Term
| Which cytokines appear early to stimulate monocytes & granulocytes to leave the bloodstream? |
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Definition
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Term
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Definition
| Bind to proteins on the surface of PMNs causing them to bind loosely to endothelium - produce integrins |
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Term
| Define the role of integrins |
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Definition
| Bind ICAMS (intercellular adhesion molecules) to generate tighet attachment between PMNs and endothelial cells - thus slowing and stopping PMNs |
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Term
| What are the 3 types of cells in host defenses? |
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Definition
1. auxiliary cells (mast, platelets, basophil) 2. phagocytes (dendridic, monocyte, PMNs, eosinophil) 3. lymphocytes (B and T cells) |
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Term
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Definition
Features of Gram + Bacteria
- TA
- Thick Peptidoglycan
- 1 membrane
- More susceptible to antibiotics that directly target the cell wall
- Less susceptible to lysis
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Term
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Definition
chemoattractant
Peptide that attracts PMNs to site where bacteria are growing |
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Term
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Definition
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Term
| LPS is associated with which toll like receptor? |
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Definition
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Term
| What PAMPS respond in the cytosol? |
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Definition
NLR - bacterial lipid/cell wall
RLR - viral RNA |
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Term
| What do NODs, NLRs, RIGs do? |
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Definition
| recognize nucleic acid, bacterial cell wall, flagellin, other PAMPs |
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Term
| TLRs 1, 2, 5, and 6 use the adaptor protein ____________ & activate the transcription factors _______ & _______. |
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Definition
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Term
| TLR3 uses the adaptor protein _______ and activates the _______ & ______ transcription factors. |
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Definition
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Term
What TLR can activate both complement pathways?
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Definition
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Term
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Definition
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Term
| how long to monocytes live? |
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Definition
| can be years in bloodstream |
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Term
| Kupffer, alveolar and speen are all types of what cell? |
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Definition
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Term
What is complement? What are the downstream consequences of complement activation?
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Definition
– Series of protein that circulate in an inactive form. – Once activated: recruit phagocytes (PMNs), promote phagocytosis (opsonize), promote inflammation, and can lyse bacteria |
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Term
| A series of proteins that circulate in plasma in an inactive form - goal is to rapidly contain infection |
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Definition
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Term
| how do we keep bacteria out? |
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Definition
•Physical barriers to infection
–Skin
–Mucosal surfaces of GI tract, the respiratory tract, the eyes
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Term
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Definition
Cysteine-rich peptides with 3 disulfide bonds.
•Epithelial cells and granules of neutrophils and Paneth cells (crypts of the small intestine)
•Cell associated or secreted
•Kill fungi and bacteria by disruption of the microbial membrane
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Term
What is Koch's 1st postulate?
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Definition
| The microbe/pathogen must be associated with symptoms of disease and present at the site of infection |
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Term
| What is Koch's 2nd Postulate? |
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Definition
| The microbe must be isolated from lesions of the disease and grown as a pure culture |
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Term
| What is Koch's 3rd Postulate? |
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Definition
| A pure culture of the microbe, when inoculated to a susceptible host, must reproduce the disease in the experimental host. |
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Term
| What is Koch's 4th Postulate? |
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Definition
| The microbe must be reisolated from the experimentally infected host |
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Term
| What is Koch's 5th (prosposed) Postulate? |
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Definition
| Elimination of the disease-causing microbe or prevention of exposure of the host to the microbe should eliminate or prevent disease |
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Term
What are Koch’s Molecular postulates?
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Definition
1. Virulence gene should only be found in disease causing strains of bacteria, not in avirulent varients
2. The gene should be "isolated" by cloning
3. Disruption of the gene should reduce virulence (attenutation)
4. Introduction of th cloned gene avirulent strain should render new strain virulent. Most stringent when complementation of original mutation with wt gene restores virulence in mutant strain. |
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Term
| What type of cells produce MHC-1 and what do they target? |
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Definition
| all nucleated cells & intracellular bacteria (cytosolic) |
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Term
| What type of cells produce MHC-II and what do they target? |
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Definition
Macrophages, DCs, and other APCS
Target: Extracellular bacteria |
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Term
| What is an APC and what are the 3 types of APCS? |
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Definition
antigen-presenting cell
macrophages, DCs, and B cells |
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Term
| Describe the MHC-II Pathway |
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Definition
| Endocytosis of protein and processed into a peptide which displaces the invariant chain of MHC-II, transported to surface and binds to TCR & CD4 of a CD4+ T cell. |
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Term
| Describe the MHC-I pathway |
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Definition
| A proteosome processes anigen in the cytosol & transports them to the ER where they enter via TAP and bind to a MHC-I. Then they are transported to the surface and bind to the TCR & CD8 of a CD8+ T cell |
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Term
| MHC-II bound to antigen peptides stimulate what type of T cells? |
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Definition
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Term
| Peptide MHC-I complex stimulate what type of T cell? |
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Definition
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Term
| T-helper cells produce and activate what? |
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Definition
Produce: IFN-y
Activate: macrophages
Stimulate (Th2): B cells to produce antibodies |
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Term
| What type of antigen would a CD1 molecule present? |
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Definition
Lipid or glycolipid
-ex. Mycobacterium tuberculosis |
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Term
| What does TCR & CTL stand for? |
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Definition
| T cell receptor & cytotoxic T lymphocyte |
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Term
| what differeniates Th0 cells into Th1 and what is Th1 used for? |
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Definition
PMNs → IL-12 which stimulates NK cells → IFN-y
Use: CTL activation, inflammation
CONTROLS INTRACELLULAR BACTERIA
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Term
| what differeniates Th0 cells into Th2 and what is Th2 used for? |
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Definition
IL-4
Use: activate eosinophils, IgG1, IgE for opsonization & some downregulation
Clears EXTRACELLULAR bacteria, parasites (metazoal) |
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Term
| For bacteria what process is the key to their success as a pathogen. |
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Definition
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Term
Mech. of Genetic Change & Diversification in Bacteria
What are some examples of slow vs rapid processes?
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Definition
slow: point mutations, gene duplication (evolutionary processes)
rapid: phase variation (slipped strand synethesis), antigenic variation (gene shuffling) conjugation, transduction |
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Term
| What is phase variation, how does it help bacteria, and list some mechanims? |
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Definition
- Regulatory mechanism for rapid alteration of bacterial gene expression (usually virulence factors)
- Allows for quick response to varying environments and conditions
Several mechanisms:
–Promoter inversion
–Slipped-strand synthesis
–Gene conversion
–Promoter methylation
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Term
| What enzyme catalyzes PROMOTER INVERSION in Salmonella? |
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Definition
ENZYME: hin (DNA invertase)
Promoter controls switch from H1 to H2 flagellin protein and back again by releasing a repressor
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Term
| what type of bacteria usegene conversion and what is it? |
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Definition
Neisseria
Carry silent copies of gene which can be incorporated into active gene
Allows permanent change of pilE |
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Term
what type of bacteria use promoter methylation?
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Definition
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Term
Define slipped-strand synthesis and give example of what bacteria use it.
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Definition
It's a reversible mutation (causes frameshift) to turn on/off toxin & other virulence factors
bordatella |
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Term
| What is HGT stand for and what are some advantages this gives to bacteria? |
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Definition
Horizontal gene transfer
-ways to acquire new genes in a matter of hour (anbiotic resistance, toxins)
-contribues to genome variability
- Transformation
- Conjugation
- Transposons
- Transduction
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Term
| how is a pathogenecity island acquired and what does this do for bacteria? |
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Definition
through HGT
Improves virulence factors (adhesion) |
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Term
| What is a "naturally competent" bacteria? Describe a famous experiment used that discovered this mode of transformation. |
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Definition
DNA taken up directly by cells (usually linear, not plasmids)
Streptoccuspneumoniae
Griffith gave R and S strain to mice found that live R strains can transform heat killed S strain = mouse dies.
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Term
| What is bacterial sex called? |
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Definition
| Conjugation (need sex pili, and conjugation bridge) |
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Term
| What are the requirements for bacterial infection & survival within a host? |
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Definition
-attach to host (COLONIZATION)
-evade innate & adaptive
outcompete commensals
-aquire limiting nutrients (iron)
-transmit to new host |
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Term
| how do bacteria evade host defenses? |
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Definition
extracellular: posess virulence factors that prevent uptake & destruction by phagocytes
intracellular: promote factors to allow survival in inhospitable environment
Or balance between location and regulate virulence factor expression |
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