ArticleBMC microbiology2008
Spatial constraints within the chlamydial host cell inclusion predict interrupted development and persistence.
Article in BMC microbiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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Who cites it
15 citing papers in PubMed, 4 citations in OpenAlex.
- Statistical analysis supports the size control mechanism of Chlamydia development.PLoS computational biology · 2025Article
- The T3SS structural and effector genes ofFrontiers in cellular and infection microbiology · 2025Article
- Nanoscale imaging of bacterial infections by sphingolipid expansion microscopy.Nature communications · 2020Article
- Single-Inclusion Kinetics ofmSystems · 2020Article
- A Chlamydia effector recruits CEP170 to reprogram host microtubule organization.Journal of cell science · 2015Article
- Mutations in hemG mediate resistance to salicylidene acylhydrazides, demonstrating a novel link between protoporphyrinogen oxidase (HemG) and Chlamydia trachomatis infectivity.Journal of bacteriology · 2013Article
- Development of Chlamydial Type III Secretion System Inhibitors for Suppression of Acute and Chronic Forms of Chlamydial Infection.Acta naturae · 2012Article
- Structural characterization of a novel Chlamydia pneumoniae type III secretion-associated protein, Cpn0803.PloS one · 2012Article
- Chlamydia Pneumoniae CdsL Regulates CdsN ATPase Activity, and Disruption with a Peptide Mimetic Prevents Bacterial Invasion.Frontiers in microbiology · 2011Article
- Exit from dormancy in microbial organisms.Nature reviews. Microbiology · 2010Review
- Interactions between flagellar and type III secretion proteins in Chlamydia pneumoniae.BMC microbiology · 2010Article
- The danger signal adenosine induces persistence of chlamydial infection through stimulation of A2b receptors.PloS one · 2009Article
- Anaplasma phagocytophilum dense-cored organisms mediate cellular adherence through recognition of human P-selectin glycoprotein ligand 1.Infection and immunity · 2009Article
- Kinematics of intracellular chlamydiae provide evidence for contact-dependent development.Journal of bacteriology · 2009Article
- Characterization of the putative type III secretion ATPase CdsN (Cpn0707) of Chlamydophila pneumoniae.Journal of bacteriology · 2008Article
Corrections and comments
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Authors and funding
4 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThe chlamydial developmental cycle involves the alternation between the metabolically inert elementary body (EB) and the replicating reticulate body (RB). The triggers that mediate the interchange between these particle types are unknown and yet this is crucial for understanding basic Chlamydia biology. PRESENTATION OF THE HYPOTHESIS: We have proposed a hypothesis to explain key chlamydial developmental events whereby RBs are replicating strictly whilst in contact with the host cell membrane-derived inclusion via type three secretion (T3S) injectisomes. As the inclusion expands, the contact between each RB and the inclusion membrane decreases, eventually reaching a threshold, beyond which T3S is inactivated upon detachment and this is the signal for RB-to-EB differentiation. TESTING THE HYPOTHESIS: We explore this hypothesis through the development of a detailed mathematical model. The model uses knowledge and data of the biological system wherever available and simulates the chlamydial developmental cycle under the assumptions of the hypothesis in order to predict various outcomes and implications under a number of scenarios. IMPLICATIONS OF THE HYPOTHESIS: We show that the concept of in vitro persistent infection is not only consistent with the hypothesis but in fact an implication of it. We show that increasing the RB radius, and/or the maximum length of T3S needles mediating contact between RBs and the inclusion membrane, and/or the number of inclusions per infected cell, will contribute to the development of persistent infection. The RB radius is the most important determinant of whether persistent infection would ensue, and subsequently, the magnitude of the EB yield. We determine relationships between the length of the T3S needle and the RB radius within an inclusion, and between the RB radius and the number of inclusions per host cell to predict whether persistent infection or normal development would occur within a host cell. These results are all testable experimentally and could lead to significantly greater understanding of one of the most crucial steps in chlamydial development.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.