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Accurate Identification of Common Pathogenic Nocardia Species: Evaluation of a Multilocus Sequence Analysis Platform and Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry

机译:准确鉴定常见病原性诺卡氏菌物种:多基因座序列分析平台和基质辅助激光解吸电离飞行时间质谱的评估

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摘要

Species identification of Nocardia is not straightforward due to rapidly evolving taxonomy, insufficient discriminatory power of conventional phenotypic methods and also of single gene locus analysis including 16S rRNA gene sequencing. Here we evaluated the ability of a 5-locus (16S rRNA, gyrB, secA1, hsp65 and rpoB) multilocus sequence analysis (MLSA) approach as well as that of matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) in comparison with sequencing of the 5’-end 606 bp partial 16S rRNA gene to provide identification of 25 clinical isolates of Nocardia. The 5’-end 606 bp 16S rRNA gene sequencing successfully assigned 24 of 25 (96%) clinical isolates to species level, namely Nocardia cyriacigeorgica (n = 12, 48%), N. farcinica (n = 9, 36%), N. abscessus (n = 2, 8%) and N. otitidiscaviarum (n = 1, 4%). MLSA showed concordance with 16S rRNA gene sequencing results for the same 24 isolates. However, MLSA was able to identify the remaining isolate as N. wallacei, and clustered N. cyriacigeorgica into three subgroups. None of the clinical isolates were correctly identified to the species level by MALDI-TOF MS analysis using the manufacturer-provided database. A small “in-house” spectral database was established incorporating spectra of five clinical isolates representing the five species identified in this study. After complementation with the “in-house” database, of the remaining 20 isolates, 19 (95%) were correctly identified to species level (score ≥ 2.00) and one (an N. abscessus strain) to genus level (score ≥ 1.70 and < 2.00). In summary, MLSA showed superior discriminatory power compared with the 5’-end 606 bp partial 16S rRNA gene sequencing for species identification of Nocardia. MALDI-TOF MS can provide rapid and accurate identification but is reliant on a robust mass spectra database.
机译:由于快速发展的分类学,常规表型方法的鉴别能力不足以及单基因座分析(包括16S rRNA基因测序),诺卡氏菌的种类鉴定并不简单。在这里,我们评估了5位点(16S rRNA,gyrB,secA1,hsp65和rpoB)多位点序列分析(MLSA)方法以及基质辅助激光解吸电离飞行时间质谱(MALDI-TOF)的能力。 MS)与5'端606 bp部分16S rRNA基因测序的比较,以鉴定25种诺卡氏菌临床分离株。 5'端606 bp 16S rRNA基因测序成功地将25种临床分离株中的24种(96%)分配给物种水平,即诺卡氏诺卡氏菌(n = 12、48%),法氏猪笼草(n = 9、36%),脓肿猪笼草(n = 2,8%)和otitidiscaviarum(n = 1,4%)。 MLSA显示与相同的24个分离株的16S rRNA基因测序结果一致。但是,MLSA能够将其余的分离株鉴定为华莱西猪笼草,并将 ciriacigeorgica 猪笼草分为三个亚组。使用制造商提供的数据库,通过MALDI-TOF MS分析,未正确鉴定出临床分离物至物种水平。建立了一个小的“内部”光谱数据库,其中包含代表本研究中鉴定的五个物种的五个临床分离株的光谱。在使用“内部”数据库进行补充之后,其余20种分离株中,正确鉴定出19种(95%)的物种水平(得分≥2.00)和一种( N )。 株)到属水平(得分≥1.70和<2.00)。综上所述,MLSA与5'-末端606 bp部分16S rRNA基因测序相比具有更好的鉴别能力,可用于鉴定诺卡氏菌。 MALDI-TOF MS可以提供​​快速,准确的鉴定,但依赖于强大的质谱数据库。

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