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Forward Genetic Approaches in Chlamydia trachomatis
Published on: October 23, 2013
Metabolic dormancy in Chlamydia trachomatis treated with different antibiotics
Daniel D Rockey1, Xisheng Wang1, Abigail Debrine1
1Department of Biomedical Sciences, Oregon State University, Corvallis, Oregon, USA.
Abstract:
Diseases caused by Chlamydia spp. are often associated with persistent infections. Chlamydial persistence is commonly associated with a unique non-infectious intracellular developmental form, termed an aberrant form. Although infectious chlamydiae can be cultured consistently in cells stressed to aberrancy, their role in persistence is not clear. Recovery from antibiotic stress was explored as a model to determine how survival of non-aberrant chlamydiae, in the presence of fully inhibitory drug concentrations, may participate in persistence. Assays included incubation in quinolones, tetracyclines, or chloramphenicol for differing lengths of time, followed by an extended recovery period in antibiotic-free media. Culturable elementary bodies were not detected during treatment with each antibiotic, but viable and culturable Chlamydia trachomatis emerged after the drug was removed. Time-lapse imaging of live, antibiotic-treated infected cells identified metabolically dormant developmental forms within cells that emerged to form typical productive inclusions. The effects of the increasing concentration of most tested antibiotics led to predictable inhibitory activity, in which the survival rate decreased with increasing drug concentration. In contrast, in fluoroquinolone-treated cells, there was a paradoxical increase in productive development that was directly correlated with drug concentration and inversely associated with aberrant form production. This model system uncovers a unique chlamydial persistence pathway that does not involve the chlamydial aberrant form. The association between productive latency and metabolic dormancy is consistent with models for many bacterial species and may lead to a different interpretation of mechanisms of chlamydial persistence in patients.IMPORTANCEThe life history of most pathogens within the genus Chlamydia relies on lengthy persistence in the host. The most generally accepted model for Chlamydia spp. persistence involves an unusual developmental stage, termed the aberrant form, which arises during conditions that mimic a stressful host environment. In this work, we provide an alternate model for chlamydial persistence in the face of antibiotic stress. This model may be relevant to antibiotic treatment failures in patients infected with C. trachomatis.
Insights
Chlamydia trachomatis can persist by entering a dormant state, not the aberrant form, during antibiotic treatment. This discovery offers a new perspective on persistence and potential treatment failures in patients.
Area of Science:
- Microbiology
- Infectious Diseases
- Bacterial Pathogenesis
Background:
- Chlamydia spp. infections are characterized by prolonged persistence within host cells.
- The established model for chlamydial persistence involves a unique non-infectious 'aberrant form'.
- The role of infectious chlamydiae in persistence, especially under antibiotic stress, remains unclear.
Purpose of the Study:
- To investigate a novel pathway for chlamydial persistence independent of the aberrant form.
- To explore the survival mechanisms of non-aberrant Chlamydia trachomatis during antibiotic exposure.
- To understand how chlamydiae recover from antibiotic stress and resume productive development.
Main Methods:
- Infection of cells with Chlamydia trachomatis followed by exposure to quinolones, tetracyclines, or chloramphenicol.
- Assessment of chlamydial viability and culturability during and after antibiotic treatment.
- Time-lapse imaging of live infected cells to observe developmental changes and metabolic activity.
Main Results:
- Culturable elementary bodies were undetectable during antibiotic treatment but reappeared post-treatment.
- Metabolically dormant forms were observed during antibiotic stress, resuming productive development upon drug removal.
- Fluoroquinolone treatment paradoxically increased productive development with increasing drug concentration, inversely correlating with aberrant form production.
Conclusions:
- A novel chlamydial persistence pathway involving metabolic dormancy and productive latency, distinct from the aberrant form, has been identified.
- This model provides an alternative explanation for chlamydial persistence and may be relevant to antibiotic treatment failures.
- Findings suggest a re-evaluation of chlamydial persistence mechanisms in clinical settings.
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