# Molecular Surveillance of Artemisinin-Resistant Plasmodium falciparum Parasites in Mining Areas of the Roraima Indigenous Territory in Brazil

**Authors:** Jacqueline de Aguiar-Barros, Fabiana Granja, Rebecca de Abreu-Fernandes, Lucas Tavares de Queiroz, Daniel da Silva e Silva, Arthur Camurça Citó, Natália Ketrin Almeida-de-Oliveira Mocelin, Cláudio Tadeu Daniel-Ribeiro, Maria de Fátima Ferreira-da-Cruz

PMC · DOI: 10.3390/ijerph21060679 · International Journal of Environmental Research and Public Health · 2024-05-25

## TL;DR

This study found no artemisinin-resistant malaria parasites in a Brazilian indigenous region affected by illegal mining.

## Contribution

The study provides molecular surveillance data on artemisinin resistance in a high-risk area for malaria transmission.

## Key findings

- All 46 parasite samples from illegal mining areas showed wild-type, artemisinin-sensitive genotypes.
- The study supports continued use of artemisinin-based therapies in Roraima for now.
- Systematic monitoring is recommended to detect resistance early in high-mobility regions like the YIL.

## Abstract

Multidrug- and artemisinin-resistant (ART-R) Plasmodium falciparum (Pf) parasites represent a challenge for malaria elimination worldwide. Molecular monitoring in the Kelch domain region (pfk13) gene allows tracking mutations in parasite resistance to artemisinin. The increase in illegal miners in the Roraima Yanomami indigenous land (YIL) could favor ART-R parasites. Thus, this study aimed to investigate ART-R in patients from illegal gold mining areas in the YIL of Roraima, Brazil. A questionnaire was conducted, and blood was collected from 48 patients diagnosed with P. falciparum or mixed malaria (Pf + P. vivax). The DNA was extracted and the pfk13 gene was amplified by PCR. The amplicons were subjected to DNA-Sanger-sequencing and the entire amplified fragment was analyzed. Among the patients, 96% (46) were from illegal mining areas of the YIL. All parasite samples carried the wild-type genotypes/ART-sensitive phenotypes. These data reinforce the continued use of artemisinin-based combination therapies (ACTs) in Roraima, as well as the maintenance of systematic monitoring for early detection of parasite populations resistant to ART, mainly in regions with an intense flow of individuals from mining areas, such as the YIL. This is especially true when the achievement of falciparum malaria elimination in Brazil is planned and expected by 2030.

## Linked entities

- **Genes:** PFK1_3 (6-phosphofructokinase, alpha subunit) [NCBI Gene 19249209]
- **Chemicals:** artemisinin (PubChem CID 68827)
- **Diseases:** malaria (MONDO:0005136), falciparum malaria (MONDO:0005920)
- **Species:** Plasmodium falciparum (taxon 5833)

## Full-text entities

- **Genes:** KLHL2 (kelch like family member 2) [NCBI Gene 11275] {aka ABP-KELCH, MAV, MAYVEN}
- **Diseases:** falciparum malaria (MESH:D016778), malaria (MESH:D008288)
- **Species:** Plasmodium vivax (malaria parasite P. vivax, species) [taxon 5855], Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC11203648/full.md

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Source: https://tomesphere.com/paper/PMC11203648