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首页> 外文期刊>Journal of Clinical Microbiology >Detecting Staphylococcus aureus Virulence and Resistance Genes: a Comparison of Whole-Genome Sequencing and DNA Microarray Technology
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Detecting Staphylococcus aureus Virulence and Resistance Genes: a Comparison of Whole-Genome Sequencing and DNA Microarray Technology

机译:检测金黄色葡萄球菌的毒力和耐药基因:全基因组测序和DNA芯片技术的比较。

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摘要

Staphylococcus aureus is a major bacterial pathogen causing a variety of diseases ranging from wound infections to severe bacteremia or intoxications. Besides host factors, the course and severity of disease is also widely dependent on the genotype of the bacterium. Whole-genome sequencing (WGS), followed by bioinformatic sequence analysis, is currently the most extensive genotyping method available. To identify clinically relevant staphylococcal virulence and resistance genes in WGS data, we developed an in silico typing scheme for the software SeqSphere+ (Ridom GmbH, Münster, Germany). The implemented target genes (n = 182) correspond to those queried by the Identibac S. aureus Genotyping DNA microarray (Alere Technologies, Jena, Germany). The in silico scheme was evaluated by comparing the typing results of microarray and of WGS for 154 human S. aureus isolates. A total of 96.8% (n = 27,119) of all typing results were equally identified with microarray and WGS (40.6% present and 56.2% absent). Discrepancies (3.2% in total) were caused by WGS errors (1.7%), microarray hybridization failures (1.3%), wrong prediction of ambiguous microarray results (0.1%), or unknown causes (0.1%). Superior to the microarray, WGS enabled the distinction of allelic variants, which may be essential for the prediction of bacterial virulence and resistance phenotypes. Multilocus sequence typing clonal complexes and staphylococcal cassette chromosome mec element types inferred from microarray hybridization patterns were equally determined by WGS. In conclusion, WGS may substitute array-based methods due to its universal methodology, open and expandable nature, and rapid parallel analysis capacity for different characteristics in once-generated sequences.
机译:金黄色葡萄球菌是引起多种疾病的主要细菌病原,从伤口感染到严重菌血症或中毒。除宿主因素外,疾病的病程和严重程度还广泛取决于细菌的基因型。全基因组测序(WGS),然后进行生物信息学序列分析,是目前最广泛的基因分型方法。为了鉴定WGS数据中临床相关的葡萄球菌毒力和耐药基因,我们为SeqSphere + 软件(Ridom GmbH,德国明斯特)开发了 insilico 分型方案。实施的靶基因( n = 182)对应于金黄色葡萄球菌基因分型DNA微阵列(Alere Technologies,Jena,Germany)查询的那些。通过比较154株人类金黄色葡萄球菌的微阵列和WGS的分型结果来评估 insilico 方案。使用微阵列和WGS可以平均鉴定出所有打字结果的96.8%( n = 27,119)(存在40.6%和不存在56.2%)。差异(总计3.2%)是由WGS错误(1.7%),微阵列杂交失败(1.3%),对歧义微阵列结果的错误预测(0.1%)或未知原因(0.1%)引起的。 WGS优于微阵列,可以区分等位基因变体,这对于预测细菌毒力和耐药性表型可能是必不可少的。通过微阵列杂交模式推断的多基因座序列分型克隆复合物和金黄色葡萄球菌盒式染色体 mec 元件类型由WGS确定。总之,WGS可以替代基于数组的方法,因为它具有通用的方法,开放和可扩展的特性以及对一旦生成的序列中的不同特征具有快速并行分析能力。

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