f Ultrastructural variation of cultured Ehrlichia chaffeensis
- Authors: V. L. Popov, Sheng-Min Chen, Hui-Min Feng, O. H. Walker*
- *Correspondence should be sent to Dr D. H. Walker.
- First Published Online: 01 December 1995, Journal of Medical Microbiology 43: 411-421, doi: 10.1099/00222615-43-6-411
- Subject: Microbial Pathogenicity
- Issue Published:
The ultrastructure of Ehrlichia chaffeensis (Arkansas strain) was studied in non-irradiated and irradiated monolayers of mouse embryo, Vero, BGM and L929 cells, and in non-irradiated DH82 cells. Within the intracellular parasitophorous vacuoles (morulae), two types of ehrlichial cells were found regularly—those with uniformly dispersed nucleoid filaments and ribosomes (reticulate cells) and smaller ones with centrally condensed nucleoid filaments and ribosomes (dense-cored cells), which represent the normal life cycle of ehrlichiae. In addition, large reticulate cells were observed, forming long projections of the cell wall, protrusions of cytoplasmic membrane into the periplasmic space, or budding of protoplast fragments (minute forms) into the periplasmic space. Ehrlichiae with abnormalities of protoplast fission were found, apparently leading to formation of giant, multilobular or elongated rod-like ehrlichiae. Morulae were usually surrounded by cisterns of granular endoplasmic reticulum and mitochondria and often contained vesicles, long tubules 25 nm in diameter, probably originating from the ehrlichial cell wall, and fibrillar ehrlichial antigen apparently shed from the surface of the cell wall. Some cells contained, in addition to normal morulae, a whole morula that had become dense and contained degenerating ehrlichiae. These results indicate that as well as normal growth and reproduction, ehrlichiae exhibit pathological events: They can be remarkably damaged inside the host cell vacuoles, presumably phagolysosomes, or enter a process morphologically similar to bacterial L-transformation.
© 1995 Pathological Society of Great Britain and Ireland | Published by the Microbiology Society
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