Use este identificador para citar ou linkar para este item: http://repositorio.ufc.br/handle/riufc/59683
Tipo: Artigo de Periódico
Título: Antimicrobial activity of synthetic Dq-3162, a 28-residue ponericin G-like dinoponeratoxin from the giant ant Dinoponera quadriceps venom, against carbapenem-resistant bactéria
Título em inglês: Antimicrobial activity of synthetic Dq-3162, a 28-residue ponericin G-like dinoponeratoxin from the giant ant Dinoponera quadriceps venom, against carbapenem-resistant bactéria
Autor(es): Lima, Hilania Valéria Doudou
Cavalcante, Carolina Sidrim de Paula
Rádis-Baptista, Gandhi
Palavras-chave: Peptídeos;Citotóxicos;Antimicrobianos
Data do documento: 2020
Instituição/Editor/Publicador: Toxicon
Citação: LIMA, Hilania Valéria Doudou; CAVALCANTE, Carolina Sidrim de Paula; RÁDIS-BAPTISTA, Gandhi. Antimicrobial activity of synthetic Dq-3162, a 28-residue ponericin G-like dinoponeratoxin from the giant ant Dinoponera quadriceps venom, against carbapenem-resistant bactéria.Toxicon, v. 187, 2020.Disponível em: https://doi.org/10.1016/j.toxicon.2020.08.015. Acesso em: 21 jul. 2021
Abstract: D. quadriceps comprises a rich blend of bioactive peptides that includes structures related to at least five classes of antimicrobial peptides. In the present study, two representative synthetic peptides, sDq-2562 and sDq-3162, belonging to the ponericin-like dinoponeratoxin family, were evaluated for their microbicide activity against antibiotic-resistant bacteria. The most effective peptide, the 28-residue sDq-3162 displayed a significant bacteriostatic and bactericidal effect with minimal inhibitory concentrations (MICs) between 5 μM and 10 μM (15.6 μg mL􀀀 1 and 31.2 μg mL􀀀 1), according to the strain of drug-resistant bacteria tested. In combination with conventional antibiotics, sDq-3162 displayed in vitro synergistic effects, reducing the MICs of antibiotics for more than 2-log against clinical isolates of carbapenem-resistant Acinetobacter baumannii, Klebsiella pneumoniae and Pseudomonas aeruginosa, with low cytotoxicity to human erythrocytes, in vitro. Since the development of molecules to circumvent the spread of antibiotic-resistant bacteria is demanding, ant venom peptides arise as useful molecular resources to contribute with the antimicrobial arsenal and therapeutic strategies to fight clinically relevant microbial infections.
URI: http://www.repositorio.ufc.br/handle/riufc/59683
ISSN: 0041-0101
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