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基于快速微阵列的大肠杆菌 DNA 基因分型。

Rapid microarray-based DNA genoserotyping of Escherichia coli.

机构信息

Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Epidemiology, Wusterhausen.

出版信息

Microbiol Immunol. 2014 Feb;58(2):77-86. doi: 10.1111/1348-0421.12120.

Abstract

In this study, an improvement in the oligonucleotide-based DNA microarray for the genoserotyping of Escherichia coli is presented. Primer and probes for additional 70 O antigen groups were developed. The microarray was transferred to a new platform, the ArrayStrip format, which allows high through-put tests in 96-well formats and fully automated microarray analysis. Thus, starting from a single colony, it is possible to determine within a few hours and a single experiment, 94 of the over 180 known O antigen groups as well as 47 of the 53 different H antigens. The microarray was initially validated with a set of defined reference strains that had previously been serotyped by conventional agglutination in various reference centers. For further validation of the microarray, 180 clinical E. coli isolates of human origin (from urine samples, blood cultures, bronchial secretions, and wound swabs) and 53 E. coli isolates from cattle, pigs, and poultry were used. A high degree of concordance between the results of classical antibody-based serotyping and DNA-based genoserotyping was demonstrated during validation of the new 70 O antigen groups as well as for the field strains of human and animal origin. Therefore, this oligonucleotide array is a diagnostic tool that is user-friendly and more efficient than classical serotyping by agglutination. Furthermore, the tests can be performed in almost every routine lab and are easily expanded and standardized.

摘要

本研究提出了一种基于寡核苷酸的 DNA 微阵列在大肠杆菌基因分型方面的改进。开发了针对另外 70 个 O 抗原群的引物和探针。微阵列被转移到一个新的平台,ArrayStrip 格式,允许在 96 孔格式中进行高通量测试和完全自动化的微阵列分析。因此,从单个菌落开始,有可能在几个小时内并通过一个单一实验确定 180 多个已知 O 抗原群中的 94 个以及 53 个不同 H 抗原中的 47 个。该微阵列最初使用一组已通过传统凝集法在不同参考中心进行血清分型的定义参考菌株进行验证。为了进一步验证微阵列,使用了 180 个人源来源的临床大肠杆菌分离株(来自尿液样本、血液培养物、支气管分泌物和伤口拭子)和 53 株来自牛、猪和家禽的大肠杆菌分离株。在验证新的 70 个 O 抗原群以及人源和动物源现场分离株时,证明了经典基于抗体的血清分型和基于 DNA 的基因分型结果之间具有高度一致性。因此,该寡核苷酸微阵列是一种比传统凝集法更具用户友好性和效率的诊断工具。此外,该测试几乎可以在每个常规实验室进行,并且易于扩展和标准化。

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