首页> 美国卫生研究院文献>Frontiers in Microbiology >Novel Degenerate PCR Method for Whole-Genome Amplification Applied to Peru Margin (ODP Leg 201) Subsurface Samples
【2h】

Novel Degenerate PCR Method for Whole-Genome Amplification Applied to Peru Margin (ODP Leg 201) Subsurface Samples

机译:用于全基因组扩增的新型简并PCR方法应用于秘鲁边缘(ODP腿201)地下样品

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A degenerate polymerase chain reaction (PCR)-based method of whole-genome amplification, designed to work fluidly with 454 sequencing technology, was developed and tested for use on deep marine subsurface DNA samples. While optimized here for use with Roche 454 technology, the general framework presented may be applicable to other next generation sequencing systems as well (e.g., Illumina, Ion Torrent). The method, which we have called random amplification metagenomic PCR (RAMP), involves the use of specific primers from Roche 454 amplicon sequencing, modified by the addition of a degenerate region at the 3′ end. It utilizes a PCR reaction, which resulted in no amplification from blanks, even after 50 cycles of PCR. After efforts to optimize experimental conditions, the method was tested with DNA extracted from cultured E. coli cells, and genome coverage was estimated after sequencing on three different occasions. Coverage did not vary greatly with the different experimental conditions tested, and was around 62% with a sequencing effort equivalent to a theoretical genome coverage of 14.10×. The GC content of the sequenced amplification product was within 2% of the predicted values for this strain of E. coli. The method was also applied to DNA extracted from marine subsurface samples from ODP Leg 201 site 1229 (Peru Margin), and results of a taxonomic analysis revealed microbial communities dominated by Proteobacteria, Chloroflexi, Firmicutes, Euryarchaeota, and Crenarchaeota, among others. These results were similar to those obtained previously for those samples; however, variations in the proportions of taxa identified illustrates well the generally accepted view that community analysis is sensitive to both the amplification technique used and the method of assigning sequences to taxonomic groups. Overall, we find that RAMP represents a valid methodology for amplifying metagenomes from low-biomass samples.
机译:开发了一种基于简并聚合酶链反应(PCR)的全基因组扩增方法,该方法旨在与454测序技术一起流畅地工作,并进行了测试,可用于深海海洋地下DNA样品。虽然在此处针对与Roche 454技术一起使用进行了优化,但所提供的通用框架也可能适用于其他下一代测序系统(例如Illumina,Ion Torrent)。我们称为随机扩增宏基因组PCR(RAMP)的方法涉及使用Roche 454扩增子测序的特异性引物,并通过在3'端添加简并区域进行修饰。它利用了PCR反应,即使经过50个PCR循环,也不会导致空白扩增。在努力优化实验条件之后,使用从培养的大肠杆菌细胞中提取的DNA对该方法进行了测试,并在三种不同的情况下进行了测序后评估了基因组覆盖率。覆盖率在不同的实验条件下变化不大,测序工作相当于理论基因组覆盖率14.10x,约为62%。测序的扩增产物的GC含量在该大肠杆菌菌株的预测值的2%以内。该方法还应用于从ODP Leg 201站点1229(秘鲁边缘)的海洋地下样本中提取的DNA,分类学分析结果表明,细菌群主要是变形杆菌,绿叶弯曲菌,Firmicutes,Euryarchaeota和Crenarchaeota。这些结果与以前从那些样品中获得的结果相似。然而,所鉴定的分类单元比例的变化很好地说明了普遍接受的观点,即群落分析对所用的扩增技术和将序列分配给分类组的方法均敏感。总体而言,我们发现RAMP代表了一种从低生物量样品中扩增基因组的有效方法。

著录项

相似文献

  • 外文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号