首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Automated comparative sequence analysis by base-specific cleavage and mass spectrometry for nucleic acid-based microbial typing
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Automated comparative sequence analysis by base-specific cleavage and mass spectrometry for nucleic acid-based microbial typing

机译:通过碱基特异性裂解和质谱法进行基于核酸的微生物分型的自动比较序列分析

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Traditional microbial typing technologies for the characterization of pathogenic microorganisms and monitoring of their global spread are often difficult to standardize and poorly portable, and they lack sufficient ease of use, throughput, and automation. To overcome these problems, we introduce the use of comparative sequencing by MALDI-TOF MS for automated high-throughput microbial DNA sequence analysis. Data derived from the public multilocus sequence typing (MLST) database (http://pubmlst.org/ neisseria) established a reference set of expected peak patterns. A model pathogen, Neisseria meningitidis, was used to validate the technology and explore its applicability as an alternative to dideoxy sequencing. One hundred N. meningitidis samples were typed by comparing MALDI-TOF MS fingerprints of the standard MLST loci to reference sequences available in the public MLST database. Identification results can be obtained in 2 working days. Results were in concordance with classical dideoxy sequencing with 98% correct automatic identification. Sequence types (STs) of 89 samples were represented in the database, seven samples revealed new STs, including three new alleles, and four samples contained mixed populations of multiple STs. The approach shows interlaboratory reproducibility and allows for the exchange of mass spectrometric fingerprints to study the geographic spread of epidemic N. meningitidis strains or other microbes of clinical importance.
机译:用于表征病原微生物和监测其全球传播的传统微生物分型技术通常难以标准化且携带不便,并且缺乏足够的易用性,通量和自动化程度。为了克服这些问题,我们介绍了使用MALDI-TOF MS进行比较测序来进行自动化的高通量微生物DNA序列分析。来自公共多基因座序列分型(MLST)数据库(http://pubmlst.org/ neisseria)的数据建立了一组预期的峰型参考。使用模型病原体脑膜炎奈瑟氏菌验证该技术并探索其作为双脱氧测序的替代方法的适用性。通过将标准MLST位点的MALDI-TOF MS指纹与公共MLST数据库中可用的参考序列进行比较,对一百个脑膜炎奈瑟氏球菌样品进行了分型。鉴定结果可在2个工作日内获得。结果与经典双脱氧测序法一致,并具有98%的正确自动识别。数据库中代表了89个样品的序列类型(ST),七个样品揭示了新的ST,包括三个新的等位基因,四个样品包含多个ST的混合种群。该方法显示了实验室间的可重复性,并允许交换质谱指纹图来研究流行性脑膜炎奈瑟氏菌菌株或其他具有临床重要性的微生物的地理分布。

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