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首页> 外文期刊>Journal of Microbiological Methods >A comparison of different pre-lysis methods and extraction kits for recovery of Streptococcus agalacticae (Lancefield group B Streptococcus) DNA from whole blood
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A comparison of different pre-lysis methods and extraction kits for recovery of Streptococcus agalacticae (Lancefield group B Streptococcus) DNA from whole blood

机译:从全血中回收无乳链球菌(兰斯菲尔德B组链球菌)DNA的不同预裂解方法和提取试剂盒的比较

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摘要

Sub-optimal recovery of bacterial DNA from whole blood samples can limit the sensitivity of molecular assays to detect pathogenic bacteria. We compared 3 different pre-lysis protocols (none, mechanical pre-lysis and achromopeptidase pre-lysis) and 5 commercially available DNA extraction platforms for direct detection of Group B Streptococcus (GBS) in spiked whole blood samples, without enrichment culture. DNA was extracted using the QIAamp Blood Mini kit (Qiagen), UCP Pathogen Mini kit (Qiagen), QuickGene DNA Whole Blood kit S (Fuji), Speed Xtract Nucleic Acid Kit 200 (Qiagen) and MagNA Pure Compact Nucleic Acid Isolation Kit I (Roche Diagnostics Corp). Mechanical pre-lysis increased yields of bacterial genomic DNA by 51.3 fold (95% confidence interval; 31.6-85.1, p 0.001) and pre-lysis with achromopeptidase by 6.1 fold (95% CI; 42-8.9, p 0.001), compared with no pre-lysis. Differences in yield due to pre-lysis were 2-3 fold larger than differences in yield between extraction methods. Including a pre-lysis step can improve the limits of detection of GBS using PCR or other molecular methods without need for culture. (C) 2016 Elsevier B.V. All rights reserved.
机译:从全血样本中回收细菌DNA的效果欠佳,这可能会限制分子分析检测病原细菌的敏感性。我们比较了3种不同的预裂解方案(无,机械预裂解和无色肽酶预裂解)和5种市售DNA提取平台,可直接检测加标全血样品中的B组链球菌(GBS),而无需富集培养。使用QIAamp Blood Mini试剂盒(Qiagen),UCP Pathogen Mini试剂盒(Qiagen),QuickGene DNA全血试剂盒S(Fuji),Speed Xtract核酸试剂盒200(Qiagen)和MagNA Pure Compact核酸分离试剂盒I(罗氏诊断公司)。机械预裂解使细菌基因组DNA的产量增加了51.3倍(95%置信区间; 31.6-85.1,p <0.001),而用染色体肽酶预裂解使6.1倍(95%CI; 42-8.9,p <0.001),与没有预裂解相比。由于预裂解造成的产量差异比萃取方法之间的产量差异大2-3倍。包括预裂解步骤可以提高使用PCR或其他分子方法无需培养而对GBS的检测限。 (C)2016 Elsevier B.V.保留所有权利。

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