MycoBiomDB – Record Details (MyCo_7161)

Biomarker Record Details

Database ID: MyCo_7161
DB IDMyCo_7161
TitleEndocytic Markers Associated with the Internalization and Processing of Aspergillus fumigatus Conidia by BEAS-2B Cells
Year2019
PMID30728282
Fungal Diseases involvedAspergillus fumigatus infection
Associated Medical ConditionNone
GenusAspergillus
Speciesfumigatus
OrganismAspergillus fumigatus
Ethical StatementAll protocols involving animals were approved by the Institutional Animal Care and Use Committee at Virginia Tech and in compliance with Public Health Service Policy (PHS [approval no. 16-085]).
Site of InfectionNone
Opportunistic invasiveInvasive/Opportunistic
Sample typeBiopsy
Sample sourceExtracted tissue
Host GroupAnimal
Host Common nameMice
Host Scientific nameMus musculus
Biomarker NameCaveolin
Biomarker Full NameCaveolin
Biomarker TypeDiagnostic
BiomoleculeProtein
Geographical LocationUSA
CohortNone
Cohort No.None
Age GroupNone
P ValueNone
SensitivityNone
SpecificityNone
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismAspergillus fumigatus is an opportunistic fungal pathogen capable of invasive pul- monary infection in a diverse array of immunocompromised individuals. Chronic exposure to A. fumigatus may also result in the development and progression of an allergic response, the most severe being acute bronchopulmonary aspergillosis (ABPA). An allergic response occurs predominately in individuals with asthma or cystic fibrosis. A. fumigatus conidia are found abundantly throughout nature and the built environment, making exposure invariable. Most inhaled conidia are thought to be removed by mucociliary clearance in respiring organisms. However, A. fumigatus conidia can easily bypass mucociliary clearance and infiltrate lung alveoli due to their small size (2 to 3 m in diameter). Airway epithelial cells (AECs) make up a large percentage of the pulmonary-air interface and are thought to play an important role in initial conidial recognition, processing, and immune signaling. There is a need to mechanistically understand how A. fumigatus conidia are processed by AECs.
TechniqueAnalytic
Analysis MethodWestern Blotting
ELISA kitsNone
Assay DataNone
Validation Techniques usedWestern Blotting, Cell-line-based conidial challenge assays
Up Regulation Down RegulationPositive
Sequence DataNone
External LinkNone