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Attachment and Entry of Chlamydia Have Distinct Requirements for Host Protein Disulfide Isomerase
by
Stephens, Richard S.
, Abromaitis, Stephanie
in
Animals
/ Anti-Bacterial Agents - pharmacology
/ Bacitracin - pharmacology
/ Bacteria
/ Bacterial Adhesion - drug effects
/ Bacterial Adhesion - physiology
/ Bacterial infections
/ Chlamydia
/ Chlamydia - pathogenicity
/ Chlamydia - physiology
/ Chlamydia infections
/ Chlamydia Infections - microbiology
/ CHO Cells
/ Cricetinae
/ Cricetulus
/ Development and progression
/ Experiments
/ HeLa Cells
/ Host-bacteria relationships
/ Humans
/ Infectious Diseases/Bacterial Infections
/ Insulin
/ Isomerases
/ Microbiology
/ Microbiology/Microbial Growth and Development
/ Microscopy, Fluorescence
/ Pathogenesis
/ Physiological aspects
/ Properties
/ Protein Disulfide-Isomerases - genetics
/ Protein Disulfide-Isomerases - metabolism
/ Proteins
/ RNA Interference
/ Sexually transmitted diseases
/ STD
2009
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Attachment and Entry of Chlamydia Have Distinct Requirements for Host Protein Disulfide Isomerase
by
Stephens, Richard S.
, Abromaitis, Stephanie
in
Animals
/ Anti-Bacterial Agents - pharmacology
/ Bacitracin - pharmacology
/ Bacteria
/ Bacterial Adhesion - drug effects
/ Bacterial Adhesion - physiology
/ Bacterial infections
/ Chlamydia
/ Chlamydia - pathogenicity
/ Chlamydia - physiology
/ Chlamydia infections
/ Chlamydia Infections - microbiology
/ CHO Cells
/ Cricetinae
/ Cricetulus
/ Development and progression
/ Experiments
/ HeLa Cells
/ Host-bacteria relationships
/ Humans
/ Infectious Diseases/Bacterial Infections
/ Insulin
/ Isomerases
/ Microbiology
/ Microbiology/Microbial Growth and Development
/ Microscopy, Fluorescence
/ Pathogenesis
/ Physiological aspects
/ Properties
/ Protein Disulfide-Isomerases - genetics
/ Protein Disulfide-Isomerases - metabolism
/ Proteins
/ RNA Interference
/ Sexually transmitted diseases
/ STD
2009
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Attachment and Entry of Chlamydia Have Distinct Requirements for Host Protein Disulfide Isomerase
by
Stephens, Richard S.
, Abromaitis, Stephanie
in
Animals
/ Anti-Bacterial Agents - pharmacology
/ Bacitracin - pharmacology
/ Bacteria
/ Bacterial Adhesion - drug effects
/ Bacterial Adhesion - physiology
/ Bacterial infections
/ Chlamydia
/ Chlamydia - pathogenicity
/ Chlamydia - physiology
/ Chlamydia infections
/ Chlamydia Infections - microbiology
/ CHO Cells
/ Cricetinae
/ Cricetulus
/ Development and progression
/ Experiments
/ HeLa Cells
/ Host-bacteria relationships
/ Humans
/ Infectious Diseases/Bacterial Infections
/ Insulin
/ Isomerases
/ Microbiology
/ Microbiology/Microbial Growth and Development
/ Microscopy, Fluorescence
/ Pathogenesis
/ Physiological aspects
/ Properties
/ Protein Disulfide-Isomerases - genetics
/ Protein Disulfide-Isomerases - metabolism
/ Proteins
/ RNA Interference
/ Sexually transmitted diseases
/ STD
2009
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Attachment and Entry of Chlamydia Have Distinct Requirements for Host Protein Disulfide Isomerase
Journal Article
Attachment and Entry of Chlamydia Have Distinct Requirements for Host Protein Disulfide Isomerase
2009
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Overview
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.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Anti-Bacterial Agents - pharmacology
/ Bacteria
/ Bacterial Adhesion - drug effects
/ Bacterial Adhesion - physiology
/ Chlamydia Infections - microbiology
/ Humans
/ Infectious Diseases/Bacterial Infections
/ Insulin
/ Microbiology/Microbial Growth and Development
/ Protein Disulfide-Isomerases - genetics
/ Protein Disulfide-Isomerases - metabolism
/ Proteins
/ Sexually transmitted diseases
/ STD
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