School of Allied Health Sciences, Walailak University, Nakhonsithammarat, Thailand.
Center of Excellence in Vector Biology and Vector-Borne Disease, Department of Parasitology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Front Cell Infect Microbiol. 2022 Sep 5;12:992741. doi: 10.3389/fcimb.2022.992741. eCollection 2022.
() is a human pathogen causing leishmaniasis and studies on the properties of metacyclic promastigotes, the parasite's infective stage, are required for a better understanding of its transmission and infection. However, information on cultivation for mass production of metacyclic promastigotes and factors that stimulate their metacyclogenesis is limited. Therefore, the objective of this study was to develop a suitable methodology for generating promastigote cultures containing a high proportion and number of metacyclic promastigotes. Various media, i.e., Schneider's insect medium, Medium 199 and Grace's insect medium, supplemented with various quantities of dithiothreitol, Basal Medium Eagle vitamins, pooled human urine, and fetal bovine serum, were optimized for metacyclogenesis. The results revealed that the optimum culture medium and conditions of those tested were Schneider's insect medium supplemented with 100 μM dithiothreitol, 1% (v/v) Basal Medium Eagle vitamins, 2% (v/v) pooled human urine, and 10% (v/v) fetal bovine serum, pH 5.0 at 26°C. We also demonstrated that metacyclic promastigotes could be purified and enriched by negative selection using peanut lectin. Under these culture conditions, the highest yield of metacyclic promastigotes was obtained with a significantly higher percentage of parasite survival, resistance to complement-mediated lysis, and infection index in THP-1 macrophage cells compared to parasites cultured without media supplements at neutral pH. This is the first report providing a reliable method for mass production of metacyclic promastigotes for infections and other experimental studies of this emerging parasite in the future.
() 是人引起利什曼病的病原体,研究循环期前体滋养体(寄生虫的感染阶段)的特性有助于更好地了解其传播和感染。然而,关于大规模生产循环期前体滋养体的培养方法以及刺激其循环期形成的因素的信息有限。因此,本研究的目的是开发一种合适的方法,用于生成含有高比例和数量的循环期前体滋养体的培养物。我们优化了各种培养基,即 Schneider 的昆虫培养基、Medium 199 和 Grace 的昆虫培养基,添加了不同量的二硫苏糖醇、基础培养基 Eagle 维生素、混合人尿和胎牛血清,以促进循环期形成。结果表明,在所测试的培养基和条件中,最佳的是含有 100 μM 二硫苏糖醇、1%(v/v)基础培养基 Eagle 维生素、2%(v/v)混合人尿和 10%(v/v)胎牛血清的 Schneider 的昆虫培养基,pH 值为 5.0,温度为 26°C。我们还证明,通过使用花生凝集素进行阴性选择,可以纯化和富集循环期前体滋养体。在这些培养条件下,与在中性 pH 值下没有培养基补充的寄生虫相比,循环期前体滋养体的产量最高,寄生虫的存活率、对补体介导的裂解的抗性和在 THP-1 巨噬细胞中的感染指数显著更高。这是首次报道提供了一种可靠的方法,用于大规模生产循环期前体滋养体,以用于 感染和未来对这种新兴寄生虫的其他实验研究。