Danforth H D, Augustine P C, Clare R A
USDA, Agricultural Research Service, Livestock and Poultry Sciences Institute, Beltsville Agricultural Research Center, MD 20705.
Parasitol Res. 1994;80(7):588-93. doi: 10.1007/BF00933007.
Transmission electron microscopy was used to study the in vitro development of Eimeria tenella in a novel established avian-derived cell line (designated CEV-1/F7) used for antigen production in chicken immunization studies. Sporozoites of E. tenella were inoculated onto cell monolayers and the cells were fixed at 24-h intervals. Large numbers of intracellular sporozoites were seen at 24 h postinoculation (p.i.), and trophozoites were identified at 24-48 h p.i. Immature schizonts, some with budding merozoites, were seen by 48 h p.i. At 72-96 h p.i., immature and mature schizonts and extracellular merozoites were observed. No merozoite invasion occurred, but immature second-generation schizogony was seen in parasitophorous vacuoles of first-generation schizonts. No further development occurred and degeneration of most schizonts was seen by 120-144 h p.i. The results confirmed synchronous development of E. tenella until 48 h p.i., followed by asynchronous development and ultrastructural degeneration with increased incubation time.
利用透射电子显微镜研究了柔嫩艾美耳球虫在一种新建立的用于鸡免疫研究中抗原生产的禽类来源细胞系(命名为CEV-1/F7)中的体外发育情况。将柔嫩艾美耳球虫的子孢子接种到细胞单层上,并每隔24小时对细胞进行固定。接种后24小时(p.i.)可见大量细胞内子孢子,接种后24 - 48小时鉴定出滋养体。接种后48小时可见未成熟裂殖体,有些带有出芽的裂殖子。接种后72 - 96小时,观察到未成熟和成熟裂殖体以及细胞外裂殖子。未见裂殖子侵入,但在第一代裂殖体的寄生泡中可见未成熟的第二代裂体增殖。未见进一步发育,接种后120 - !44小时可见大多数裂殖体退化。结果证实,柔嫩艾美耳球虫在接种后48小时内发育同步,随后随着培养时间延长出现异步发育和超微结构退化。