Winstanley C, Hales B A, Corkill J E, Gallagher M J, Hart C A
Department of Biomedical Sciences, University of Bradford, West Yorkshire.
J Med Microbiol. 1998 Aug;47(8):689-94. doi: 10.1099/00222615-47-8-689.
The flagellin gene sequence from a clinical isolate of Burkholderia pseudomallei was used to design oligonucleotide primers for PCR/RFLP analysis of flagellin gene variation among clinical and environmental isolates of B. pseudomallei. Genes from four clinical and six environmental isolates were amplified and compared by RFLP. The clinical isolates were indistinguishable, but variation was detected among some of the environmental isolates. Sequence analysis of flagellin gene amplified products demonstrated high levels of conservation amongst the flagellin genes of clinical isolates (>99% similarity), compared to the variation observed between the clinical isolates and one of the environmental isolates (<90% similarity). Genomic comparisons with pulsed-field gel electrophoresis (PFGE) revealed differences between the relationships inferred by flagellin genotyping and PFGE, suggesting that a combination of molecular methods may be useful for the subtyping of B. pseudomallei strains.
来自一株伯克霍尔德菌临床分离株的鞭毛蛋白基因序列被用于设计寡核苷酸引物,以对伯克霍尔德菌临床和环境分离株中的鞭毛蛋白基因变异进行PCR/RFLP分析。对来自4株临床分离株和6株环境分离株的基因进行扩增,并通过RFLP进行比较。临床分离株无法区分,但在一些环境分离株中检测到了变异。与临床分离株和一株环境分离株之间观察到的变异(<90%相似性)相比,鞭毛蛋白基因扩增产物的序列分析表明临床分离株的鞭毛蛋白基因之间具有高度保守性(>99%相似性)。用脉冲场凝胶电泳(PFGE)进行的基因组比较揭示了鞭毛蛋白基因分型和PFGE推断的关系之间的差异,这表明分子方法的组合可能有助于伯克霍尔德菌菌株的亚型分析。