Graf J
Institute for Medical Microbiology, University of Berne, CH-3010 Berne, Switzerland.
J Clin Microbiol. 1999 Oct;37(10):3194-7. doi: 10.1128/JCM.37.10.3194-3197.1999.
Restriction fragment length polymorphism analysis after PCR amplification (RFLP-PCR) of the 16S rRNA gene has been previously proposed as a rapid method to identify Aeromonas species. In the present study, the precision of RFLP-PCR was evaluated with 62 Aeromonas reference strains. The analysis revealed that Aeromonas veronii biovar sobria strains produce various patterns, possibly leading to its misidentification as an environmental species. For most other Aeromonas species little variation was noted. This study supports the usefulness of RFLP-PCR analysis to separate three clinically important species but also reveals possible misidentifications that necessitate further biochemical tests to validate the preliminary identification.
此前已提出,对16S rRNA基因进行聚合酶链反应(PCR)扩增后的限制性片段长度多态性分析(RFLP-PCR)是一种鉴定气单胞菌属菌种的快速方法。在本研究中,利用62株气单胞菌参考菌株对RFLP-PCR的准确性进行了评估。分析表明,维氏气单胞菌温和生物变种菌株产生多种图谱,可能导致其被误鉴定为环境菌种。对于大多数其他气单胞菌属菌种,未观察到明显变异。本研究支持RFLP-PCR分析在区分三种临床重要菌种方面的实用性,但也揭示了可能的误鉴定情况,这就需要进一步进行生化试验以验证初步鉴定结果。