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The Chlamydia trachomatis inclusion membrane protein CT006 associates with lipid droplets in eukaryotic cells
Chlamydia trachomatis causes genital and ocular infections in humans. This bacterial pathogen multiplies exclusively within host cells in a characteristic vacuole (inclusion) and delivers proteins such as inclusion membrane proteins (Incs) into the host cell. Here, we identified CT006 as a novel C....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863265/ https://www.ncbi.nlm.nih.gov/pubmed/35192658 http://dx.doi.org/10.1371/journal.pone.0264292 |
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author | Bugalhão, Joana N. Luís, Maria P. Pereira, Inês S. da Cunha, Maria Pais, Sara V. Mota, Luís Jaime |
author_facet | Bugalhão, Joana N. Luís, Maria P. Pereira, Inês S. da Cunha, Maria Pais, Sara V. Mota, Luís Jaime |
author_sort | Bugalhão, Joana N. |
collection | PubMed |
description | Chlamydia trachomatis causes genital and ocular infections in humans. This bacterial pathogen multiplies exclusively within host cells in a characteristic vacuole (inclusion) and delivers proteins such as inclusion membrane proteins (Incs) into the host cell. Here, we identified CT006 as a novel C. trachomatis protein that when expressed ectopically eukaryotic cells can associate with lipid droplets (LDs). A screen using Saccharomyces cerevisiae identified two Incs causing vacuolar protein sorting defects and seven Incs showing tropism for eukaryotic organelles. Ectopic expression in yeast and mammalian cells of genes encoding different fragments of CT006 revealed tropism for the endoplasmic reticulum and LDs. We identified a LD-targeting region within the first 88 amino acid residues of CT006, and positively charged residues important for this targeting. Comparing with the parental wild-type strain, cells infected by a newly generated C. trachomatis strain overproducing CT006 with a double hemagglutinin tag showed a slight increase in the area occupied by LDs within the inclusion region. However, we could not correlate this effect with the LD-targeting regions within CT006. We further showed that both the amino and carboxy-terminal regions of CT006, flanking the Inc-characteristic bilobed hydrophobic domain, are exposed to the host cell cytosol during C. trachomatis infection, supporting their availability to interact with host cell targets. Altogether, our data suggest that CT006 might participate in the interaction of LDs with C. trachomatis inclusions. |
format | Online Article Text |
id | pubmed-8863265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-88632652022-02-23 The Chlamydia trachomatis inclusion membrane protein CT006 associates with lipid droplets in eukaryotic cells Bugalhão, Joana N. Luís, Maria P. Pereira, Inês S. da Cunha, Maria Pais, Sara V. Mota, Luís Jaime PLoS One Research Article Chlamydia trachomatis causes genital and ocular infections in humans. This bacterial pathogen multiplies exclusively within host cells in a characteristic vacuole (inclusion) and delivers proteins such as inclusion membrane proteins (Incs) into the host cell. Here, we identified CT006 as a novel C. trachomatis protein that when expressed ectopically eukaryotic cells can associate with lipid droplets (LDs). A screen using Saccharomyces cerevisiae identified two Incs causing vacuolar protein sorting defects and seven Incs showing tropism for eukaryotic organelles. Ectopic expression in yeast and mammalian cells of genes encoding different fragments of CT006 revealed tropism for the endoplasmic reticulum and LDs. We identified a LD-targeting region within the first 88 amino acid residues of CT006, and positively charged residues important for this targeting. Comparing with the parental wild-type strain, cells infected by a newly generated C. trachomatis strain overproducing CT006 with a double hemagglutinin tag showed a slight increase in the area occupied by LDs within the inclusion region. However, we could not correlate this effect with the LD-targeting regions within CT006. We further showed that both the amino and carboxy-terminal regions of CT006, flanking the Inc-characteristic bilobed hydrophobic domain, are exposed to the host cell cytosol during C. trachomatis infection, supporting their availability to interact with host cell targets. Altogether, our data suggest that CT006 might participate in the interaction of LDs with C. trachomatis inclusions. Public Library of Science 2022-02-22 /pmc/articles/PMC8863265/ /pubmed/35192658 http://dx.doi.org/10.1371/journal.pone.0264292 Text en © 2022 Bugalhão et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Bugalhão, Joana N. Luís, Maria P. Pereira, Inês S. da Cunha, Maria Pais, Sara V. Mota, Luís Jaime The Chlamydia trachomatis inclusion membrane protein CT006 associates with lipid droplets in eukaryotic cells |
title | The Chlamydia trachomatis inclusion membrane protein CT006 associates with lipid droplets in eukaryotic cells |
title_full | The Chlamydia trachomatis inclusion membrane protein CT006 associates with lipid droplets in eukaryotic cells |
title_fullStr | The Chlamydia trachomatis inclusion membrane protein CT006 associates with lipid droplets in eukaryotic cells |
title_full_unstemmed | The Chlamydia trachomatis inclusion membrane protein CT006 associates with lipid droplets in eukaryotic cells |
title_short | The Chlamydia trachomatis inclusion membrane protein CT006 associates with lipid droplets in eukaryotic cells |
title_sort | chlamydia trachomatis inclusion membrane protein ct006 associates with lipid droplets in eukaryotic cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863265/ https://www.ncbi.nlm.nih.gov/pubmed/35192658 http://dx.doi.org/10.1371/journal.pone.0264292 |
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