Literature DB >> 15972482

Development of secondary inclusions in cells infected by Chlamydia trachomatis.

Robert J Suchland1, Daniel D Rockey, Sara K Weeks, Damir T Alzhanov, Walter E Stamm.   

Abstract

The chlamydiae are obligate intracellular bacteria that occupy a non-acidified vacuole (the inclusion) during their entire developmental cycle. These bacteria produce a set of proteins (Inc proteins) that localize to the surface of the inclusion within infected cells. Chlamydia trachomatis IncA is also commonly found in long fibers that extend away from the inclusion. We used standard and confocal immunofluorescence microscopy to demonstrate that these fibers extend to newly developed inclusions, termed secondary inclusions, within infected cells. Secondary inclusions observed at early time points postinfection were devoid of chlamydial reticulate bodies. Later in the developmental cycle, secondary inclusions containing variable numbers of reticulate bodies were common. Reticulate bodies were also observed within the IncA-laden fibers connecting primary and secondary inclusions. Quantitative differences in secondary inclusion formation were found among clinical isolates, and these differences were associated with serovar. Isolates of serovar G consistently produced secondary inclusions at the highest frequency (P < 0.0001). Similar quantitative studies demonstrated that secondary inclusion formation was associated with segregation of inclusions to daughter cells following cytokinesis. We conclude that the production of secondary inclusions via IncA-laden fibers allows chlamydiae to generate an expanded intracellular niche in which they can grow and may provide a means for continuous infection within progeny cells following cell division.

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Year:  2005        PMID: 15972482      PMCID: PMC1168544          DOI: 10.1128/IAI.73.7.3954-3962.2005

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


  28 in total

Review 1.  Proteins in the chlamydial inclusion membrane.

Authors:  Daniel D Rockey; Marci A Scidmore; John P Bannantine; Wendy J Brown
Journal:  Microbes Infect       Date:  2002-03       Impact factor: 2.700

2.  Determination of the physical environment within the Chlamydia trachomatis inclusion using ion-selective ratiometric probes.

Authors:  Scott Grieshaber; Joel A Swanson; Ted Hackstadt
Journal:  Cell Microbiol       Date:  2002-05       Impact factor: 3.715

3.  Chlamydial antigens colocalize within IncA-laden fibers extending from the inclusion membrane into the host cytosol.

Authors:  W J Brown; Y A W Skeiky; P Probst; D D Rockey
Journal:  Infect Immun       Date:  2002-10       Impact factor: 3.441

4.  Longitudinal assessment of infecting serovars of Chlamydia trachomatis in Seattle public health clinics: 1988-1996.

Authors:  Robert J Suchland; Linda O Eckert; Stephen E Hawes; Walter E Stamm
Journal:  Sex Transm Dis       Date:  2003-04       Impact factor: 2.830

5.  Epidemiology of anorectal chlamydial and gonococcal infections among men having sex with men in Seattle: utilizing serovar and auxotype strain typing.

Authors:  William M Geisler; William L H Whittington; Robert J Suchland; Walter E Stamm
Journal:  Sex Transm Dis       Date:  2002-04       Impact factor: 2.830

6.  The Chlamydia trachomatis IncA protein is required for homotypic vesicle fusion.

Authors:  T Hackstadt; M A Scidmore-Carlson; E I Shaw; E R Fischer
Journal:  Cell Microbiol       Date:  1999-09       Impact factor: 3.715

7.  A secondary structure motif predictive of protein localization to the chlamydial inclusion membrane.

Authors:  J P Bannantine; R S Griffiths; W Viratyosin; W J Brown; D D Rockey
Journal:  Cell Microbiol       Date:  2000-02       Impact factor: 3.715

8.  Global stage-specific gene regulation during the developmental cycle of Chlamydia trachomatis.

Authors:  Tracy L Nicholson; Lynn Olinger; Kimberley Chong; Gary Schoolnik; Richard S Stephens
Journal:  J Bacteriol       Date:  2003-05       Impact factor: 3.490

9.  Inhibition of host cell cytokinesis by Chlamydia trachomatis infection.

Authors:  Whitney Greene; Guangming Zhong
Journal:  J Infect       Date:  2003-07       Impact factor: 6.072

10.  Genomic transcriptional profiling of the developmental cycle of Chlamydia trachomatis.

Authors:  Robert J Belland; Guangming Zhong; Deborah D Crane; Daniel Hogan; Daniel Sturdevant; Jyotika Sharma; Wandy L Beatty; Harlan D Caldwell
Journal:  Proc Natl Acad Sci U S A       Date:  2003-06-18       Impact factor: 12.779

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  15 in total

1.  The broad-spectrum antiviral compound ST-669 restricts chlamydial inclusion development and bacterial growth and localizes to host cell lipid droplets within treated cells.

Authors:  Kelsi M Sandoz; William G Valiant; Steven G Eriksen; Dennis E Hruby; Robert D Allen; Daniel D Rockey
Journal:  Antimicrob Agents Chemother       Date:  2014-04-28       Impact factor: 5.191

Review 2.  Emancipating Chlamydia: Advances in the Genetic Manipulation of a Recalcitrant Intracellular Pathogen.

Authors:  Robert J Bastidas; Raphael H Valdivia
Journal:  Microbiol Mol Biol Rev       Date:  2016-03-30       Impact factor: 11.056

3.  Distinct intensity of host-pathogen interactions in Chlamydia psittaci- and Chlamydia abortus-infected chicken embryos.

Authors:  Maria Braukmann; Konrad Sachse; Ilse D Jacobsen; Martin Westermann; Christian Menge; Hans-Peter Saluz; Angela Berndt
Journal:  Infect Immun       Date:  2012-06-11       Impact factor: 3.441

Review 4.  Host Organelle Hijackers: a similar modus operandi for Toxoplasma gondii and Chlamydia trachomatis: co-infection model as a tool to investigate pathogenesis.

Authors:  Julia D Romano; Isabelle Coppens
Journal:  Pathog Dis       Date:  2013-07-22       Impact factor: 3.166

5.  In contrast to Chlamydia trachomatis, Waddlia chondrophila grows in human cells without inhibiting apoptosis, fragmenting the Golgi apparatus, or diverting post-Golgi sphingomyelin transport.

Authors:  Stephanie Dille; Eva-Maria Kleinschnitz; Collins Waguia Kontchou; Thilo Nölke; Georg Häcker
Journal:  Infect Immun       Date:  2015-06-08       Impact factor: 3.441

6.  Global Mapping of the Inc-Human Interactome Reveals that Retromer Restricts Chlamydia Infection.

Authors:  Kathleen M Mirrashidi; Cherilyn A Elwell; Erik Verschueren; Jeffrey R Johnson; Andrew Frando; John Von Dollen; Oren Rosenberg; Natali Gulbahce; Gwendolyn Jang; Tasha Johnson; Stefanie Jäger; Anusha M Gopalakrishnan; Jessica Sherry; Joe Dan Dunn; Andrew Olive; Bennett Penn; Michael Shales; Jeffery S Cox; Michael N Starnbach; Isabelle Derre; Raphael Valdivia; Nevan J Krogan; Joanne Engel
Journal:  Cell Host Microbe       Date:  2015-06-25       Impact factor: 21.023

7.  Genome sequencing of recent clinical Chlamydia trachomatis strains identifies loci associated with tissue tropism and regions of apparent recombination.

Authors:  Brendan M Jeffrey; Robert J Suchland; Kelsey L Quinn; John R Davidson; Walter E Stamm; Daniel D Rockey
Journal:  Infect Immun       Date:  2010-03-22       Impact factor: 3.441

8.  Fierce competition between Toxoplasma and Chlamydia for host cell structures in dually infected cells.

Authors:  Julia D Romano; Catherine de Beaumont; Jose A Carrasco; Karen Ehrenman; Patrik M Bavoil; Isabelle Coppens
Journal:  Eukaryot Cell       Date:  2012-12-14

9.  Salmonella-containing vacuoles display centrifugal movement associated with cell-to-cell transfer in epithelial cells.

Authors:  Jason Szeto; Anton Namolovan; Suzanne E Osborne; Brian K Coombes; John H Brumell
Journal:  Infect Immun       Date:  2008-12-22       Impact factor: 3.441

10.  Population genomics of Chlamydia trachomatis: insights on drift, selection, recombination, and population structure.

Authors:  Sandeep J Joseph; Xavier Didelot; James Rothschild; Henry J C de Vries; Servaas A Morré; Timothy D Read; Deborah Dean
Journal:  Mol Biol Evol       Date:  2012-08-13       Impact factor: 16.240

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