# First report of a Plasmodium malariae SSU rRNA gene variant in Africa associated with reduced amplification by nested PCR

**Authors:** Maki Goto, Kei Yamamoto, Kanako Komaki-Yasuda, Shigeyuki Kano, Norio Ohmagari

PMC · DOI: 10.1186/s41182-025-00787-5 · 2025-08-04

## TL;DR

A new Plasmodium malariae gene variant in Africa may cause missed detection by standard PCR tests, highlighting the need for improved diagnostic methods.

## Contribution

The study reports a novel SSU rRNA gene variant in African P. malariae linked to reduced PCR amplification efficiency.

## Key findings

- A four-base deletion in the SSU rRNA gene of P. malariae was found to reduce amplification in nested PCR.
- The deletion is located in the primer-binding site of species-specific reverse primers used in secondary PCR.
- Cytochrome b gene sequencing confirmed the sample was P. malariae despite the PCR anomaly.

## Abstract

Nested polymerase chain reaction (PCR) targeting the small subunit ribosomal ribonucleic acid (SSU rRNA, 18S rRNA) region is widely used to differentiate Plasmodium species. We identified a variant of the Plasmodium malariae SSU rRNA gene that suggests nested PCR may fail to detect P. malariae strains with unknown mutations.

A 56-year-old Japanese man developed a fever 2 months after returning from a 2-month stay in Sierra Leone. Quartan malaria was suspected based on blood smear findings, and nested PCR confirmed P. malariae infection. However, the secondary PCR band obtained using P. malariae-specific primers was fainter than the primary PCR band amplified with universal primers—a reversal of the typical pattern. Sequence analysis revealed a four-base deletion in the SSU rRNA gene within the primer-binding site of the species-specific reverse primer used in the secondary PCR, suggesting that mutations in this region may partially impair amplification and hinder species identification. Cytochrome b gene sequencing confirmed 100% identity with P. malariae.

These findings underscore the need for continued molecular surveillance and sequence-based validation to ensure accurate diagnosis of Plasmodium infections, particularly in regions where genetic variants and zoonotic strains are emerging.

## Linked entities

- **Genes:** ssu rRNA (s-rRNA) [NCBI Gene 17098817], Cytochrome B (cytochrome b) [NCBI Gene 79504804]
- **Diseases:** malaria (MONDO:0005136), quartan malaria (MONDO:0001943)
- **Species:** Plasmodium malariae (taxon 5858), Plasmodium (taxon 5820)

## Full-text entities

- **Genes:** CYTB (cytochrome b) [NCBI Gene 4519] {aka MTCYB}, rRNA [NCBI Gene 29295223]
- **Diseases:** jaundice (MESH:D007565), renal impairment (MESH:D007674), non-falciparum malaria (MESH:D016778), Infectious Diseases (MESH:D003141), hyperbilirubinemia (MESH:D006932), metabolic acidosis (MESH:D000138), Malaria (MESH:D008288), fever (MESH:D005334), hypoglycemia (MESH:D007003), hepatosplenomegaly (MESH:C535727)
- **Chemicals:** artemether-lumefantrine (MESH:D000077611), LC859864 (-), doxycycline (MESH:D004318), Giemsa (MESH:D001399), agarose (MESH:D012685)
- **Species:** Homo sapiens (human, species) [taxon 9606], Plasmodium (subgenus) [taxon 418103], Plasmodium ovale wallikeri (subspecies) [taxon 864142], Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Hominidae (great apes, family) [taxon 9604], Platyrrhini (monkey, parvorder) [taxon 9479], Pan troglodytes (chimpanzee, species) [taxon 9598], Plasmodium malariae (species) [taxon 5858], Plasmodium knowlesi (species) [taxon 5850], Plasmodium vivax (malaria parasite P. vivax, species) [taxon 5855], Plasmodium ovale curtisi (subspecies) [taxon 864141]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12323105/full.md

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Source: https://tomesphere.com/paper/PMC12323105