Plasmodium falciparum AMA1 and CSP antigen diversity in parasite isolates from southern Ghana

Front Cell Infect Microbiol. 2024 May 13:14:1375249. doi: 10.3389/fcimb.2024.1375249. eCollection 2024.

Abstract

Introduction: Diversity in malarial antigens is an immune evasion mechanism that gives malaria parasites an edge over the host. Immune responses against one variant of a polymorphic antigen are usually not fully effective against other variants due to altered epitopes. This study aimed to evaluate diversity in the Plasmodium falciparum antigens apical membrane antigen 1 (PfAMA1) and circumsporozoite protein (PfCSP) from circulating parasites in a malaria-endemic community in southern Ghana and to determine the effects of polymorphisms on antibody response specificity.

Methods: The study involved 300 subjects, whose P. falciparum infection status was determined by microscopy and PCR. Diversity within the two antigens was evaluated by msp2 gene typing and molecular gene sequencing, while the host plasma levels of antibodies against PfAMA1, PfCSP, and two synthetic 24mer peptides from the conserved central repeat region of PfCSP, were measured by ELISA.

Results: Of the 300 subjects, 171 (57%) had P. falciparum infection, with 165 of the 171 (96.5%) being positive for either or both of the msp2 allelic families. Gene sequencing of DNA from 55 clonally infected samples identified a total of 56 non-synonymous single nucleotide polymorphisms (SNPs) for the Pfama1 gene and these resulted in 44 polymorphic positions, including two novel positions (363 and 365). Sequencing of the Pfcsp gene from 69 clonal DNA samples identified 50 non-synonymous SNPs that resulted in 42 polymorphic positions, with half (21) of these polymorphic positions being novel. Of the measured antibodies, only anti-PfCSP antibodies varied considerably between PCR parasite-positive and parasite-negative persons.

Discussion: These data confirm the presence of a considerable amount of unique, previously unreported amino acid changes, especially within PfCSP. Drivers for this diversity in the Pfcsp gene do not immediately seem apparent, as immune pressure will be expected to drive a similar level of diversity in the Pfama1 gene.

Keywords: Ghana; PFCSP; PfAMA1; malaria; plasmodium; polymorphism.

MeSH terms

  • Adolescent
  • Adult
  • Antibodies, Protozoan* / blood
  • Antibodies, Protozoan* / immunology
  • Antigenic Variation
  • Antigens, Protozoan* / genetics
  • Antigens, Protozoan* / immunology
  • Child
  • Child, Preschool
  • DNA, Protozoan / genetics
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Genetic Variation
  • Ghana
  • Humans
  • Malaria, Falciparum* / immunology
  • Malaria, Falciparum* / parasitology
  • Male
  • Membrane Proteins* / genetics
  • Membrane Proteins* / immunology
  • Middle Aged
  • Plasmodium falciparum* / genetics
  • Plasmodium falciparum* / immunology
  • Polymerase Chain Reaction
  • Protozoan Proteins* / genetics
  • Protozoan Proteins* / immunology
  • Sequence Analysis, DNA
  • Young Adult

Substances

  • Antigens, Protozoan
  • Protozoan Proteins
  • Membrane Proteins
  • apical membrane antigen I, Plasmodium
  • Antibodies, Protozoan
  • circumsporozoite protein, Protozoan
  • merozoite surface protein 2, Plasmodium
  • DNA, Protozoan

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was funded by the Congressionally Directed Medical Research Program (CDMRP; CDMRPL-19-0-PR180876 and W81XH-19-1-0020) awarded jointly to MS and KAK. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.