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February 26, 2026PLoS ONE0 citationsOpen Access

Distribution of falciparum and non-falciparum malaria among symptomatic malaria patients in Dschang, West Region of Cameroon

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PTPacome V. K. TchuenkamLMLethicia K. MafoVPVarun R. Potlapalli

Key Points

  • Investigate the prevalence of various malaria parasite species in symptomatic patients in Dschang, Cameroon.
  • Cross-sectional facility-based study conducted in 2020
  • Recruited 431 suspected malaria cases from three health centres
  • Collected socio-demographic and clinical data, as well as dried blood spots (DBS)
  • Used real-time PCR for amplification of malaria species-specific DNA including P. falciparum, P. ovale, P. malariae, and P. vivax
  • Sub-classified P. ovale into curtisi and wallikeri using qPCR.
  • Overall malaria prevalence was 54.8% among sampled patients
  • 53.4% of infections were P. falciparum, 4% P. ovale, and 0.9% P. malariae
  • No cases of P. vivax detected
  • Mixed infections were found in 8.9% of cases
  • Both subspecies of P. ovale were present, with genotyping revealing 6 P. ovale curtisi and 3 P. ovale wallikeri.

Abstract

Background Malaria is a vector-borne parasitic disease that continues to be a global public health threat. Five different species of the genus Plasmodium ( P. falciparum , P. malariae, P. ovale curtisi, P. ovale wallikeri, and P. vivax) cause malaria in Sub-Saharan Africa. Previous cross-sectional surveys from 2013 and 2017 indicated the circulation of P. vivax in the West region of Cameroon, prompting an investigation into the prevalence of all falciparum and non-falciparum malaria parasite species in this region. Methods A cross-sectional facility-based study targeting both adult and children in which we recruited 431 clinically suspected cases of malaria from three health centres in the West region of Cameroon in 2020. Socio-demographic, clinical data, and dried blood spots (DBS) were collected from all consenting patients. Parasite DNA was extracted from DBS for real-time PCR amplification of species-specific Plasmodium 18S rRNA for P. falciparum, P. ovale, P. malariae, and P. vivax . In addition, P. ovale was further sub-classified into P. ovale curtisi or P. ovale wallikeri using qPCR. The prevalence of different species was measured. Results Among the 431 samples, the overall malaria prevalence was 54.8% 95% CI: 50.1–59.8 (236/431). Of these, 53.4% 95% CI: 48.7–58.5 were infected with P. falciparum , 4% 95%CI: 2.2–5.6 with P. ovale , and 0.9% 95% CI: 0.2–1.7 with P. malariae . No P. vivax was detected. Mixed infections were common, with 8.9% of the infections harbouring more than one Plasmodium species. A total of 5 P. ovale and 1 P. malariae mono-infections were detected. Of the 17 P. ovale infections, 12 were successfully genotyped, with 6 P. ovale curtisi , 3 P. ovale wallikeri, and 3 a mixture of the species. Conclusions While falciparum remains the dominant malaria parasite species among acute febrile illness cases, non-falciparum malaria is also commonly found in Dschang, both as a co-infection with P. falciparum and as mono-infections. Both subspecies of P. ovale are present in the region. Continued monitoring of non-falciparum species is needed for understanding malaria burden in West Cameroon.

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Cite This Study

Tchuenkam et al. (2026) studied this question.

synapsesocial.com/papers/699fe37b95ddcd3a253e7702https://doi.org/10.1371/journal.pone.0340824
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