<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14</volume><submitter>Yi W</submitter><pubmed_abstract>&lt;i>Aspergillus fumigatus&lt;/i> keratitis is a potential blinding disease associated with &lt;i>A. fumigatus&lt;/i> invasion and excessive inflammatory response. Benzyl isothiocyanate (BITC) is a secondary metabolite with broad antibacterial and anti-inflammatory activity extracted from cruciferous species. However, the role of BITC in &lt;i>A. fumigatus&lt;/i> keratitis has not been discovered yet. This study aims to explore the antifungal and anti-inflammatory effects and mechanisms of BITC in &lt;i>A. fumigatus&lt;/i> keratitis. Our results provided evidences that BITC exerted antifungal effects against &lt;i>A. fumigatus&lt;/i> by damaging cell membranes, mitochondria, adhesion, and biofilms in a concentration-dependent manner. &lt;i>In vivo&lt;/i>, fungal load and inflammatory response including inflammatory cell infiltration and pro-inflammatory cytokine expression were reduced in BITC-treated &lt;i>A. fumigatus&lt;/i> keratitis. Additionally, BITC significantly decreased Mincle, IL-1β, TNF-α, and IL-6 expression in RAW264.7 cells that stimulated by &lt;i>A. fumigatus&lt;/i> or Mincle ligand trehalose-6,6-dibehenate. In summary, BITC possessed fungicidal activities and could improve the prognosis of &lt;i>A. fumigatus&lt;/i> keratitis by reducing fungal load and inhibiting the inflammatory response mediated by Mincle.</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>1119568</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9978348</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Benzyl isothiocyanate improves the prognosis of &lt;i>Aspergillus fumigatus&lt;/i> keratitis by reducing fungal load and inhibiting Mincle signal pathway.</pubmed_title><pmcid>PMC9978348</pmcid><pubmed_authors>Chi M</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Diao W</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Qi Y</pubmed_authors><pubmed_authors>Gu L</pubmed_authors><pubmed_authors>Zhao G</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Yin M</pubmed_authors><pubmed_authors>Yi W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Benzyl isothiocyanate improves the prognosis of &lt;i>Aspergillus fumigatus&lt;/i> keratitis by reducing fungal load and inhibiting Mincle signal pathway.</name><description>&lt;i>Aspergillus fumigatus&lt;/i> keratitis is a potential blinding disease associated with &lt;i>A. fumigatus&lt;/i> invasion and excessive inflammatory response. Benzyl isothiocyanate (BITC) is a secondary metabolite with broad antibacterial and anti-inflammatory activity extracted from cruciferous species. However, the role of BITC in &lt;i>A. fumigatus&lt;/i> keratitis has not been discovered yet. This study aims to explore the antifungal and anti-inflammatory effects and mechanisms of BITC in &lt;i>A. fumigatus&lt;/i> keratitis. Our results provided evidences that BITC exerted antifungal effects against &lt;i>A. fumigatus&lt;/i> by damaging cell membranes, mitochondria, adhesion, and biofilms in a concentration-dependent manner. &lt;i>In vivo&lt;/i>, fungal load and inflammatory response including inflammatory cell infiltration and pro-inflammatory cytokine expression were reduced in BITC-treated &lt;i>A. fumigatus&lt;/i> keratitis. Additionally, BITC significantly decreased Mincle, IL-1β, TNF-α, and IL-6 expression in RAW264.7 cells that stimulated by &lt;i>A. fumigatus&lt;/i> or Mincle ligand trehalose-6,6-dibehenate. In summary, BITC possessed fungicidal activities and could improve the prognosis of &lt;i>A. fumigatus&lt;/i> keratitis by reducing fungal load and inhibiting the inflammatory response mediated by Mincle.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-21T23:51:06.282Z</modification><creation>2025-04-05T19:15:23.841Z</creation></dates><accession>S-EPMC9978348</accession><cross_references><pubmed>36876115</pubmed><doi>10.3389/fmicb.2023.1119568</doi></cross_references></HashMap>