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1.
Glycobiology ; 34(9)2024 Jul 26.
Article in English | MEDLINE | ID: mdl-39088584

ABSTRACT

The limited availability of efficient treatments for Candida infections and the increased emergence of antifungal-resistant strains stimulates the search for new antifungal agents. We have previously isolated a sunflower mannose-binding lectin (Helja) with antifungal activity against Candida albicans, capable of binding mannose-bearing oligosaccharides exposed on the cell surface. This work aimed to investigate the biological and biophysical basis of Helja's binding to C. albicans cell wall mannans and its influence on the fungicidal activity of the lectin. We evaluated the interaction of Helja with the cell wall mannans extracted from the isogenic parental strain (WT) and a glycosylation-defective C. albicans with altered cell wall phosphomannosylation (mnn4∆ null mutants) and investigated its antifungal effect. Helja exhibited stronger antifungal activity on the mutant strain, showing greater inhibition of fungal growth, loss of cell viability, morphological alteration, and formation of clusters with agglutinated cells. This differential biological activity of Helja was correlated with the biophysical parameters determined by solid phase assays and isothermal titration calorimetry, which demonstrated that the lectin established stronger interactions with the cell wall mannans of the mnn4∆ null mutant than with the WT strain. In conclusion, our results provide new evidence on the nature of the Helja molecular interactions with cell wall components, i.e. phosphomannan, and its impact on the antifungal activity. This study highlights the relevance of plant lectins in the design of effective antifungal therapies.


Subject(s)
Antifungal Agents , Candida albicans , Cell Wall , Antifungal Agents/pharmacology , Antifungal Agents/chemistry , Candida albicans/drug effects , Cell Wall/drug effects , Cell Wall/metabolism , Plant Lectins/chemistry , Plant Lectins/pharmacology , Helianthus/chemistry , Mannans/chemistry , Mannans/pharmacology , Mannans/metabolism , Microbial Sensitivity Tests
2.
J Plant Physiol ; 162(6): 618-24, 2005 Jun.
Article in English | MEDLINE | ID: mdl-16008084

ABSTRACT

Nonspecific lipid transfer proteins (nsLTPs) belong to a large family of plant proteins whose function in vivo remains unknown. In this research, we studied a LTP previously isolated from sunflower seeds (Ha-AP10), which displays strong antimicrobial activity against a model fungus. The protein is present during at least the first 5 days of germination, and tissue printing experiments revealed the homogeneous distribution of the protein in the cotyledons. Here we report that Ha-AP10 exerts a weak inhibitory effect on the growth of Alternaria alternata, a fungus that naturally attacks sunflower seeds. These data put into question the contribution of Ha-AP10 as an antimicrobial protein of direct effect on pathogenic fungus, and rather suggest a function related to the mobilization of lipid reserves. We also show that the levels of Ha-AP10 in germinating seeds increase upon salt stress, fungal infection and ABA treatment, indicating that it somehow participates in the adaptative responses of germinating sunflower seeds.


Subject(s)
Antifungal Agents/pharmacology , Carrier Proteins/biosynthesis , Carrier Proteins/physiology , Gene Expression Regulation, Developmental , Gene Expression Regulation, Plant , Helianthus/physiology , Plant Proteins/biosynthesis , Plant Proteins/physiology , Abscisic Acid/pharmacology , Alternaria/drug effects , Antifungal Agents/metabolism , Carrier Proteins/pharmacology , Germination , Plant Diseases/microbiology , Plant Proteins/pharmacology , Sodium Chloride/pharmacology
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