Suppr超能文献

使用DNA微阵列和DNA测序进行细菌鉴定和亚型分析。

Bacterial identification and subtyping using DNA microarray and DNA sequencing.

作者信息

Al-Khaldi Sufian F, Mossoba Magdi M, Allard Marc M, Lienau E Kurt, Brown Eric D

机构信息

Division of Microbiology, Office of Regulatory Science, Center for Food Safety and Applied Nutrition, Food and Drug Administration, College Park, MD, USA.

出版信息

Methods Mol Biol. 2012;881:73-95. doi: 10.1007/978-1-61779-827-6_4.

Abstract

The era of fast and accurate discovery of biological sequence motifs in prokaryotic and eukaryotic cells is here. The co-evolution of direct genome sequencing and DNA microarray strategies not only will identify, isotype, and serotype pathogenic bacteria, but also it will aid in the discovery of new gene functions by detecting gene expressions in different diseases and environmental conditions. Microarray bacterial identification has made great advances in working with pure and mixed bacterial samples. The technological advances have moved beyond bacterial gene expression to include bacterial identification and isotyping. Application of new tools such as mid-infrared chemical imaging improves detection of hybridization in DNA microarrays. The research in this field is promising and future work will reveal the potential of infrared technology in bacterial identification. On the other hand, DNA sequencing by using 454 pyrosequencing is so cost effective that the promise of $1,000 per bacterial genome sequence is becoming a reality. Pyrosequencing technology is a simple to use technique that can produce accurate and quantitative analysis of DNA sequences with a great speed. The deposition of massive amounts of bacterial genomic information in databanks is creating fingerprint phylogenetic analysis that will ultimately replace several technologies such as Pulsed Field Gel Electrophoresis. In this chapter, we will review (1) the use of DNA microarray using fluorescence and infrared imaging detection for identification of pathogenic bacteria, and (2) use of pyrosequencing in DNA cluster analysis to fingerprint bacterial phylogenetic trees.

摘要

在原核细胞和真核细胞中快速准确发现生物序列基序的时代已经到来。直接基因组测序和DNA微阵列策略的共同发展不仅将识别、确定病原体的同种型和血清型,还将通过检测不同疾病和环境条件下的基因表达来帮助发现新的基因功能。微阵列细菌鉴定在处理纯细菌样本和混合细菌样本方面取得了巨大进展。技术进步已从细菌基因表达扩展到包括细菌鉴定和同种型鉴定。诸如中红外化学成像等新工具的应用提高了DNA微阵列中杂交检测的能力。该领域的研究前景广阔,未来的工作将揭示红外技术在细菌鉴定中的潜力。另一方面,使用454焦磷酸测序进行DNA测序成本效益极高,每个细菌基因组序列1000美元的目标正成为现实。焦磷酸测序技术是一种易于使用的技术,能够快速对DNA序列进行准确的定量分析。大量细菌基因组信息在数据库中的存储正在催生指纹系统发育分析,这最终将取代诸如脉冲场凝胶电泳等多种技术。在本章中,我们将综述:(1)使用基于荧光和红外成像检测的DNA微阵列来鉴定病原菌;(2)在DNA聚类分析中使用焦磷酸测序来构建细菌系统发育树的指纹图谱。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验