Literature DB >> 4127629

Fine structures of cell envelopes of Chlamydia organisms as revealed by freeze-etching and negative staining techniques.

A Matsumoto.   

Abstract

The cell walls of Chlamydia psittaci (meningopneumonitis strain) were examined by the freeze-etching and negative staining techniques. It was observed that the cleaved convex surface of the developmental, reticulate body was covered with numerous non-etchable particles 9 to 10 nm in diameter, these particles being rarely seen on the concave surface. Similarly, the convex surface of the mature, elementary body (EB) was covered with many particles but the concavity lacked these particles. After etching, the smooth concave surface of the EB appeared to have a hexagonally arrayed subunit structure, on which the button structure (B structure) was observed. Each B structure had a diameter of 27 nm and several B structures were grouped together in a hexagonal arrangement with a center-to-center spacing of 45 nm. In a limited area of the negatively stained EB cell wall, hexagonally arrayed rosette structures were present, with a center-to-center spacing similar to the B structures seen in the freeze-etched preparation. Each rosette, about 19 to 20 nm in diameter, appeared to be composed of a radial arrangement of nine subunits. The freeze-fractured cell wall-cytoplasmic membrane complexes indicated that the outer surface of the cytoplasmic membrane which appeared as the convex surface was covered with the fine particles, and thus it was likely that frozen EB was cleaved at the gap between the cell wall and ctyoplasmic membrane. On the cleaved inclusion, several groups of fine particles were observed. In each group, the particles were arranged hexagonally with the spacing ranging from 20 to 50 nm.

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Year:  1973        PMID: 4127629      PMCID: PMC246495          DOI: 10.1128/jb.116.3.1355-1363.1973

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  8 in total

1.  PURIFICATION AND CHEMICAL COMPOSITION OF MENINGOPNEUMONITIS VIRUS.

Authors:  A TAMURA; N HIGASHI
Journal:  Virology       Date:  1963-08       Impact factor: 3.616

2.  ELECTRON MICROSCOPIC STUDIES ON THE MODE OF REPRODUCTION OF TRACHOMA VIRUS AND PSITTACOSIS VIRUS IN CELL CULTURES.

Authors:  N HIGASHI
Journal:  Exp Mol Pathol       Date:  1965-02       Impact factor: 3.362

3.  Developmental cycle and reproductive mechanism of the meningopneumonitis virus in strain L cells.

Authors:  N HIGASHI; A TAMURA; M IWANAGA
Journal:  Ann N Y Acad Sci       Date:  1962-03-05       Impact factor: 5.691

4.  Electron microscopic observations on the structure of the envelopes of mature elementary bodies and developmental reticulate forms of Chlamydia psittaci.

Authors:  A Tamura; A Matsumoto; G P Manire; N Higashi
Journal:  J Bacteriol       Date:  1971-01       Impact factor: 3.490

5.  Purification and chemical composition of reticulate bodies of the meningopneumonitis organisms.

Authors:  A Tamura; A Matsumoto; N Higashi
Journal:  J Bacteriol       Date:  1967-06       Impact factor: 3.490

6.  Electron Microscopic Observations on the Fine Structure of Cell Walls of Chlamydia psittaci.

Authors:  A Matsumoto; G P Manire
Journal:  J Bacteriol       Date:  1970-12       Impact factor: 3.490

7.  Electron microscopic observations on the effects of penicillin on the morphology of Chlamydia psittaci.

Authors:  A Matsumoto; G P Manire
Journal:  J Bacteriol       Date:  1970-01       Impact factor: 3.490

8.  Effect of penicillin on the multiplication of meningopneumonitis organisms (Chlamydia psittaci).

Authors:  A Tamura; G P Manire
Journal:  J Bacteriol       Date:  1968-10       Impact factor: 3.490

  8 in total
  15 in total

1.  Chlamydia parasitism: ultrastructural characterization of the interaction between the chlamydial cell envelope and the host cell.

Authors:  E M Peterson; L M de la Maza
Journal:  J Bacteriol       Date:  1988-03       Impact factor: 3.490

Review 2.  The chlamydia: molecular biology of procaryotic obligate parasites of eucaryocytes.

Authors:  Y Becker
Journal:  Microbiol Rev       Date:  1978-06

3.  Ultrastucture of the surface of Rickettsia prowazeki and Rickettsia akari.

Authors:  E L Palmer; M L Martin; L Mallavia
Journal:  Appl Microbiol       Date:  1974-10

4.  Isolation and electron microscopic observations of intracytoplasmic inclusions containing Chlamydia psittaci.

Authors:  A Matsumoto
Journal:  J Bacteriol       Date:  1981-01       Impact factor: 3.490

5.  Surface projections of Chlamydia psittaci elementary bodies as revealed by freeze-deep-etching.

Authors:  A Matsumoto
Journal:  J Bacteriol       Date:  1982-08       Impact factor: 3.490

6.  Protection of sheep against Chlamydia psittaci infection with a subcellular vaccine containing the major outer membrane protein.

Authors:  T W Tan; A J Herring; I E Anderson; G E Jones
Journal:  Infect Immun       Date:  1990-09       Impact factor: 3.441

7.  Electron tomography and cryo-SEM characterization reveals novel ultrastructural features of host-parasite interaction during Chlamydia abortus infection.

Authors:  M Wilkat; E Herdoiza; V Forsbach-Birk; P Walther; A Essig
Journal:  Histochem Cell Biol       Date:  2014-02-13       Impact factor: 4.304

8.  Electron microscopic observations of surface projections on Chlamydia psittaci reticulate bodies.

Authors:  A Matsumoto
Journal:  J Bacteriol       Date:  1982-04       Impact factor: 3.490

9.  Chlamydia trachomatis has penicillin-binding proteins but not detectable muramic acid.

Authors:  A G Barbour; K Amano; T Hackstadt; L Perry; H D Caldwell
Journal:  J Bacteriol       Date:  1982-07       Impact factor: 3.490

10.  Modifications of the envelope of Chlamydia psittaci during its developmental cycle: freeze-fracture study of complementary replicas.

Authors:  C Louis; G Nicolas; F Eb; J F Lefebvre; J Orfila
Journal:  J Bacteriol       Date:  1980-02       Impact factor: 3.490

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