Fernandes O, Degrave W, Campbell D A
Department of Microbiology and Immunology, University of California, Los Angeles 90024.
Parasitology. 1993 Sep;107 ( Pt 3):219-24. doi: 10.1017/s003118200007918x.
The mini-exon gene repeats from three different strains of Endotrypanum schaudinni have been amplified by the polymerase chain reaction (PCR). Sequence analysis of the cloned products shows the gene and intergenic region to be identical in two of the strains (LV86 and M6159); the intergenic region from the mini-exon gene of the third strain (LV59) is significantly different. The LV86 gene and an intergenic probe from the LV59 mini-exon gene do not cross-hybridize with the mini-exon gene from New World Leishmania species. These data provide the basis of a PCR assay to detect E. schaudinni and distinguish it from New World Leishmania species, and which should be applicable to epidemiological studies in insect vectors and mammalian reservoirs. The identification of two different mini-exon gene repeats in E. schaudinni isolates is indicative of further strain variation within this species.
通过聚合酶链反应(PCR)扩增了来自三种不同绍丁氏内锥虫菌株的小外显子基因重复序列。对克隆产物的序列分析表明,其中两个菌株(LV86和M6159)的基因和基因间区域相同;第三个菌株(LV59)的小外显子基因的基因间区域有显著差异。LV86基因和来自LV59小外显子基因的基因间探针与新大陆利什曼原虫物种的小外显子基因不发生交叉杂交。这些数据为检测绍丁氏内锥虫并将其与新大陆利什曼原虫物种区分开来的PCR检测方法提供了基础,该方法应适用于昆虫媒介和哺乳动物宿主中的流行病学研究。在绍丁氏内锥虫分离株中鉴定出两种不同的小外显子基因重复序列,表明该物种内存在进一步的菌株变异。