Bone Marrow Is a Major Parasite Reservoir in Plasmodium Vivax Infection
Overview
Authors
Affiliations
causes heavy burdens of disease across malarious regions worldwide. Mature asexual and transmissive gametocyte stages occur in the blood circulation, and it is often assumed that accumulation/sequestration in tissues is not an important phase in their development. Here, we present a systematic study of stage distributions in infected tissues of nonhuman primate (NHP) malaria models as well as in blood from human infections. In a comparative analysis of the transcriptomes of and blood-stage parasites, we found a conserved cascade of stage-specific gene expression despite the greatly different gametocyte maturity times of these two species. Using this knowledge, we validated a set of conserved asexual- and gametocyte-stage markers both by quantitative real-time PCR and by antibody assays of peripheral blood samples from infected patients and NHP ( sp.). Histological analyses of parasites in organs of 13 infected NHP ( and species) demonstrated a major fraction of immature gametocytes in the parenchyma of the bone marrow, while asexual schizont forms were enriched to a somewhat lesser extent in this region of the bone marrow as well as in sinusoids of the liver. These findings suggest that the bone marrow is an important reservoir for gametocyte development and proliferation of malaria parasites. malaria continues to cause major public health burdens worldwide. Yet, significant knowledge gaps in the basic biology and epidemiology of malaria remain, largely due to limited available tools for research and diagnostics. Here, we present a systematic examination of tissue sequestration during infection. Studies of nonhuman primates and malaria patients revealed enrichment of developing sexual stages (gametocytes) and mature replicative stages (schizonts) in the bone marrow and liver, relative to those present in peripheral blood. Identification of the bone marrow as a major tissue reservoir has important implications for parasite diagnosis and treatment.
Dao F, Niangaly A, Sogore F, Wague M, Dabitao D, Goita S PLoS Negl Trop Dis. 2025; 19(1):e0012790.
PMID: 39761327 PMC: 11735006. DOI: 10.1371/journal.pntd.0012790.
Exploring the naturally acquired response to Pvs47 gametocyte antigen.
Soares da Veiga G, Donassolo R, Forcellini S, Ferraboli J, Kujbida Junior M, Nisimura L Front Immunol. 2024; 15:1455454.
PMID: 39450180 PMC: 11499161. DOI: 10.3389/fimmu.2024.1455454.
Rodolphi C, Soares I, da Silva Matos A, Rodrigues-da-Silva R, Urbano Ferreira M, Pratt-Riccio L Antibodies (Basel). 2024; 13(3).
PMID: 39189240 PMC: 11348034. DOI: 10.3390/antib13030069.
Pestana K, Ford A, Rama R, Abagero B, Kepple D, Tomida J J Infect Dis. 2024; 230(4):1004-1012.
PMID: 39102894 PMC: 11481331. DOI: 10.1093/infdis/jiae388.
The impact of Plasmodium-driven immunoregulatory networks on immunity to malaria.
Boyle M, Engwerda C, Jagannathan P Nat Rev Immunol. 2024; 24(9):637-653.
PMID: 38862638 PMC: 11688169. DOI: 10.1038/s41577-024-01041-5.