Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/70211
Title: Unveiling the properties of thai stingless bee propolis via diminishing cell wall-associated cryptococcal melanin and enhancing the fungicidal activity of macrophages
Authors: Ketsaya Mamoon
Patcharin Thammasit
Anupon Iadnut
Kuntida Kitidee
Usanee Anukool
Yingmanee Tragoolpua
Khajornsak Tragoolpua
Keywords: Biochemistry, Genetics and Molecular Biology
Immunology and Microbiology
Medicine
Pharmacology, Toxicology and Pharmaceutics
Issue Date: 1-Jul-2020
Abstract: © 2020 by the authors. Licensee MDPI, Basel, Switzerland. . Cryptococcus neoformans, a life-threatening human yeast pathogen, has the ability to produce melanin, which is one of the common virulence factors contributing to cryptococcal pathogenesis. This virulence factor is closely associated with the cryptococcal cell wall, specifically chitin and chitosan polysaccharides, a complex structure that is essential for maintaining cellular structure and integrity. In this study, we aim to investigate the effects of two stingless bee (SLB) propolis from Tetragonula laeviceps and Tetrigona melanoleuca against cell wall-associated melanin in C. neoformans, and its immune response in RAW 264.7 macrophage. The ethanolic extract of SLB propolis (EEP) has strongly exhibited anti-cryptococcal activity. Moreover, EEP from both sources reduced chitin/chitosan and melanin production against C. neoformans in a dose-dependent manner. Likewise, the mRNA expression level of CDA1, IPC1-PKC1 and LAC1 genes involved in the cryptococcal melanization pathway was significantly decreased at 2 mg/mL in EEP treatment. Additionally, pretreatment with EEP prior to yeast infection dramatically reduced intracellular replication of C. neoformans in RAW 264.7 macrophages in a dose-dependent manner. This study might be a new insight to use a natural powerful source, not only acting to target cell wall-associated molecules, but also being capable to explore a novel strategy by which dysregulation of these molecules leads to promote immunomodulatory activity.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85088528493&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/70211
ISSN: 20796382
Appears in Collections:CMUL: Journal Articles

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