Chemical composition of essential oils of Eugenia caryophylla and Mentha sp cf Piperita and their in vitro antifungal activities on six human pathogenic fungi

Background: Many fungal infections are responsible for human skin damages, to control their negative action, some aromatic and medicinal plants are traditionally used by local population in Cameroon. The present study was carried out to determine the chemical composition of essential oils of Eugenia caryophylla and Mentha sp cf piperita and their antifungal activity on some human pathogenic fungi.Materials and methods: Essential oils from Eugenia caryophylla and Mentha sp cf piperita were extracted by steam distillation using Clevenger apparatus and the antifungal activity was evaluated on six human pathogenic fungal strains; two yeasts (Candida albicans 1 and Candida albicans 2) and four dermatophytes (Tricophyton rubrum 1, T. rubrum 2, T. violaceum, and T. soudanensis) using modified broth microdilution method M27-A3 and M38-A respectively.Results: The essential oils obtained yielded of 5.9 for Eugenia caryophylla and 0.2% Mentha sp cf piperita respectively. The chemical composition was assigned by GC and GC/SM and showed that E. caryophylla was mainly composed of eugenol (80.0 %), E-caryophyllene (8.3%), and eugenol acetate (6.7%) while Mentha sp cf piperita was characterized by piperitone (67.5 %), menthol (10.0 %) and ß-phellandrene (5.8%). The result showed that essential oil of E. caryophylla exhibit the highest antifungal activity with MICs and MFC of 0.25μL/mL and 0.125μL/mL for filamentous fungi and MIC of 0.5 μL/mL for both yeast strains while MFC value was 1 μL/mL for one yeast strain and not determined for the second. MFCs Mentha sp cf piperita essential oil showed a weak activity with a MIC of 2.5 μL/mL on Tricophyton strains while no activity was exhibited on Candida albicans strains.Conclusion: The results of this work can be used to confirm their traditional uses and can also be proposed as natural ingredients to some industries to treat superficial infections.Keys words: Essential oil, Eugenia caryophylla, Mentha sp cf piperita, antifungal activity, Human pathogenic strains, fungistatic and fungicide

One-step immunopurification and lectinochemical characterization of the Duffy atypical chemokine receptor from human erythrocytes

Duffy antigen/receptor for chemokines (DARC) is a glycosylated seven-transmembrane protein acting as a blood group antigen, a chemokine binding protein and a receptor for Plasmodium vivax malaria parasite. It is present on erythrocytes and endothelial cells of postcapillary venules. The N-terminal extracellular domain of the Duffy glycoprotein carries Fya/Fyb blood group antigens and Fy6 linear epitope recognized by monoclonal antibodies. Previously, we have shown that recombinant Duffy protein expressed in K562 cells has three N-linked oligosaccharide chains, which are mainly of complex-type. Here we report a one-step purification method of Duffy protein from human erythrocytes. DARC was extracted from erythrocyte membranes in the presence of 1% n-dodecyl-β-D-maltoside (DDM) and 0.05% cholesteryl hemisuccinate (CHS) and purified by affinity chromatography using immobilized anti-Fy6 2C3 mouse monoclonal antibody. Duffy glycoprotein was eluted from the column with synthetic DFEDVWN peptide containing epitope for 2C3 monoclonal antibody. In this single-step immunoaffinity purification method we obtained highly purified DARC, which migrates in SDS-polyacrylamide gel as a major diffuse band corresponding to a molecular mass of 40–47 kDa. In ELISA purified Duffy glycoprotein binds anti-Duffy antibodies recognizing epitopes located on distinct regions of the molecule. Results of circular dichroism measurement indicate that purified DARC has a high content of α-helical secondary structure typical for chemokine receptors. Analysis of DARC glycans performed by means of lectin blotting and glycosidase digestion suggests that native Duffy N-glycans are mostly triantennary complex-type, terminated with α2-3- and α2-6-linked sialic acid residues with bisecting GlcNAc and α1-6-linked fucose at the core