Olivares-Fuster Oscar, Shoemaker Craig A, Klesius Phillip H, Arias Covadonga R
Department of Fisheries and Allied Aquacultures, Auburn University, Auburn, AL 36849, USA.
FEMS Microbiol Lett. 2007 Apr;269(1):63-9. doi: 10.1111/j.1574-6968.2006.00605.x. Epub 2007 Jan 11.
Flavobacterium columnare intraspecies diversity was revealed by analyzing the 16S rRNA gene and the 16S-23S internal spacer region (ISR). Standard restriction fragment length polymorphism (RFLP) of these sequences was compared with single-strand conformation polymorphism (SSCP). Diversity indexes showed that both 16S-SSCP and ISR-SSCP improved resolution (D>or=0.9) when compared with standard RFLP. ISR-SSCP offered a simpler banding pattern than 16S-SSCP while providing high discrimination between isolates. SSCP analysis of rRNA genes proved to be a simple, rapid, and cost-effective method for routine fingerprinting of F. columnare.
通过分析16S rRNA基因和16S - 23S内部间隔区(ISR)揭示了柱状黄杆菌种内多样性。将这些序列的标准限制性片段长度多态性(RFLP)与单链构象多态性(SSCP)进行比较。多样性指数表明,与标准RFLP相比,16S - SSCP和ISR - SSCP均提高了分辨率(D≥0.9)。ISR - SSCP提供了比16S - SSCP更简单的条带模式,同时在分离株之间具有高鉴别力。rRNA基因的SSCP分析被证明是一种用于柱状黄杆菌常规指纹图谱分析的简单、快速且经济高效的方法。