6.3 - Defence against infectious diseases Flashcards

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1
Q

what is a disease?

A
  • the condition that negatively affects the structure or function of an organism.
  • Sometimes, the microorganism is opportunistic whilst others are highly specialised
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2
Q

what are the Microorganisms that cause disease?

A
  • in the host (the one who is being infected) is called a pathogen
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3
Q

what are humans primary defence system?

A
  • against pathogens is the skin and mucous membranes as it prevents majority of pathogens from entering the body.
  • It acts as physical barrier
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4
Q

how does the skin protect the body from pathogens?

A
  • it is extremely tough by providing both a physical and chemical barrier
  • skin contains sebaceous glands that secrete sebum to maintain skin moisture and lowers the skin pH slightly to inhibit the growth of bacteria and fungi
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5
Q

what are Mucous membranes?

A
  • are thinner and softer than skin
  • Mucous membranes secrete mucous and this acts as a barrier by trapping and either swallowing or expelling pathogens and harmful particles
  • Mucous contains antibacterial enzyme lysozyme that has antiseptic properties
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6
Q

what do cuts do?

A
  • when tissues are injured, the break in the physical barrier allows pathogens to enter
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7
Q

what do clots do?

A
  • blood vessels are also commonly injured
  • A non-specific defence takes place called clotting
  • Clotting serves to seal up the wound and it prevents further loss of blood and blood pressure
  • Clotting is also important as it temporarily reseals the damaged site on the skin and prevent further entry of pathogens
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8
Q

how does blood clotting work?

A
  • involves a cascade of reactions (at least 12), where each produces a product that catalyses the next reaction
  • tightly controlled and very quick so there are no clots in vessles
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9
Q

how do blood clots form?

A
  • blood contains two components that form clots: thrombocytes and fibrinogen.
  • Thrombocytes, also called platelets, are fragments of cytoplasm pinched off from larger cells in the bone marrow.
  • Platelets will aggregate at the site of a cut to form a temporary plug that prevents any further bleeding, so then triggers the release of clotting factors that triggers the clotting process
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10
Q

what is Fibrin production?

A
  • platelets release the enzyme and the enzyme together with clotting factors in the plasma convert a plasma protein called prothrombin to its active form thrombin
  • final reaction involves thrombin, which converts soluble fibrinogen protein into strands of insoluble fibrin.
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11
Q

what is Fibrinogen?

A
  • Fibrinogen is a membrane-wrapped protein found in blood plasma, which is the liquid part of blood
  • Fibrin forms a mesh of fibres across the wound that traps platelets and blood cells to form a semi-solid clot or scab at the surface of the skin as it is air-dried
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12
Q

what is Coronary thrombosis?

A
  • arteries with atherosclerosis have a rough inner surface and this tends to cause blood clots to form
  • arteries with atherosclerosis have a rough inner surface and this tends to cause blood clots to form
  • deprives the heart of oxygen and other nutrients, and the cells in this area of the heart are unable to
    respire to produce ATP
  • the heart becomes irregular or stops
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13
Q

what happens because of Coronary thrombosis?

A
  • The wall of the heart makes quivering movements called fibrillation that do not pump blood effectively
  • can be fatal unless stent insertion
  • Atherosclerosis causes occlusion in the coronary arteries, and it may lead to a myocardial infarction (MI) or a heart attack
  • factors that are correlated with an increased risk of coronary thrombosis and heart attacks include: smoking, high blood cholesterol concentration, high blood pressure, diabetes, obesity and a lack of exercise
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14
Q

what are Phagocytes?

A
  • they are white blood cells that are the next line of defence
  • a non-specific response to pathogens
  • can move through the capillary pores (extravasation) and into sites of infection to ingest the pathogen
  • A phagosome is formed around the pathogen, and it fuses with lysosomes that contain digestive enzymes that destroy the foreign pathogen.
  • Waste material is expelled - pus
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15
Q

what is phagocytosis?

A
  • Phagocytes recognise and engulf pathogens by a transport mechanisms known as endocytosis
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16
Q

what is an antigen?

A
  • a foreign substance that stimulates a specific immune response
  • they can be molecules on the surface of viruses or foreign cells, or toxins produced by microorganisms
  • When the immune response detects an antigen, it produces proteins called antibodies (Ab)
17
Q

what are antibodies?

A
  • part of the specific immune response
  • a protein found in blood plasma that recognises and binds to a specific antigen and helps to counter its effects by clearing the pathogen
18
Q

how are antigens fought in the body?

A
  • enters body and is recognised by white blood cell called a B-cell with a specific receptor to the antigen
  • B-cell matures and produces antigen-specific antibodies
  • Antigen-presenting cells (macrophages and dendritic cells) can activate helper T-cells (TH cells)
  • Another white blood cell - TH cells gives processed antigen to the B-cell as a foreign antigen. TH cells also secrete chemicals (cytokines) to activate B-cells
  • compatible B-cell is activated and it undergoes proliferation (increase in cell numbers) and differentiates into plasma cells and memory B-cells
  • plasma B-cells produce antibodies that destroy the antigen. These are shortlived cells
  • memory B-cells remain in circulation for many years to provide immunity against the same antigen if it is encountered again by proliferating and differentiating into plasma cells very rapidly
19
Q

what are antigen-presenting cells?

A
  • macrophages and dendritic cells
20
Q

what is HIV?

A
  • Human immunodeficiency virus (HIV) is a retrovirus that infects helper T-cells - essential for production of antibodies
  • Antibody production involves complex processes and uses different types of lymphocytes: B and T cells
21
Q

what does HIV do?

A
  • the virus undergoes a period of clinical latency where it is inactive
  • virus becomes active and spreads where it destroys helper T-cells and stops production of antibodies
  • Without a functioning immune system, the body is vulnerable to pathogens that would
    normally be effectively controlled,
  • prone to opportunistic pathogens
22
Q

what happens because of HIV?

A
  • secondary infection such as pneumonia that results in death because immune system is down
23
Q

where did HIV come from?

A
  • a global issue especially in developing countries.
  • It was first identified in 1983.
  • HIV is a retrovirus with RNA as its genetic material.
  • It uses reverse transcription during the replication phase in host cells.
  • It embeds its genetic material in the host’s DNA to avoid host detection
  • HIV is transmitted through the exchange of body fluids
  • antivirals can be taken to slow down infection
24
Q

what do antibiotics do?

A
  • inhibit the growth of microorganisms
  • blocks specific metabolic pathways just for bacteria and not eukaryotes such as bacterial DNA replication, transcription, translation, ribosome functions and cell wall formation
  • Most antibiotics destroy bacterial cells by disrupting the cell membranes or puncturing a hole (lysis).
  • Antibiotics do not inhibit eukaryotic cell functions, and therefore it can be used to treat bacterial infections in humans without causing any harm.
25
Q

how were antibiotics discovered?

A
  • discovered in saprotrophic fungi that compete with saprotrophic bacteria for dead organic matter
26
Q

how was penicillin found?

A
  • by Scottish scientist Alexander Fleming in 1928 in the fungus Penicillium rubens
  • development of penicillin as an antibiotic used in medicine was Australian scientist Howard Florey and German scientist Ernst Chain
27
Q

how did they test penicillin?

A
  • 1939-1940, Florey and Chain tested the effect of penicillin on bacterial infections in mice (in vivo)
  • Eight mice were infected with Streptococcus bacteria with a known concentration to cause death from pneumonia, of which, four were injected with penicillin.
  • Within 24 hours, the 4 untreated mice died whilst the 4 penicillin-treated mice remained healthy
  • then tested on human and it worked
28
Q

what is a virus?

A
  • Viruses are non-living and must exist inside host cells.
  • Viruses do not have cell walls and rely on host cell’s metabolic pathways to reproduce as they lack a metabolism.
  • viruses are not affected by antibiotics but antivirals will inhibit some viruses’ disease progression in hosts
  • if use antibiotic for virus it kills good bacteria
  • Overuse of antibiotics may potentially develop antibiotic-resistant strains of bacteria
29
Q

what is antibiotic resistance?

A
  • because of evolution the bacteria can resist the antibiotics
  • Golden Staph, Staphylococcus aureus (MRSA) which has infected the blood or surgical wounds of hospital patients and resists all commonly used antibiotics
  • Another example is MDR—TB.
  • The problem is certainly avoidable if:
  • Doctors prescribe antibiotics only for serious bacterial infections.
  • If patients complete full courses of antibiotics.
  • If hospital staff maintain high standards of hygiene.
  • If farmers do not use antibiotics in livestock feed.