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通过在塑料DNA阵列上进行伴侣蛋白60分化来鉴定致病性幽门螺杆菌菌种

Identification of pathogenic Helicobacter species by chaperonin-60 differentiation on plastic DNA arrays.

作者信息

Masson Luke, Maynard Christine, Brousseau Roland, Goh Swee-Han, Hemmingsen Sean M, Hill Janet E, Paccagnella Ana, Oda Ryuichi, Kimura Naoki

机构信息

Biotechnology Research Institute, National Research Council of Canada, Montréal, QC, Canada.

出版信息

Genomics. 2006 Jan;87(1):104-12. doi: 10.1016/j.ygeno.2005.06.014. Epub 2005 Nov 21.

Abstract

A microarray method for bacterial species identification based on cpn60 and 16S rDNA hybridization was developed. Specific cpn60 or 16S rDNA oligonucleotides from various Helicobacter or Campylobacter species were printed and immobilized onto a proprietary plastic solid support. Using universal primers, fragments derived from either cpn60 or 16S rDNA genes from single isolates or from a complex human waste sludge DNA sample spiked with Helicobacter pylori were biotinylated and hybridized to the plastic slide. Subsequent querying with a streptavidin-horseradish peroxidase conjugate followed by color development using tetramethylbenzidine resulted in accurate Helicobacter species identification with no cross-hybridization to either the 16S rDNA or the cpn60 sequence of a closely related strain of Campylobacter jejuni. The combination of a nonfluorescence visual detection system with a polymer-based DNA microarray slide has resulted in a molecular tool that should prove useful in numerous applications requiring rapid, low-cost bacterial species identification.

摘要

开发了一种基于cpn60和16S rDNA杂交的细菌物种鉴定微阵列方法。将来自各种幽门螺杆菌或弯曲杆菌物种的特异性cpn60或16S rDNA寡核苷酸打印并固定在一种专有的塑料固体支持物上。使用通用引物,将来自单个分离株或掺有幽门螺杆菌的复杂人类粪便污泥DNA样品的cpn60或16S rDNA基因片段进行生物素化,并与塑料载玻片杂交。随后用链霉亲和素 - 辣根过氧化物酶缀合物进行检测,再用四甲基联苯胺进行显色,从而准确鉴定幽门螺杆菌物种,且不会与空肠弯曲杆菌的密切相关菌株的16S rDNA或cpn60序列发生交叉杂交。非荧光视觉检测系统与基于聚合物的DNA微阵列载玻片的结合产生了一种分子工具,该工具在许多需要快速、低成本细菌物种鉴定的应用中应会证明是有用的。

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