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Differential growth of Legionella pneumophila in guinea pig versus mouse macrophage cultures

Insights

Guinea pig macrophages normally support Legionella pneumophila growth, unlike mouse macrophages. Lymphokines from stimulated guinea pig lymphocytes can induce macrophages to restrict L. pneumophila, revealing a key mechanism in host resistance.

Area of Science:

  • Immunology
  • Microbiology
  • Cell Biology

Background:

  • Legionella pneumophila (L. pneumophila) is an intracellular bacterium with varying susceptibility across host species.
  • Guinea pigs are generally susceptible to L. pneumophila infections, while mice are considered resistant.
  • The underlying mechanisms for differential host susceptibility remain unclear.

Purpose of the Study:

  • To investigate the differential growth restriction of L. pneumophila in macrophages from guinea pigs and mice.
  • To explore the role of lymphokines and immune serum in modulating macrophage permissiveness to L. pneumophila.

Main Methods:

  • Comparative analysis of L. pneumophila replication in peritoneal macrophages from guinea pigs (strain 2) and mice (BDF1).
  • Assessment of macrophage uptake of L. pneumophila and growth of Listeria monocytogenes as controls.
  • Evaluation of the effect of immune guinea pig serum and supernatants from activated guinea pig splenocytes on L. pneumophila growth in macrophages.

Main Results:

  • L. pneumophila replicated well in guinea pig macrophages but was restricted in mouse macrophages, irrespective of infectivity ratio.
  • Macrophage uptake of L. pneumophila was similar in both species.
  • Preincubation of guinea pig macrophages with lymphokine-containing supernatants induced L. pneumophila growth restriction, mimicking mouse macrophage resistance. Immune serum did not confer this restriction.

Conclusions:

  • Macrophage permissiveness to L. pneumophila is linked to host susceptibility.
  • Lymphokines derived from stimulated lymphocytes can transform permissive macrophages into non-permissive ones.
  • Opsonization with immune serum does not induce growth restriction, highlighting the critical role of cell-mediated immune factors.

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