Conrad P A, Thomford J W, Marsh A, Telford S R, Anderson J F, Spielman A, Sabin E A, Yamane I, Persing D H
Department of Veterinary Microbiology and Immunology, University of California, Davis 95616.
J Clin Microbiol. 1992 May;30(5):1210-5. doi: 10.1128/jcm.30.5.1210-1215.1992.
The objective of this study was to determine whether different isolates of Babesia microti could be distinguished from morphologically similar isolates of B. gibsoni by using a ribosomal DNA (rDNA) probe. A Babesia-specific rDNA probe was obtained by polymerase chain reaction amplification of sequences from B. microti DNA using universal primers directed against highly conserved portions of the eukaryotic 16S-like rRNA gene. The chemiluminescent rDNA probe hybridized to Southern blots of restriction endonuclease-digested DNA preparations of different isolates of B. gibsoni from infected dogs and B. microti from infected humans and white-footed mice. Restriction fragment length polymorphisms served to differentiate these species. Although the hybridization patterns seen with DNAs from six B. microti isolates did not vary, those of the five B. gibsoni isolates did indicate genotypic variation. We concluded that isolates of B. microti and B. gibsoni can be differentiated on the basis of restriction fragment length polymorphism detected with a chemiluminescent rDNA probe.
本研究的目的是确定能否通过核糖体DNA(rDNA)探针,将微小巴贝斯虫的不同分离株与形态相似的吉氏巴贝斯虫分离株区分开来。通过聚合酶链反应,使用针对真核生物16S样rRNA基因高度保守区域的通用引物,对微小巴贝斯虫DNA的序列进行扩增,从而获得巴贝斯虫特异性rDNA探针。该化学发光rDNA探针与经限制性内切酶消化的感染犬的不同吉氏巴贝斯虫分离株、感染人类和白足鼠的微小巴贝斯虫的DNA制备物的Southern印迹杂交。限制性片段长度多态性可用于区分这些物种。虽然来自6株微小巴贝斯虫分离株的DNA的杂交模式没有变化,但5株吉氏巴贝斯虫分离株的杂交模式确实表明存在基因型变异。我们得出结论,微小巴贝斯虫和吉氏巴贝斯虫分离株可根据化学发光rDNA探针检测到的限制性片段长度多态性进行区分。