一步多重PCR检测方法的开发。
J Clin Microbiol. 2017 Sep;55(9):2736-2751. doi: 10.1128/JCM.00549-17. Epub 2017 Jun 28.
10
Nucleic acid detection with CRISPR-Cas13a/C2c2.利用CRISPR-Cas13a/C2c2进行核酸检测。
Science. 2017 Apr 28;356(6336):438-442. doi: 10.1126/science.aam9321. Epub 2017 Apr 13.