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In vitro characterisation of koala Chlamydia pneumoniae: Morphology, inclusion development and doubling time

Candice M. Mitchell a, Sarah A. Mathews a, Christina Theodoropoulos b, Peter Timms a,*

a Institute of Health and Biomedical Innovation, School of Life Sciences, Queensland University of Technology, Corner of Musk Avenue and Blamey St., Kelvin Grove, Queensland 4059, Australia

b Analytical Electron Microscopy Facility, Queensland University of Technology, Brisbane, Queensland 4001, Australia

ABSTRACT

Chlamydia pneumoniae is a common human and animal pathogen associated with upper and lower respiratory tract infections. Of the animal C. pneumoniae isolates, the koala nasal isolate (LPCoLN) is by far the best genetically characterised. This current study was designed to characterise the morphology and developmental events for the LPCoLN isolate, and our results showed several striking in vitro growth differences when compared to the human isolate, AR39. The LPCoLN inclusion size and morphology was distinct from AR39, and a much faster doubling time (3.4–4.9 h versus 5.9–8.7 h doubling time) was observed when grown in HEp-2 cell monolayers. Confocal and electron microscopy of LPCoLN confirmed large (9–30 mm in diameter) inclusions, that were heterogeneously shaped, compared to the small (5–9 mm in diameter), uniformly shaped inclusions of AR39. The morphology of the LPCoLN elementary body was round, and had a narrow or nonexistent periplasmic space, compared to the ‘pear-shaped’ morphology of AR39 EBs. While both isolates showed evidence of inclusion fusion, the level of fusion was much higher for LPCoLN (100%) compared to AR39 (30–40%). Our findings have provided new insights and identified key differences in the in vitro doubling time, size and morphology of an animal C.

  • All
  • 2013
  • Biogeography
  • Biology
  • Chlamydia
  • Diet
  • Disease
  • Ecology
  • Ellis
  • Eucalyptus
  • Genetics
  • Habitat
  • Infection
  • Interventions
  • Koala
  • Lunney
  • Threats
  • Timms
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