TY - JOUR
T1 - Plasmodium falciparum expresses fewer var genes at lower levels during asymptomatic dry season infections than clinical malaria cases
AU - Ceesay, Sukai
AU - Kampmann, Martin
AU - Votborg-Novél, Lasse
AU - Hansson, Helle Smedegaard
AU - Jensen, Rasmus Weisel
AU - Carrasquilla, Manuela
AU - Cisse, Hamidou
AU - Turner, Louise
AU - Dabbas, Usama
AU - Ntalla, Christina
AU - Bandermann, Silke
AU - Doumbo, Safiatou
AU - Doumtabe, Didier
AU - Ongoiba, Aissata
AU - Kayentao, Kassoum
AU - Traore, Boubacar
AU - Crompton, Peter D.
AU - Lavstsen, Thomas
AU - Portugal, Silvia
N1 - Publisher Copyright:
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
PY - 2025/6
Y1 - 2025/6
N2 - In seasonal transmission areas, clinical malaria occurs during the wet season when mosquitoes are present, while in the dry season, malaria transmission is interrupted and clinical cases are rare. In Mali, Plasmodium falciparum can persist in low parasitaemic asymptomatic individuals through the six-month dry season and shows circulation of more developed parasite stages compared to clinical malaria cases, indicative of reduced cytoadhesion of infected erythrocytes. How prolonged circulation of infected erythrocytes is achieved remains unknown. Here, we explored var gene expression in subclinical infections and clinical malaria cases of Malian children, collected during the dry and wet seasons. We sequenced expressed var DBLα-tags, used bioinformatic tools to predict their domain composition, binding phenotype and upstream sequence type; and determined their relationship to seasonality and clinical presentation. We found that parasites of asymptomatic infections expressed fewer var genes, with a larger proportion of var transcripts attributed to one or a few vars. In contrast, clinical cases exhibited expression of many var genes at lower proportions. We found that parasites of asymptomatic carriers expressed a mixture of CD36- and EPCR-binding PfEMP1, which changed over time. We confirmed that vars encoding CD36-binding PfEMP1 dominated in non-severe malaria cases, and found no significant difference in expressed var types between dry and wet seasons. Asymptomatic carriers were older, had higher titers of anti-P. falciparum antibodies, and broader reactivity to PfEMP1, suggesting that host immunity was the main determinant limiting var transcript variation in asymptomatic carriers. However, qRT-PCR analyses also indicated higher total var transcript levels in malaria cases compared to asymptomatic carriers, suggesting that in addition to the parasite’s switching and the host’s immune selection of expressed var genes, parasites able to sustain long-term infections may be poised for reduced PfEMP1 expression.
AB - In seasonal transmission areas, clinical malaria occurs during the wet season when mosquitoes are present, while in the dry season, malaria transmission is interrupted and clinical cases are rare. In Mali, Plasmodium falciparum can persist in low parasitaemic asymptomatic individuals through the six-month dry season and shows circulation of more developed parasite stages compared to clinical malaria cases, indicative of reduced cytoadhesion of infected erythrocytes. How prolonged circulation of infected erythrocytes is achieved remains unknown. Here, we explored var gene expression in subclinical infections and clinical malaria cases of Malian children, collected during the dry and wet seasons. We sequenced expressed var DBLα-tags, used bioinformatic tools to predict their domain composition, binding phenotype and upstream sequence type; and determined their relationship to seasonality and clinical presentation. We found that parasites of asymptomatic infections expressed fewer var genes, with a larger proportion of var transcripts attributed to one or a few vars. In contrast, clinical cases exhibited expression of many var genes at lower proportions. We found that parasites of asymptomatic carriers expressed a mixture of CD36- and EPCR-binding PfEMP1, which changed over time. We confirmed that vars encoding CD36-binding PfEMP1 dominated in non-severe malaria cases, and found no significant difference in expressed var types between dry and wet seasons. Asymptomatic carriers were older, had higher titers of anti-P. falciparum antibodies, and broader reactivity to PfEMP1, suggesting that host immunity was the main determinant limiting var transcript variation in asymptomatic carriers. However, qRT-PCR analyses also indicated higher total var transcript levels in malaria cases compared to asymptomatic carriers, suggesting that in addition to the parasite’s switching and the host’s immune selection of expressed var genes, parasites able to sustain long-term infections may be poised for reduced PfEMP1 expression.
KW - Humans
KW - Plasmodium falciparum/genetics
KW - Malaria, Falciparum/parasitology
KW - Protozoan Proteins/genetics
KW - Seasons
KW - Mali/epidemiology
KW - Child, Preschool
KW - Child
KW - Asymptomatic Infections/epidemiology
KW - Female
KW - Male
KW - Infant
UR - https://www.scopus.com/pages/publications/105007749854
U2 - 10.1371/journal.ppat.1013210
DO - 10.1371/journal.ppat.1013210
M3 - Journal article
C2 - 40493675
AN - SCOPUS:105007749854
SN - 1553-7366
VL - 21
JO - PLOS Pathogens
JF - PLOS Pathogens
IS - 6
M1 - e1013210
ER -