Temporal analysis of the developing Chlamydia psittaci inclusion by use of fluorescence and electron microscopy

Infection and Immunity

Volumn 64, Issue 10, 1996, Pages 4269-4278

  Rockey, Daniel D ^a   Fischer, Elizabeth R ^a   Hackstadt, Ted ^a  

^a NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BACTERIAL GROWTH; CELL ULTRASTRUCTURE; CHLAMYDOPHILA PSITTACI; FLUORESCENCE MICROSCOPY; HELA CELL; NONHUMAN; PRIORITY JOURNAL;

EID: 0029842450     PISSN: 00199567     EISSN: None     Source Type: Journal    
DOI: 10.1128/iai.64.10.4269-4278.1996     Document Type: Article

References (25)

1. Anderson, D. R., H. E. Hops, M. F. Barile, and B. C. Bernheim. 1965. Comparison of the ultrastructure of several rickettsiae, ornithosis virus, and Mycoplasma in tissue culture. J. Bacteriol. 90:1387-1403.
2. Caldwell, H. D., J. Kromhout, and J. Schachter. 1981. Purification and partial characterization of the major outer membrane protein of Chlamydia trachomatis. Infect. Immun. 31:1161-1176.
3. Campbell, S., S. J. Richmond, and P. Yates. 1989. The development of Chlamydia trachomatis inclusions within the host eukaryotic cell during interphase and mitosis. J. Gen. Microbiol. 135:1153-1165.
4. Friis, R. R. 1972. Interaction of L cells and Chlamydia psittaci: entry of the parasite and host response to its development. J. Bacteriol. 110:706-721.
5. Hackstadt, T., D. D. Rockey, R. A. Heinzen, and M. A. Scidmore. 1996. Chlamydia trachomatis interrupts an exocytic pathway to acquire endogenously synthesized sphingomyelin in transit from the Golgi apparatus to the plasma membrane. EMBO J. 15:964-977.
6. Hackstadt, T., M. A. Scidmore, and D. D. Rockey. 1995. Lipid metabolism in Chlamydia trachomatis infected cells: directed trafficking of Golgi-derived sphingolipids to the chlamydial inclusion. Proc. Natl. Acad. Sci. USA 92:4877-4881.
7. Heinzen, R. A., M. A. Scidmore, D. D. Rockey, and T. Hackstadt. 1996. Lysosomal glycoproteins and the vacuolar-type (H+)-ATPase differentiate the parasitophorous vacuoles of Coxiella burnetii and Chlamydia trachomatis. Infect. Immun. 64:796-809.
8. Higashi, N. 1965. Electron microscopic studies on the mode of reproduction of trachoma virus and psittacosis virus in cell culture. Exp. Mol. Pathol. 4:24-39.
9. Hodinka, R. L., C. H. Davis, J. Choong, and P. B. Wyrick. I988. Ultrastructural study of endocytosis of Chlamydia trachomatis by McCoy cells. Infect. Immun. 56:1456-1463.
10. Lepinay, A., J. Orfila, A. Anteunis, J. M. Boutry, L. Orme-Roselli, and R. Robineaux. 1970. Etude en microscopic electronique du developpement et de la morphologie de Chlamydia psittaci dans les macrophages de souris. Ann. Inst. Pasteur 119:222-231.
11. Lipsky, N. G., and R. E. Pagano. 1985. Intracellular translocation of fluorescent sphingolipids in cultured fibroblasts: endogenously synthesized sphingomyelin and glucocerebrocide analogues pass through the Golgi apparatus en route to the plasma membrane. J. Cell Biol. 100:27-34.
12. Matsumoto, A. 1988. Structural characteristics of chlamydial bodies, p. 21-46. In A. L. Barron (ed.). Microbiology of Chlamydia. CRC Press, Boca Raton, Fla.
13. Matsumoto, A., I. Bessho, K. Uehira, and T. Suda. 1991. Morphological studies of the association of mitochondria with chlamydial inclusions and the fusion of chlamydial inclusions. J. Electron Microsc. 40:356-36.3.
14. McDonald, K. 1984. Osmium ferricyanide fixation improves microfilament preservation and membrane visualization in a variety of animal cell types. J. Ultrastruct. Res. 86:107-118.
15. Moulder, J. W. 1991. Interaction of chlamydiac and host cells in vitro. Microbiol. Rev. 55:143-190.
16. Patton, D. L., and C. C. Kuo. 1990. Cinematographic observations of growth of Chlamydia pneumonias in primary cultures of monkey conjunctival and human amniotic epithelial cells, p. 20-23. In W. R. Bowie et al. (ed.). Chlamydial infections. Cambridge University Press, Cambridge.
17. Reynolds, E. S. 1963. The use of lead citrate at high pH as an electronopaque stain in electron microscopy. J. Cell Biol. 17:208-213.
18. Ridderhof, J. C., and R. C. Barnes. 1989. Fusion of inclusions following superinfection of HeLa cells by two serovars of Chlamydia trachomatis. Infect. Immun. 57:31 3189-3193.
19. Rockey, D. D., R. A. Heinzen, and T. Hackstadt. 1995. Cloning and characterization of a Chlamydia psittaci gene coding for a protein localized in the inclusion membrane of infected cells. Mol. Microbiol. 15:617-626.
20. Rockey, D. D., and J. L. Rosquist. 1994. Protein antigens of Chlamydia psittaci present in infected cells but not detected in the infectious elementary body. Infect. Immun. 62:1116-112.
21. Schramm, N., and P. B. Wyrick. 1995. Cytoskeletal requirements in Chlamydia trachomatis infection of host cells. Infect. Immun. 63:324-332.
22. Spears, P., and J. Storz. 1979. Biotyping of Chlamydia psittaci bused on inclusion morphology and response to diethylaminoethyl-dextran and cycloheximide. Infect. Immun. 24:224-232.
23. Virtanen, I., P. Ekblom, and P. Laurila. 1980. Subcellular compartmenlalization of saccharide moieties in cultured normal and malignant cells. J. Cell Biol. 85:429-434.
24. Ward, M. E. 1983. Chlamydial classification, development and structure. Br. Med. Bull. 39:109-115.
25. Wyrick, P. B., and E. A. Brownridge. 1978. Growth of Chlamydia psittaci in macrophages. Infect. Immun. 19:1054-1060.