Blanco A, Montamat E E
Cátedra de Química Biológica, Facultad de Ciencias Médicas, Universidad Nacional de Córdoba, Argentina.
J Exp Zool. 1998;282(1-2):62-70.
The analysis of enzyme electrophoretic patterns in 141 extracts of Trypanosoma cruzi isolated from humans and domesticated and wild animals from the endemic zone of Chagas' disease in Argentina allowed their characterization into 12 different "isozymic strains" or zymodemes (Z1 to Z12). In humans, the parasites most frequently found belong to Z1 and Z12. These zymodemes differ significantly in pathogenic activity, Z1 having fewer deleterious effects than Z12. Because of the good correlation existing between zymodemes and the groups of parasites characterized by the study of kinetoplast DNA (kDNA), it is possible to identify zymodemes by analyzing kDNA. A 270-base-pair probe of the highly variable region of minicircles (HVRm) of kDNA, purified from Z1 and Z12 reference stocks, hybridized specifically with PCR-amplified HVRm from T. cruzi isolates, allowing identification of the "major natural clones." It is suggested that this technique of zymodeme identification could be useful for the prognosis of the probable evolution of the disease.
对从阿根廷恰加斯病流行区的人类、家畜和野生动物中分离出的141份克氏锥虫提取物进行酶电泳图谱分析,可将它们分为12种不同的“同工酶株”或酶型(Z1至Z12)。在人类中,最常发现的寄生虫属于Z1和Z12。这些酶型在致病活性上有显著差异,Z1的有害影响比Z12少。由于酶型与通过动基体DNA(kDNA)研究表征的寄生虫群体之间存在良好的相关性,因此可以通过分析kDNA来鉴定酶型。从Z1和Z12参考菌株中纯化出的kDNA小环高变区(HVRm)的270个碱基对探针,与克氏锥虫分离株经PCR扩增的HVRm特异性杂交,从而能够鉴定“主要天然克隆”。有人提出,这种酶型鉴定技术可能有助于预测疾病可能的发展。