Total parasite biomass but not peripheral parasitaemia is associated with endothelial and haematological perturbations in Plasmodium vivax patients

Autor(es):Mostrar menos -

Silva-Filho, Joao L. ^{[1, 2]} ; Dos-Santos, Joao C. K. ^{[2, 3]} ; Judice, Carla ^[2] ; Beraldi, Dario ^[1] ; Venugopal, Kannan ^[1] ; Lima, Diogenes ^[4] ; Nakaya, I, Helder ; De Paula, V, Erich ; Lopes, Stefanie C. P. ^{[5, 6, 7]} ; Lacerda, Marcus V. G. ^{[5, 7]} ; Marti, Matthias ^[1] ; Costa, Fabio T. M. ^[2]

Afiliação do(s) autor(es)

^[1] Univ Glasgow, Wellcome Ctr Integrat Parasitol, Inst Infect Immun & Inflammat, Glasgow, Lanark - Scotland

^[2] Univ Estadual Campinas, Inst Biol, Dept Genet Evolut Microbiol & Immunol, Lab Trop Dis Prof Luiz Jacintho da Silva, Campinas - Brazil

^[3] Univ Estadual Campinas, Sch Med Sci, Postgrad Med Pathophysiol, Campinas - Brazil

^[4] I, Univ Sao Paulo, Sch Pharmaceut Sci, Sao Paulo - Brazil

^[5] Fiocruz MS, Inst Leonidas & Maria Deane, Manaus, Amazonas - Brazil

^[6] De Paula, Erich, V, Univ Estadual Campinas, Sch Med Sci, Dept Clin Pathol, Campinas - Brazil

^[7] Trop Med Fdn Dr Heitor Vieira Dourado, Manaus, Amazonas - Brazil

• Tipo de documento: Artigo Científico
• Fonte: eLIFE; v. 10, SEP 29 2021.
• Citações Web of Science: 0

Resumo

Plasmodium vivax is the major cause of human malaria in the Americas. How P. vivax infection can lead to poor clinical outcomes, despite low peripheral parasitaemia, remains a matter of intense debate. Estimation of total P. vivax biomass based on circulating markers indicates existence of a predominant parasite population outside of circulation. In this study, we investigate associations between both peripheral and total parasite biomass and host response in vivax malaria. We analysed parasite and host signatures in a cohort of uncomplicated vivax malaria patients from Manaus, Brazil, combining clinical and parasite parameters, multiplexed analysis of host responses, and ex vivo assays. Patterns of clinical features, parasite burden, and host signatures measured in plasma across the patient cohort were highly heterogenous. Further data deconvolution revealed two patient clusters, here termed Vivax(low) and Vivax(high). These patient subgroups were defined based on differences in total parasite biomass but not peripheral parasitaemia. Overall Vivax(low) patients clustered with healthy donors and Vivax(high) patients showed more profound alterations in haematological parameters, endothelial cell (EC) activation, and glycocalyx breakdown and levels of cytokines regulating different haematopoiesis pathways compared to Vivax(low). Vivax(high) patients presented more severe thrombocytopenia and lymphopenia, along with enrichment of neutrophils in the peripheral blood and increased neutrophil-to-lymphocyte ratio (NLCR). When patients' signatures were combined, high association of total parasite biomass with a subset of markers of EC activation, thrombocytopenia, and lymphopenia severity was observed. Finally, machine learning models defined a combination of host parameters measured in the circulation that could predict the extent of parasite infection outside of circulation. Altogether, our data show that total parasite biomass is a better predictor of perturbations in host homeostasis in P. vivax patients than peripheral parasitaemia. This supports the emerging paradigm of a P. vivax tissue reservoir, particularly in the haematopoietic niche of bone marrow and spleen. (AU)

• Processo FAPESP: 16/12855-9 - Mecanismo de ação da lipoxina na proteção do desenvolvimento da malária cerebral experimental
• Beneficiário: João Luiz da Silva Filho
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado
• Processo FAPESP: 19/01578-2 - Interação parasito-hospedeiro na medula óssea: papel chave na patogênese da Malária
• Beneficiário: João Luiz da Silva Filho
• Modalidade de apoio: Bolsas no Exterior - Estágio de Pesquisa - Pós-Doutorado
• Processo FAPESP: 17/18611-7 - Desenvolvimento de novas ferramentas para busca e validação de alvos moleculares para terapia contra Plasmodium vivax
• Beneficiário: Fabio Trindade Maranhão Costa
• Modalidade de apoio: Auxílio à Pesquisa - Temático