# Evidence for infectious merozoites of Plasmodium falciparum from natural isolates of cultured hepatoma cells infected with sporozoites

**Authors:** Olumide Adeyemi, Akinniyi Osuntoki, Olubunmi Magbagbeola, Muzamil Mahdi Abdel Hamid, Arwa Elaagip, Ann-Kristin Mueller, Muntaser Ibrahim

PMC · DOI: 10.1371/journal.pone.0319901 · PLOS One · 2025-03-19

## TL;DR

Researchers showed that Plasmodium falciparum can fully develop in HepG2 cells, producing infective merozoites that start a blood infection, which is important for malaria research.

## Contribution

The study demonstrates full intra-hepatic maturation of natural P. falciparum isolates in HepG2 cells, yielding infective merozoites.

## Key findings

- HepG2 cells supported full maturation of P. falciparum parasites from natural isolates.
- Infective merozoites were produced and successfully infected O+ erythrocytes.
- RNA analysis confirmed the parasites were P. falciparum.

## Abstract

Previous cell culture systems using various human hepatoma cell lines established that the intra-hepatic stages of Plasmodium falciparum could be studied ex vivo. However, only one of these culture systems yielded infective merozoites that subsequently completed the parasite’s life cycle outside a human host. We hypothesized that a major limitation is the use of laboratory-adapted P. falciparum blood stages for sporozoites generation. Plasmodium falciparum sporozoites were generated by membrane-feeding of gametocyte-infected blood samples from hospital patients to Anopheles arabiensis. Subsequently, cultured HepG2 cells were infected with the sporozoites. From 6 days post-sporozoite inoculation, liver merozoites could be harvested from the cell supernatants. When co-cultured with O + erythrocytes, these merozoites established a blood infection and yielded erythrocytic stage parasites that re-infected erythrocytes. To confirm that the erythrocytic parasites generated were P. falciparum, RNA expressed by the erythrocytic parasites was isolated and used as control in microarray analysis against RNA expressed by irradiated erythrocytic parasites; subsequently, P. falciparum genes were identified. The cultured HepG2 cells permitted the full intra-hepatic maturation of P. falciparum parasites from natural isolates. Infective merozoites were yielded which gave rise to the erythrocytic stage P. falciparum post-infection into O + erythrocytes. The full intra-hepatic maturation of the naturally isolated P. falciparum parasites in a HepG2 cell culture system is possible. This finding has important implications for malaria research and vaccine development.

## Linked entities

- **Diseases:** malaria (MONDO:0005136)
- **Species:** Plasmodium falciparum (taxon 5833), Anopheles arabiensis (taxon 7173), Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** malaria (MESH:D008288), hepatoma (MESH:D006528)
- **Chemicals:** O (MESH:D010100)
- **Species:** Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Anopheles arabiensis (species) [taxon 7173], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11922282/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC11922282/full.md

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Source: https://tomesphere.com/paper/PMC11922282