Module 4 Section 1: Disease and the Immune System Flashcards

1
Q

What is a disease

A

A condition that impairs the normal functioning of an organism
Can affect plants and animals

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2
Q

What is a pathogen

A

An organism that causes a disease

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3
Q

What are the different types of pathogens

A

Bacteria
Viruses
Fungi
Protoctista
Prion (don’t need to know)

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4
Q

What is a communicable disease

A

A disease that can spread between organisms

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5
Q

Diseases caused by bacteria

A

Tuberculosis (TB)
Bacterial meningitis
Ring rot

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6
Q

Diseases caused by viruses

A

HIV/AIDS
Influenza
Tobacco mosaic virus

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7
Q

Diseases caused by fungi

A

Black Sigatoka
Ringworm
Athletes foot

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8
Q

Diseases caused by a protoctist

A

Potato/tomato late blight
Malaria

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9
Q

Tuberculosis (TB)

A

Bacterium
Affects animals typically humans and cattle
Caused by bacterium mycobacterium tuberculosis
Damages and destroys lung tissue and suppresses immune system
Curable by antibiotics and preventable by improving living conditions

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10
Q

Bacterial meningitis

A

Bacterium
Affects humans
Caused by streptococcus pneumoniae or neisseria meningitidis
Affects meninges of the brain (protective membranes of brain surface) which can spread to rest of the body causing blood poisoning (septicaemia)
Cured by antibiotics if delivered early

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11
Q

Ring rot

A

Bacterium
Affects potatoes, tomatoes
Caused by clavibacter michiganensis
Damages leaves, tubers and fruit

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12
Q

HIV/AIDS

A

Virus
Affects humans
Pathogen called Human Immunodeficiency Virus
Disease: Acquired Immunodeficiency Syndrome (AIDS)
Destroys immune system so people are vulnerable to other diseases
Passed through exchange of body fluids (sex) and blood (needles)
No vaccine or cure but drugs can slow progress of disease

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13
Q

Influenza

A

Virus
Affects animals including humans
Caused by orthomyxoviridae spp
Attacks and kills ciliated epithelial cells leaving them open to secondary infection
No cure but people can be vaccinated annually

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14
Q

Tobacco mosaic

A

Virus
Affects tobacco plants, tomatoes, peppers, cucumbers, petunias
Caused by Tomabovirus (?)
Damages leaves, flowers, fruit
Stunts growth and reduces yield
No cure

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15
Q

Black Sigatoka

A

Fungi
Affects banana plants
Caused by mycophaerella fijiensis
Attacks and destroys leaves turning them black
No cure but fungicide can be used to control spread

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16
Q

Ringworm

A

Fungi
Affects cattle
Caused by Trycophyton verrucosum
Causes grey-white, crusty circular areas of skin in cattle
Cured using antifungal creams

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17
Q

Athlete’s foot

A

Fungi
Affects humans
Caused by Tinia Pedia
Grows on and digests warm, moist skin between toes causing cracking and scaling which can be itchy and sore
Cured using antifungals creams

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18
Q

Malaria

A

Protoctist
Affects animals including humans
Caused by Protoctista plasmodium spread by bites of infected mosquitoes (vector)
Invades red blood cells, liver and brain
No vaccine and limited cures

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19
Q

Potato/tomato blight

A

Protoctist
Affects potatoes and tomatoes
Oomycete phytophthora
Destroys leaves, tubers and fruit
No cure

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20
Q

How can communicable diseases be transmitted

A

Directly transmission
Indirectly transmission

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21
Q

How are diseases spread by direct transmission

A

When a disease is transmitted directly from one organism to another
Can be done through:
Direct contact
Inoculation
Ingestion

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22
Q

How are diseases spread directly by contact

A

Contact with body fluids of another person
E.g. bacterial meningitis or STIs

Direct skin to skin contact
E.g. ring worm, athletes foot

Microorganisms from faeces transmitted on hands
E.g. diarrhoeal diseases

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23
Q

How can diseases be transmitted indirectly

A

When a disease is transmitted from one organism via an intermediate
Intermediates include:
Fomites
Droplet infection
Vectors

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24
Q

Examples of disease that can be transmitted indirectly

A

Potato/tomato late blight is spread when spores are carried between plants - first in the air , then in the water
Malaria is spread between animals via mosquitoes
Mosquitoes act as vectors - they don’t cause malaria themselves, they just spread the Protoctista that cause it

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25
What conditions can affect disease transmission
Living conditions Climate Social factors
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How can living conditions affect disease transmission
Overcrowded living conditions increase the transmission of many diseases E.g. TB is spread directly via droplet infection, can also be spread indirectly because the bacteria can remain in the air and infect new people so the risk of infection is increased when lots of people live crowded together
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How can climate affect disease transmission
Potato/tomato late blight is especially common during wet summers because the spores need water to spread Malaria is most common in tropical countries, which are humid and hot This is because these are the ideal conditions for mosquitoes to breed
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How can social factors affect how disease is spread in humans
Risk of HIV infection is high in places where there’s limited access to: Healthcare: people are less likely to be diagnosed and treated for HIV and anti-HIV drugs are less likely to be available, so the virus is more likely to be passed on to others Health education: to inform people about how HIV is transmitted and how it can be avoided (e.g. through safe sex practices like using condoms)
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How can bacteria be classified
By their shape By their cell wall
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What are the different shapes available for bacteria
Bacillus/ chain of bacilli (rod) Coccus/ pair, chain or cluster (sphere) Vibrio (comma) Spirillum (spiral) Spirochaete (corkscrew)
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How to test for the different types of bacterial cell wall
Gram staining Different structures of cell wall react differently with the stain
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Results of gram staining for bacteria
Gram positive appear purple/blue under light microscope Gram negative appear red under light microscope
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How can different types of cell walls affect how bacteria are treated
The type of cell wall affects how bacteria react to different antibiotics
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How do bacteria reproduce
Binary fission
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Characteristics of viruses
Protein shell Genetic information as RNA or DNA 0.02-0.3 micrometers No organelles Rapidly evolve Non living Always pathogenic
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How do viruses replicate
Invade other cells using attachment proteins Hijack biochemistry of the cell Insert viral DNA into host DNA Host cell transcribes and translates viral DNA Host cell copies viruses
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How do the different pathogens damage the body
Viruses: hijack and destroy cells Bacteria: produce toxins Protists: digest cell contents Fungi: saprotrophic feeding and digestion of cells
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What are protists
Eukaryotes Single celled or colonies Parasitic Often require vector Do not fall into any other categories
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What are fungi
Multicellular Fungi can be saprophytes: feed on dead organisms Fungi can be parasitic: pathogenic fungi which causes disease Fungi reproduce by making millions of spores which can spread
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How do fungi feed
Saprotrophic feeding Secrete enzymes onto surface of food Extracellular feeding Enzymes digest food leaving nutrients Fungi absorbs nutrients left by enzymes
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How to prevent malaria
Preventative measures can be used such as mosquito nets, window and door screens and long sleeves to prevent bites Preventative measures also include controlling the vector by using insecticides and removing standing water
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How are diseases spread directly by inoculation
Through a break in the skin E.g. during sex (HIV) From an animal bite E.g. rabies Through a wound or through sharing needles E.g. septicaemia
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How are diseases spread directly by ingestion
Taking in contaminated food or drink, or transferring pathogens to the mouth from the hands E.g. dysentery, diarrhoeal diseases
44
How are diseases spread indirectly by fomites
Inanimate objects such as bedding, socks or cosmetics can transfer pathogens E.g. athletes foot
45
How are diseases spread indirectly by droplet infection
Droplets of saliva and mucus enter the air through talking, coughing or sneezing If they contain pathogens and are breathed in by people then they can become infected E.g. influenza, tuberculosis
46
How are diseases spread indirectly by vectors
Vectors transmit communicable pathogens from one host or another These are often but not always animals E.g. mosquitoes (malaria), rat fleas (plague) Water can also act as a vector of disease
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How are plant diseases spread by direct transmission
Direct contact of a healthy plant with any part of a diseased plant E.g. ring rot, TMV, tomato and potato blight and black sigatoka
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How are plant diseases spread by indirect transmission
Soil contamination Vectors
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How is plant disease spread by soil contamination
Infected plants often leave pathogens or reproductive spores from protoctista or fungi in the soil These infect the next crop E.g. black sigatoka spores, ring rot bacteria and TMV
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How is plant disease spread by vectors
Wind: pathogens can be carried by the wind Water: spores swim in the surface film of water on leaves Animals: insects and birds carry pathogens and spores from one plant to another as they feed Humans: pathogens and spores are transmitted by hands, clothing, fomites, farming practices and through transporting plants around the world
51
Factors that affect the transmission of communicable diseases in plants
Planting crops that are susceptible to disease Over crowding plants Poor mineral nutrition reduces resistance of plants Damp, warm conditions increase the survival and spread of pathogens and spores Climate change causing increased rain and wind promotes the spread of disease, changing conditions allow animal vectors to spread to new areas
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How do plants recognise and respond to pathogens
Receptors in plant cells respond to molecules from the pathogens or to chemicals produces when the plant cell wall is attacked The stimulates the release of signalling molecules that switch on genes in the nucleus This triggers cellular responses such as: Producing defensive chemicals Sending alarm signals to unaffected cells to trigger their defences Physically strengthening cell walls
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Physical defences of plants
Waxy cuticles: provide barrier against pathogen entry and stops water containing pathogens from collecting on leaf Cell walls: physical barrier against pathogens that make it through waxy cuticle Plant produce callose: makes it harder for viruses to spread and enter cells
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Functions of callose
Synthesised within minutes of the attack and is deposited between the cell walls and cell membrane in cells next to the infected cells These callose papillae act as barriers to prevent the pathogens entering the plant cells around the site of infection Large amounts of callose continue to be deposited in cell walls after the initial infection Lignin is added to make the mechanical barrier to invasion thicker and stronger Blocks sieve plates in the phloem, sealing off the infected part and preventing the spread of pathogens Deposited in the plasmodesmata between infected cells and their neighbours, sealing them off from the healthy cells and helping to prevent the pathogen from spreading
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How do plants use chemicals to defend against pathogens
Plants produce powerful chemicals to either repel insect vectors of disease or kill invading pathogens
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How can plant chemical defences be utilised by humans
These chemicals can be used by humans to help control insects, fungi and bacteria
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Examples of chemicals used in plant defence
Insect repellants: pine resin Insecticides: caffeine Antibacterial compounds (including antibiotics): defensins Antifungal compounds: chitinases Anti-oomycetes: glucanases General toxins: cyanide
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How do plants respond to pathogen infection internally
Waxy cuticle thickens Cell walls get stronger Guard cells close stomata in the leaf If microbes are attacking one section of the plant, the surrounding cells self destruct to quarantine the infection
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How do animals prevent pathogens getting into the body
Animals have a range of primary, non specific defences to prevent pathogens entering the body
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How does skin act as a defence against pathogens
Physical barrier Blocks pathogens from entering body Can act as chemical barrier by producing chemicals that are antimicrobial and can lower pH to inhibit the growth of pathogens Has skin flora of healthy microorganisms that outcompete pathogens for space on body surface Produces sebum, oily substances that inhibits growth of pathogens
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How do mucous membranes act as a defence against pathogens
Protect body openings that are exposed to the environment (e.g. mouth, nostrils, ears, genitals and anus 👅) Some membranes secrete mucus - sticky substance that traps pathogens and contains lysozymes and phagocytes
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How does blood clotting act as a defence against pathogens
Blood clots are a mesh of protein (fibrin) fibres The clots plug wounds to prevent pathogen entry and blood loss Formed by a series of chemical reactions that occur when platelets are exposed to collagen from damaged blood vessels Platelets release: Thromboplastin: trigger series of reactions resulting in blood clot formation (thrombus) Serotonin: causes smooth muscle in blood vessel walls contract to reduce blood flow to the area
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How does inflammation act as a defence against pathogens
The swelling helps to isolate pathogens that may have entered the damaged tissue The vasodilation increases blood flow to the area which brings white blood cells to the area to fight off present pathogens
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How does inflammation occur
Signs include swelling, pain, heat and redness Triggered by mast cells in damaged tissue which releases: Histamines: makes blood vessels dilate causing localised heat and redness, raised temperature helps prevent pathogens reproducing Histamines make vessel walls leaky so blood plasma is forced out to become tissue fluid (tissue fluid causes swelling and pain) Cytokines: attract white blood cells (phagocytes) to the site to dispose of pathogens by phagocytosis
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How does wound repair act as a defence against pathogens
Skin is able to repair itself in the event of injury and re-form a barrier against pathogen entry
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How are wounds repaired
Epidermal cells below scab start to grow to seal the wound Damaged blood vessels regrow Tissue below the wound contracts to bring the edges of the wound closer together Wound is repaired using collagen fibres - too many collagen fibres causes a scar to form
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How do expulsive reflexes repair act as a defence against pathogens
E.g. coughing, sneezing, vomiting, diarrhoea Sneezes happen when the mucous membranes in the nostrils are irritated by dust or dirt Coughing stems from irritation in respiratory tract Both coughing and sneezing aim to expel foreign objects, including pathogens, from the body Happen automatically Vomiting and diarrhoea expel contents of the gut along with any pathogens
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How do tears, urine and stomach act as defence systems
Tears and urine contain lysozymes Acid in the stomach Helps prevent pathogens entering the body
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How do fevers help kill pathogens inside the body
Normal body temperature is around 37°C and is maintained by the hypothalamus When pathogens invades the body the cytokines stimulate hypothalamus to increase temperature Higher temperatures inhibit pathogen reproduction Specific immune system works faster at higher temperatures
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What are phagocytes and how do they kill pathogens
Phagocytes are white blood cells that engulf and destroy pathogens Two main types: neutrophils and macrophages Phagocytes build up at the site of infection and attack pathogens Pus building up in wound is a result of dead neutrophils and pathogens
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Stages of phagocytosis
Pathogens produces chemicals that attract phagocytes Phagocytes recognise non-human proteins on the pathogens This response is not specific to a type of pathogen, instead it’s against any cell or organism that is non-self Phagocyte engulfs the pathogen and encloses it in a vacuole called phagosome Phagosome combines with a lysosome to form phagolysosome Enzymes from the lysosome digest and destroy pathogen
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Difference between neutrophil’s and macrophages’ times to digest pathogens
Neutrophils take under 10 mins to engulf and destroy a bacterium whereas macrophages take longer as they have a more complex process
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How do macrophages digest pathogens
When a macrophage has digested a pathogen, it combines antigens from the pathogen surface membrane with glycoproteins in the cytoplasm called the major histocompatibility complex (MHC) MHC complex moves these pathogens antigens to the macrophage’s own surface membrane It becomes an antigen presenting cell (APC) These antigens now stimulate other cells involved in the specific immune system response
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What are cytokines and when are they produced
Produced when phagocytes have engulfed a pathogen They are chemicals that act as cell signalling molecules Inform other phagocytes that the body is under attack and stimulates them to move to the site of infection or inflammation Can also increase body temperature and stimulate the specific immune system
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What are opsonins
Bind to pathogens and tags them so they can be more easily recognised by phagocytes Phagocytes have receptors on their cell membranes that bind to common opsonins The phagocyte then engulfs the pathogen
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Different types of opsonins
Many different types Antibodies such as immunoglobulin G (IgG) and immunoglobulin M (IgM) have the strongest effect
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How to examine blood under a microscope
Smear sample Spreading a drop of blood thinly across the slide Can be stained to show nuclei of lymphocytes Identifying the number of different types of lymphocytes in a blood smear indicates if a non specific or specific immune response is taking place
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What are T cells
T cells Mature in the thymus Have highly specific receptors in their membranes Respond to 'changed' cells (infected cells, antigen-presenting cells, 'non-self' cells, mutated cells) - this is the Cell-Mediated Response Selection of correct T cell leads to expansion by mitosis, then differentiation into variety of T cells ('T helper', 'T killer', 'T memory', 'T regulator' T cells play key roles in control and coordination of immune response
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What are B cells
B cells Remain in bone marrow until mature Congregate in lymph nodes and spleen, forming the 'humoral response' - roaming protection in the fluids.  Have highly specific antibodies in their membrane - each B cell can only produce one type of antibody and each B cell is unique.  Selection of correct B cell leads to expansion by mitosis, then differentiation into plasma/effector cells (which produce antibodies) and memory cells. 
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Different types of T lymphocyte cells
T helper cells T killer cells T memory cells T regulator cells
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Different types of B lymphocyte cells
Plasma cells B effector cells B memory cells
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T killer cells
T killer cells: Destroy the pathogen carrying the antigen Produce a chemical Perforin which kills the pathogen by making holes in the cell membrane so it’s freely permeable
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T memory cells
T memory cells: Live for a long time and are part of the immunological memory If they meet an antigen a second time, they divide rapidly to form a huge number of cloned T killer cells that destroy the pathogen
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T helper cells
T helper cells: Have CD4 receptors on their cell surface membrane which bind to the surface antigens on APCs Produce interleukins (type of cytokine) Interleukins made by T helper cells stimulate the activity of B cells, which increases antibody production Stimulates production of other types of T cells Attracts and stimulates macrophages to ingest pathogen with antigen-antibody complexes
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T regulator cells
T regulator cells: Suppress immune system, acting to control and regulate it They stop the immune response once a pathogen has been eliminated They make sure the body recognises self antigens and does not set up an autoimmune response Interleukins are important in this control
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What are plasma cells
Plasma cells: Produce antibodies to a particular antigen and release them into circulation Produced from B effector cells An active plasma cell lives for a few days but produces around 2000 antibodies per second while it’s alive and active
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What are B memory cells
B memory cells: Live for a long time and provide the immunological memory They are programmed to remember a specific antigen and enable the body to make a rapid response when a pathogen carrying that antigen is encountered again
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What are B effector cells
Divide to form the plasma cell clones
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Structure of antibodies
Y shaped glycoproteins called immunoglobulins Two identical long polypeptide chains called the heavy chains 4 polypeptide chains held together by disulfide bridges Also disulfide bridges within polypeptide chains holding them in shape Hinge region of antibody provides flexibility and allows it to bind two separate antigens, one at each of its antigen binding sites Made up of constant region which is same on all antibodies and allows attachment to phagocytes and contains only heavy chains Heavy chains extend into variable region which contains light chains and gives specificity
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Function of antibodies
Produced by B cells in response to antigens Bind to specific antigen on pathogen or toxin that has triggered immune response Bind to antigens with a lock and key mechanism
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What is it called when an antibody binds to an antigen
Forms an antigen-antibody complex
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Structure of antibody binding site
Area of 110 amino acids on both heavy and light chains Known as variable region since its different on each antibody and gives them their specificity
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How do antibodies defend the body
Antibody in antigen-antibody complex acts as an Opsonins so complex is easily engulfed by phagocytes Most pathogens cannot invade host cells once they are part of an antigen-antibody complex Mostly done through antibodies acting alone Act as agglutinins causing pathogens carrying antigen- antibody complexes to clump together, helps prevent them spreading through body and makes it easier for phagocytes to engulf multiple pathogens at the same time Done by antibodies acting in complex Act as antitoxins by binding to toxins produced and making them harmless
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What is cell-mediated immunity
Where T-lymphocytes respond to the cells of an organisms that have been changed E.g. by a virus, antigen processing, mutation or cells from transplanted tissue
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Process of cell mediated immunity
1. In the non-specific defence system, macrophages engulf and digest pathogens in phagocytosis Process the antigens from the surface of pathogen and form antigen presenting cells (APCs) 2. Receptors on some T helper cells fit the antigens (clonal selection) These T helper cells are activated to produce interleukins These stimulate more T cells to divide rapidly by mitosis (clonal expansion) Form clones of identical T helper cells that all carry the antigen to bind to a specific pathogen 3. The cloned T cells can: Develop into T memory cells to respond rapidly on second infection Produce interleukins that stimulate phagocytosis Produce interleukins that stimulate B cells to divide Stimulate development of a clone of T killer cells that are specific for the presented antigen and then destroy infected cells
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What happens in humoral immunity
The body responds to antigens found outside the cells E.g. bacteria, fungi and APCs Humoral immune system produces antibodies that are soluble in the blood and tissue fluid and not attached to cells
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How do antibodies and pathogen antigens interact in humoral immunity
B lymphocytes have antibodies on their cell surface membrane (immunoglobulin M) Pathogens entering the body carry specific antigens or produce toxins that act as antigens B cells with the complimentary antibodies will bind to the antigens on the pathogen or to free antigens The B cells engulfs and processes the antigens to become an APC
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Process of humoral immunity
Activated T helper cells bind to B cell APC This is clonal selection: the point when the B cell with the correct antibody to overcome a particular antigen is selected for cloning Interleukins produced by the activated T helper cells activate the B cells Activated B cell divides by mitosis to give clones of plasma cells and B memory cells This is clonal expansion Cloned plasma cells produce antibodies that fit antigens on pathogen surface They bind to and disable antigens or act as opsonins and agglutanins This is primary immune response Some cloned B cells develop into B memory cells If body is infected by the same pathogen again, B memory cells divide rapidly to form plasma cell clones which produce right antibody to kill pathogen quickly This is secondary immune response
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Why do we get ill during an infection
Primary immune response takes days or weeks to become fully effective against pathogen Symptoms are a results of the body reacting when pathogens are dividing freely, before the primary immune response is fully operational
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What are autoimmune diseases
When the immune system stops recognising self cells and attack healthy body tissue Can be caused by genetics, immune system responding abnormally to mild pathogen or normal bodily microorganisms or T regulator cells do not work effectively
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Examples of autoimmune diseases
Rheumatoid arthritis Lupus
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What is rheumatoid arthritis
Immune system attacks cells in joints Affects joints such as hands, wrists, ankles, feet No cure Treatment includes: immunosuppressants, pain relief
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What is lupus
Affect skin and joints causing fatigue Immune system attacks cells in connective tissue Can attack any organ in the body such as liver, lungs or brain No cure Treatments include: immunosuppressants, steroids
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How do plants respond to pathogen infection externally
An area of a plant that is under attack can warn separate areas of the infection via hormones, electrical signals or airborne compounds When the areas detect these signals, they increase production of defensive compounds This can also alert separate neighbouring plants of the infection as well Plants under attack from insects can release chemicals into the air This attract other insects (e.g. wasps) that can deter the attacking insects
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What are antigens
Molecules that can stimulate an immune response Our own antigens are recognised as ‘self’, foreign antigens stimulate the production of antibodies Specific to the organism
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Simple structure of antigens
Usually protein or glycoproteins with specific structure On or inside the cell surface membrane
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When does natural active immunity occur
Body produces T and B memory cells after being infected with pathogen If you meet a pathogen for a second time, your immune system recognises the antigens more quickly and launches a secondary immune response before the pathogen causes disease
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When does active artificial immunity occur
Active artificial immunity occurs when you become immune after you’ve been given a vaccination containing a harmless dose of antigen
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When does artificial passive immunity occur
Artificial passive immunity is when you become immune after being injected with antibodies from someone else E.g. being given antibodies to beat a disease via blood donation
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What is passive immunity
Passive immunity is when you are given antibodies made by a different organism - your immune system doesn’t produce any antibodies of its own
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When does natural passive immunity occur
Natural passive immunity is when a baby becomes immune due to the antibodies it receives from its mother, through the placenta and in breast milk This lasts until the immune system of the baby begins to make its own antibodies The antibodies received are likely to be relevant to pathogens in its environment
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What is active immunity
Natural Active immunity results from having actually been infected by a pathogen. This activates the immune system, leading to antibodies being formed by B cells.
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Active immunity summary
Requires exposure to antigen Takes a while for protection to develop Protection is long term Memory cells are produced
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Passive immunity summary
No exposure to antigens Protection is immediate Protection is short term Memory cells aren’t produced
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What could a vaccine contain
Killed or inactivated bacteria and viruses Attenuated (weakened) strains of live bacteria or viruses Toxin molecules that have been altered and detoxified Isolated antigens extracted from the pathogen Genetically engineered antigens
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Process of vaccination
Pathogen is made harmless so that the antigens are intact but there is no risk of infection Small amounts of the safe antigen, known as the vaccine, are injected into the blood The primary immune response is triggered by the foreign antigens and your body produces antibodies and memory cells as if you were infected with a live pathogen If you come into contact with a live pathogen, the secondary immune response is triggered and you destroy the pathogen rapidly before you suffer symptoms of the disease
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What is an epidemic
When a communicable disease spreads rapidly to a lot of people at a local or national level
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What is an pandemic
When a disease spreads rapidly across a number of countries and continents
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Why is mass vaccination usually most effective at the start of an epidemic
This prevents the spread of the pathogen into the wider population When vaccines are being deployed to prevent epidemics, they often have to be changed regularly to remain effective
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What is herd immunity
This is when a significant number of people in the population have been vaccinated This gives protection to those who do not have immunity There is minimal opportunity for an outbreak to occur
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Why are booster vaccines given later
These make sure that memory cells are produced These can be given several years after first vaccination
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How is vaccination different from immunisation
Vaccination is the administration of a substance designed to stimulate the immune system Immunisation is the process by why you develop immunity Vaccination causes immunity
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What are some routine vaccines offered to everyone
MMR: Protects against measles, mumps and rubella and is given to children as an injection at around a year old and again before they start school Contains attenuated measles, mumps and rubella viruses Meningitis C vaccine: Protects against bacteria that cause meningitis C First given as an injection at 3 months and boosters are given to 1 year olds and teenagers
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Why can vaccines change with the influenza vaccine for example
The flu vaccine changes every year This is because antigens on the surface of the influenza virus change regularly to form new strains of the virus Memory cells produced from vaccination with one strain of the flu will not recognise other strains with different antigens (strains are immunologically distinct) Every year there are different trains of the influenza virus circulating in the population This means a different vaccine must be made
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Why may vaccine programmes change along with the vaccine (e.g. influenza vaccine)
Laboratories collect samples of these different strains Organisations, such as the WHO (world health organisation) and CDC (centre for disease control), test the effectiveness of different influenza vaccines against them New vaccines are developed and one is chosen every year that is most effective against the recently circulating influenza viruses Governments and health authorities then implement a programme of vaccination using the most suitable vaccine
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Why may someone be vaccinated when they are travelling
Sometimes people are given a vaccine that protects them from a strain causing an epidemic in another country This helps stop the strain spreading globally
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What is antigenic shift
The process by which two or more different strains of a virus, or strains of two or more different viruses, combine to form a new subtype having a mixture of the surface antigens of the two or more original strains
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What is antigenic drift
A gradual process of genetic change that leads to more variety for each type of influenza virus due to there being different types of antigens on the surface
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What happens in the primary response
When a pathogen enters the body for the first time, the antigens on its surface activate the immune system as the primary response This response is slow because there aren’t many B lymphocytes that can make the antibody needed to bind to it Eventually the body will produce enough of the right antibody to overcome the infection, this means that the person will show symptoms T and B lymphocytes produce memory cells, which remains in the body for a long time and can remember the specific antigen and will recognise it the second time. This means that the person is now immune
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Why is the secondary response faster
If the same pathogen enters the body, the immune system will produce a quicker, stronger immune response (secondary response) Clonal selection happens faster as memory B lymphocytes are activated and divide into plasma cells that produce the right antibody to the antigen Memory T lymphocytes are activated and divided into the correct type of T lymphocytes to kill the cell carrying the antigen This gets rid of the pathogen before you begin to show any symptoms
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Summarised primary response
Pathogen enters first time Slow response B and T lymphocytes activated Show symptoms
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Summarised secondary responses
Pathogen enters for 2nd time Response is fast Memory cells activated No symptoms
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How are many medicinal drugs manufactured
Many are manufactured using natural compounds found in plants, animals or microorganisms E.g. penicillin is obtained from penicillium fungus, cancer drugs can be made using soil bacteria, daffodils are now grown to produce a drug used to treat Alzheimer’s disease Organisms that have already been studied could still prove to be useful sources of medicines as new techniques are developed for identifying, purifying and testing compounds
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Why is maintaining biodiversity important for drug development
Species could die out before we get a chance to study them and we may never create cures for diseases such as AIDS
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What are pharmocogenetics
This is a combination of drugs that work with your individual combination of DNA Doctors can analyse your genetics and only prescribe drugs which will be most effective for you This can mean that more effective drugs can be manufactured in the future using this information
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How do genetics impact medication
Your genes determine how your body responds to certain drugs and different people respond to the same drug in different ways This determines whether a drug is more effective or not
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What is synthetic biology
This involves using technology to design and make things like artificial proteins, cells and even microorganisms This can be applied to medicine where scientists can engineer bacteria to destroy cancer cells, while leaving healthy body cells intact by producing drugs which would otherwise be too rare, expensive or unavailable
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How is nanotechnology involved in synthetic biology
This can also use nanotechnology where tiny, non natural particles are used for biological purposes e.g. to deliver drugs to specific sites within cells of pathogens or tumours
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Stages of drug development
Phase 1: small number of healthy volunteers (establish how drug works and likely dose required Phase 2: small number of patients (can be controlled, double blind or randomised experiments) Phase 3: larger study of patients (assess and compare drug to existing treatments) Licensing: if drug appears to have high efficacy, is safe, and meets manufacturing standards then it can be sold by licence holder in regions covered by regulatory authority
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What are antibiotics
Chemicals which kill or inhibit the growth of bacteria Used by humans as drugs to treat bacterial infections They target bacteria cells without damaging body cells
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Why have the deaths from bacterial infections dropped recently
We have been able to beat bacterial infections easily using antibiotics so the death rate has fallen This have been happening since the discovery of penicillin (from penicillium mould) by Alexander Fleming and the chemical’s use during the Second World War
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Possible risks from using antibiotics
Can develop severe allergic reactions in some people Antibiotic resistance
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How do bacteria become resistant to antibiotics
There is genetic variation in a population of bacteria Genetic mutations make some bacteria naturally resistant to an antibiotic The ability to resist an antibiotic is an advantage over competition as the bacteria are able to survive in a more hostile environment (due to antibiotics providing selection pressure) so they live longer and reproduce by binary fission Resistance alleles are also passed laterally through the population by conjugation in the form of plasmids The allele for antibiotic resistance is passed on to lots of offspring So resistance spreads and becomes more common in a population of bacteria over time
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Why is antibiotic resistance a problem for patients of bacterial infections
If the bacteria has developed resistance then the infection cannot be treated as easily using antibiotics so the infection can become more severe which could lead to death
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What can be a product of antibiotic resistance
Can lead to the development of superbugs that are resistant to most known antibiotics These are becoming more common We are less able to treat some potentially life threatening bacterial infections
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What is MRSA
Stands for Meticillin resistant staphylococcus aureus This causes serious wound infections such as septicaemia It is resistant to several antibiotics (including meticillin) Carried by up to 30% of population on skin or in nose
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What is C. difficile
Clostridium difficile Infects the digestive system which causes problems in people who have already been treated with antibiotics Could be caused by harmless bacteria that are present in the digestive system which are killed by the antibiotics, which C. difficile is resistant to Causes C.difficile to flourish due to lack of competition It produces a toxin causing severe diarrhoea, fever or cramps
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How to help prevent bacterial antibiotic resistance
Doctors should not prescribe antibiotics for minor infections Should not prescribe them to prevent future infections (except patients with weak immune systems, e.g, elderly people or HIV patients) Patients should take all the antibiotics they’re prescribed to fully clear the infection and all bacteria are killed
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B lymphocyte diagram
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Phagocytes diagram
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Primary and secondary response graph
Primary response starts around the 5th - 10th day Secondary starts around 25-28 days
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What type of molecule is callose
Polysaccharide
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T lymphocyte diagram