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用于常见沙门氏菌血清群分子测定的多重珠基悬浮阵列。

Multiplex, bead-based suspension array for molecular determination of common Salmonella serogroups.

作者信息

Fitzgerald Collette, Collins Marcus, van Duyne Susan, Mikoleit Matthew, Brown Teresa, Fields Patricia

机构信息

Enteric Diseases Laboratory Preparedness Branch, Division of Foodborne, Bacterial and Mycotic Diseases, National Center for Zoonotic, Vector-Borne and Enteric Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.

出版信息

J Clin Microbiol. 2007 Oct;45(10):3323-34. doi: 10.1128/JCM.00025-07. Epub 2007 Jul 18.

Abstract

We report the development and evaluation of a Salmonella O-group-specific Bio-Plex assay to detect the six most common serogroups in the United States (B, C(1), C(2), D, E, and O13) plus serotype Paratyphi A. The assay is based on rfb gene targets directly involved in O-antigen biosynthesis; it can be completed 45 min post-PCR amplification. The assay correctly and specifically identified 362 of 384 (94.3%) isolates tested in comparison to traditional serotyping. Seventeen isolates (4.4%) produced results consistent with what is known about the molecular basis for serotypes but different from the results of traditional serotyping, and five isolates (1.3%) generated false-negative results. Molecular determination of the serogroup for rough isolates was consistent with a common serotype in most instances, indicating that this approach has the potential to provide O-group information for isolates that do not express an O antigen. We also report the sequence of the O-antigen-encoding rfb gene cluster from Salmonella enterica serotype Poona (serogroup O13). Compared with other, previously characterized rfb regions, the O13 rfb gene cluster was most closely related to Escherichia coli O127 and O86. The O-group Bio-Plex assay described here provides an easy-to-use, high-throughput system for rapid detection of common Salmonella serogroups.

摘要

我们报告了一种沙门氏菌O群特异性生物芯片检测方法的开发与评估,该方法用于检测美国六种最常见的血清群(B、C(1)、C(2)、D、E和O13)以及甲型副伤寒血清型。该检测方法基于直接参与O抗原生物合成的rfb基因靶点;在PCR扩增后45分钟即可完成检测。与传统血清分型相比,该检测方法正确且特异性地鉴定了384株测试菌株中的362株(94.3%)。17株菌株(4.4%)产生的结果与已知的血清型分子基础一致,但与传统血清分型结果不同,5株菌株(1.3%)产生了假阴性结果。在大多数情况下,粗糙菌株血清群的分子测定与常见血清型一致,这表明该方法有可能为不表达O抗原的菌株提供O群信息。我们还报告了肠炎沙门氏菌波纳血清型(血清群O13)编码O抗原的rfb基因簇序列。与其他先前已表征的rfb区域相比,O13 rfb基因簇与大肠杆菌O127和O86关系最为密切。本文所述的O群生物芯片检测方法提供了一种易于使用的高通量系统,用于快速检测常见的沙门氏菌血清群。

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