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Article

Chlamydia Uses K+ Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation

by
Susan C. Andrew
1,2,†,
Maud Dumoux
1,3,*,† and
Richard D. Hayward
1,4,*
1
Institute of Structural and Molecular Biology, University College London & Birkbeck, Malet Street, London WC1E 7HX, UK
2
Mint Diagnostics, Unit 1093b Kent Science Park, Sittingbourne ME9 8GA, UK
3
Rosalind Franklin Institute, Harwell Campus, Didcot OX11 0DE, UK
4
Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK
*
Authors to whom correspondence should be addressed.
Co-first authors.
Microorganisms 2021, 9(1), 173; https://doi.org/10.3390/microorganisms9010173
Submission received: 16 December 2020 / Revised: 8 January 2021 / Accepted: 8 January 2021 / Published: 15 January 2021

Abstract

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.
Keywords: Chlamydia; host-pathogen interactions; cell-to-cell communications and community Chlamydia; host-pathogen interactions; cell-to-cell communications and community

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MDPI and ACS Style

Andrew, S.C.; Dumoux, M.; Hayward, R.D. Chlamydia Uses K+ Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation. Microorganisms 2021, 9, 173. https://doi.org/10.3390/microorganisms9010173

AMA Style

Andrew SC, Dumoux M, Hayward RD. Chlamydia Uses K+ Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation. Microorganisms. 2021; 9(1):173. https://doi.org/10.3390/microorganisms9010173

Chicago/Turabian Style

Andrew, Susan C., Maud Dumoux, and Richard D. Hayward. 2021. "Chlamydia Uses K+ Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation" Microorganisms 9, no. 1: 173. https://doi.org/10.3390/microorganisms9010173

APA Style

Andrew, S. C., Dumoux, M., & Hayward, R. D. (2021). Chlamydia Uses K+ Electrical Signalling to Orchestrate Host Sensing, Inter-Bacterial Communication and Differentiation. Microorganisms, 9(1), 173. https://doi.org/10.3390/microorganisms9010173

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