Piarroux R, Azaiez R, Lossi A M, Reynier P, Muscatelli F, Gambarelli F, Fontes M, Dumon H, Quilici M
Laboratoire de Parasitologie, Faculte de Medecine, Marseille, France.
Am J Trop Med Hyg. 1993 Sep;49(3):364-9. doi: 10.4269/ajtmh.1993.49.364.
To construct a DNA probe specific for protozoa that cause visceral leishmaniasis, we cloned Pst I fragments of Leishmania infantum genomic DNA into a Bluescript II SK vector. A clone of 4.3 kb that contained a highly repetitive sequence was isolated and cut with three restriction enzymes: Hae III, Rsa I, and Sau 3A. After a new molecular cloning step, we isolated and sequenced a 140-basepair (bp) fragment. Two oligonucleotides were synthesized to be used as primers for a polymerase chain reaction. Using this probe, we detected an amount of DNA equivalent to one promastigote of L. infantum. This probe showed a high specificity; all protozoa tested that cause visceral leishmaniasis and L. major (one of the causative agents of Old World cutaneous leishmaniasis) showed a 100-bp amplified sequence, whereas other Leishmania strains showed a signal of a different size or else no signal. Moreover, no amplified sequence was obtained with other pathogenic parasites tested (Trypanosoma brucei, T. cruzi, Plasmodium falciparum, Pneumocystis carinii, and Toxoplasma gondii).
为构建针对引起内脏利什曼病的原生动物的DNA探针,我们将婴儿利什曼原虫基因组DNA的Pst I片段克隆到pBluescript II SK载体中。分离出一个包含高度重复序列的4.3 kb克隆,并使用三种限制性内切酶(Hae III、Rsa I和Sau 3A)进行切割。经过新一轮分子克隆步骤后,我们分离并测序了一个140碱基对(bp)的片段。合成了两条寡核苷酸用作聚合酶链反应的引物。使用该探针,我们检测到相当于一个婴儿利什曼原虫前鞭毛体的DNA量。该探针显示出高度特异性;所有检测的引起内脏利什曼病的原生动物以及硕大利什曼原虫(旧世界皮肤利什曼病的病原体之一)均显示出100 bp的扩增序列,而其他利什曼原虫菌株则显示出不同大小的信号或无信号。此外,对其他测试的致病寄生虫(布氏锥虫、克氏锥虫、恶性疟原虫、卡氏肺孢子虫和刚地弓形虫)未获得扩增序列。