Adapting Eimeria tenella to Grow in Primary Chicken Kidney Cells Following Repeated Passages between Cell Culture and Chickens

1997 ◽  
Vol 41 (1) ◽  
pp. 111 ◽  
Author(s):  
Jianfei Zhang ◽  
Eric Wilson ◽  
Shiguang Yang ◽  
Mark C. Healey
Parasitology ◽  
1981 ◽  
Vol 82 (2) ◽  
pp. 189-194 ◽  
Author(s):  
Catriona Urquhart

SUMMARYThe pattern of DNA synthesis in chicken kidney (CK) cells parasitized by Eimeria tenella was altered; a 2-fold increase in the uptake of [3H]-thymidine occurred in these cells compared with that shown by the controls. This difference was significantly different at 16 h post-inoculation (p.i.) and reached a peak at 20 h p.i. Non-parasitized cells in co-culture with parasitized cells showed a level of incorporation intermediate between that of the parasitized and non-parasitized mono- cultures. It was shown that this stimulation was due to a factor released into the medium by the parasite or the parasitized cell. A possible course of events leading to induced and prolonged DNA synthesis by the host cell and the significance of this change in the life-cycle of the parasite is discussed.


Parasite ◽  
2021 ◽  
Vol 28 ◽  
pp. 11
Author(s):  
Xinlei Yan ◽  
Wenying Han ◽  
Xianyong Liu ◽  
Xun Suo

Egress plays a vital role in the life cycle of apicomplexan parasites including Eimeria tenella, which has been attracting attention from various research groups. Many recent studies have focused on early egress induced by immune molecules to develop a new method of apicomplexan parasite elimination. In this study, we investigated whether nitric oxide (NO), an immune molecule produced by different types of cells in response to cytokine stimulation, could induce early egress of eimerian sporozoites in vitro. Eimeria tenella sporozoites were extracted and cultured in primary chicken kidney cells. The number of sporozoites egressed from infected cells was analyzed by flow cytometry after treatment with NO released by sodium nitroferricyanide (II) dihydrate. The results showed that exogenous NO stimulated the rapid egress of E. tenella sporozoites from primary chicken kidney cells before replication of the parasite. We also found that egress was dependent on intra-parasitic calcium ion (Ca2+) levels and no damage occurred to host cells after egress. The virulence of egressed sporozoites was significantly lower than that of fresh sporozoites. The results of this study contribute to a novel field examining the interactions between apicomplexan parasites and their host cells, as well as that of the clearance of intracellular pathogens by the host immune system.


1996 ◽  
Vol 40 (1) ◽  
pp. 63 ◽  
Author(s):  
Jianfei Zhang ◽  
Eric Wilson ◽  
Shiguang Yang ◽  
Mark C. Healey

Parasitology ◽  
1972 ◽  
Vol 65 (1) ◽  
pp. 131-136 ◽  
Author(s):  
B. Klimes ◽  
D. G. Rootes ◽  
Zabel Tanielian

In chickens kidney-cell culture gametogony of E. tenella usually occurs in a limited number of selected cells in the form of nests of gametocytes. Some cells contain only macrogametocytes, others only microgametocytes and some cells contain both sexes together. Mixed nests of gametocytes are evidence for genetic sex determination. By using PAS staining the origin of macrogametocytes and microgametocytes can be retraced to the merozoites and schizonts of the last generation, which are differentiated by this technique.


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