1/61
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced |
---|
No study sessions yet.
Disease
Type of illness w/ characteristic symptoms
Causes (4)
1. Genetic - genetic disorders
2. environmental - toxins/radiation
3. Pathogens - organisms and viruses
4. Prion - Proteins that cause other proteins to misfold
Pathogens
Microorganisms that pass from one infected organism to another, they enter, multiply, and cause harm
Pathogen Types (4)
1. Bacteria - tuberculosis, leprosy
2. Fungi - athlete's foot
3. Protista (single-celled prokaryote) - malaria, sleeping sickness
4. Viruses (non-living) - influenza, measles, ebola
First Line of Defense
includes skin and mucus membranes
Skin
physical barrier that keeps pathogens out, layer of dry/thick/dead cells containing keratin
Sabaceous Glands
secretes lactic acid to make skin slightly acidic and inhibit microbial growth
Mucus Membranes
protects internal structures (ex. esophagus, trachea, genitals)
they are ciliated and secrete mucus (to trap and swallow/expel)
Ciliated
property of mucus membranes, have little cilila to move stuff and remove pathogens via coughing
Lysozyme
mucus membrane contains these, they are antiseptic that causes lysis in bacteria cell walls
Blood Clotting (hemostasis)
repairs damaged blood vessels in a cut, prevents blood loss and limits pathogen entry
Platelets
First step of blood clotting, they are blood cell fragments that change structurally to form a temporary "plug" of sticky, semi-solid gel
*they release clotting factors that eventually form insoluble mesh (scab)*
Coagulation Cascade Process
1. inactive prothrombin becomes active thrombin
2. thrombin converts soluble fibrinogen to insoluble fibrin
3. fibrin forms a blood clot that traps cells and seals wound
4. when exposed to air, blood clot forms a scab
5. after damage repaired, plasmin dissolves clot and scab
Leukocytes
white blood cells
Second Line of Defense (2)
Non-specific - responds to broad array of pathogens
Non-adaptive - responds in the same way, every time
Phagocytes
type of leukocyte that patrols blood and eats pathogens via endocytosis
ex. macrophage
Endocytosis
process by which a cell takes material into the cell by infolding of the cell membrane
Histamine
a compound that is released by cells in response to injury and in allergic and inflammatory reactions, causing contraction of smooth muscle and dilation of capillaries.
Chemotaxis
movement by a cell or organism in reaction to a chemical stimulus
Second Line of Defense Process
1. Phagocyte's pseudopodia engulfs pathogens
2. traps pathogens in vesicles
3. Fuses vesicle w/ lysosomes to form phagolysosomes (dissolves bacteria)
4. presents antigens (fragments of pathogen) on surface to initiate 3rd line of defense
Pseudopodia
part of phagocytes that helps to entrap pathogen
Phagolysosome
fusion of vesicle w/ pathogen and lysosome, allows of pathogen destruction
3rd Line of Defense (2)
Specific - differentiates between pathogens and alters response
Adaptive - builds memory to respond faster to same pathogen
*lymphocytes*
Lymphatic System
where white blood cells travel, consists of nodes and vessels
Function: manage fluid levels in body, returns fluid (lymph) leaked from circulatory system back to it via nodes
Antigen vs. Antibody
Antigen: "them"
-glycoproteins found on pathogen/cell surface, elicits immune response (antibody production)
Antibodies: "us"
-protein made by lymphocytes
-complimentary in shape and charge to antigens
-binding between the two is irreversible
More on Antibodies
-produced by lymphocytes, each lymphocyte can only produce one type (b/c clone)
-made up of 4 polypeptides
-makes pathogen more recognizable to phagocytes
-prevents viruses from docking to host cells
Opsonization
An immune response in which the binding of antibodies to the surface of a microbe facilitates phagocytosis of the the microbe by a macrophage
Opsonin
an antibody or other substance that binds to foreign microorganisms or cells, making them more susceptible to phagocytosis.
Antibody Regions (2)
Hypervariable: binding site of antigens from phagocytes or pathogens or random antigens floating around
Constant: helps body fight pathogen (able to be recognized by B-cell)
Types of Lymphocytes
1. B-cells, made in bone marrow, produces antibodies
2. Helper T-cells, matures in Thymus, activates B-cells and cytotoxic T-cells
3. Cytotoxic T-cells, destroys body's own cells that have been infected or become cancerous
After Antigen Presentation in Phagocytes...
antigens bind to and activate specific helper-t cells that have complimentary antigen receptors
activated helper t-cells then activate helper specific B-cells
How do Helper T-cells activate B-cells?
By releasing cytokines or through direct contact
Cytokines
type of ligand released by Helper-T cell to activate B-cell
Activated B-cell Differentiation
Plasma B-Cells or Memory B-cells
Effector Cell
A short-lived cell, what a Plasma B-cell is
Plasma B-cell
A short lived cell that produces high amounts of specific antibodies
They develop extensive rER and golgi to assist in protein synthesis
*die after infection overcome*
Memory B-cells
Remain inactive until same pathogen enters system, then activate and respond rapidly by stimulating production of Plasma B-cells
Immunity
Either having antibodies to pathogen or memory B-cells that can rapidly produce antibodies
Cytotoxic T-cells
destroys pathogens and body's own infected cells by secreting perforating proteins to puncture cell membrane and induce cell lysis
Antibody Relevance in pathogen removal
Produced by plasma b-cells, then tag antigens of pathogens by binding to it with hypervariable region. Constant region then attracts macrophages (phagocytes) for pathogen destruction
HIV Transmission
Occurs via exchange of body fluids
1. unprotected sex w/ abrasions
2. shared usage of hypodermic needles
3. blood transfusions or blood products
4. childbirth and breastfeeding
HIV (General Facts)
A RNA retrovirus that synthesizes DNA with reverse transcriptase
How to inhibit HIV (2)
1. Use antiretroviral drugs to inhibit reverse transcriptase
2. Use drugs that target HIV enzymes utilizes in DNA entry
How HIV affects the immune system
It destroys Helper T-cells, meaning that the CD4+ receptor can no longer recognize antigens on pathogens
Therefore no activated B-cells (no antibodies) or no activated cytotoxic T-cells
Host eventually killed by opportunistic infections (bc can no longer respond normal infections w/ 3rd line of defense)
AIDS
Acquired immunodeficiency syndrome
Syndrome is a collection of symptoms and infections
Kaposi's Sarcoma, a marker disease (if u have Kaposi's Sarcoma, then u likely have HIV)
Bactericidal vs. Bacteriostatic
Bactericidal - Kills bacteria
Bacteriostatic - Inhibits bacterial growth
Antibiotics
Kill and/or inhibit growth of bacteria
Target prokaryotic DNA replication, protein synthesis, enzymes, 70S ribosomes, and cell wall formation
*don't affect eukaryotes bc of structural and metabolic differences*
*don't affect viruses bc viruses are non-living and have no metabolism*
Narrow vs Broad Spectrum
Narrow Spectrum - effective against specific bacteria
Broad Spectrum - effective against many types of bacteria
Fleming (1928)
Identified penicillin, first chemical antibiotic
Penicillin
Produced by saprotrophic fungi that competed with saprotrophic bacteria, inhibits bacterial competitors via secretion
Florey and Chain (1940)
first clinical trials of penicillin
Antibiotic Resistance
Only a concern if strains with multiple resistances develop (such things are now widespread.
Easy for bacteria to get bc of horizontal gene transfer using plasmids (can just transfer resistance gene)
MRSA
Methicillin-resistant Staphylococcus aureus)
Example of strain with multiple resistances
**superbacteria**
Measures to Prevent Antibiotic Resistance (5)
1. Prescribe antiobiotics for only serios bacteria
2. Maintain high level of hygiene to prevent cross infection
3. Farmers must exclude antibiotics from animal feeds
4. Develop new antibiotics
5. Do not overuse antibiotic products
Zoonoses
Type of pathogen that can cross from species (zoonotic pathogen)
*most pathogens species specific*
Zoonoses Examples
Mycobacterium bovis (cows)
Lyssaviruses (rabies)
COVID-19 (bats)
Immunity Xtra Info
Having Memory B-cells that, if second infection, can quickly produce plasma B-cells to produce antibodies
Prevents disease from really developing
Vaccinations
Promotes immunity by producing memory B-cells
given via intramuscular or subcutaneous (skin) injections
Contains some form of pathogen (weakened/killed pathogen, subunits of pathogen like antigen, or mRNA that codes for antigen)
Epidemic
increase in prevalence of infection within a region
Pandemic
Epidemic that has spread over a larger area
Herd Immunity
Spread of pathogen is impeded because of its repeated encounters with people who are immune, can protect individuals that cannot be vaccinated.
Created via vaccination or those who have already had the disease
Herd Immunity Equation
(1-1/r) * 100%
R is the average number of people that the infected person infects