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Survival of Listeria monocytogenes in experimentally infected mice

Applied Microbiology
|January 1, 1971
PubMed

Insights

Physiological saline harms Listeria monocytogenes survival. Peptone solutions improved viability, and spleen tissue did not inhibit Listeria in infected mice.

Area of Science:

  • Microbiology
  • Immunology
  • Pathogen Survival

Background:

  • Listeria monocytogenes is a significant foodborne pathogen.
  • Understanding factors affecting Listeria monocytogenes viability is crucial for food safety and public health.
  • The role of physiological fluids and host tissues in pathogen survival requires further investigation.

Purpose of the Study:

  • To investigate the effect of physiological saline and peptone solutions on Listeria monocytogenes viability.
  • To determine if normal splenic tissue inhibits Listeria monocytogenes survival.
  • To assess the in vivo survival of Listeria monocytogenes in experimentally infected mice.

Main Methods:

  • In vitro assessment of Listeria monocytogenes viability in different suspending fluids (saline vs. peptone).
  • In vitro co-culture experiments with Listeria monocytogenes and normal splenic tissue.
  • Experimental infection of mice to evaluate Listeria monocytogenes survival in the peritoneal cavity and spleen.

Main Results:

  • Physiological saline was found to be detrimental to Listeria monocytogenes viability.
  • The median lethal dose (LD50) of Listeria monocytogenes was significantly lower in peptone than in saline.
  • Normal splenic tissue did not inhibit the survival of Listeria monocytogenes.
  • Listeria monocytogenes survived for 8 days in the peritoneal cavity and at least 11 days in the spleen of experimentally infected mice.

Conclusions:

  • The composition of the suspending fluid significantly impacts Listeria monocytogenes viability.
  • Host splenic tissue does not appear to be an inhibitory environment for Listeria monocytogenes.
  • Listeria monocytogenes exhibits prolonged survival in vivo, highlighting its persistence potential in infected hosts.

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