Chlamydophila pneumoniae in human immortal Jurkat cells and primary lymphocytes uncontrolled by interferon-γ

Microbes Infect. 2013 Mar;15(3):192-200. doi: 10.1016/j.micinf.2012.11.006. Epub 2012 Nov 20.

Abstract

Lymphocytes are a potential host cell for Chlamydophila pneumoniae, although why the bacteria must hide in lymphocytes remains unknown. Meanwhile, interferon (IFN)-γ is a crucial factor for eliminating chlamydiae from infected cells through indoleamine 2,3-dioxygenase (IDO) expression, resulting in depletion of tryptophan. We therefore assessed if lymphocytes could work as a shelter for the bacteria to escape IFN-γ. C. pneumoniae grew normally in human lymphoid Jurkat cells, even in the presence of IFN-γ or under stimulation with phorbol myristate acetate plus ionomycin. Although Jurkat cells expressed IFN-γ receptor CD119, their lack of IDO expression was confirmed by RT-PCR and western blotting. Also, C. pneumoniae survived in enriched human peripheral blood lymphocytes, even in the presence of IFN-γ. Furthermore, C. pneumoniae in spleen cells obtained from IFN-γ knockout mice with C57BL/6 background was maintained in a similar way to wild-type mice, supporting a minimal role of IFN-γ-related response for eliminating C. pneumoniae from lymphocytes. Thus, we concluded that IFN-γ did not remove C. pneumoniae from lymphocytes, possibly providing a shelter for C. pneumoniae to escape from the innate immune response, which has direct clinical significance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chlamydophila Infections / immunology
  • Chlamydophila Infections / microbiology
  • Chlamydophila pneumoniae / drug effects
  • Chlamydophila pneumoniae / immunology*
  • Female
  • HeLa Cells
  • Humans
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / metabolism
  • Interferon gamma Receptor
  • Interferon-gamma / immunology*
  • Interferon-gamma / pharmacology
  • Jurkat Cells
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / microbiology*
  • Lymphocytes / metabolism
  • Lymphocytes / microbiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microbial Viability
  • Receptors, Interferon / immunology
  • Spleen / cytology

Substances

  • Indoleamine-Pyrrole 2,3,-Dioxygenase
  • Receptors, Interferon
  • Interferon-gamma