MycoBiomDB – Record Details (MyCo_2346)

Biomarker Record Details

Database ID: MyCo_2346
DB IDMyCo_2346
TitleDetection of Rhizopus-specific antigen in human and murine serum and bronchoalveolar lavage
Year2020
PMID32060526
Fungal Diseases involvedMucormycosis
Associated Medical ConditionNone
GenusNone
SpeciesNone
OrganismNone
Ethical StatementThe experimental protocol was approved by the Animal Experiment Ethics Committee of Osaka City University, Japan.
Site of InfectionNone
Opportunistic invasiveOpportunistic
Sample typeBody fluid
Sample sourcebronchoalveolar lavage fluid (BALF)
Host GroupAnimal
Host Common nameMice
Host Scientific nameMus musculus
Biomarker NameRSA-specific rabbit monoclonal antibodies
Biomarker Full NameRhizopus-specific antigen (RSA)-specific rabbit monoclonal antibodies
Biomarker TypeDiagnostic
BiomoleculeProtein
Geographical LocationJapan
CohortFor examinations, mice were euthanized on days 1 to 4. On day 1, 5 control mice and 5 inoculated mice were euthanatized, on day 2, 3, 4, and 5 inoculated mice were euthanized.
Cohort No.None
Age GroupNone
P ValueNone
SensitivityNone
SpecificityNone
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismMucormycosis is an infection caused mainly by fungi, such as Rhizopus, Mucor, Rhizomucor, Lichtheimia, and Cunninghamella, which are widely found in the soil and on the surface of plants. Cases of mucormycosis are classified into six groups depending on the site of infection, namely, nasal cerebral, pulmonary, gastrointestinal, cutaneous, disseminated, and uncommon. Although mucormycosis is extremely rare in humans with normal immunity levels, it results in poor prognosis in immunocompromised patients, making it an important disease. Pulmonary mucormycosis occurs most frequently in patients with hematological malignancy. In order to improve its prognosis, treatment with single or multidrug combination antifungal agents, surgical removal of the lesion, and amelioration of the immunosuppressive state are necessary. Delayed diagnosis and treatment doubles the mortality compared to that associated with early treatment, which is especially important in patients with hematological malignancies. Thus, there is a need to develop early detection systems to improve the prognosis.
TechniqueELISA
Analysis MethodELISA Based
ELISA kitsNone
Assay DataNone
Validation Techniques usedELISA, Immunohistochemistry
Up Regulation Down RegulationIncrease
Sequence DataNone
External LinkNone