Attachment and entry of Chlamydia have distinct requirements for host protein disulfide isomerase.

Chlamydia is an obligate intracellular pathogen that causes a wide range of diseases in humans. Attachment and entry are key processes in infectivity and subsequent pathogenesis of Chlamydia, yet the mechanisms governing these interactions are unknown. It was recently shown that a cell line, CHO6, t...

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Main Authors: Stephanie Abromaitis, Richard S Stephens
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-04-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC2655716?pdf=render
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spelling doaj-559b60972ece4fedbefaffe777c752462020-11-25T01:30:56ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742009-04-0154e100035710.1371/journal.ppat.1000357Attachment and entry of Chlamydia have distinct requirements for host protein disulfide isomerase.Stephanie AbromaitisRichard S StephensChlamydia is an obligate intracellular pathogen that causes a wide range of diseases in humans. Attachment and entry are key processes in infectivity and subsequent pathogenesis of Chlamydia, yet the mechanisms governing these interactions are unknown. It was recently shown that a cell line, CHO6, that is resistant to attachment, and thus infectivity, of multiple Chlamydia species has a defect in protein disulfide isomerase (PDI) N-terminal signal sequence processing. Ectopic expression of PDI in CHO6 cells led to restoration of Chlamydia attachment and infectivity; however, the mechanism leading to this recovery was not ascertained. To advance our understanding of the role of PDI in Chlamydia infection, we used RNA interference to establish that cellular PDI is essential for bacterial attachment to cells, making PDI the only host protein identified as necessary for attachment of multiple species of Chlamydia. Genetic complementation and PDI-specific inhibitors were used to determine that cell surface PDI enzymatic activity is required for bacterial entry into cells, but enzymatic function was not required for bacterial attachment. We further determined that it is a PDI-mediated reduction at the cell surface that triggers bacterial uptake. While PDI is necessary for Chlamydia attachment to cells, the bacteria do not appear to utilize plasma membrane-associated PDI as a receptor, suggesting that Chlamydia binds a cell surface protein that requires structural association with PDI. Our findings demonstrate that PDI has two essential and independent roles in the process of chlamydial infectivity: it is structurally required for chlamydial attachment, and the thiol-mediated oxido-reductive function of PDI is necessary for entry.http://europepmc.org/articles/PMC2655716?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Stephanie Abromaitis
Richard S Stephens
spellingShingle Stephanie Abromaitis
Richard S Stephens
Attachment and entry of Chlamydia have distinct requirements for host protein disulfide isomerase.
PLoS Pathogens
author_facet Stephanie Abromaitis
Richard S Stephens
author_sort Stephanie Abromaitis
title Attachment and entry of Chlamydia have distinct requirements for host protein disulfide isomerase.
title_short Attachment and entry of Chlamydia have distinct requirements for host protein disulfide isomerase.
title_full Attachment and entry of Chlamydia have distinct requirements for host protein disulfide isomerase.
title_fullStr Attachment and entry of Chlamydia have distinct requirements for host protein disulfide isomerase.
title_full_unstemmed Attachment and entry of Chlamydia have distinct requirements for host protein disulfide isomerase.
title_sort attachment and entry of chlamydia have distinct requirements for host protein disulfide isomerase.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2009-04-01
description Chlamydia is an obligate intracellular pathogen that causes a wide range of diseases in humans. Attachment and entry are key processes in infectivity and subsequent pathogenesis of Chlamydia, yet the mechanisms governing these interactions are unknown. It was recently shown that a cell line, CHO6, that is resistant to attachment, and thus infectivity, of multiple Chlamydia species has a defect in protein disulfide isomerase (PDI) N-terminal signal sequence processing. Ectopic expression of PDI in CHO6 cells led to restoration of Chlamydia attachment and infectivity; however, the mechanism leading to this recovery was not ascertained. To advance our understanding of the role of PDI in Chlamydia infection, we used RNA interference to establish that cellular PDI is essential for bacterial attachment to cells, making PDI the only host protein identified as necessary for attachment of multiple species of Chlamydia. Genetic complementation and PDI-specific inhibitors were used to determine that cell surface PDI enzymatic activity is required for bacterial entry into cells, but enzymatic function was not required for bacterial attachment. We further determined that it is a PDI-mediated reduction at the cell surface that triggers bacterial uptake. While PDI is necessary for Chlamydia attachment to cells, the bacteria do not appear to utilize plasma membrane-associated PDI as a receptor, suggesting that Chlamydia binds a cell surface protein that requires structural association with PDI. Our findings demonstrate that PDI has two essential and independent roles in the process of chlamydial infectivity: it is structurally required for chlamydial attachment, and the thiol-mediated oxido-reductive function of PDI is necessary for entry.
url http://europepmc.org/articles/PMC2655716?pdf=render
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