Leishmania amazonensis from distinct clinical forms/hosts has polymorphisms in Lipophosphoglycans, displays variations in immunomodulatory properties and, susceptibility to antileishmanial drugs.

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Autor(es): dc.creatorRêgo, Felipe Dutra-
Autor(es): dc.creatorCardoso, Camila Almeida-
Autor(es): dc.creatorMoreira, Paulo Otávio Lourenço-
Autor(es): dc.creatorNogueira, Paula Monalisa-
Autor(es): dc.creatorAraújo, Márcio Sobreira Silva-
Autor(es): dc.creatorBorges, Valéria Matos-
Autor(es): dc.creatorLaurenti, Marcia Dalastra-
Autor(es): dc.creatorBartholomeu, Daniella Castanheira-
Autor(es): dc.creatorReis, Alexandre Barbosa-
Autor(es): dc.creatorMonte Neto, Rubens Lima do-
Autor(es): dc.creatorSoares, Rodrigo Pedro Pinto-
Data de aceite: dc.date.accessioned2025-08-21T15:45:05Z-
Data de disponibilização: dc.date.available2025-08-21T15:45:05Z-
Data de envio: dc.date.issued2023-10-06-
Data de envio: dc.date.issued2023-10-06-
Data de envio: dc.date.issued2021-
Fonte completa do material: dc.identifierhttp://www.repositorio.ufop.br/jspui/handle/123456789/17533-
Fonte completa do material: dc.identifierhttps://doi.org/10.1002/cbin.11880-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/1023251-
Descrição: dc.descriptionLipophosphoglycan (LPG), the major Leishmania glycoconjugate, induces pro‐ inflammatory/immunosuppressive innate immune responses. Here, we evaluated functional/biochemical LPG properties from six Leishmania amazonensis strains from different hosts/clinical forms. LPGs from three strains (GV02, BA276, and LV79) had higher pro‐inflammatory profiles for most of the mediators, including tumor necrosis factor alpha and interleukin 6. For this reason, glycoconjugates from all strains were biochemically characterized and had polymorphisms in their repeat units. They consisted of three types: type I, repeat units devoid of side chains; type II, containing galactosylated side chains; and type III, containing glucosylated side chains. No relationship was observed between LPG type and the pro‐inflammatory properties. Finally, to evaluate the susceptibility against antileishmanial agents, two strains with high (GV02, BA276) and one with low (BA336) pro‐inflammatory activity were selected for chemotherapeutic tests in THP‐1 cells. All analyzed strains were susceptible to amphotericin B (AmB) but displayed various responses against miltefosine (MIL) and glucantime (GLU). The GV02 strain (canine visceral leishmaniasis) had the highest IC50 for MIL (3.34 μM), whereas diffuse leishmaniasis strains (BA276 and BA336) had a higher IC50 for GLU (6.87–12.19 mM). The highest IC50 against MIL shown by the GV02 strain has an impact on clinical management. Miltefosine is the only drug approved for dog treatment in Brazil. Further studies into drug susceptibility of L. amazonensis strains are warranted, especially in areas where dog infection by this species overlaps with those caused by Leishmania infantum.-
Formato: dc.formatapplication/pdf-
Idioma: dc.languageen-
Direitos: dc.rightsaberto-
Direitos: dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. Fonte: PDF do artigo.-
Palavras-chave: dc.subjectAntileishmanial agents-
Palavras-chave: dc.subjectGlycoconjugates-
Palavras-chave: dc.subjectInnate immunity-
Palavras-chave: dc.subjectLeishmania amazonensis-
Palavras-chave: dc.subjectLipophosphoglycan-
Título: dc.titleLeishmania amazonensis from distinct clinical forms/hosts has polymorphisms in Lipophosphoglycans, displays variations in immunomodulatory properties and, susceptibility to antileishmanial drugs.-
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