Plasma Lysophosphatidylcholine and Phospholipase A 2 Activity in Chagas Disease Patients: A Comparative Analysis
- 1 Laboratório de Bioquímica de Lipídios e Lipoproteínas, Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
- 2 Instituto Nacional de Ciência e Tecnologia em Entomologia Molecular (INCT-EM), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
- 3 Instituto Nacional de Ciência e Tecnologia em Entomologia Molecular (INCT-EM), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
- 4 Laboratório de Bioquímica de Lipídios e Lipoproteínas, Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
- 5 Laboratório de Sinalização Celular, Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
Abstract
Chagas disease (CD) affects 21 countries in the Americas and is caused by the parasite Trypanosoma cruzi . A key molecule involved in CD is lysophosphatidylcholine (LPC), which has been studied in various contexts: in the saliva of insect vectors, during the establishment of infection in the vertebrate host, and for the parasite itself. This lipid can be produced by the action of phospholipases A 2 (PLA 2 ), enzymes that catalyze the hydrolysis of phospholipids releasing fatty acids and lysophospholipids, such as LPC. This study investigates LPC levels and PLA 2 activities in the plasma of CD patients and compares these levels with those in healthy individuals and patients with idiopathic dilated cardiomyopathy (IDCM). Plasma from 64 CD patients, 54 healthy individuals, and 16 IDCM patients were analyzed. LPC levels and the activity of two types of phospholipase A 2 : secreted (sPLA 2 ) and lipoprotein-associated (Lp-PLA 2 ) were measured. LPC levels and sPLA 2 activity were similar between CD patients and the control groups. However, there were notable differences in LPC levels and sPLA 2 activity between subgroups of CD patients and IDCM patients. This study is the first to identify LPC in patients with CD across various stages of the disease. It also offers new insights into the biochemical changes observed in the plasma of patients with IDCM.
- Organization, P.A.H.O. Chagas Disease 2024.
- Nouvellet, P., Cucunubá, Z.M. and Gourbière, S. (2015) Ecology, Evolution and Control of Chagas Disease: A Century of Neglected Modelling and a Promising Future. Advances in Parasitology , 87, 135-191. https://doi.org/10.1016/bs.apar.2014.12.004
- Coura, J.R. and Dias, J.C.P. (2009) Epidemiology, Control and Surveillance of Chagas Disease: 100 Years after Its Discovery. Memórias do Instituto Oswaldo Cruz , 104, 31-40. https://doi.org/10.1590/s0074-02762009000900006
- Gourbière, S., Dorn, P., Tripet, F. and Dumonteil, E. (2011) Genetics and Evolution of Triatomines: From Phylogeny to Vector Control. Heredity , 108, 190-202. https://doi.org/10.1038/hdy.2011.71
- Andrade, L.O. and Andrews, N.W. (2005) The Trypanosoma cruzi —Host-Cell Interplay: Location, Invasion, Retention. Nature Reviews Microbiology , 3, 819-823. https://doi.org/10.1038/nrmicro1249
- Echavarría, N.G., Echeverría, L.E., Stewart, M., Gallego, C. and Saldarriaga, C. (2021) Chagas Disease: Chronic Chagas Cardiomyopathy. Current Problems in Cardiology , 46, Article 100507. https://doi.org/10.1016/j.cpcardiol.2019.100507
- Khan, S.A. and Ilies, M.A. (2023) The Phospholipase A2 Superfamily: Structure, Isozymes, Catalysis, Physiologic and Pathologic Roles. International Journal of Molecular Sciences , 24, Article 1353. https://doi.org/10.3390/ijms24021353
- Golodne, D.M., Monteiro, R.Q., Graça-Souza, A.V., Silva-Neto, M.A.C. and Atella, G.C. (2003) Lysophosphatidylcholine Acts as an Anti-Hemostatic Molecule in the Saliva of the Blood-Sucking Bug Rhodnius Prolixus. Journal of Biological Chemistry , 278, 27766-27771. https://doi.org/10.1074/jbc.m212421200
- Lima, M.S., Carneiro, A.B., Souto-Padron, T., Jurberg, J., Silva-Neto, M.A.C. and Atella, G.C. (2018) Triatoma Infestans Relies on Salivary Lysophosphatidylcholine to Enhance Trypanosoma Cruzi Transmission. Acta Tropica , 178, 68-72. https://doi.org/10.1016/j.actatropica.2017.10.022
- Mesquita, R.D., Carneiro, A.B., Bafica, A., Gazos-Lopes, F., Takiya, C.M., Souto-Padron, T., et al . (2008) Trypanosoma cruzi Infection Is Enhanced by Vector Saliva through Immunosuppressant Mechanisms Mediated by Lysophosphatidylcholine. Infection and Immunity , 76, 5543-5552. https://doi.org/10.1128/iai.00683-08
- Gazos-Lopes, F., Oliveira, M.M., Hoelz, L.V.B., Vieira, D.P., Marques, A.F., Nakayasu, E.S., et al . (2014) Structural and Functional Analysis of a Platelet-Activating Lysophosphatidylcholine of Trypanosoma Cruzi . PLOS Neglected Tropical Diseases , 8, e3077. https://doi.org/10.1371/journal.pntd.0003077