Evidence map›Paper›PMID 38775551›Full record

ArticleMemorias do Instituto Oswaldo Cruz2024

Leishmania (Sauroleishmania) tarentolae versus pathogenic species: comparative evaluation of protease activity, glycoconjugates, resistance to complement and metabolome composition.

Filipe Fideles Duarte Andrade, Jéssica Gardone Vitório, Gisele André Baptista Canuto, Fernanda Freire Campos Nunes, Isabela Aurora Rodrigues, Ana Paula Martins Morais Almeida, Frederico Crepaldi Nascimento, Adriana Oliveira Costa, Tamara da Silva Vieira, Ana Carolina Carvalho Silva and 6 more

Abstract readComparative Study
In one paragraph

Article in Memorias do Instituto Oswaldo Cruz, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. LABCG1 AffectsACS infectious diseases · 2026
    Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Filipe Fideles Duarte AndradeUniversidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Departamento de Biologia Geral, Belo Horizonte, MG, Brasil.
Jéssica Gardone VitórioUniversidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
Gisele André Baptista CanutoUniversidade Federal da Bahia, Instituto de Química, Departamento de Química Analítica, Salvador, BA, Brasil.
Fernanda Freire Campos NunesUniversidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
Isabela Aurora RodriguesUniversidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
Ana Paula Martins Morais AlmeidaUniversidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
Frederico Crepaldi NascimentoUniversidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
Adriana Oliveira CostaUniversidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
Tamara da Silva VieiraFundação Oswaldo Cruz-Fiocruz, Instituto René Rachou, Grupo Biotecnologia Aplicada ao Estudo de Patógenos, Belo Horizonte, MG, Brasil.
Ana Carolina Carvalho SilvaUniversidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Departamento de Biologia Geral, Belo Horizonte, MG, Brasil.
Leiliane Coelho AndréUniversidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
Célia Maria Ferreira GontijoFundação Oswaldo Cruz-Fiocruz, Instituto René Rachou, Grupo Biotecnologia Aplicada ao Estudo de Patógenos, Belo Horizonte, MG, Brasil.
Caroline JunqueiraFundação Oswaldo Cruz-Fiocruz, Instituto René Rachou, Grupo Biotecnologia Aplicada ao Estudo de Patógenos, Belo Horizonte, MG, Brasil.
Juliano Simões de ToledoUniversidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Análises Clínicas e Toxicológicas, Belo Horizonte, MG, Brasil.
Ana Paula FernandesUniversidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Departamento de Biologia Geral, Belo Horizonte, MG, Brasil.ORCID http://orcid.org/0000-0002-6208-548X
Rodrigo Pedro SoaresFundação Oswaldo Cruz-Fiocruz, Instituto René Rachou, Grupo Biotecnologia Aplicada ao Estudo de Patógenos, Belo Horizonte, MG, Brasil.ORCID http://orcid.org/0000-0002-7966-3629

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeishmania 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.

objectivesWe 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).

methodsParasites 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.

findingsLeishmania 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

conclusionsThe 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.

Indexed as

GlycoconjugatesLeishmaniaMetabolomePeptide HydrolasesAnimalsComplement System ProteinsGlycosphingolipidsComplement System ProteinsGlycoconjugatesGlycosphingolipidslipophosphonoglycanPeptide Hydrolases

Identifiers

PMID38775551
PMCPMC11111114

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.