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Complexity of the genomic diversity in enterohemorrhagic Escherichia coli O157 revealed by the combinational use of the O157 Sakai OligoDNA microarray and the Whole Genome PCR scanning.通过组合使用O157阪崎寡核苷酸DNA微阵列和全基因组PCR扫描揭示的肠出血性大肠杆菌O157基因组多样性的复杂性
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Highly accurate genome sequences of Escherichia coli K-12 strains MG1655 and W3110.大肠杆菌K-12菌株MG1655和W3110的高精度基因组序列。
Mol Syst Biol. 2006;2:2006.0007. doi: 10.1038/msb4100049. Epub 2006 Feb 21.
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High-resolution analysis of genomic alterations and human papillomavirus integration in anal intraepithelial neoplasia.肛管上皮内瘤变中基因组改变和人乳头瘤病毒整合的高分辨率分析
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A comparison study: applying segmentation to array CGH data for downstream analyses.一项比较研究:将分割应用于阵列比较基因组杂交数据以进行下游分析。
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Diversity and host range of Shiga toxin-encoding phage.产志贺毒素噬菌体的多样性及宿主范围
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用于比较基因组分析的七基因组大肠杆菌微阵列设计

Design of a seven-genome Escherichia coli microarray for comparative genomic profiling.

作者信息

Willenbrock Hanni, Petersen Anne, Sekse Camilla, Kiil Kristoffer, Wasteson Yngvild, Ussery David W

机构信息

Center for Biological Sequence Analysis, Technical University of Denmark, Building 301, DK-2800 Kgs. Lyngby, Denmark.

出版信息

J Bacteriol. 2006 Nov;188(22):7713-21. doi: 10.1128/JB.01043-06. Epub 2006 Sep 8.

DOI:10.1128/JB.01043-06
PMID:16963574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1636325/
Abstract

We describe the design and evaluate the use of a high-density oligonucleotide microarray covering seven sequenced Escherichia coli genomes in addition to several sequenced E. coli plasmids, bacteriophages, pathogenicity islands, and virulence genes. Its utility is demonstrated for comparative genomic profiling of two unsequenced strains, O175:H16 D1 and O157:H7 3538 (Deltastx(2)::cat) as well as two well-known control strains, K-12 W3110 and O157:H7 EDL933. By using fluorescently labeled genomic DNA to query the microarrays and subsequently analyze common virulence genes and phage elements and perform whole-genome comparisons, we observed that O175:H16 D1 is a K-12-like strain and confirmed that its phi3538 (Deltastx(2)::cat) phage element originated from the E. coli 3538 (Deltastx(2)::cat) strain, with which it shares a substantial proportion of phage elements. Moreover, a number of genes involved in DNA transfer and recombination was identified in both new strains, providing a likely explanation for their capability to transfer phi3538 (Deltastx(2)::cat) between them. Analyses of control samples demonstrated that results using our custom-designed microarray were representative of the true biology, e.g., by confirming the presence of all known chromosomal phage elements as well as 98.8 and 97.7% of queried chromosomal genes for the two control strains. Finally, we demonstrate that use of spatial information, in terms of the physical chromosomal locations of probes, improves the analysis.

摘要

我们描述了一种高密度寡核苷酸微阵列的设计,并评估了其用途。该微阵列除覆盖几个已测序的大肠杆菌质粒、噬菌体、致病岛和毒力基因外,还涵盖了七个已测序的大肠杆菌基因组。通过对两个未测序菌株O175:H16 D1和O157:H7 3538(Deltastx(2)::cat)以及两个著名的对照菌株K-12 W3110和O157:H7 EDL933进行比较基因组分析,证明了该微阵列的实用性。通过使用荧光标记的基因组DNA查询微阵列,随后分析常见的毒力基因和噬菌体元件并进行全基因组比较,我们观察到O175:H16 D1是一种类似K-12的菌株,并证实其phi3538(Deltastx(2)::cat)噬菌体元件源自大肠杆菌3538(Deltastx(2)::cat)菌株,二者共享相当比例的噬菌体元件。此外,在这两个新菌株中均鉴定出了一些参与DNA转移和重组的基因,这可能解释了它们在彼此之间转移phi3538(Deltastx(2)::cat)的能力。对照样品分析表明,使用我们定制设计的微阵列得到的结果代表了真实生物学情况,例如,通过确认两个对照菌株中所有已知的染色体噬菌体元件以及98.8%和97.7%的被查询染色体基因的存在。最后,我们证明,利用探针在染色体上的物理位置等空间信息可改善分析。