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采用聚合酶链反应-限制性片段长度多态性分析及毛细管电泳法检测罕见分枝杆菌和诺卡菌属的hsp65基因模式。

The hsp65 gene patterns of less common Mycobacterium and Nocardia spp. by polymerase chain reaction-restriction fragment length polymorphism analysis with capillary electrophoresis.

作者信息

Chang Po-Ling, Hsieh Wen-Shyang, Chiang Chia-Lien, Tuohy Marion J, Hall Gerri S, Procop Gary W, Chang Huan-Tsung, Ho Hsin-Tsung

机构信息

Department of Chemistry, National Taiwan University, Taipei, Taiwan.

出版信息

Diagn Microbiol Infect Dis. 2007 Jul;58(3):315-23. doi: 10.1016/j.diagmicrobio.2007.02.004. Epub 2007 Mar 26.

Abstract

To rapidly identify Mycobacterium and Nocardia spp. without costly probes, we had implemented capillary electrophoresis (CE) in polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) analysis to analyze their 65-kDa heat shock protein (hsp65) gene. The PCR-RFLP analysis with CE (PRACE) involved only one restriction enzyme, HaeIII, and a single electrophoretic separation less than 10 min. Full-range (10-200 bp) RFLP patterns of 12 less common Mycobacterium and 7 Nocardia spp. were investigated. A good agreement was observed between the sizes of restriction fragments resolved by CE and the real sizes deduced from sequence analysis. Including hsp65 gene patterns of 12 Mycobacterium spp. published earlier, differentiation was distinct among 24 Mycobacterium and 7 Nocardia spp. Some closely related species exhibiting similar biochemical characteristics could be well discriminated by an extra HaeIII digestion site. Thus, PRACE offers a nonprobe alternative for rapid identification of various cultured Mycobacterium and Nocardia to the species level.

摘要

为了在不使用昂贵探针的情况下快速鉴定分枝杆菌属和诺卡菌属,我们在聚合酶链反应(PCR)-限制性片段长度多态性(RFLP)分析中采用毛细管电泳(CE)来分析它们的65-kDa热休克蛋白(hsp65)基因。采用CE的PCR-RFLP分析(PRACE)仅涉及一种限制性内切酶HaeIII,且单次电泳分离时间不到10分钟。研究了12种较不常见分枝杆菌和7种诺卡菌属的全范围(10 - 200 bp)RFLP图谱。通过CE解析的限制性片段大小与序列分析推导的实际大小之间观察到良好的一致性。包括早期发表的12种分枝杆菌属的hsp65基因图谱,24种分枝杆菌和7种诺卡菌属之间的区分明显。一些具有相似生化特征的密切相关物种可以通过额外的HaeIII酶切位点得到很好的区分。因此,PRACE为将各种培养的分枝杆菌和诺卡菌快速鉴定到种水平提供了一种无需探针的替代方法。

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