Acanthamoeba castellanii is not be an adequate model to study human adenovirus interactions with macrophagic cells

Elodie Maisonneuve1, Estelle Cateau1,2, Nicolas Leveque3,4

  • 1Laboratoire Ecologie et Biologie des Interactions, Equipe Microbiologie de l'Eau, UMR CNRS 7267, Université de Poitiers, Poitiers, France.

Plos One
|June 8, 2017
PubMed

Insights

Free-living amoebae (FLA) like Acanthamoeba castellanii share similarities with macrophages. However, this study found Acanthamoeba is not a suitable in vitro model for adenovirus-macrophage interactions, as viruses only replicated in macrophages.

Area of Science:

  • Microbiology
  • Cell Biology
  • Immunology

Background:

  • Free-living amoebae (FLA), such as Acanthamoeba castellanii, exhibit similarities to macrophages in cellular structure and function.
  • These similarities have led to the hypothesis that FLA could serve as an in vitro model for studying host-pathogen interactions, particularly involving macrophages.

Purpose of the Study:

  • To compare the interactions between a human adenovirus strain and Acanthamoeba castellanii versus THP-1 macrophagic cells.
  • To determine the relevance of Acanthamoeba castellanii as an in vitro model for investigating adenovirus-macrophage relationships.

Main Methods:

  • Co-culture experiments involving human adenovirus and either Acanthamoeba castellanii or THP-1 macrophagic cells.
  • Molecular and microscopy techniques were employed to analyze viral presence, replication, and host cell viability.

Main Results:

  • Adenovirus infection significantly decreased the viability of THP-1 macrophages.
  • Acanthamoeba castellanii viability remained unaffected by the adenovirus.
  • Viral replication was exclusively observed in the THP-1 macrophagic cells, not in Acanthamoeba castellanii.

Conclusions:

  • Acanthamoeba castellanii does not support human adenovirus replication.
  • The study concludes that Acanthamoeba castellanii is not a relevant in vitro model for exploring the interactions between adenoviruses and macrophages.