Sterols
Lanosterol
Antifungal Agents
Nystatin
Drug Resistance, Fungal
Sterol 14-Demethylase
Candida albicans
Saccharomyces cerevisiae
Cholestanes
Fluconazole
Amphotericin B
Ketoconazole
Dehydrocholesterols
Saccharomyces
Steroid Isomerases
Squalene Monooxygenase
Farnesyl-Diphosphate Farnesyltransferase
Natamycin
Filipin
Fungicides, Industrial
Oxidoreductases
Gene Expression Regulation, Fungal
Naphthalenes
Allylamine
Methyltransferases
Ergocalciferols
Clotrimazole
Lipid Bilayers
Fungi
Cholesterol
1,2-Dipalmitoylphosphatidylcholine
Mitosporic Fungi
Trichophyton
Agaricales
Candida
Chromatography, Thin Layer
Saccharomyces cerevisiae Proteins
Microbial Sensitivity Tests
Gas Chromatography-Mass Spectrometry
Ketosteroids
Candida glabrata
Sphingolipids
Trypanocidal Agents
Stachybotrys
Dimyristoylphosphatidylcholine
Calcium Sulfate
Aspergillus
Biomass
Membrane Fluidity
Itraconazole
Reishi
Anaerobiosis
Cell Membrane
Yeast, Dried
Mutation
Pimpinella
Chromatography, Gas
Poria
Drug Resistance, Multiple, Fungal
Thymol
Membrane Lipids
Intramolecular Transferases
Polyporus
Liposomes
Culture Media
Lipids
Sitosterols
Muramic Acids
Rhizopus
Vacuoles
Candidiasis
Molecular Structure
Membrane Microdomains
Ethylene Oxide
Cytochrome P-450 Enzyme System
Hydroxymethylglutaryl-CoA-Reductases, NADP-dependent
Cordyceps
Phosphatidylcholines
Tricarboxylic Acids
Agaricus
Penicillium
Cladosporium
Fatty Acids
Phospholipids
Temperature
Vitamin D
Aspergillus fumigatus
Spheroplasts
Membranes, Artificial
Drug Resistance, Microbial
Deuterium
Spectrum Analysis
RNA, Fungal
Magnetic Resonance Spectroscopy
Biosynthetic Pathways
Yeasts
Sterol Regulatory Element Binding Proteins
Gene Deletion
Amino Acid Transport Systems
Cell Membrane Permeability
Phenylalanine Ammonia-Lyase
Pichia
Trypanosoma cruzi
Hydroxymethylglutaryl CoA Reductases
Ethanol
Cryptococcus neoformans
Spectrophotometry, Ultraviolet
Calorimetry, Differential Scanning
Cotyledon
Carbon Isotopes
Molecular Sequence Data
Alkenes
Fusarium
Models, Chemical
Mycology
Phosphatidylethanolamines
Methylation
Anisotropy
Fermentation
Lipid Metabolism
Lovastatin
Membranes
Amiodarone
Oxygen
beta-N-Acetylhexosaminidases
Schizosaccharomyces
Acyltransferases
Spectrophotometry
Genetic Complementation Test
Acetates
Tryptophan
Membrane Fusion
Heme
Microsomes
Permeability
Chemistry
Cholesterol Side-Chain Cleavage Enzyme
Chemical Phenomena
Vacuolar Proton-Translocating ATPases
Cell Wall
Ultraviolet Rays
Mass Spectrometry
Chitosan
Pyrimidines
Membrane Proteins
Spectroscopy, Fourier Transform Infrared
Biological Transport
Structure-Activity Relationship
Mitochondria
Base Sequence
Homeostasis
Protein Transport
Gene Expression Profiling
Amino Acid Sequence
DNA Primers
Cloning, Molecular
Enzyme Inhibitors
HT29 Cells
Cell-Free System
Vesicular Transport Proteins
Membrane Transport Proteins
Adenosine Triphosphatases
Colony Count, Microbial
Transcriptional regulation of the squalene synthase gene (ERG9) in the yeast Saccharomyces cerevisiae. (1/600)
The ergosterol biosynthetic pathway is a specific branch of the mevalonate pathway. Since the cells requirement for sterols is greater than for isoprenoids, sterol biosynthesis must be regulated independently of isoprenoid biosynthesis. In this study we explored the transcriptional regulation of squalene synthase (ERG9) in Saccharomyces cerevisiae, the first enzyme dedicated to the synthesis of sterols. A mutant search was performed to identify genes that were involved in the regulation of the expression of an ERG9-lacZ promoter fusion. Mutants with phenotypes consistent with known sterol biosynthetic mutations (ERG3, ERG7, ERG24) increased expression of ERG9. In addition, treatment of wild-type cells with the sterol inhibitors zaragozic acid and ketoconazole, which target squalene synthase and the C-14 sterol demethylase respectively, also caused an increase in ERG9 expression. The data also demonstrate that heme mutants increased ERG9 expression while anaerobic conditions decreased expression. Additionally, the heme activator protein transcription factors HAP1 and HAP2/3/4, the yeast activator protein transcription factor yAP-1, and the phospholipid transcription factor complex INO2/4 regulate ERG9 expression. ERG9 expression is decreased in hap1, hap2/3/4, and yap-1 mutants while ino2/4 mutants showed an increase in ERG9 expression. This study demonstrates that ERG9 transcription is regulated by several diverse factors, consistent with the idea that as the first step dedicated to the synthesis of sterols, squalene synthase gene expression and ultimately sterol biosynthesis is highly regulated. (+info)The yeast multidrug resistance pump, Pdr5p, confers reduced drug resistance in erg mutants of Saccharomyces cerevisiae. (2/600)
Mutants of Saccharomyces cerevisiae bearing lesions in the ergosterol biosynthetic pathway exhibit a pleiotropic drug-sensitive phenotype. This has been reported to result from an increased permeability of the membranes of the mutant strains to different drugs. As disruption of the yeast multidrug resistance protein, Pdr5p, results in a similar pleiotropic drug-sensitive phenotype, the possibility that Pdr5p may be functioning with a reduced efficiency in these altered sterol backgrounds was examined. To do this, the function of Pdr5p in isogenic strains of S. cerevisiae that have disruptions in the late stages of the ergosterol biosynthesis pathway (ERG6, ERG2, ERG3, ERG4) was studied. A reduced ability of Pdr5p to confer resistance to different drugs in these strains was observed, which did not appear to be dependent solely on the permeability of the membrane towards the drug. A simultaneous examination was made of how the lipid composition might be altering the efficiency of Pdr5p by similar studies in strains lacking phosphatidylserine synthase (encoded by CHO1). The results indicated that the drug sensitivity of the erg strains is, to a significant extent, a result of the reduced efficiency of the Pdr5p efflux pump, and that the membrane environment plays an important role in determining the drug resistance conferred by Pdr5p. (+info)Comprehensive evaluation of isoprenoid biosynthesis regulation in Saccharomyces cerevisiae utilizing the Genome Reporter Matrix. (3/600)
Gene expression profiling is rapidly becoming a mainstay of functional genomic studies. However, there have been relatively few studies of how the data from expression profiles integrate with more classic approaches to examine gene expression. This study used gene expression profiling of a portion of the genome of Saccharomyces cerevisiae to explore the impact of blocks in the isoprenoid biosynthetic pathway on the expression of genes and the regulation of this pathway. Approximately 50% of the genes whose expression was altered by blocks in isoprenoid biosynthesis were genes previously known to participate in the pathway. In contrast to this simple correspondence, the regulatory patterns revealed by different blocks, and in particular by antifungal azoles, was complex in a manner not anticipated by earlier studies. (+info)Differential inhibitory effects of protoberberines on sterol and chitin biosyntheses in Candida albicans. (4/600)
The anti-Candida potentials of 12 Korean medicinal plants were explored: methanol extracts from Coptis rhizoma and Phellodendron amurense caused significant inhibition of growth of Candida albicans, Candida glabrata, Candida krusei and Candida parapsilosis. The predominant active components of the extracts were the protoberberines berberine and palmatine; the most potent inhibition of growth was exhibited by berberine on C. krusei (MIC <4 mg/L) and palmatine on C. parapsilosis (MIC 16 mg/L). Both berberine and palmatine inhibited the in-vivo rate of incorporation of L-[methyl-14C]methionine into C-24 of ergosterol in C. albicans (50% inhibition concentration (IC50 values), 25 microM and 300 microM, respectively); this result suggests that sterol 24-methyl transferase (24-SMT) is one of the cellular targets for the antifungal activity of the protoberberines. In-vitro 24-SMT activity in microsomes from the yeast growth form of C. albicans was inhibited by both berberine (inhibition constant (Ki) 232 microM) and palmatine (Ki 257 microM) in a non-competitive manner; inhibition of 24-SMT was more marked for the mycelial form than for the yeast growth form of this organism. Palmatine inhibited chitin synthase from both the yeast and mycelial growth phases of C. albicans in a non-competitive manner (Ki 780 microM). The effects of protoberberines, extracted from established medicinal plants, on both sterol and cell wall biosyntheses in pathogenic fungi indicate that the potential of these compounds, or their semi-synthetic derivatives, as a novel class of antifungal agents should be investigated more fully. (+info)Microscopic fungi in dwellings and their health implications in humans. (5/600)
The article reviews the quantitative and qualitative incidence of microscopic filamentous fungi in dwellings, methods for their detection, mycotoxins, glucans and volatile organic compounds produced by microscopic fungi in the indoor air of homes. Characteristics and properties of the most important species of fungi in dwellings (Alternaria spp., Aspergillus spp., Cladosporium spp., Fusarium spp., Penicillium spp., Stachybotrys spp., and Wallemia spp.) and the health problems of occupants of the "moldy homes are also discussed. (+info)The 2.1 A structure of an elicitin-ergosterol complex: a recent addition to the Sterol Carrier Protein family. (6/600)
Elicitins, produced by most of the phytopathogenic fungi of the genus Phytophthora, provoke in tobacco both remote leaf necrosis and the induction of a resistance against subsequent attack by various microorganisms. Despite the recent description of the three-dimensional crystal structure of cryptogein (CRY), the molecular basis of the interactions between Phytophthora and plants largely remains unknown. The X-ray crystal structure, refined at 2.1 A, of a ligand complexed, mutated CRY, K13H, is reported. Analysis of this structure reveals that CRY is able to encapsulate a ligand that induces only a minor conformational change in the protein structure. The ligand has been identified as an ergosterol by gas chromatographic analysis coupled with mass spectrometry analysis. This result is consistent with biochemical data that have shown that elicitins are a distinct class of Sterol Carrier Proteins (SCP). Data presented here provide the first structural description of the pertinent features of the elicitin sterol interaction and permit a reassessment of the importance of both the key residue 13 and the mobility of the omega loop for the accessibility of the sterol to the cavity. The biological implications thereof are discussed. This paper reports the first structure of a SCP/sterol complex. (+info)5-Fluorocytosine antagonizes the action of sterol biosynthesis inhibitors in Candida glabrata. (7/600)
The concentration-dependent antagonistic interaction between 5-fluorocytosine and a sterol biosynthesis inhibitor (SBI) was studied using intact cells and cell-free extracts of Candida glabrata. 5-Fluorocytosine promoted incorporation of radioactivity into 4-desmethylsterols (P < 0.01), and enhanced the relative and absolute increases of ergosterol (P < 0.05) in C. glabrata incubated aerobically with an SBI (miconazole or amorolfine). Further aerobic incubation of C. glabrata with combinations of a nucleic acid or protein synthesis inhibitor (rifampicin or chlortetracycline) and an SBI (miconazole) promoted a similar increase in ergosterol biosynthesis. In contrast, 5-fluorocytosine reduced the incorporation of radioactivity into 4,4-dimethylsterols (P < 0.01), but had no obvious effect on the absolute ergosterol level in C. glabrata incubated statically with miconazole. In cell-free extracts of cultures previously incubated with 5-fluorocytosine, ergosterol synthesis was less sensitive to the action of miconazole. Antagonism between 5-fluorocytosine and the SBI is thus mediated by a reversal of inhibition of intracellular ergosterol synthesis. The possible mechanisms underlying antagonism between 5-fluorocytosine and SBIs that inhibit different sites of the sterol biosynthesis pathway, as well as its clinical relevance to combination therapy, are discussed. (+info)Elicitins trap and transfer sterols from micelles, liposomes and plant plasma membranes. (8/600)
Using elicitins, proteins secreted by some phytopathogenic Oomycetes (Phytophthora) known to be able to transfer sterols between phospholipid vesicles, the transfer of sterols between micelles, liposomes and biological membranes was studied. Firstly, a simple fluorometric method to screen the sterol-carrier capacity of proteins, avoiding the preparation of sterol-containing phospholipidic vesicles, is proposed. The transfer of sterols between DHE micelles (donor) and stigmasterol or cholesterol micelles (acceptor) was directly measured, as the increase in DHE fluorescence signal. The results obtained with this rapid and easy method lead to the same conclusions as those previously reported, using fluorescence polarization of a mixture of donor and acceptor phospholipid vesicles, prepared in the presence of different sterols. Therefore, the micelles method can be useful to screen proteins for their sterol carrier activity. Secondly, elicitins are shown to trap sterols from purified plant plasma membranes and to transfer sterols from micelles to these biological membranes. This property should contribute to understand the molecular mechanism involved in sterol uptake by Phytophthora. It opens new perspectives concerning the role of such proteins in plant-microorganism interactions. (+info)Types of candidiasis:
1. Vulvovaginal candidiasis (VVC): a common infection that affects the vagina and vulva; symptoms include itching, burning, and abnormal discharge.
2. Oral thrush (OT): an infection that affects the mouth, often seen in infants and people with weakened immune systems; symptoms include white patches on the tongue and inside the cheeks.
3. Invasive candidiasis (IC): a severe infection that can spread throughout the body, often seen in people with weakened immune systems, such as those with HIV/AIDS or undergoing chemotherapy; symptoms include fever, chills, and difficulty breathing.
4. Candidal balanitis: an infection of the foreskin and glans of the penis; symptoms include redness, swelling, and pain.
5. Diaper rash: a common skin infection that affects infants who wear diapers; symptoms include redness, swelling, and irritability.
Causes and risk factors:
1. Overgrowth of Candida fungus due to an imbalance of the normal flora.
2. Use of antibiotics or steroids that can disrupt the balance of the body's natural flora.
3. Weakened immune system, such as in people with HIV/AIDS or undergoing chemotherapy.
4. Poor hygiene and sanitation.
5. Diabetes mellitus.
6. Pregnancy.
7. Obesity.
Diagnosis:
1. Physical examination and medical history.
2. Microscopic examination of a scraping or biopsy specimen.
3. Cultures of skin, blood, or other body fluids.
4. Polymerase chain reaction (PCR) or other molecular diagnostic techniques to detect the presence of the fungus.
Treatment:
1. Topical antifungal medications, such as clotrimazole, miconazole, or terbinafine, applied directly to the affected area.
2. Oral antifungal medications, such as fluconazole or itraconazole, for more severe infections or those that do not respond to topical treatment.
3. Antibiotics if there is a secondary bacterial infection.
4. Supportive care, such as pain management and wound care.
5. Proper hygiene and sanitation practices.
6. In severe cases, hospitalization may be necessary for intravenous antifungal medications and close monitoring.
Prevention:
1. Practice good hygiene and sanitation.
2. Avoid sharing personal items, such as towels or clothing.
3. Wash hands before touching the affected area.
4. Keep the affected area clean and dry.
5. Use of antifungal powders or sprays on the affected area.
6. Avoid using harsh soaps or cleansers that can irritate the skin.
7. Wear shoes in public areas to prevent exposure to fungal spores.
8. Avoid sharing bathing or showering facilities with others.
9. Dry thoroughly after bathing or swimming.
10. Use of antifungal medications as a prophylactic measure in high-risk individuals, such as those with weakened immune systems.
It's important to note that the best treatment and prevention strategies will depend on the specific type of fungus causing the infection, as well as the severity and location of the infection. It is essential to consult a healthcare professional for proper diagnosis and treatment.
The symptoms of aspergillosis depend on the location and severity of the infection. In the lungs, it may cause coughing, fever, chest pain, and difficulty breathing. In the sinuses, it can cause headaches, facial pain, and nasal congestion. In the brain, it can cause seizures, confusion, and weakness.
Aspergillosis is typically diagnosed through a combination of imaging tests such as chest X-rays, CT scans, and MRI scans, along with a biopsy to confirm the presence of Aspergillus fungi.
Treatment of aspergillosis depends on the severity and location of the infection. In mild cases, treatment may involve antifungal medications and supportive care such as oxygen therapy and pain management. In severe cases, treatment may require hospitalization and intravenous antifungal medications.
Preventive measures for aspergillosis include avoiding exposure to dusty or damp environments, managing chronic conditions such as asthma and COPD, and taking antifungal medications as prescribed.
Aspergillosis can be a serious condition, especially in people with weakened immune systems, such as those with cancer, HIV/AIDS, or taking immunosuppressive drugs. In severe cases, aspergillosis can lead to life-threatening complications such as respiratory failure, sepsis, and organ damage.
In conclusion, aspergillosis is a common fungal infection that can affect various parts of the body, and it can be serious and potentially life-threatening, especially in people with weakened immune systems. Early diagnosis and appropriate treatment are essential to prevent complications and improve outcomes.
Ergosterol
Ergosterol peroxide
Ergocalciferol
Hericium erinaceus
Cerevisterol
Phytosterol
Amanita caesarea
Terbinafine
Microsporum audouinii
Squalene
Lipid
Myclobutanil
Topical antifungal drugs
Lipopeptide
Calcium deficiency (plant disorder)
Sertaconazole
Beta-Sitosterol
Lichtheimia corymbifera
Steroid
Proteolipid
Ecklonia cava
Plant disease resistance
Episterol
Tolciclate
C-5 sterol desaturase
Mary Peters Fieser
Tolnaftate
Alternaria brassicicola
Amphotericin B
Nystatin
The genome and transcriptome of |i|Sarocladium terricola|/i| provide insight into ergosterol biosynthesis. | Front Cell Infect...
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Synthesis3
- Furthermore, transcriptome analyses of differentially expressed genes suggested that the ergosterol synthesis genes ERG3, ERG5, and ERG25 were significantly up-regulated in potato dextrose media. (bvsalud.org)
- A synthetic triazole antifungal agent that inhibits fungal cell growth by inhibiting the cytochrome P-450-dependent synthesis of ergosterol, a vital component of fungal cell membranes. (medscape.com)
- It blocks ergosterol synthesis by inhibiting the enzyme lanosterol 14-alpha-demethylase and sterol precursor accumulation. (medscape.com)
Sterols3
- Antifungal activity of amphotericin B results from its ability to insert itself into fungal cytoplasmic membrane at sites that contain ergosterol or other sterols. (medscape.com)
- Amphotericin B binds to sterols (eg, ergosterol) in the fungal cell membrane, causing intracellular components to leak with subsequent fungal cell death. (medscape.com)
- The accumulation of 14 alpha-methyl sterols correlates with the subsequent loss of ergosterol in the fungal cell wall and may be responsible for the fungistatic activity of econazole. (empr.com)
Lanosterol2
- It is a triazole antifungal that inhibits fungal CYP450-mediated 14 alpha-lanosterol demethylation, which is essential in fungal ergosterol biosynthesis. (medscape.com)
- This enzyme functions to convert lanosterol to ergosterol. (empr.com)
Yeast3
- Vitamin D2 is produced by UV irradiation of ergosterol, which occurs in molds, yeast, and higher-order plants. (cdc.gov)
- Ergosterol or provitamin D 2 is found in plants and yeast and has no antirachitic activity. (nih.gov)
- Additionally, aeration affected ergosterol formation in yeast cell membrane at high ethanol concentrations, whereas trehalose content under all conditions was not different. (ejbiotechnology.info)
Endotoxin4
- Personal exposure of dairy workers to dust, endotoxin, muramic acid, ergosterol, and ammonia on large-scale dairies in the high plains Western United States. (cdc.gov)
- To characterize the levels and types of exposures, 115 dairy workers grouped into three task categories on nine farm s in the high plains western United States underwent personal monitoring for inhalable dust, endotoxin, 3-hydroxy fatty acids (3- OHFA), muramic acid, ergosterol, and ammonia over one work shift. (cdc.gov)
- This study was among the first to concurrently evaluate occupational exposure to assayable endotoxin (lipid A), 3-hydroxy fatty acids or 3-OHFA (a chemical measure of cell bound and non-cell-bound endotoxins), muramic acid, ergosterol, and ammonia among workers on western U.S. dairies. (cdc.gov)
- Biological activity such as ergosterol, spore count, and endotoxin levels were higher on the first floor of the Hall of Education and in the Stadium Hall, both areas where high numbers of animals were housed. (cdc.gov)
Dust3
- Residential culturable fungi, (1-3, 1-6)-β-d-glucan, and ergosterol concentrations in dust are not associated with asthma, rhinitis, or eczema diagnoses in children. (nih.gov)
- In the homes of 198 multiple allergic case children and 202 controls in Sweden, we cultivated culturable fungi by directly plating dust, and quantified (1-3, 1-6)-β-D-glucan and ergosterol in dust samples from the child's bedroom. (nih.gov)
- Culturable fungi, (1-3, 1-6)-β-D-glucan, and ergosterol in dust were not associated with qualitative markers of indoor dampness or mold or indoor humidity. (nih.gov)
Binds2
- type is the antifungal agent amphotericin B, which binds to a specific molecule (ergosterol) found in fungal cells. (britannica.com)
- Fluconazole binds to the fungal p450 enzymes and stops the cells making ergosterol, the main component of the cell wall. (dermnetnz.org)
Concentrations1
- There were no differences in concentrations of the individual or the total summed culturable fungi, (1-3, 1-6)-β-D-glucan, and ergosterol between the controls and the multiple allergic case children, or individual diagnosis of asthma, rhinitis, or eczema. (nih.gov)
Light1
- It is created from viosterol, which in turn is created when ultraviolet light activates ergosterol. (hmdb.ca)
Found1
- Spore counts and ergosterol levels were consistent with the levels found in other studies where adverse health effects had occurred. (cdc.gov)
Double1
- We also determined that the ergosterol content of S. terricola was synthesized to nearly double levels when cultured in potato dextrose media compared to bean media (4509 mg/kg vs. 2382 mg/kg). (bvsalud.org)
Results1
- These results will help us to recognize metabolic pathway of ergosterol biosynthesis of S. terricloa comprehensivelly. (bvsalud.org)
Sterol4
- The sterol composition of Aspergillus fumigatus for the biosynthesis of ergosterol is of interest since this pathway is the target for many antifungal drugs in clinical use. (nih.gov)
- Also, sterols were analyzed in several A. fumigatus mutant strains deficient in enzymatic steps of the ergosterol biosynthesis pathway such as 14-alpha sterol demethylases (Cyp51A and Cyp51B) and C-5 sterol desaturases (Erg3A, Erg3B and Erg3C). (nih.gov)
- The analysis of the sterol composition in these mutant strains led to a better understanding of the ergosterol biosynthesis pathway in this important fungus. (nih.gov)
- All the azole antifungals inhibit the cytochrome P450-dependent, 14 alpha-demethylase, a key enzyme in the synthesis of ergosterol, the main sterol in most fungal cells. (nih.gov)
Synthesis2
- Blocks ergosterol synthesis by inhibiting squalene epoxidase. (medscape.com)
- Currently, representatives of two classes of EBI antifungals are available: the squalene epoxidase inhibitors and those that interfere with cytochrome P450-dependent ergosterol synthesis. (nih.gov)
Fungal cells1
- In a previous study, the team found that AmB initially binds a molecule called ergosterol on the outer membrane of fungal cells. (nih.gov)
Fungi10
- We examined associations of total fungi, hydrophilic fungi (requiring water activity ≥ 0.9) , and ergosterol with the health outcomes using logistic regression models. (medscape.com)
- In models adjusted for demographics, respiratory illnesses showed significant linear exposure-response relationships to total culturable fungi [interquartile range odds ratios (IQR-OR) = 1.37-1.72], hydrophilic fungi (IQR-OR = 1.45-2.19), and ergosterol (IQR-OR = 1.54-1.60) in floor and chair dusts. (medscape.com)
- Ergosterol levels in floor dust were significantly associated with epidemiologic asthma independent of culturable fungi (IQR-OR = 1.54-1.55). (medscape.com)
- Hydrophilic fungi and ergosterol as measures of fungal biomass may have promise as markers of risk of building-related respiratory diseases in damp indoor environments. (medscape.com)
- In this study we focused on examining associations of hydrophilic fungi and ergosterol with respiratory health outcomes among employees in a 20-story office building in the northeastern United States. (medscape.com)
- To find out which mechanism-the ergosterol binding itself or the subsequent channel formation-kills the fungi, the researchers created AmB-like compounds that could bind ergosterol without forming channels. (nih.gov)
- Residential culturable fungi, (1-3, 1-6)-β-d-glucan, and ergosterol concentrations in dust are not associated with asthma, rhinitis, or eczema diagnoses in children. (nih.gov)
- In the homes of 198 multiple allergic case children and 202 controls in Sweden, we cultivated culturable fungi by directly plating dust, and quantified (1-3, 1-6)-β-D-glucan and ergosterol in dust samples from the child's bedroom. (nih.gov)
- There were no differences in concentrations of the individual or the total summed culturable fungi, (1-3, 1-6)-β-D-glucan, and ergosterol between the controls and the multiple allergic case children, or individual diagnosis of asthma, rhinitis, or eczema. (nih.gov)
- Culturable fungi, (1-3, 1-6)-β-D-glucan, and ergosterol in dust were not associated with qualitative markers of indoor dampness or mold or indoor humidity. (nih.gov)
Cell1
- Ergosterol is essentially the fungal equivalent of cholesterol and is vital for fungal cell survival. (nih.gov)
Levels1
- Spore counts and ergosterol levels were consistent with the levels found in other studies where adverse health effects had occurred. (cdc.gov)
Similar1
- The scientists noted that both molecules shared a similar ergosterol binding arm, but that AmB alone had an element required for channel formation. (nih.gov)
Important1
- The ergosterol biosynthesis-inhibiting (EBI) antifungals constitute the most important group of compounds developed for the control of fungal diseases in man. (nih.gov)