Fukushima Masao, Kakinuma Kenichi, Hayashi Hiroshi, Nagai Hiroko, Ito Kunihiko, Kawaguchi Ryuji
Genomics Research Institute, SRL, Inc., 5-6-50 Shinmachi, Hino-shi, Tokyo 191-0002, Japan.
J Clin Microbiol. 2003 Jun;41(6):2605-15. doi: 10.1128/JCM.41.6.2605-2615.2003.
Rapid identification of Mycobacterium species isolates is necessary for the effective management of tuberculosis. Recently, analysis of DNA gyrase B subunit (gyrB) genes has been identified as a suitable means for the identification of bacterial species. We describe a microarray assay based on gyrB gene sequences that can be used for the identification of Mycobacteria species. Primers specific for a gyrB gene region common to all mycobacteria were synthesized and used for PCR amplification of DNA purified from clinical samples. A set of oligonucleotide probes for specific gyrB gene regions was developed for the identification of 14 Mycobacterium species. Each probe was spotted onto a silylated glass slide with an arrayer and used for hybridization with fluorescently labeled RNA derived from amplified sample DNA to yield a pattern of positive spots. This microarray produced unique hybridization patterns for each species of mycobacteria and could differentiate closely related bacterial species. Moreover, the results corresponded well with those obtained by the conventional culture method for the detection of mycobacteria. We conclude that a gyrB-based microarray can rapidly detect and identify closely related mycobacterial species and may be useful in the diagnosis and effective management of tuberculosis.
快速鉴定分枝杆菌属分离株对于结核病的有效管理至关重要。最近,DNA促旋酶B亚基(gyrB)基因分析已被确定为鉴定细菌种类的合适方法。我们描述了一种基于gyrB基因序列的微阵列分析方法,可用于鉴定分枝杆菌种类。合成了针对所有分枝杆菌共有的gyrB基因区域的特异性引物,并用于从临床样本中纯化的DNA的PCR扩增。开发了一组用于特定gyrB基因区域的寡核苷酸探针,用于鉴定14种分枝杆菌。每个探针用阵列仪点样到硅烷化玻片上,并用于与源自扩增样本DNA的荧光标记RNA杂交,以产生阳性斑点模式。这种微阵列对每种分枝杆菌产生独特的杂交模式,并且可以区分密切相关的细菌种类。此外,结果与通过传统培养方法检测分枝杆菌所获得的结果非常吻合。我们得出结论,基于gyrB的微阵列可以快速检测和鉴定密切相关的分枝杆菌种类,并且可能在结核病的诊断和有效管理中有用。