Upton S J, Tilley M, Brillhart D B
Division of Biology, Kansas State University, Manhattan 66506.
J Clin Microbiol. 1995 Feb;33(2):371-5. doi: 10.1128/jcm.33.2.371-375.1995.
Surface-sterilized oocysts of Cryptosporidium parvum were applied to subconfluent monolayers of human adenocarcinoma (HCT-8) cells grown on coverslips in six-well cluster plates. Parasite-infected cultures were then incubated in RPMI 1640 with 10% fetal bovine serum, 15 mM HEPES (N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid) buffer, and antibiotics at 37 degrees C in a 5% CO2-95% air incubator for 2 h to allow sporozoites to excyst and enter cells. After cultures were washed free of debris, fresh cell culture media containing select supplements were added and cultures were reincubated. Parasite growth was assessed 66 h later by counting the number of parasite developmental stages in 25 random x 100 oil fields by Nomarski interference-contrast microscopy. Four vitamin supplements, calcium pantothenate, L-ascorbic acid, folic acid, and 4-(para)-aminobenzoic acid, each resulted in a significant increase in parasite numbers in vitro. The addition of insulin and the sugars glucose, galactose, and maltose also had a positive effect on parasite growth, although the effect was less pronounced than with any of the vitamins. Using the above information, we developed a supplemental medium formulation consisting of RPMI 1640 with 10% fetal bovine serum, 15 mM HEPES, 50 mM glucose, and 35 micrograms of ascorbic acid, 1.0 micrograms of folic acid, 4.0 micrograms of 4-aminobenzoic acid, 2.0 micrograms of calcium pantothenate, 0.1 U of insulin, 100 U of penicillin G, 100 micrograms of streptomycin, and 0.25 microgram of amphotericin B (Fungizone) per ml (pH 7.4). The growth of c. parvum in this medium was found to be enhanced approximately 10-fold compared with that in control medium without additional glucose, insulin, or vitamins.
将经表面消毒的微小隐孢子虫卵囊接种到六孔板盖玻片上生长的人腺癌(HCT-8)细胞亚汇合单层培养物中。然后将感染寄生虫的培养物在含有10%胎牛血清、15 mM HEPES(N-2-羟乙基哌嗪-N'-2-乙磺酸)缓冲液和抗生素的RPMI 1640中,于37℃、5%二氧化碳-95%空气培养箱中孵育2小时,以使子孢子脱囊并进入细胞。培养物清洗去除碎片后,加入含有特定补充剂的新鲜细胞培养基并重新孵育。66小时后,通过Nomarski干涉相差显微镜在25个随机的×100油镜视野中计数寄生虫发育阶段的数量来评估寄生虫生长情况。四种维生素补充剂,泛酸钙、L-抗坏血酸、叶酸和4-(对)氨基苯甲酸,每种都导致体外寄生虫数量显著增加。添加胰岛素以及糖葡萄糖、半乳糖和麦芽糖对寄生虫生长也有积极影响,尽管其效果不如任何一种维生素明显。利用上述信息,我们开发了一种补充培养基配方,由含有10%胎牛血清、15 mM HEPES、50 mM葡萄糖、35微克抗坏血酸、1.0微克叶酸、4.0微克4-氨基苯甲酸、2.0微克泛酸钙、0.1 U胰岛素、100 U青霉素G、100微克链霉素和每毫升0.25微克两性霉素B(两性霉素)(pH 7.4)的RPMI 1640组成。发现微小隐孢子虫在这种培养基中的生长与不含额外葡萄糖、胰岛素或维生素的对照培养基相比增强了约10倍。