학술논문

Parasite genetic diversity reflects continued residual malaria transmission in Vhembe District, a hotspot in the Limpopo Province of South Africa
Document Type
article
Source
Malaria Journal. 20(1)
Subject
Biological Sciences
Biomedical and Clinical Sciences
Genetics
Clinical Sciences
Medical Microbiology
Infectious Diseases
Vector-Borne Diseases
Malaria
Rare Diseases
2.2 Factors relating to the physical environment
Aetiology
Infection
Good Health and Well Being
Adult
Aged
Female
Genetic Variation
Humans
Malaria
Falciparum
Male
Middle Aged
Plasmodium falciparum
South Africa
Young Adult
Genetic diversity
Microsatellites
Multiplicity of infection
Residual transmission
Vhembe District
Limpopo
Microbiology
Public Health and Health Services
Tropical Medicine
Medical microbiology
Public health
Language
Abstract
BackgroundSouth Africa aims to eliminate malaria transmission by 2023. However, despite sustained vector control efforts and case management interventions, the Vhembe District remains a malaria transmission hotspot. To better understand Plasmodium falciparum transmission dynamics in the area, this study characterized the genetic diversity of parasites circulating within the Vhembe District.MethodsA total of 1153 falciparum-positive rapid diagnostic tests (RDTs) were randomly collected from seven clinics within the district, over three consecutive years (2016, 2017 and 2018) during the wet and dry malaria transmission seasons. Using 26 neutral microsatellite markers, differences in genetic diversity were described using a multiparameter scale of multiplicity of infection (MOI), inbreeding metric (Fws), number of unique alleles (A), expected heterozygosity (He), multilocus linkage disequilibrium (LD) and genetic differentiation, and were associated with temporal and geospatial variances.ResultsA total of 747 (65%) samples were successfully genotyped. Moderate to high genetic diversity (mean He = 0.74 ± 0.03) was observed in the parasite population. This was ascribed to high allelic richness (mean A = 12.2 ± 1.2). The majority of samples (99%) had unique multi-locus genotypes, indicating high genetic diversity in the sample set. Complex infections were observed in 66% of samples (mean MOI = 2.13 ± 0.04), with 33% of infections showing high within-host diversity as described by the Fws metric. Low, but significant LD (standardised index of association, ISA = 0.08, P