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Chlamydia Uses K(+) Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation
Prokaryotic communities coordinate quorum behaviour in response to external stimuli to control fundamental processes including inter-bacterial communication. The obligate intracellular bacterial pathogen Chlamydia adopts two developmental forms, invasive elementary bodies (EBs) and replicative retic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830353/ https://www.ncbi.nlm.nih.gov/pubmed/33467438 http://dx.doi.org/10.3390/microorganisms9010173 |
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author | Andrew, Susan C. Dumoux, Maud Hayward, Richard D. |
author_facet | Andrew, Susan C. Dumoux, Maud Hayward, Richard D. |
author_sort | Andrew, Susan C. |
collection | PubMed |
description | Prokaryotic communities coordinate quorum behaviour in response to external stimuli to control fundamental processes including inter-bacterial communication. The obligate intracellular bacterial pathogen Chlamydia adopts two developmental forms, invasive elementary bodies (EBs) and replicative reticulate bodies (RBs), which reside within a specialised membrane-bound compartment within the host cell termed an inclusion. The mechanisms by which this bacterial community orchestrates different stages of development from within the inclusion in coordination with the host remain elusive. Both prokaryotic and eukaryotic kingdoms exploit ion-based electrical signalling for fast intercellular communication. Here we demonstrate that RBs specifically accumulate potassium (K(+)) ions, generating a gradient. Disruption of this gradient using ionophores or an ion-channel inhibitor stalls the Chlamydia lifecycle, inducing persistence. Using photobleaching approaches, we establish that the RB is the master regulator of this [K(+)] differential and observe a fast K(+) exchange between RBs revealing a role for this ion in inter-bacterial communication. Finally, we demonstrate spatio-temporal regulation of bacterial membrane potential during RB to EB differentiation within the inclusion. Together, our data reveal that Chlamydia harnesses K(+) to orchestrate host sensing, inter-bacteria communication and pathogen differentiation. |
format | Online Article Text |
id | pubmed-7830353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78303532021-01-26 Chlamydia Uses K(+) Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation Andrew, Susan C. Dumoux, Maud Hayward, Richard D. Microorganisms Article Prokaryotic communities coordinate quorum behaviour in response to external stimuli to control fundamental processes including inter-bacterial communication. The obligate intracellular bacterial pathogen Chlamydia adopts two developmental forms, invasive elementary bodies (EBs) and replicative reticulate bodies (RBs), which reside within a specialised membrane-bound compartment within the host cell termed an inclusion. The mechanisms by which this bacterial community orchestrates different stages of development from within the inclusion in coordination with the host remain elusive. Both prokaryotic and eukaryotic kingdoms exploit ion-based electrical signalling for fast intercellular communication. Here we demonstrate that RBs specifically accumulate potassium (K(+)) ions, generating a gradient. Disruption of this gradient using ionophores or an ion-channel inhibitor stalls the Chlamydia lifecycle, inducing persistence. Using photobleaching approaches, we establish that the RB is the master regulator of this [K(+)] differential and observe a fast K(+) exchange between RBs revealing a role for this ion in inter-bacterial communication. Finally, we demonstrate spatio-temporal regulation of bacterial membrane potential during RB to EB differentiation within the inclusion. Together, our data reveal that Chlamydia harnesses K(+) to orchestrate host sensing, inter-bacteria communication and pathogen differentiation. MDPI 2021-01-15 /pmc/articles/PMC7830353/ /pubmed/33467438 http://dx.doi.org/10.3390/microorganisms9010173 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Andrew, Susan C. Dumoux, Maud Hayward, Richard D. Chlamydia Uses K(+) Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation |
title | Chlamydia Uses K(+) Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation |
title_full | Chlamydia Uses K(+) Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation |
title_fullStr | Chlamydia Uses K(+) Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation |
title_full_unstemmed | Chlamydia Uses K(+) Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation |
title_short | Chlamydia Uses K(+) Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation |
title_sort | chlamydia uses k(+) electrical signalling to orchestrate host sensing, inter-bacterial communication and differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830353/ https://www.ncbi.nlm.nih.gov/pubmed/33467438 http://dx.doi.org/10.3390/microorganisms9010173 |
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