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快速检测鼻疽伯克霍尔德菌的侧向流动重组酶聚合酶扩增检测法。

Rapid detection of Burkholderia pseudomallei with a lateral flow recombinase polymerase amplification assay.

机构信息

Department of Pestis, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Changping, Beijing, China.

Department of Diarrheal Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Changping, Beijing, China.

出版信息

PLoS One. 2019 Jul 8;14(7):e0213416. doi: 10.1371/journal.pone.0213416. eCollection 2019.

Abstract

Melioidosis is a severe infectious disease caused by gram-negative, facultative intracellular pathogen Burkholderia pseudomallei (B. pseudomallei). Although cases are increasing reported from other parts of the world, it is an illness of tropical and subtropical climates primarily found in southeast Asia and northern Australia. Because of a 40% mortality rate, this life-threatening disease poses a public health risk in endemic area. Early detection of B. pseudomallei infection is vital for prognosis of a melioidosis patient. In this study, a novel isothermal recombinase polymerase amplification combined with lateral flow dipstick (LF-RPA) assay was established for rapid detection of B. pseudomallei. A set of primer-probe targeting orf2 gene within the putative type III secretion system (T3SS) cluster genes was generated and parameters for the LF-RPA assay were optimized. Result can be easy visualized in 30 minutes with the limit of detection (LOD) as low as 20 femtogram (fg) (ca. 25.6 copies) of B. pseudomallei genomic DNA without a specific equipment. The assay is highly specific as no cross amplification was observed with Burkholderia mallei, members of the Burkholderia cepacia-complex and 35 non-B. pseudomallei bacteria species. Moreover, isolates from patients in Hainan (N = 19), Guangdong (N = 1), Guangxi (N = 3) province of China as well as in Australia (N = 3) and Thailand (N = 1) were retrospectively confirmed by the newly developed method. LODs for B. pseudomallei-spiked soil and blood samples were 2.1×103 CFU/g and 4.2×103 CFU/ml respectively. The sensitivity of the LF-RPA assay was comparable to TaqMan Real-Time PCR (TaqMan PCR). In addition, the LF-RPA assay exhibited a better tolerance to inhibitors in blood than TaqMan PCR. Our results showed that the LF-RPA assay is an alternative to existing PCR-based methods for detection of B. pseudomallei with a potentiality of early accurate diagnosis of melioidosis at point of care or in-field use.

摘要

类鼻疽是一种由革兰氏阴性、兼性细胞内病原体伯克霍尔德菌假单胞菌(B. pseudomallei)引起的严重传染病。尽管世界各地越来越多的报告病例,但这种疾病主要发生在东南亚和澳大利亚北部的热带和亚热带气候地区。由于 40%的死亡率,这种危及生命的疾病在流行地区构成了公共卫生风险。早期检测 B. pseudomallei 感染对类鼻疽患者的预后至关重要。在这项研究中,建立了一种新的等温重组酶聚合酶扩增结合侧流试纸(LF-RPA)检测方法,用于快速检测 B. pseudomallei。针对假定的 III 型分泌系统(T3SS)簇基因中的 orf2 基因设计了一组引物-探针,并对 LF-RPA 检测方法的参数进行了优化。结果可以在 30 分钟内轻松可视化,检测限(LOD)低至 20 飞克(fg)(约 25.6 拷贝)的 B. pseudomallei 基因组 DNA,无需特定设备。该检测方法具有高度特异性,因为与 Burkholderia mallei、伯克霍尔德菌洋葱伯克霍尔德菌复合群成员以及 35 种非 B. pseudomallei 细菌物种均无交叉扩增。此外,从中国海南(N=19)、广东(N=1)、广西(N=3)以及澳大利亚(N=3)和泰国(N=1)的患者中分离的菌株也通过新开发的方法得到了回顾性确认。B. pseudomallei 污染土壤和血液样本的 LOD 分别为 2.1×103 CFU/g 和 4.2×103 CFU/ml。LF-RPA 检测方法的灵敏度与 TaqMan 实时 PCR(TaqMan PCR)相当。此外,LF-RPA 检测方法在血液中对抑制剂的耐受性优于 TaqMan PCR。我们的结果表明,LF-RPA 检测方法是现有基于 PCR 的方法的替代方法,可用于检测 B. pseudomallei,具有在床边或现场进行早期准确诊断类鼻疽的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df7d/6613700/545c32153f2d/pone.0213416.g001.jpg

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