Kallel K, Pratlong F, Haouas N, Kaouech E, Belhadj S, Anane S, Dedet J P, Babba H, Chaker E
Laboratoire de Parasitologie, Hôpital La Rabta, 1007 Tunis, Tunisia.
Acta Trop. 2008 May;106(2):132-6. doi: 10.1016/j.actatropica.2008.02.006. Epub 2008 Feb 29.
The different clinical forms of leishmaniasis are the result of both the immunological status of individuals and the species of the parasite causing the infection. In Mediterranean countries, the Leishmania infantum complex groups zymodemes which are responsible for visceral, cutaneous and exceptionally cutaneomucosal or mucosal leishmaniasis. We report in this study a synthesis concerning 254 cases of L. infantum that have been characterized at the "Laboratoire de Parasitologie" of the Rabta Hospital. The strains were isolated from human cases of visceral leishmaniasis (VL) and cutaneous leishmaniasis (CL) by culture on NNN medium: 156 VL cases and 98 CL cases. The isoenzymatic characterization revealed three zymodemes of L. infantum. * L. infantum MON 1, a common zymodeme of VL,occurred in 154 cases (61%): 147 VL (95%) and 7 CL (5%). All CL cases were from the northern provinces, six of them occurring during an epidemic disease in 2001. * L. infantum MON 24, a common zymodeme of CL in the north, occurred in 98 cases (38.5%): 91 CL (93%) and 7 VL (7%). The seven VL cases were immunocompetent children aged from 8 months to 9 years and native of northern Tunisia. Two of the CL cases were from central regions of the country. This is the first time that cases from these regions are reported. * L. infantum MON 80, an uncommon zymodeme in Tunisia, occurred in two VL cases (0.5%): two children aged 7 and 5. The small number of strains of this zymodeme does not allow understanding of its epidemiological role. The results of this study indicate a low enzymatic variability of L. infantum in the country. However, our study includes only human strains and should be extended to animal ones (dogs, rodents and sand flies). This would lead to a better understanding of the epidemiology of leishmaniasis in Tunisia.
利什曼病的不同临床形式是个体免疫状态和引起感染的寄生虫种类共同作用的结果。在地中海国家,婴儿利什曼原虫复合体包含一些酶谱型,它们可导致内脏利什曼病、皮肤利什曼病,偶尔也会引起皮肤黏膜或黏膜利什曼病。在本研究中,我们报告了拉卜塔医院“寄生虫学实验室”对254例婴儿利什曼原虫病例的综合研究情况。这些菌株通过在NNN培养基上培养,从内脏利什曼病(VL)和皮肤利什曼病(CL)的人类病例中分离得到:156例VL病例和98例CL病例。同工酶特征分析显示婴儿利什曼原虫有三种酶谱型。
婴儿利什曼原虫MON 1,一种常见的VL酶谱型,出现于154例(61%):147例VL(95%)和7例CL(5%)。所有CL病例均来自北部省份,其中6例发生在2001年的一次流行病期间。
婴儿利什曼原虫MON 24,北部常见的CL酶谱型,出现于98例(38.5%):91例CL(93%)和7例VL(7%)。7例VL病例为免疫功能正常的儿童,年龄在8个月至9岁之间,来自突尼斯北部。2例CL病例来自该国中部地区。这是首次报告来自这些地区的病例。
婴儿利什曼原虫MON 80,在突尼斯是一种不常见的酶谱型,出现于2例VL病例(0.5%):2名分别为7岁和5岁的儿童。该酶谱型的菌株数量较少,无法了解其流行病学作用。本研究结果表明该国婴儿利什曼原虫的酶变异性较低。然而,我们的研究仅包括人类菌株,应扩展至动物菌株(狗、啮齿动物和白蛉)。这将有助于更好地了解突尼斯利什曼病的流行病学情况。