Anti-staphylococcal, antibiofilm and trypanocidal activities of CrataBL encapsulated into liposomes: Lectin with potential against infectious diseases

The present study aimed to evaluate the anti-staphylococcal, antibiofilm, cytotoxicity and trypanocidal activity, mechanisms of parasite death and immunomodulatory effect of CrataBL encapsulated into liposomes (CrataBL-Lipo). CrataBL-Lipo were prepared by the freeze-thaw technique and characterized....

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Veröffentlicht in:Microbial pathogenesis 2024-11, Vol.196, p.107007, Article 107007
Hauptverfasser: Almeida Campos, Luís André de, Costa Junior, Sérgio Dias da, Santos, João Victor de Oliveira, Souza, Zion Nascimento de, da Silva, Carlos Eduardo Sales, Cristovão-Silva, Ana Catarina, Brelaz-de-Castro, Maria Carolina Accioly, Pereira, Valéria Rêgo Alves, Paiva, Patrícia Maria Guedes, Santos Correia, Maria Tereza dos, Santos-Magalhães, Nereide Stela, Cavalcanti, Isabella Macário Ferro
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Sprache:eng
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Zusammenfassung:The present study aimed to evaluate the anti-staphylococcal, antibiofilm, cytotoxicity and trypanocidal activity, mechanisms of parasite death and immunomodulatory effect of CrataBL encapsulated into liposomes (CrataBL-Lipo). CrataBL-Lipo were prepared by the freeze-thaw technique and characterized. Anti-staphylococcal and antibiofilm activities of CrataBL and CrataBL-Lipo were evaluated against standard and clinical strains of Staphylococcus aureus susceptible and resistant. Thus, broth microdilution method was performed to determine the Minimum Inhibitory Concentration (MIC). Antibiofilm activity at subinhibitory concentrations was evaluated using the crystal violet staining method. Cytotoxicity of CrataBL-Lipo was verified in L929 fibroblasts and J774A.1 macrophages by determining the inhibitory concentration necessary to kill 50 % of cells (IC50). Trypanocidal activities of CrataBL-Lipo was evaluated in Trypanosoma cruzi and the efficacy was expressed as the concentration necessary to kill 50 % of parasites (EC50). The mechanisms of parasite death and immunomodulatory effect of CrataBL-Lipo were evaluated using flow cytometry analysis. CrataBL-Lipo presented Ø of 101.9 ± 1.3 nm (PDI = 0.245), ζ of +33.8 ± 1.3 mV and %EE = 80 ± 0.84 %. CrataBL-Lipo presented anti-staphylococcal activity (MIC = 0.56 mg/mL to 0.72 mg/mL). CrataBL-Lipo inhibited 45.4 %–75.6 % of biofilm formation. No cytotoxicity of CrataBL-Lipo was found (IC50 > 100 mg/L). CrataBL-Lipo presented EC50 of 1.1 mg/L, presenting autophagy, apoptosis and necrosis as death profile. In addition, CrataBL-Lipo reduced the production of IL-10 and TNF-α levels, causing an immunomodulatory effect. CrataBL-Lipo has a therapeutic potential for the treatment of staphylococcal infections and Chagas disease exhibiting a high degree of selectivity for the microorganism, and immunomodulatory properties. [Display omitted] •CrataBL-Lipo presented the physicochemical characteristics appropriate for in vivo application.•CrataBL-Lipo inhibited bacterial growth, prevented and eradicated biofilm produced by Staphylococcus aureus strains.•CrataBL-Lipo exhibits EC50 of 1.1 μg/ml.•CrataBL-Lipo induces parasite death by autophagy, apoptosis and necrosis pathways.•CrataBL-Lipo revealed immunomodulatory effects with reduction of IL-10 and TNF-α levels.
ISSN:0882-4010
1096-1208
1096-1208
DOI:10.1016/j.micpath.2024.107007