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Identification of Chlamydia trachomatis CT621, a protein delivered through the type III secretion system to the host cell cytoplasm and nucleus

Chlamydiae are obligate intracellular bacteria, developing inside host cells within chlamydial inclusions. From these inclusions, the chlamydiae secrete proteins into the host cell cytoplasm. A pathway through which secreted proteins can be delivered is the type III secretion system (T3SS). The T3SS...

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Autores principales: Hobolt-Pedersen, Anne-Sofie, Christiansen, Gunna, Timmerman, Evy, Gevaert, Kris, Birkelund, Svend
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2784215/
https://www.ncbi.nlm.nih.gov/pubmed/19682078
http://dx.doi.org/10.1111/j.1574-695X.2009.00581.x
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author Hobolt-Pedersen, Anne-Sofie
Christiansen, Gunna
Timmerman, Evy
Gevaert, Kris
Birkelund, Svend
author_facet Hobolt-Pedersen, Anne-Sofie
Christiansen, Gunna
Timmerman, Evy
Gevaert, Kris
Birkelund, Svend
author_sort Hobolt-Pedersen, Anne-Sofie
collection PubMed
description Chlamydiae are obligate intracellular bacteria, developing inside host cells within chlamydial inclusions. From these inclusions, the chlamydiae secrete proteins into the host cell cytoplasm. A pathway through which secreted proteins can be delivered is the type III secretion system (T3SS). The T3SS is common to several gram-negative bacteria and the secreted proteins serve a variety of functions often related to the modulation of host signalling. To identify new potentially secreted proteins, the cytoplasm was extracted from Chlamydia trachomatis L2-infected HeLa cells, and two-dimensional polyacrylamide gel electrophoresis profiles of [(35)S]-labelled chlamydial proteins from this extract were compared with profiles of chlamydial proteins from the lysate of infected cells. In this way, CT621 was identified. CT621 is a member of a family of proteins containing a domain of unknown function DUF582 that is only found within the genus Chlamydia. Immunofluorescence microscopy and immunoblotting demonstrated that CT621 is secreted late in the chlamydial developmental cycle and that it is the first chlamydial protein found to be localized within both the host cell cytoplasm and the nucleus. To determine whether CT621 is secreted through the T3SS, an inhibitor of this apparatus was added to the infection medium, resulting in retention of the protein inside the chlamydiae. Hence, the so far uncharacterized CT621 is a new type III secretion effector protein.
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spelling pubmed-27842152009-11-28 Identification of Chlamydia trachomatis CT621, a protein delivered through the type III secretion system to the host cell cytoplasm and nucleus Hobolt-Pedersen, Anne-Sofie Christiansen, Gunna Timmerman, Evy Gevaert, Kris Birkelund, Svend FEMS Immunol Med Microbiol Research Articles Chlamydiae are obligate intracellular bacteria, developing inside host cells within chlamydial inclusions. From these inclusions, the chlamydiae secrete proteins into the host cell cytoplasm. A pathway through which secreted proteins can be delivered is the type III secretion system (T3SS). The T3SS is common to several gram-negative bacteria and the secreted proteins serve a variety of functions often related to the modulation of host signalling. To identify new potentially secreted proteins, the cytoplasm was extracted from Chlamydia trachomatis L2-infected HeLa cells, and two-dimensional polyacrylamide gel electrophoresis profiles of [(35)S]-labelled chlamydial proteins from this extract were compared with profiles of chlamydial proteins from the lysate of infected cells. In this way, CT621 was identified. CT621 is a member of a family of proteins containing a domain of unknown function DUF582 that is only found within the genus Chlamydia. Immunofluorescence microscopy and immunoblotting demonstrated that CT621 is secreted late in the chlamydial developmental cycle and that it is the first chlamydial protein found to be localized within both the host cell cytoplasm and the nucleus. To determine whether CT621 is secreted through the T3SS, an inhibitor of this apparatus was added to the infection medium, resulting in retention of the protein inside the chlamydiae. Hence, the so far uncharacterized CT621 is a new type III secretion effector protein. Blackwell Publishing Ltd 2009-10 2009-08-14 /pmc/articles/PMC2784215/ /pubmed/19682078 http://dx.doi.org/10.1111/j.1574-695X.2009.00581.x Text en © 2009 The Authors. Journal compilation © 2009 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Research Articles
Hobolt-Pedersen, Anne-Sofie
Christiansen, Gunna
Timmerman, Evy
Gevaert, Kris
Birkelund, Svend
Identification of Chlamydia trachomatis CT621, a protein delivered through the type III secretion system to the host cell cytoplasm and nucleus
title Identification of Chlamydia trachomatis CT621, a protein delivered through the type III secretion system to the host cell cytoplasm and nucleus
title_full Identification of Chlamydia trachomatis CT621, a protein delivered through the type III secretion system to the host cell cytoplasm and nucleus
title_fullStr Identification of Chlamydia trachomatis CT621, a protein delivered through the type III secretion system to the host cell cytoplasm and nucleus
title_full_unstemmed Identification of Chlamydia trachomatis CT621, a protein delivered through the type III secretion system to the host cell cytoplasm and nucleus
title_short Identification of Chlamydia trachomatis CT621, a protein delivered through the type III secretion system to the host cell cytoplasm and nucleus
title_sort identification of chlamydia trachomatis ct621, a protein delivered through the type iii secretion system to the host cell cytoplasm and nucleus
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2784215/
https://www.ncbi.nlm.nih.gov/pubmed/19682078
http://dx.doi.org/10.1111/j.1574-695X.2009.00581.x
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