Frontiers in Cellular and Infection Microbiology (Dec 2019)

Mapping Alterations Induced by Long-Term Axenic Cultivation of Leishmania amazonensis Promastigotes With a Multiplatform Metabolomic Fingerprint Approach

  • Frederico Crepaldi,
  • Frederico Crepaldi,
  • Juliano Simões de Toledo,
  • Juliano Simões de Toledo,
  • Anderson Oliveira do Carmo,
  • Leopoldo Ferreira Marques Machado,
  • Daniela Diniz Viana de Brito,
  • Angela Vieira Serufo,
  • Ana Paula Martins Almeida,
  • Leandro Gonzaga de Oliveira,
  • Tiago Queiroga Nery Ricotta,
  • Douglas de Souza Moreira,
  • Silvane Maria Fonseca Murta,
  • Ariane Barros Diniz,
  • Gustavo Batista Menezes,
  • Ángeles López-Gonzálvez,
  • Coral Barbas,
  • Ana Paula Fernandes

DOI
https://doi.org/10.3389/fcimb.2019.00403
Journal volume & issue
Vol. 9

Abstract

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Leishmaniases are widespread neglected diseases with an incidence of 1.6 million new cases and 40 thousand deaths per year. Leishmania parasites may show distinct, species-specific patterns of virulence that lead to different clinical manifestations. It is well known that successive in vitro passages (SIVP) lead to the attenuation of virulence, but neither the metabolism nor the pathways involved in these processes are well understood. Herein, promastigotes of a virulent L. amazonensis strain recently isolated from mice was compared to SIVP derived and attenuated promastigotes, submitted to 10, 40, and 60 axenic passages and named R10, R40, and R60, respectively. In vitro assays and in vivo tests were performed to characterize and confirmed the attenuation profiles. A metabolomic fingerprint comparison of R0, R10, and R60 was performed by means of capillary electrophoresis, liquid and gas chromatography coupled to mass spectrometry. To validate the metabolomic data, qPCR for selected loci, flow cytometry to measure aPS exposure, sensitivity to antimony tartrate and ROS production assays were conducted. The 65 identified metabolites were clustered in biochemical categories and mapped in eight metabolic pathways: ABC transporters; fatty acid biosynthesis; glycine, serine and threonine metabolism; β-alanine metabolism; glutathione metabolism; oxidative phosphorylation; glycerophospholipid metabolism and lysine degradation. The obtained metabolomic data correlated with previous proteomic findings of the SVIP parasites and the gene expression of 13 selected targets. Late SIVP cultures were more sensitive to SbIII produced more ROS and exposed less phosphatidylserine in their surface. The correspondent pathways were connected to build a biochemical map of the most significant alterations involved with the process of attenuation of L. amazonensis. Overall, the reported data pointed out to a very dynamic and continuous metabolic reprogramming process, accompanied by changes in energetic, lipid and redox metabolisms, membrane remodeling and reshaping of parasite-host cells interactions, causing impacts in chemotaxis, host inflammatory responses and infectivity at the early stages of infection.

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