A Derivative of Butyric Acid, the Fermentation Metabolite of Staphylococcus epidermidis , Inhibits the Growth of a Staphylococcus aureus Strain Isolated from Atopic Dermatitis Patients
The microbiome is a rich source of metabolites for the development of novel drugs. Butyric acid, for example, is a short-chain fatty acid fermentation metabolite of the skin probiotic bacterium ( ). Glycerol fermentation of resulted in the production of butyric acid and effectively hindered the grow...
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Published in | Toxins Vol. 11; no. 6; p. 311 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
31.05.2019
MDPI |
Subjects | |
Online Access | Get full text |
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Summary: | The microbiome is a rich source of metabolites for the development of novel drugs. Butyric acid, for example, is a short-chain fatty acid fermentation metabolite of the skin probiotic bacterium
(
). Glycerol fermentation of
resulted in the production of butyric acid and effectively hindered the growth of a
(
) strain isolated from skin lesions of patients with atopic dermatitis (AD) in vitro and in vivo. This approach, however, is unlikely to be therapeutically useful since butyric acid is malodorous and requires a high concentration in the mM range for growth suppression of AD
. A derivative of butyric acid, BA-NH-NH-BA, was synthesized by conjugation of two butyric acids to both ends of an -NH-O-NH- linker. BA-NH-NH-BA significantly lowered the concentration of butyric acid required to inhibit the growth of AD
. Like butyric acid, BA-NH-NH-BA functioned as a histone deacetylase (HDAC) inhibitor by inducing the acetylation of Histone H3 lysine 9 (AcH3K9) in human keratinocytes. Furthermore, BA-NH-NH-BA ameliorated AD
-induced production of pro-inflammatory interleukin (IL)-6 and remarkably reduced the colonization of AD
in mouse skin. These results describe a novel derivative of a skin microbiome fermentation metabolite that exhibits anti-inflammatory and
bactericidal activity. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2072-6651 2072-6651 |
DOI: | 10.3390/toxins11060311 |