Gomes M A, Silva E F, Macedo A M, Vago A R, Melo M N
Departamento de Parasitologia, Universidade Federal de Minas Gerais, Brasil.
Parasitology. 1997 Jun;114 ( Pt 6):517-20.
Strains of Entamoeba histolytica isolated in Brazil were characterized using the Low-Stringency Single Specific Primer PCR (LSSP-PCR), that detects single or multiple mutations in gene size DNA fragments. Using this technique, a 482-bp genomic DNA fragment from a structural gene in 8 strains and 2 clones of E. histolytica, isolated from symptomatic and asymptomatic patients in Brazil, including pathogenic and non-pathogenic zymodemes were studied. The results obtained indicate that LSSP-PCR is a valuable method for differentiating strains of E. histolytica. Moreover, the results are consistent with the concept that pathogenic and non-pathogenic strains of E. histolytica may represent distinct species or subspecies and are in accord with phenotypically characteristic isoenzyme patterns.
使用低严谨度单特异性引物PCR(LSSP-PCR)对在巴西分离出的溶组织内阿米巴菌株进行特征分析,该技术可检测基因大小DNA片段中的单突变或多突变。利用此技术,对从巴西有症状和无症状患者中分离出的8株溶组织内阿米巴菌株及2个克隆的一个结构基因的482 bp基因组DNA片段进行了研究,其中包括致病和非致病酶谱型。所得结果表明,LSSP-PCR是区分溶组织内阿米巴菌株的一种有价值的方法。此外,这些结果与溶组织内阿米巴致病和非致病菌株可能代表不同物种或亚种的概念一致,并且与表型特征性同工酶模式相符。