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首页> 外文期刊>FEMS Microbiology Letters >Development of a single-tube loop-mediated isothermal amplification assay for detection of four pathogens of bacterial meningitis
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Development of a single-tube loop-mediated isothermal amplification assay for detection of four pathogens of bacterial meningitis

机译:用于检测细菌性脑膜炎的四种病原体的单管环介导的等温扩增测定法的开发

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Several loop-mediated isothermal amplification (LAMP) assays have been developed to detect common causative pathogens of bacterial meningitis (BM). However, no LAMP assay is reported to detect Streptococcus agalactiae and Streptococcus suis, which are also among common pathogens of BM. Moreover, it is laborious and expensive by performing multiple reactions for each sample to detect bacterial pathogen. Thus, we aimed to design and develop a single-tube LAMP assay capable of detecting multiple bacterial species, based on the nucleotide sequences of the 16S rRNA genes of the bacteria. The nucleotide sequences of the 16S rRNA genes of main pathogens involved in BM were aligned to identify conserved regions, which were further used to design broad range specific LAMP assay primers. We successfully designed a set of broad range specific LAMP assay primers for simultaneous detection of four species including Staphylococcus aureus, Streptococcus pneumoniae, S. suis and S. agalactiae. The broad range LAMP assay was highly specific without cross-reactivity with other bacteria including Haemophilus influenzae, Neisseria meningitidis and Escherichia coli. The sensitivity of our LAMP assay was 100-1000 times higher compared with the conventional PCR assay. The bacterial species could be identified after digestion of the LAMP products with restriction endonuclease DdeI and HaeIII.
机译:已经开发了几种环介导的等温扩增(LAMP)测定法,以检测细菌性脑膜炎(BM)的常见病原体。但是,尚无LAMP检测方法可以检测无乳链球菌和猪链球菌,它们也是BM的常见病原体。此外,通过对每个样品进行多种反应以检测细菌病原体是费力且昂贵的。因此,我们旨在基于细菌的16S rRNA基因的核苷酸序列设计和开发一种能够检测多种细菌的单管LAMP检测方法。将与BM相关的主要病原体的16S rRNA基因的核苷酸序列进行比对,以鉴定保守区域,将其进一步用于设计广泛范围的特异性LAMP分析引物。我们成功设计了一套广泛的特异性LAMP分析引物,用于同时检测四个物种,包括金黄色葡萄球菌,肺炎链球菌,猪链球菌和无乳链球菌。广泛的LAMP分析具有高度特异性,并且与其他细菌(包括流感嗜血杆菌,脑膜炎奈瑟氏球菌和大肠杆菌)没有交叉反应。我们的LAMP分析的灵敏度是传统PCR分析的100-1000倍。用限制性核酸内切酶DdeI和HaeIII消化LAMP产物后,可以鉴定出细菌种类。

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