Howe D K, Vodkin M H, Novak R J, Visvesvara G, McLaughlin G L
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110-1093, USA.
Parasitol Res. 1997;83(4):345-8. doi: 10.1007/s004360050259.
Species-level identification of Acanthamoeba isolates is difficult and gives little or no indication of the isolate's pathogenicity. We identified two amplification-based genetic markers that were highly correlated with pathogenicity in Acanthamoeba spp. One marker, designed to amplify a 485-bp fragment of the small-subunit ribosomal RNA gene (ssrDNA), was preferentially amplified from the nonpathogenic strains; amplifications from the pathogenic strains yielded anomalous fragments of 650 and 900 bp. A second marker was developed on the basis of the anomalous 650-bp fragment. Primers to this sequence preferentially amplified a noncoding locus (called Ac6) only from the pathogenic strains. These two genetic markers may be useful for identification of pathogenic Acanthamoeba spp. strains.
棘阿米巴分离株的种水平鉴定很困难,且几乎无法或根本无法表明分离株的致病性。我们鉴定出两种基于扩增的遗传标记,它们与棘阿米巴属的致病性高度相关。一种标记设计用于扩增小亚基核糖体RNA基因(ssrDNA)的485bp片段,优先从非致病菌株中扩增出来;致病菌株的扩增产生了650bp和900bp的异常片段。基于650bp的异常片段开发了第二种标记。针对该序列的引物仅从致病菌株中优先扩增出一个非编码位点(称为Ac6)。这两种遗传标记可能有助于鉴定致病性棘阿米巴属菌株。