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An Electron Microscopic Study of Babesia Microti Invading Erythrocytes

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Journal Cell Tissue Res
Date 1976 Jun 28
PMID 820430
Citations 33
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Abstract

Intracellular sporozoan parasites invade the host cell through the invagination of the plasma membrane of the host and a vacuole is formed which accommodates the entering parasite. The vacuole may disappear and the invaginated membrane of the host then becomes closely apposed to that of the parasite's own membrane. As a result the parasite is covered by two membranes. Members of the class Piroplasmea differ from other Sporozoa in that their trophozoites are covered by a single membrane. By screening numerous sections of intraerythrocytic Babesia microti belonging to the class Piroplasmea, it was found that merozoites of Babesia enter the erythrocytes of hamsters in the same way as those of the other Sporozoa. When a merozoite touches the red blood cell with its anterior end it becomes attached to the membrane of the host, which starts to invaginate and a parasitophorous vacuole is formed. The vacuolar space disappears rapidly and the membrane of the vacuole and that of the parasite become closely adjacent. At this stage the parasite is surrounded by two plasma membranes. The outer membrane derived from the invaginated host membrane disintegrates quickly and the parasite is left with a single membrane throughout its life span.

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References
1.
Kilejian A . Does a histidine-rich protein from Plasmodium lophurae have a function in merozoite penetration?. J Protozool. 1976; 23(2):272-7. DOI: 10.1111/j.1550-7408.1976.tb03768.x. View

2.
RUDZINSKA M . The fine structure of malaria parasites. Int Rev Cytol. 1969; 25:161-99. DOI: 10.1016/s0074-7696(08)60203-x. View

3.
Smith K, BROCKLESBY D, Bland P, Purnell R, Brown C, Payne R . The fine structure of intra-erythrocytic stages of Theileria gorgonis and a strain of Anaplasma marginale isolated from wildebeest (Connochaetes taurinus). Tropenmed Parasitol. 1974; 25(3):293-300. View

4.
Weidner E . Ultrastructural study of microsporidian invasion into cells. Z Parasitenkd. 1972; 40(3):227-42. DOI: 10.1007/BF00329623. View

5.
RUDZINSKA M . Ultrastructure of intraerythrocytic Babesia microti with emphasis on the feeding mechanism. J Protozool. 1976; 23(2):224-33. DOI: 10.1111/j.1550-7408.1976.tb03759.x. View