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Leishmania (Sauroleishmania) tarentolae versus pathogenic species: comparative evaluation of protease activity, glycoconjugates, resistance to complement and metabolome composition.
Andrade, Filipe Fideles Duarte; Vitório, Jéssica Gardone; Canuto, Gisele André Baptista; Nunes, Fernanda Freire Campos; Rodrigues, Isabela Aurora; Almeida, Ana Paula Martins Morais; Nascimento, Frederico Crepaldi; Costa, Adriana Oliveira; Vieira, Tamara da Silva; Silva, Ana Carolina Carvalho; André, Leiliane Coelho; Gontijo, Célia Maria Ferreira; Junqueira, Caroline; Toledo, Juliano Simões de; Fernandes, Ana Paula; Soares, Rodrigo Pedro.
Affiliation
  • Andrade FFD; Universidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Departamento de Biologia Geral, Belo Horizonte, MG, Brasil.
  • Vitório JG; Universidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
  • Canuto GAB; Universidade Federal da Bahia, Instituto de Química, Departamento de Química Analítica, Salvador, BA, Brasil.
  • Nunes FFC; Universidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
  • Rodrigues IA; Universidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
  • Almeida APMM; Universidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
  • Nascimento FC; Universidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
  • Costa AO; Universidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
  • Vieira TDS; Fundação Oswaldo Cruz-Fiocruz, Instituto René Rachou, Grupo Biotecnologia Aplicada ao Estudo de Patógenos, Belo Horizonte, MG, Brasil.
  • Silva ACC; Universidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Departamento de Biologia Geral, Belo Horizonte, MG, Brasil.
  • André LC; Universidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
  • Gontijo CMF; Fundação Oswaldo Cruz-Fiocruz, Instituto René Rachou, Grupo Biotecnologia Aplicada ao Estudo de Patógenos, Belo Horizonte, MG, Brasil.
  • Junqueira C; Fundação Oswaldo Cruz-Fiocruz, Instituto René Rachou, Grupo Biotecnologia Aplicada ao Estudo de Patógenos, Belo Horizonte, MG, Brasil.
  • Toledo JS; Universidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
  • Fernandes AP; Universidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Departamento de Biologia Geral, Belo Horizonte, MG, Brasil.
  • Soares RP; Fundação Oswaldo Cruz-Fiocruz, Instituto René Rachou, Grupo Biotecnologia Aplicada ao Estudo de Patógenos, Belo Horizonte, MG, Brasil.
Mem Inst Oswaldo Cruz ; 119: e230243, 2024.
Article in En | MEDLINE | ID: mdl-38775551
ABSTRACT

BACKGROUND:

Leishmania tarentolae is a non-pathogenic species found in lizards representing an important model for Leishmania biology. However, several aspects of this Sauroleishmania remain unknown to explain its low level of virulence.

OBJECTIVES:

We reported several aspects of L. tarentolae biology including glycoconjugates, proteolytic activities and metabolome composition in comparison to pathogenic species (Leishmania amazonensis, Leishmania braziliensis, Leishmania infantum and Leishmania major).

METHODS:

Parasites were cultured for extraction and purification of lipophosphoglycan (LPG), immunofluorescence probing with anti-gp63 and resistance against complement. Parasite extracts were also tested for proteases activity and metabolome composition.

FINDINGS:

Leishmania tarentolae does not express LPG on its surface. It expresses gp63 at lower levels compared to pathogenic species and, is highly sensitive to complement-mediated lysis. This species also lacks intracellular/extracellular activities of proteolytic enzymes. It has metabolic differences with pathogenic species, exhibiting a lower abundance of metabolites including ABC transporters, biosynthesis of unsaturated fatty acids and steroids, TCA cycle, glycine/serine/threonine metabolism, glyoxylate/dicarboxylate metabolism and pentose-phosphate pathways. MAIN

CONCLUSIONS:

The non-pathogenic phenotype of L. tarentolae is associated with alterations in several biochemical and molecular features. This reinforces the need of comparative studies between pathogenic and non-pathogenic species to elucidate the molecular mechanisms of virulence during host-parasite interactions.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Hydrolases / Glycoconjugates / Metabolome / Leishmania Limits: Animals Language: En Journal: Mem Inst Oswaldo Cruz Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Hydrolases / Glycoconjugates / Metabolome / Leishmania Limits: Animals Language: En Journal: Mem Inst Oswaldo Cruz Year: 2024 Document type: Article Affiliation country: Country of publication: