Literature DB >> 3131245

Ultrastructural study of endocytosis of Chlamydia trachomatis by McCoy cells.

R L Hodinka1, C H Davis, J Choong, P B Wyrick.   

Abstract

The entry of Chlamydia trachomatis into McCoy cells (fibroblasts) was studied by transmission electron microscopy. On adsorption of elementary bodies (EBs) to host cells at 37 degrees C, the EBs were bound primarily to preexisting cell-surface microvilli. They were also observed in coated pits located at the bases of the microvilli and along smooth surfaces of the host cells and were internalized within coated vesicles at this temperature. Postembedding immunogold labeling on Lowicryl thin sections with anti-clathrin antibody as the primary reagent revealed the gold marker localized in pits and vesicles containing chlamydiae. Some EBs were present in smooth-surfaced invaginations at or near the bases of microvilli and in vesicles devoid of distinguishable coat material. A similar entry process was observed with centrifugation-assisted inoculation of EBs onto the McCoy cells. Individual EBs were initially internalized into tightly bound endocytic vesicles. However, within 1 to 3 h postinfection, multiple C. trachomatis EBs were observed in large, loosely bound vesicles. Evidence suggests that vesicles containing C. trachomatis may have fused with one another early in the infectious process. These results indicate that chlamydiae can exploit the specific process of adsorptive endocytosis for entry into host cells and for translocation to a given intracellular destination, which may be different for each species.

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Year:  1988        PMID: 3131245      PMCID: PMC259421          DOI: 10.1128/iai.56.6.1456-1463.1988

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  36 in total

Review 1.  Endocytosis.

Authors:  S C Silverstein; R M Steinman; Z A Cohn
Journal:  Annu Rev Biochem       Date:  1977       Impact factor: 23.643

2.  Interaction of Chlamydia psittaci reticulate bodies with mouse peritoneal macrophages.

Authors:  E Brownridge; P B Wyrick
Journal:  Infect Immun       Date:  1979-06       Impact factor: 3.441

3.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

4.  Growth of Chlamydia psittaci in macrophages.

Authors:  P B Wyrick; E A Brownridge
Journal:  Infect Immun       Date:  1978-03       Impact factor: 3.441

5.  Interaction of Chlamydia trachomatis organisms and HeLa 229 cells.

Authors:  C C Kuo; T Grayston
Journal:  Infect Immun       Date:  1976-04       Impact factor: 3.441

6.  Coated pits, coated vesicles, and receptor-mediated endocytosis.

Authors:  J L Goldstein; R G Anderson; M S Brown
Journal:  Nature       Date:  1979-06-21       Impact factor: 49.962

7.  Effect of polycations, polyanions and neuraminidase on the infectivity of trachoma-inclusin conjunctivitis and lymphogranuloma venereum organisms HeLa cells: sialic acid residues as possible receptors for trachoma-inclusion conjunction.

Authors:  C C Kuo; S P Wang; J T Grayston
Journal:  Infect Immun       Date:  1973-07       Impact factor: 3.441

8.  Parasite-specified phagocytosis of Chlamydia psittaci and Chlamydia trachomatis by L and HeLa cells.

Authors:  G I Byrne; J W Moulder
Journal:  Infect Immun       Date:  1978-02       Impact factor: 3.441

9.  Interaction of Chlamydia psittaci with mouse peritoneal macrophages.

Authors:  P B Wyrick; E A Brownridge; B E Ivins
Journal:  Infect Immun       Date:  1978-03       Impact factor: 3.441

10.  Ultrastructural study of mode of entry of Chlamydia psittaci into L-929 cells.

Authors:  R L Hodinka; P B Wyrick
Journal:  Infect Immun       Date:  1986-12       Impact factor: 3.441

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  41 in total

1.  Ultrastructural analysis of developmental events in Chlamydia pneumoniae-infected cells.

Authors:  K Wolf; E Fischer; T Hackstadt
Journal:  Infect Immun       Date:  2000-04       Impact factor: 3.441

2.  Normal IncA expression and fusogenicity of inclusions in Chlamydia trachomatis isolates with the incA I47T mutation.

Authors:  Y Pannekoek; A van der Ende; P P Eijk; J van Marle; M A de Witte; J M Ossewaarde; A J van den Brule; S A Morré; J Dankert
Journal:  Infect Immun       Date:  2001-07       Impact factor: 3.441

3.  Development of a rickettsia isolated from an aborted bovine fetus.

Authors:  K M Kocan; T B Crawford; P M Dilbeck; J F Evermann; T C McGuire
Journal:  J Bacteriol       Date:  1990-10       Impact factor: 3.490

Review 4.  Hijacking the endocytic machinery by microbial pathogens.

Authors:  Ann En-Ju Lin; Julian Andrew Guttman
Journal:  Protoplasma       Date:  2010-06-25       Impact factor: 3.356

5.  Initial Characterization of the Two ClpP Paralogs of Chlamydia trachomatis Suggests Unique Functionality for Each.

Authors:  Nicholas A Wood; Krystal Y Chung; Amanda M Blocker; Nathalia Rodrigues de Almeida; Martin Conda-Sheridan; Derek J Fisher; Scot P Ouellette
Journal:  J Bacteriol       Date:  2018-12-20       Impact factor: 3.490

Review 6.  Interaction of chlamydiae and host cells in vitro.

Authors:  J W Moulder
Journal:  Microbiol Rev       Date:  1991-03

7.  Interaction of outer envelope proteins of Chlamydia psittaci GPIC with the HeLa cell surface.

Authors:  L M Ting; R C Hsia; C G Haidaris; P M Bavoil
Journal:  Infect Immun       Date:  1995-09       Impact factor: 3.441

8.  Fusion of inclusions following superinfection of HeLa cells by two serovars of Chlamydia trachomatis.

Authors:  J C Ridderhof; R C Barnes
Journal:  Infect Immun       Date:  1989-10       Impact factor: 3.441

9.  Sulfated polyanions block Chlamydia trachomatis infection of cervix-derived human epithelia.

Authors:  F R Zaretzky; R Pearce-Pratt; D M Phillips
Journal:  Infect Immun       Date:  1995-09       Impact factor: 3.441

10.  Cytoskeletal requirements in Chlamydia trachomatis infection of host cells.

Authors:  N Schramm; P B Wyrick
Journal:  Infect Immun       Date:  1995-01       Impact factor: 3.441

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