Cysne-Finkelstein L, Temporal R M, Alves F A, Leon L L
Department of Protozoology, FIOCRUZ, Manguinhos,Brazil.
Exp Parasitol. 1998 May;89(1):58-62. doi: 10.1006/expr.1998.4276.
Axenic Leishmania amazonensis cultures were obtained (with 2 years of follow-up) in Schneider's medium at pH 5.5 and a temperature of 32 degrees C. Differentiation of promastigotes into amastigotes is directly associated with the metacyclogenesis rate of the original promastigotes. Promastigote cultures containing different percentages of metacyclic forms, as evaluated by the complement lysis test, resulted in axenic amastigote cultures containing a variable amount of undifferentiated forms. We observed that a culture originally containing a large amount of metacyclic forms (73%) underwent a complete differentiation process, resulting in a 100% amastigote culture with no promastigote forms. All other cultures (with a decreasing amount of metacyclic forms: 50% and fewer) failed to differentiate completely, resulting in cultures with increasing percentages of promastigote contamination. The amastigote/promastigote rate in these cultures has been maintained at the same level thus far. The axenic Leishmania amazonensis amastigotes were cryopreserved, thawed as such, and successfully cultivated under appropriately defined growth conditions.
在pH 5.5和32摄氏度的条件下,于施奈德培养基中获得了无共生体的亚马逊利什曼原虫培养物(随访2年)。前鞭毛体向无鞭毛体的分化与原始前鞭毛体的循环后期发育率直接相关。通过补体溶解试验评估,含有不同百分比循环后期形式的前鞭毛体培养物,产生了含有不同数量未分化形式的无共生体无鞭毛体培养物。我们观察到,最初含有大量循环后期形式(73%)的培养物经历了完全分化过程,产生了100%无鞭毛体培养物,没有前鞭毛体形式。所有其他培养物(循环后期形式数量逐渐减少:50%及以下)未能完全分化,导致前鞭毛体污染百分比增加的培养物。到目前为止,这些培养物中的无鞭毛体/前鞭毛体比率一直保持在同一水平。无共生体的亚马逊利什曼原虫无鞭毛体被冷冻保存,原样解冻,并在适当定义的生长条件下成功培养。