Target type: biologicalprocess
Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus from a Gram-positive bacterium. [PMID:23664307]
The response to Gram-positive bacteria is a complex and multifaceted process that involves a coordinated effort by the host's innate and adaptive immune systems. Upon encountering Gram-positive bacteria, the host initiates a series of events aimed at recognizing, containing, and eliminating the invading pathogens.
**Recognition:**
- Pattern Recognition Receptors (PRRs): The immune system recognizes Gram-positive bacteria through PRRs, which are specialized receptors expressed on immune cells. These PRRs bind to specific molecular patterns present on the bacterial surface, such as peptidoglycan, lipoteichoic acid (LTA), and flagellin.
- Toll-like receptors (TLRs): TLR2 and TLR4 are key TLRs involved in recognizing Gram-positive bacteria. TLR2 specifically recognizes peptidoglycan and LTA, while TLR4 recognizes LTA and other bacterial components.
**Initiation of Immune Response:**
- Activation of signaling pathways: Upon binding to PRRs, signaling pathways are activated within the immune cells. These pathways lead to the production of various signaling molecules, including cytokines and chemokines.
- Cytokine and chemokine production: Cytokines like TNF-α, IL-1β, and IL-6 are released, triggering inflammation and activating other immune cells. Chemokines attract neutrophils and macrophages to the site of infection.
**Recruitment of Immune Cells:**
- Neutrophils: These are the first line of defense against Gram-positive bacteria. They are recruited to the site of infection by chemokines and phagocytose the bacteria.
- Macrophages: Macrophages also phagocytose bacteria and present bacterial antigens to T lymphocytes, initiating the adaptive immune response.
**Adaptive Immune Response:**
- Antigen presentation: Macrophages and dendritic cells present bacterial antigens to T lymphocytes, leading to activation of specific T cells.
- T helper (Th) cells: Th1 cells produce cytokines that stimulate the production of antibodies and activate macrophages.
- B cells: B cells differentiate into plasma cells that produce antibodies specific to bacterial antigens. These antibodies neutralize the bacteria, promote phagocytosis by immune cells, and activate the complement system.
**Effector Mechanisms:**
- Phagocytosis: Neutrophils and macrophages engulf and destroy bacteria within their phagosomes.
- Complement activation: The complement system is a cascade of proteins that can directly kill bacteria, promote inflammation, and facilitate phagocytosis.
- Antibody-dependent cell-mediated cytotoxicity (ADCC): Antibodies can bind to bacteria and target them for destruction by natural killer (NK) cells.
**Resolution of Infection:**
- Clearance of bacteria: The immune response eventually eliminates the bacteria, leading to resolution of the infection.
- Tissue repair: The damaged tissue is repaired, and the immune system returns to its resting state.
This detailed response provides a comprehensive overview of the biological processes involved in the response to Gram-positive bacteria. The process is complex and involves multiple cell types, signaling pathways, and effector mechanisms. The successful response to Gram-positive bacteria depends on the coordinated action of both innate and adaptive immunity.'
"
Protein | Definition | Taxonomy |
---|---|---|
Cadherin-1 | A cadherin-1 that is encoded in the genome of human. [PRO:WCB, UniProtKB:P12830] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
salvin | salvin: a biocyclic diterpenoid; from sage and rosemary (Lamiaceae) | abietane diterpenoid; carbotricyclic compound; catechols; monocarboxylic acid | angiogenesis modulating agent; anti-inflammatory agent; antineoplastic agent; antioxidant; apoptosis inducer; food preservative; HIV protease inhibitor; plant metabolite |
toxoflavin | toxoflavin : A pyrimidotriazine that is 1,6-dimethyl-1,5,6,7-tetrahydropyrimido[5,4-e][1,2,4]triazine with oxo groups at positions 5 and 7. toxoflavin: azapteridine antibiotic; structure | carbonyl compound; pyrimidotriazine | antibacterial agent; antineoplastic agent; apoptosis inducer; bacterial metabolite; toxin; virulence factor; Wnt signalling inhibitor |
cercosporin | cercosporin : An organic heterohexacyclic compound that is perylo[1,12-def][1,3]dioxepine-6,11-dione substituted by hydroxy groups at positions 5 and 12, by methoxy groups at positions 7 and 10, and by 2-hydroxypropyl groups at positions 8 and 9 (the R,R-stereoisomer). It is a phytotoxin which was first isolated from the pathogenic soybean fungus, Cercospora kikuchii and later found in multiple members of the genus Cercospora. cercosporin: phyytotoxin from Cercospora beticola Sacc; posses photodynamic action on mice, bacteria & plants | ||
ucn 1028 c | calphostin C: structure given in first source; isolated from Cladosporium cladosporioides |