wgSNP

wgSNP
  • 文章类型: Journal Article
    通过全基因组测序进行细菌基因分型在公共卫生实验室的疾病监测和疫情调查中起着至关重要的作用。这项研究评估了牛津纳米孔技术(ONT)测序在单核细胞增生李斯特菌和肠炎沙门氏菌基因分型中的有效性。我们的结果表明,ONT序列,使用R10.4.1流动池生成,并使用Dorado0.5.0超精确4.3模型进行基础处理,表现出与Illumina序列相当的准确性,有效区分来自爆发的细菌菌株。这些发现表明,ONT测序有可能成为公共卫生实验室中用于流行病学调查的细菌病原体快速全基因组测序的有希望的工具。
    目的:这项研究揭示了牛津纳米孔技术测序,本身,在公共卫生实验室中具有作为基于全基因组测序的基因分型工具的潜力,能够对细菌分离株进行常规亚型分型,用于疾病监测和疫情调查。
    Bacterial genotyping through whole-genome sequencing plays a crucial role in disease surveillance and outbreak investigations in public health laboratories. This study assessed the effectiveness of Oxford Nanopore Technologies (ONT) sequencing in the genotyping of Listeria monocytogenes and Salmonella enterica serovar Enteritidis. Our results indicated that ONT sequences, generated with the R10.4.1 flow cell and basecalled using the Dorado 0.5.0 Super Accurate 4.3 model, exhibited comparable accuracy to Illumina sequences, effectively discriminating among bacterial strains from outbreaks. These findings suggest that ONT sequencing has the potential to be a promising tool for rapid whole-genome sequencing of bacterial pathogens in public health laboratories for epidemiological investigations.
    OBJECTIVE: This study unveils that Oxford Nanopore Technologies sequencing, by itself, holds the potential to serve as a whole-genome sequencing-based genotyping tool in public health laboratories, enabling routine subtyping of bacterial isolates for disease surveillance and outbreak investigations.
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  • 文章类型: Case Reports
    除了典型的肺炎表现外,嗜肺军团菌还可引起大量症状。在这里,我们介绍了一个在随后的免疫功能低下患者中致命的医院蜂窝织炎的病例,一年后,同一病房的第二例军团病。虽然根据症状出现的日期,第一例很容易被认为是医院感染,第二种情况需要明确的分型结果被分配为医院和与第一种情况相同的环境来源,或社区获得。为了解开这个具体的问题,我们应用核心基因组多位点分型(MLST),使用文献中推荐的阈值和基于当地流行病学数据的定制阈值,对36个比利时和41个国际序列1型(ST1)分离株进行全基因组单核苷酸多态性和全基因组MLST方法.根据应用于集群隔离的阈值,这三种方法给出了不同的结果,对于第二例病例的医院设置没有得出确切的结论。我们的数据表明,尽管在疫情研究和大规模流行病学调查中取得了有希望的结果,应用于ST1疫情调查的下一代测序分型方法在湿实验室方案和生物信息学方面仍需要标准化.还需要对嗜肺乳杆菌进化时钟进行更深入的评估,以增加我们对在临床感染期间和环境中采样的分离株之间的基因组差异的理解。
    Legionella pneumophila can cause a large panel of symptoms besides the classic pneumonia presentation. Here we present a case of fatal nosocomial cellulitis in an immunocompromised patient followed, a year later, by a second case of Legionnaires\' disease in the same ward. While the first case was easily assumed as nosocomial based on the date of symptom onset, the second case required clear typing results to be assigned either as nosocomial and related to the same environmental source as the first case, or community acquired. To untangle this specific question, we applied core-genome multilocus typing (MLST), whole-genome single nucleotide polymorphism and whole-genome MLST methods to a collection of 36 Belgian and 41 international sequence-type 1 (ST1) isolates using both thresholds recommended in the literature and tailored threshold based on local epidemiological data. Based on the thresholds applied to cluster isolates together, the three methods gave different results and no firm conclusion about the nosocomial setting of the second case could been drawn. Our data highlight that despite promising results in the study of outbreaks and for large-scale epidemiological investigations, next-generation sequencing typing methods applied to ST1 outbreak investigation still need standardization regarding both wet-lab protocols and bioinformatics. A deeper evaluation of the L. pneumophila evolutionary clock is also required to increase our understanding of genomic differences between isolates sampled during a clinical infection and in the environment.
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  • 文章类型: Journal Article
    The present study was designed to identify nine Arcanobacterium phocae strains isolated from cases of mink dermatitis of a single farm in Finland and characterize the strains for epidemiological relationships. All nine strains and previously described A. phocae used for comparative purposes were identified and further characterized phenotypically, by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS), by Fourier Transform Infrared Spectroscopy (FT-IR) and genotypically by detection of phocaelysin encoding gene phl with a previously developed loop-mediated isothermal amplification (LAMP) assay and by sequencing 16S rRNA gene and gene phl, the elongation factor tu encoding gene tuf and the β subunit of bacterial RNA polymerase encoding gene rpoB. Genetic relatedness among isolates was determined using whole-genome single nucleotide polymorphism (wgSNP) analysis. The wgSNP results, partly the MALDI-TOF MS and FT-IR analyses and sequencing of the genes, revealed that the nine A. phocae strains recovered from a single farm showed close sequence similarities among each other and differed from previously investigated A. phocae strains isolated from other farms and animals in Finland and from the A. phocae type strain. This indicated a close epidemiological relationship of the A. phocae strains isolated from a single farm and that the nine A. phocae strains of the present study might have developed from a common ancestor.
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