Abstract
Plasmodium elongatum, an avian malarial parasite, differs from other such parasites by infecting both the circulating red blood cells and the hematopoietic cells. The exoerythrocytic development of P. elongatum occurs mainly in these red cell precursors. The fine structure of the asexual stages of P. elongatum has been studied in the bone marrow and peripheral blood of canaries and compared with that of the asexual stages of other avian malarial parasites. With minor differences, the merozoites of P. elongatum possess the same organelles as those in the exoerythrocytic merozoites of P. fallax and the erythrocytic stages of P. cathemerium, P. lophurae, P. fallax, and P. gallinaceum. The developmental sequence is also essentially similar to that of other avian malarial parasites, in that upon entry into a new host cell, the dedifferentiation, growth, and redifferentiation phases take place. However, we have found some important differences in the feeding mechanism of P. elongatum. The cytostome is involved in the ingestion of host cell cytoplasm in both exoerythrocytic and erythrocytic stages, in contrast to P. fallax, in which the cytostome is inactive in the exoerythrocytic stages. In P. elongatum, host cell cytoplasm is ingested through the cytostome, and "boluses" are formed and incorporated into a large digestive vacuole. Subsequently, the digestion of the boluses takes place in this digestive vacuole. Thus, in regard to the function of the cytostome, the exoerythrocytic stages of P. elongatum appear to be closely related to the erythrocytic stage which has a feeding mechanism similar to that of the erythrocytic stage of other avian malarial parasites.
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Selected References
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- Aikawa M., Hepler P. K., Huff C. G., Sprinz H. The feeding mechanism of avian malarial parasites. J Cell Biol. 1966 Feb;28(2):355–373. doi: 10.1083/jcb.28.2.355. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Aikawa M. The fine structure of the erythrocytic stages of three avian malarial parasites, Plasmodium fallax, P. lophurae, and P. cathemerium. Am J Trop Med Hyg. 1966 Jul;15(4):449–471. doi: 10.4269/ajtmh.1966.15.449. [DOI] [PubMed] [Google Scholar]
- COOK L., GRANT P. T., KERMACK W. O. Proteolytic enzymes of the erythrocytic forms of roden and simian species of malarial plasmodia. Exp Parasitol. 1961 Nov;11:372–379. doi: 10.1016/0014-4894(61)90041-8. [DOI] [PubMed] [Google Scholar]
- Elliott A. M., Clemmons G. L. An ultrastructural study of ingestion and digestion in Tetrahymena pyriformis. J Protozool. 1966 May;13(2):311–323. doi: 10.1111/j.1550-7408.1966.tb01912.x. [DOI] [PubMed] [Google Scholar]
- GARNHAM P. C., BIRD R. G., BAKER J. R. Electron microscope studies of motile stages of malaria parasites. I. The fine structure of the sporozoites of Haemamoeba (Plasmodium) gallinacea. Trans R Soc Trop Med Hyg. 1960 May;54:274–278. doi: 10.1016/0035-9203(60)90075-4. [DOI] [PubMed] [Google Scholar]
- GRASSO J. A., SWIFT H., ACKERMAN G. A. Observations on the development of erythrocytes in mammalian fetal liver. J Cell Biol. 1962 Aug;14:235–254. doi: 10.1083/jcb.14.2.235. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hepler P. K., Huff C. G., Sprinz H. The fine structure of the exoerythrocytic stages of Plasmodium fallax. J Cell Biol. 1966 Aug;30(2):333–358. doi: 10.1083/jcb.30.2.333. [DOI] [PMC free article] [PubMed] [Google Scholar]
- NOVIKOFF A. B., ESSNER E., QUINTANA N. GOLGI APPARATUS AND LYSOSOMES. Fed Proc. 1964 Sep-Oct;23:1010–1022. [PubMed] [Google Scholar]
- PALADE G. E. A small particulate component of the cytoplasm. J Biophys Biochem Cytol. 1955 Jan;1(1):59–68. doi: 10.1083/jcb.1.1.59. [DOI] [PMC free article] [PubMed] [Google Scholar]
- REYNOLDS E. S. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963 Apr;17:208–212. doi: 10.1083/jcb.17.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Robinow C. F., Marak J. A fiber apparatus in the nucleus of the yeast cell. J Cell Biol. 1966 Apr;29(1):129–151. doi: 10.1083/jcb.29.1.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
- STRAUS W. Colorimetric analysis with N, N-dimethyl-p-phenylenediamine of the uptake of intravenously injected horseradish peroxidase by various tissues of the rat. J Biophys Biochem Cytol. 1958 Sep 25;4(5):541–550. doi: 10.1083/jcb.4.5.541. [DOI] [PMC free article] [PubMed] [Google Scholar]
- THEG D. E., BECKER C., BEARD J. W. VIRUS OF AVIAN MYELOBLASTOSIS (BAI STRAIN A). XXV. ULTRACYTOCHEMICAL STUDY OF VIRUS AND MYELOBLAST PHOSPHATASE ACTIVITY. J Natl Cancer Inst. 1964 Jan;32:201–235. [PubMed] [Google Scholar]
- Takeuchi A. Electron microscope studies of experimental Salmonella infection. I. Penetration into the intestinal epithelium by Salmonella typhimurium. Am J Pathol. 1967 Jan;50(1):109–136. [PMC free article] [PubMed] [Google Scholar]
