Garfinkel L I, Giladi M, Huber M, Gitler C, Mirelman D, Revel M, Rozenblatt S
MacArthur Center for Molecular Biology of Parasitic Diseases, Weizmann Institute of Science, Rehovot, Israel.
Infect Immun. 1989 Mar;57(3):926-31. doi: 10.1128/iai.57.3.926-931.1989.
A number of DNA probes which hybridize to highly abundant DNA sequences of Entamoeba histolytica were developed. Variations in the hybridization patterns of different E. histolytica strains were detected with selected probes. Four types of restriction fragment length patterns were obtained. Of these, the first class belonged to E. invadens and E. histolytica-like var. Laredo. The next two classes consisted of various strains of E. histolytica which were originally isolated from symptomatic patients and possessed pathogenic patterns of isoenzymes (zymodemes), whereas the fourth group contained E. histolytica strains with nonpathogenic zymodemes obtained from asymptomatic carriers. DNA probes, based on DNA sequences specific to E. histolytica isolates with pathogenic and nonpathogenic zymodemes were isolated, and their nucleotide sequences were determined. These probes (P145 and B133) hybridized selectively to DNA of isolates possessing either pathogenic or nonpathogenic isoenzyme patterns. The newly developed probes could be useful for diagnostic purposes and could serve as tools to investigate the molecular basis of pathogenicity and the genetic mechanisms which regulate the variable aggressive behavior of the parasite.
开发了许多与溶组织内阿米巴高度丰富的DNA序列杂交的DNA探针。用选定的探针检测不同溶组织内阿米巴菌株杂交模式的差异。获得了四种类型的限制性片段长度模式。其中,第一类属于侵袭内阿米巴和类溶组织内阿米巴变种拉雷多。接下来的两类由最初从有症状患者中分离出的各种溶组织内阿米巴菌株组成,这些菌株具有同工酶(酶型)的致病模式,而第四组包含从无症状携带者中获得的具有非致病酶型的溶组织内阿米巴菌株。基于具有致病和非致病酶型的溶组织内阿米巴分离株特异性DNA序列的DNA探针被分离出来,并确定了它们的核苷酸序列。这些探针(P145和B133)选择性地与具有致病或非致病同工酶模式的分离株的DNA杂交。新开发的探针可用于诊断目的,并可作为研究致病性分子基础和调节寄生虫可变侵袭行为的遗传机制的工具。