Page last updated: 2024-10-24

detection of fungus

Definition

Target type: biologicalprocess

The series of events in which a stimulus from a fungus is received and converted into a molecular signal. [GOC:hb]

Fungus detection is a complex biological process involving a series of steps initiated by the host's immune system and often assisted by symbiotic microorganisms. The process begins with recognition of fungal components by host immune cells, such as macrophages, neutrophils, and dendritic cells. This recognition can occur through various mechanisms:

1. **Pattern Recognition Receptors (PRRs):** These receptors, located on the surface of immune cells, bind to specific fungal molecules called Pathogen-Associated Molecular Patterns (PAMPs). Examples of PAMPs include:
* **β-glucans:** Found in the cell walls of many fungi.
* **Chitin:** A structural polysaccharide present in fungal cell walls.
* **Mannan:** A sugar molecule found in fungal cell walls.
* **Lipoproteins:** Lipid-protein complexes present in fungal membranes.

2. **Toll-like receptors (TLRs):** TLRs are a type of PRR that recognize specific PAMPs and trigger downstream signaling pathways leading to immune responses. For example, TLR2 recognizes zymosan, a component of fungal cell walls, while TLR4 recognizes fungal lipopolysaccharides (LPS).

3. **Complement System:** The complement system is a part of the innate immune system that can directly kill fungi or enhance the immune response. Certain complement proteins bind to fungal cell walls, triggering a cascade of events that lead to the lysis of fungal cells.

4. **Antigen Presentation:** Once fungal components are recognized, immune cells like dendritic cells process and present fungal antigens to T lymphocytes (T cells). This process activates specific T cells, which then orchestrate the immune response.

5. **Cytokine Production:** Activated immune cells release cytokines, signaling molecules that coordinate the immune response. Some key cytokines involved in fungal detection include:
* **Interleukin-1β (IL-1β):** Induces inflammation.
* **Tumor necrosis factor-α (TNF-α):** Contributes to inflammation and immune cell recruitment.
* **Interleukin-6 (IL-6):** Promotes immune cell differentiation and activation.

6. **Immune Cell Recruitment:** Cytokines attract various immune cells, including neutrophils, macrophages, and lymphocytes, to the site of infection. These cells engulf and destroy fungal cells through phagocytosis.

7. **Antibody Production:** B lymphocytes (B cells) produce antibodies specific to fungal antigens. These antibodies can neutralize fungal toxins, facilitate phagocytosis, and activate the complement system.

8. **Adaptive Immune Response:** The adaptive immune system develops memory cells specific to the invading fungus. This allows for a faster and more efficient response upon subsequent exposure to the same fungus.

The specific immune response to a particular fungus can vary depending on factors such as the fungal species, the host's immune status, and the site of infection. However, the fundamental mechanisms of recognition, activation, and response remain consistent.'
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Proteins (1)

ProteinDefinitionTaxonomy
Toll-like receptor 4A Toll-like receptor 4 that is encoded in the genome of human. [PRO:CNA, UniProtKB:O00206]Homo sapiens (human)

Compounds (5)

CompoundDefinitionClassesRoles
carvedilolcarbazoles;
secondary alcohol;
secondary amino compound
alpha-adrenergic antagonist;
antihypertensive agent;
beta-adrenergic antagonist;
cardiovascular drug;
vasodilator agent
methotrexatedicarboxylic acid;
monocarboxylic acid amide;
pteridines
abortifacient;
antimetabolite;
antineoplastic agent;
antirheumatic drug;
dermatologic drug;
DNA synthesis inhibitor;
EC 1.5.1.3 (dihydrofolate reductase) inhibitor;
immunosuppressive agent
parthenolidesesquiterpene lactonedrug allergen;
inhibitor;
non-narcotic analgesic;
non-steroidal anti-inflammatory drug;
peripheral nervous system drug
resatorvid
crx-526CRX-526: aminoalkyl-glucosaminide-phosphate; lipid A-mimetic with anti-inflammatory properties; structure in first source