Temperature and host cell-dependent changes in virulence of Chlamydia pneumoniae CWL029 in an optimized mouse

Katrin Janik1, Jenny Bode1, Pavel Dutow1

  • 1Institute of Medical Microbiology and Hospital Epidemiology, Hannover Medical School (MHH), Carl-Neuberg-Str. 1, D-30625 Hannover, Germany.

Pathogens and Disease
|April 9, 2015
PubMed

Insights

Culturing Chlamydia pneumoniae at 37°C, closer to host body temperature, enhances its lung colonization and virulence in mice. This temperature-dependent virulence shift, observed in specific cell lines, offers insights into chlamydial pathogenicity.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Pathogenesis

Background:

  • Chlamydia pneumoniae (Cpn) is an obligate intracellular bacterium causing respiratory infections and linked to vascular diseases.
  • Understanding factors influencing Cpn virulence is crucial for disease management and research.

Purpose of the Study:

  • To investigate how temperature and host cell type during propagation affect Cpn virulence.
  • To establish an optimized mouse model for studying Cpn lung infections.

Main Methods:

  • Cpn CWL0129 cultured at 35°C or 37°C in BHK-21 or HeLa cells.
  • Infection of mice with differentially propagated Cpn.
  • Assessment of clinical scores, body weight, lung inflammation, and cytokine induction.
  • Transcriptome analysis of Cpn.

Main Results:

  • Cpn cultured at 37°C in BHK-21 cells showed faster lung colonization, stronger symptoms, and increased cytokine induction compared to Cpn cultured at 35°C.
  • Temperature-triggered virulence alteration was not observed in HeLa cells.
  • Observed virulence changes were independent of host cell protein synthesis and not explained by Cpn gene expression alterations.

Conclusions:

  • Pre-culturing Cpn at a temperature mimicking host body temperature (37°C) can enhance its virulence.
  • These findings suggest a novel, non-transcriptional regulatory mechanism for Cpn virulence.
  • The study provides a basis for further unraveling Cpn pathogenicity and optimizing infection models.

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