Fosmidomycin Uptake into Plasmodium and Babesia-Infected Erythrocytes Is Facilitated by Parasite-Induced New Permeability Pathways
2011

Fosmidomycin Uptake into Infected Erythrocytes

publication 10 minutes Evidence: moderate

Author Information

Author(s): Stefan Baumeister, Jochen Wiesner, Armin Reichenberg, Martin Hintz, Sven Bietz, Omar S. Harb, David S. Roos, Maximilian Kordes, Johannes Friesen, Kai Matuschewski, Klaus Lingelbach, Hassan Jomaa, Frank Seeber

Primary Institution: Philipps-Universität, Marburg, Germany

Hypothesis

The drugs fosmidomycin and its derivative FR900098 are taken up only by erythrocytes infected with Plasmodium.

Conclusion

The study found that only erythrocytes infected with Plasmodium or Babesia exhibit increased permeability that allows for the uptake of fosmidomycin and FR900098.

Supporting Evidence

  • Fosmidomycin and FR900098 showed parasiticidal activity against Plasmodium falciparum.
  • Increased permeability of erythrocyte membranes was observed in infected cells.
  • Toxoplasma gondii-infected cells did not take up the drugs.
  • Uptake of FR was significantly inhibited by NPP inhibitors.

Takeaway

Infected red blood cells can absorb certain drugs better than healthy ones, which helps fight malaria, but some parasites are resistant.

Methodology

The study used radiolabeled drugs to measure uptake in infected and non-infected erythrocytes and assessed permeability changes.

Limitations

The study did not explore the molecular mechanisms behind the new permeability pathways in detail.

Statistical Information

P-Value

0.011

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0019334

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