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Malaria merozoite surface protein antisense oligodeoxynucleotides lack antisense activity but function as polyanions

R Kanagaratnam1, K Misiura, G Rebowski

  • 1Division of Life Sciences, Institute of Fundamental Studies, Kandy, Sri Lanka.

Insights

Antisense and sense oligonucleotides, charged molecules, were found to inhibit malaria parasite invasion of red blood cells. This suggests polyanions could be a novel therapeutic approach for malaria.

Area of Science:

  • Parasitology
  • Molecular Biology
  • Drug Discovery

Background:

  • Malaria remains a significant global health challenge, necessitating novel therapeutic strategies.
  • Merozoite surface proteins are crucial for malaria parasite invasion of red blood cells.

Purpose of the Study:

  • To investigate the effects of antisense and sense oligodeoxynucleoside phosphorothioates on malaria parasite growth and red blood cell invasion.
  • To explore the potential of polyanionic compounds as antimalarial agents.

Main Methods:

  • Oligodeoxynucleoside phosphorothioates targeting merozoite surface protein mRNA were synthesized.
  • Inhibition of merozoite invasion was assessed using microscopy and [3H]hypoxanthine incorporation.
  • The role of oligonucleotide charge was investigated using cationic liposomes.

Main Results:

  • Specific antisense effects were not demonstrated during parasite schizogony.
  • Both antisense and sense oligonucleotides inhibited merozoite invasion of red blood cells.
  • Neutralizing the negative charge of oligonucleotides with cationic liposomes abolished the inhibitory effect.

Conclusions:

  • Oligonucleotides, due to their polyanionic nature, interfere with merozoite binding to red blood cells.
  • Polyanions show promise as a potential therapeutic strategy for malaria treatment.

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