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Forward Genetic Approaches in Chlamydia trachomatis
Published on: October 23, 2013
Selective cyclooxygenase inhibitors prevent the growth of Chlamydia pneumoniae in HL cells
Ying Yan1, Sylvi Silvennoinen-Kassinen, Liisa Törmäkangas
1Department of Medical Microbiology, University of Oulu, Aapistie 5A, Oulu, Finland. ying.yan@oulu.fi
Abstract:
The effects of the selective cyclooxygenase (COX) inhibitors SC-560 and PTPBS were studied in Chlamydia pneumoniae-infected HL cell cultures. Chlamydia pneumoniae growth and viability were assessed by quantifying inclusions and re-passages. COX-1 and COX-2 mRNA expression in HL cells during chlamydial infection was quantified with real-time polymerase chain reaction. SC-560 (10 microg/mL) and PTPBS (18 microg/mL) completely inhibited the growth of C. pneumoniae and the effect was dose-dependent between 4-9 microg/mL and 2-16 microg/mL, respectively. Inclusion size was reduced from 11.5+/-1.3 microm to 1.9+/-0.7 microm in the presence of the drugs. Removing the drugs returned the size to normal and increased the number of inclusions. Selective COX inhibitors appear to have a chlamydiostatic but not chlamydiacidic effect; they inhibit the growth of C. pneumoniae in vitro but do not prevent infection or eradicate C. pneumoniae from host cells.
Insights
Selective cyclooxygenase (COX) inhibitors SC-560 and PTPBS demonstrated a dose-dependent inhibition of Chlamydia pneumoniae growth in cell cultures. These compounds exhibit a chlamydiostatic effect, slowing but not eliminating the infection.
Area of Science:
- Microbiology
- Pharmacology
Background:
- Chlamydia pneumoniae is a significant human pathogen.
- Cyclooxygenase (COX) enzymes play roles in inflammatory and infectious processes.
Purpose of the Study:
- To investigate the impact of selective COX inhibitors on Chlamydia pneumoniae growth and viability.
- To assess the effects of SC-560 and PTPBS on C. pneumoniae in HL cell cultures.
Main Methods:
- Quantification of Chlamydia pneumoniae inclusions and re-passages to assess growth and viability.
- Real-time polymerase chain reaction (PCR) to measure COX-1 and COX-2 mRNA expression.
- Treatment of infected HL cell cultures with varying concentrations of SC-560 and PTPBS.
Main Results:
- SC-560 and PTPBS completely inhibited C. pneumoniae growth in a dose-dependent manner.
- Inclusion size was significantly reduced in the presence of the drugs.
- Removal of the inhibitors restored inclusion size and increased their number, indicating a reversible effect.
Conclusions:
- Selective COX inhibitors display a chlamydiostatic, not chlamydiacidic, effect against Chlamydia pneumoniae in vitro.
- These agents inhibit C. pneumoniae growth but do not prevent infection or eradicate the bacteria from host cells.
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