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Replication-dependent size reduction precedes differentiation in Chlamydia trachomatis

Chlamydia trachomatis is the most common cause of bacterial sexually transmitted infection. It produces an unusual intracellular infection in which a vegetative form, called the reticulate body (RB), replicates and then converts into an elementary body (EB), which is the infectious form. Here we use...

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Autores principales: Lee, Jennifer K., Enciso, Germán A., Boassa, Daniela, Chander, Christopher N., Lou, Tracy H., Pairawan, Sean S., Guo, Melody C., Wan, Frederic Y. M., Ellisman, Mark H., Sütterlin, Christine, Tan, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752669/
https://www.ncbi.nlm.nih.gov/pubmed/29298975
http://dx.doi.org/10.1038/s41467-017-02432-0
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author Lee, Jennifer K.
Enciso, Germán A.
Boassa, Daniela
Chander, Christopher N.
Lou, Tracy H.
Pairawan, Sean S.
Guo, Melody C.
Wan, Frederic Y. M.
Ellisman, Mark H.
Sütterlin, Christine
Tan, Ming
author_facet Lee, Jennifer K.
Enciso, Germán A.
Boassa, Daniela
Chander, Christopher N.
Lou, Tracy H.
Pairawan, Sean S.
Guo, Melody C.
Wan, Frederic Y. M.
Ellisman, Mark H.
Sütterlin, Christine
Tan, Ming
author_sort Lee, Jennifer K.
collection PubMed
description Chlamydia trachomatis is the most common cause of bacterial sexually transmitted infection. It produces an unusual intracellular infection in which a vegetative form, called the reticulate body (RB), replicates and then converts into an elementary body (EB), which is the infectious form. Here we use quantitative three-dimensional electron microscopy (3D EM) to show that C. trachomatis RBs divide by binary fission and undergo a sixfold reduction in size as the population expands. Conversion only occurs after at least six rounds of replication, and correlates with smaller RB size. These results suggest that RBs only convert into EBs below a size threshold, reached by repeatedly dividing before doubling in size. A stochastic mathematical model shows how replication-dependent RB size reduction produces delayed and asynchronous conversion, which are hallmarks of the Chlamydia developmental cycle. Our findings support a model in which RB size controls the timing of RB-to-EB conversion without the need for an external signal.
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spelling pubmed-57526692018-01-13 Replication-dependent size reduction precedes differentiation in Chlamydia trachomatis Lee, Jennifer K. Enciso, Germán A. Boassa, Daniela Chander, Christopher N. Lou, Tracy H. Pairawan, Sean S. Guo, Melody C. Wan, Frederic Y. M. Ellisman, Mark H. Sütterlin, Christine Tan, Ming Nat Commun Article Chlamydia trachomatis is the most common cause of bacterial sexually transmitted infection. It produces an unusual intracellular infection in which a vegetative form, called the reticulate body (RB), replicates and then converts into an elementary body (EB), which is the infectious form. Here we use quantitative three-dimensional electron microscopy (3D EM) to show that C. trachomatis RBs divide by binary fission and undergo a sixfold reduction in size as the population expands. Conversion only occurs after at least six rounds of replication, and correlates with smaller RB size. These results suggest that RBs only convert into EBs below a size threshold, reached by repeatedly dividing before doubling in size. A stochastic mathematical model shows how replication-dependent RB size reduction produces delayed and asynchronous conversion, which are hallmarks of the Chlamydia developmental cycle. Our findings support a model in which RB size controls the timing of RB-to-EB conversion without the need for an external signal. Nature Publishing Group UK 2018-01-03 /pmc/articles/PMC5752669/ /pubmed/29298975 http://dx.doi.org/10.1038/s41467-017-02432-0 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lee, Jennifer K.
Enciso, Germán A.
Boassa, Daniela
Chander, Christopher N.
Lou, Tracy H.
Pairawan, Sean S.
Guo, Melody C.
Wan, Frederic Y. M.
Ellisman, Mark H.
Sütterlin, Christine
Tan, Ming
Replication-dependent size reduction precedes differentiation in Chlamydia trachomatis
title Replication-dependent size reduction precedes differentiation in Chlamydia trachomatis
title_full Replication-dependent size reduction precedes differentiation in Chlamydia trachomatis
title_fullStr Replication-dependent size reduction precedes differentiation in Chlamydia trachomatis
title_full_unstemmed Replication-dependent size reduction precedes differentiation in Chlamydia trachomatis
title_short Replication-dependent size reduction precedes differentiation in Chlamydia trachomatis
title_sort replication-dependent size reduction precedes differentiation in chlamydia trachomatis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752669/
https://www.ncbi.nlm.nih.gov/pubmed/29298975
http://dx.doi.org/10.1038/s41467-017-02432-0
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