Eddaikra Naouel, Kherachi Djenad Ihcene, Benbetka Sihem, Benikhlef Razika, Aït-Oudhia Khatima, Moulti-Mati Farida, Oury Bruno, Sereno Denis, Harrat Zoubir
Laboratoire d'Eco-Épidemiologie Parasitaire et Génétique des Populations, Institut Pasteur d'Algerie, Route de Petit Staouéli, Dely Brahim, Algiers, Algeria; Unité Mixte de Recherche IRD 224 MiVegec (Maladies Infectieuses et Vecteurs: Écologie, Génétique, Évolution et Contrôle), Institut de Recherche pour le Développement (IRD), BP 64501, 34394 Montpellier Cedex 5, France; Laboratoire de Biochimie Analytique et Biotechnologies, Université Mouloud Mameri de Tizi-Ouzou, Algeria.
Laboratoire d'Eco-Épidemiologie Parasitaire et Génétique des Populations, Institut Pasteur d'Algerie, Route de Petit Staouéli, Dely Brahim, Algiers, Algeria.
Biomed Res Int. 2016;2016:7985104. doi: 10.1155/2016/7985104. Epub 2016 Feb 2.
In Algeria, Leishmania infantum, Leishmania major, and Leishmania killicki (Leishmania tropica) are responsible for cutaneous leishmaniosis. We established a murine model of L. killicki infection to investigate its infective capacity, some immunophysiopathological aspects, and its suitability for pharmacological purposes. Following the injection of L. major or L. killicki metacyclic promastigotes in the ear dermis of BALB/c mice, the course of infection was followed. The infection with L. killicki caused slower lesion formation than with L. major. The presence of L. killicki or L. major DNA and parasites was detected in the ear dermis and in lymph nodes, spleen, and liver. Lesions induced by L. killicki were nonulcerative in their aspect, whereas those caused by L. major were highly ulcerative and necrotic, which matches well with the lesion phenotype reported in humans for L. killicki and L. major, respectively. The treatment of L. killicki lesions by injection of Glucantime® significantly reduced the lesion thickness and parasite burden. Ear dermal injection of BALB/c mice constitutes a model to study lesions physiopathology caused by L. killicki and presents interest for in vivo screening of new compounds against this pathogen, emerging in Algeria.
在阿尔及利亚,婴儿利什曼原虫、硕大利什曼原虫和基利克氏利什曼原虫(热带利什曼原虫)是皮肤利什曼病的病原体。我们建立了基利克氏利什曼原虫感染的小鼠模型,以研究其感染能力、一些免疫生理病理学方面以及其在药理学上的适用性。在BALB/c小鼠耳部真皮注射硕大利什曼原虫或基利克氏利什曼原虫的后鞭毛体前鞭毛体后,对感染过程进行了跟踪。与硕大利什曼原虫相比,基利克氏利什曼原虫感染导致病变形成较慢。在耳部真皮以及淋巴结、脾脏和肝脏中检测到了基利克氏利什曼原虫或硕大利什曼原虫的DNA和寄生虫。基利克氏利什曼原虫引起的病变外观无溃疡,而硕大利什曼原虫引起的病变则高度溃疡和坏死,这与人类中分别由基利克氏利什曼原虫和硕大利什曼原虫引起的病变表型非常吻合。通过注射葡糖胺锑钠治疗基利克氏利什曼原虫病变可显著降低病变厚度和寄生虫负荷。对BALB/c小鼠进行耳部真皮注射构成了一个研究基利克氏利什曼原虫引起的病变生理病理学的模型,并且对于体内筛选针对这种在阿尔及利亚出现的病原体的新化合物具有重要意义。