TY - JOUR
T1 - High genetic diversity of Plasmodium falciparum in the low transmission setting of the Kingdom of Eswatini
AU - Roh, Michelle E.
AU - Tessema, Sofonias K.
AU - Murphy, Maxwell
AU - Nhlabathi, Nomcebo
AU - Mkhonta, Nomcebo
AU - Vilakati, Sibonakaliso
AU - Ntshalintshali, Nyasatu
AU - Saini, Manik
AU - Maphalala, Gugu
AU - Chen, Anna
AU - Wilheim, Jordan
AU - Prach, Lisa
AU - Gosling, Roly
AU - Kunene, Simon
AU - Hsiang, Michelle
AU - Greenhouse, Bryan
N1 - Publisher Copyright:
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2019/1/17
Y1 - 2019/1/17
N2 - ABSTRACT Background To better understand transmission dynamics, we characterized Plasmodium falciparum (Pf) genetic diversity in Eswatini, where transmission is low and sustained by importation. Methods 26 Pf microsatellites were genotyped in 66% of all confirmed cases from 2014-2016 (n=582). Population and within-host diversity were used to characterize differences between imported and locally-acquired infections, as determined by travel history. Logistic regression was used to assess the added value of diversity metrics to classify imported and local infections beyond epidemiology data alone. Results The parasite population in Eswatini was highly diverse (HE=0.75) and complex, with 67% polyclonal infections, a mean MOI of 2.2, and mean FWS of 0.84. Imported cases had comparable diversity to local cases, but exhibited higher MOI (2.4 versus 2.0; p=0.004) and lower mean FWS (0.82 vs. 0.85; p=0.03). Addition of MOI and FWS to multivariate analyses did not increase discrimination between imported and local infections. Discussion In contrast to the commonly held perception that Pf diversity declines with decreasing transmission intensity, isolates from Eswatini exhibited high parasite diversity consistent with high rates of malaria importation and limited local transmission. Estimates of malaria transmission intensity from genetic data need to consider the effect of importation, especially as countries near elimination.
AB - ABSTRACT Background To better understand transmission dynamics, we characterized Plasmodium falciparum (Pf) genetic diversity in Eswatini, where transmission is low and sustained by importation. Methods 26 Pf microsatellites were genotyped in 66% of all confirmed cases from 2014-2016 (n=582). Population and within-host diversity were used to characterize differences between imported and locally-acquired infections, as determined by travel history. Logistic regression was used to assess the added value of diversity metrics to classify imported and local infections beyond epidemiology data alone. Results The parasite population in Eswatini was highly diverse (HE=0.75) and complex, with 67% polyclonal infections, a mean MOI of 2.2, and mean FWS of 0.84. Imported cases had comparable diversity to local cases, but exhibited higher MOI (2.4 versus 2.0; p=0.004) and lower mean FWS (0.82 vs. 0.85; p=0.03). Addition of MOI and FWS to multivariate analyses did not increase discrimination between imported and local infections. Discussion In contrast to the commonly held perception that Pf diversity declines with decreasing transmission intensity, isolates from Eswatini exhibited high parasite diversity consistent with high rates of malaria importation and limited local transmission. Estimates of malaria transmission intensity from genetic data need to consider the effect of importation, especially as countries near elimination.
KW - Eswatini
KW - malaria
KW - malaria elimination
KW - microsatellite genotyping
KW - parasite diversity
KW - population genetics
KW - Swaziland
KW - transmission intensity
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U2 - 10.1101/522896
DO - 10.1101/522896
M3 - Article
AN - SCOPUS:85095626475
JO - Seminars in Fetal and Neonatal Medicine
JF - Seminars in Fetal and Neonatal Medicine
SN - 1744-165X
ER -