Biology  by Bradford
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C3.2 Defence against disease: revision map

The subtopic in the middle and 13 tasks round it: label three diagrams, complete three tables, put a process in order and fill 68 gaps. Every box is standard level. Type into the blanks and check them, or print it on A4, Letter or A3 with an answer key.

C3.2 practice questionsThe whole C3 map

C3.2

Defence against disease

1 of 2Organisms · Interaction and interdependenceName

C3.2.4, C3.2.7Innate and adaptive

Innate systemAdaptive system
Responds tobroad categories of pathogen pathogens
Cells
Over a lifetimedoes not changebuilds up a of pathogens met, so it becomes more effective

The adaptive system recognises : mostly on a pathogen's outer surface. Those on red blood cells can trigger antibody production after a transfusion of the wrong .

C3.2.6, C3.2.8, C3.2.9From one cell to many

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Lymphocytes circulate in the blood and also collect in . The body has a vast number of B-cells, each able to make one type of antibody. A B-cell is activated only when it binds the molecule it matches and is touched by a lymphocyte activated by that same molecule. It then divides by into a clone.

C3.2.1Causes of infection

Disease-causing organisms, or , include viruses, bacteria, and protists. No are known to cause disease in humans. Careful observation drove progress: Semmelweis cut deaths from childbed fever in Vienna by making doctors wash their , and John Snow traced a cholera outbreak in London to one water .

C3.2.2First line of defence

The skin is a barrier: its outer layer is tough, dry and made of dead cells packed with . It is also a barrier, as its secretions are slightly and contain substances that kill bacteria. Mucous membranes line the airways and gut, where sticky traps pathogens.

C3.2Defence against disease

C3.2.10, C3.2.16A second encounter

1st2ndtimeantibody

Immunity is the ability to eliminate an infectious disease. It comes from long-lived : on a second exposure they make the specific antibody and in greater amounts. A vaccine contains , or coding for them, so it builds immunity without causing the disease.

C3.2.3Sealing a cut

Number the steps in order.

  1. Platelets at the wound release clotting factors.
  2. The clotting factors set off a cascade of reactions.
  3. Fibrin threads form a mesh that traps erythrocytes: a clot.
  4. The cascade activates the enzyme thrombin.
  5. Thrombin converts soluble fibrinogen into insoluble fibrin.

Because each step activates the next, the clot forms , sealing the skin against .

C3.2.5A phagocyte at work

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Phagocytes squeeze out of the blood and reach the site of infection by movement. They recognise foreign cells, engulf them by and digest them with .

Word bank acidicamoeboidantigenantigensarchaeabacteriumblood groupchemicalendocytosisfasterfungiglycoproteinshandshelper T-cellhydrolytic enzymeskeratinlymph nodeslymphocyteslysosomememorymemory cellmemory cellsmitosismucusnucleic acidnucleuspathogensphagocytesphysicalplasma cellpseudopodiumpumprapidlyspecificvesicle
C3.2

Defence against disease

2 of 2Organisms · Interaction and interdependenceName

C3.2.13, C3.2.14Antibiotics

Antibiotics block processes in bacteria that do not happen in cells, such as building a bacterial cell . They cannot control viruses, which have no of their own and use the host cell's. Each use of an antibiotic resistant bacteria, which survive and multiply, so careful use is needed to slow the rise of strains.

C3.2.15From animals to us

DiseasePathogenHow it reaches humans
Tuberculosisunpasteurised milk or air breathed out by infected cattle
Rabiesvirusa from an infected mammal, often a dog
Japanese encephalitisvirusthe bite of a that fed on infected pigs or birds
COVID-19virus (SARS-CoV-2)crossed recently from another species; now spreads between people in airborne

Infectious diseases that pass to humans from other species are : they are common, and most newly emerging human diseases start this way.

C3.2.11, C3.2.12Infected by HIV

HIV passes between people in body fluids: in semen and vaginal fluid during unprotected , in blood on shared , and from mother to baby during pregnancy or birth, or in . It infects and kills , so fewer B-cells are activated and fewer antibodies are made. Opportunistic infections take hold: develops.

C3.2Defence against disease

C3.2.17When most are immune

If a high enough of a population is immune, an infected person rarely meets a one, so transmission is impeded and an cannot take hold. This also shields people who cannot be vaccinated. Vaccines are rigorously tested: the risk of side effects is very small, but not .

C3.2.18COVID-19 by numbers

WeekNew cases in one townPercentage change on the week before
11600(first week)
22400 %
31800 %
41440 %

Percentage change = change ÷ × 100. In week 4, 30 in every 100 000 vaccinated people caught it, against 120 in every 100 000 unvaccinated: taken relative to the unvaccinated rate, a percentage difference of %.

C3.2 examSome of the cells and molecules present in a lymph

Some of the cells and molecules present in a lymph12345
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Word bank +50−20−2575AIDSantibodyantigenB-lymphocytebacteriumbitebreast milkdropletsepidemiceukaryotichelper T-cellsherd immunitymetabolismmosquitomultiresistantneedlesoriginal valuepercentageplasma cellselects forsexsusceptibleT-lymphocytewallzerozoonoses

Answer key

Every box on the sheet with its gaps filled in, as the subtopic reads in full.
  1. GapsCauses of infection

    Disease-causing organisms, or pathogens, include viruses, bacteria, fungi and protists. No archaea are known to cause disease in humans. Careful observation drove progress: Semmelweis cut deaths from childbed fever in Vienna by making doctors wash their hands, and John Snow traced a cholera outbreak in London to one water pump.

  2. GapsFirst line of defence

    The skin is a physical barrier: its outer layer is tough, dry and made of dead cells packed with keratin. It is also a chemical barrier, as its secretions are slightly acidic and contain substances that kill bacteria. Mucous membranes line the airways and gut, where sticky mucus traps pathogens.

  3. OrderSealing a cut

    1. Platelets at the wound release clotting factors.
    2. The clotting factors set off a cascade of reactions.
    3. The cascade activates the enzyme thrombin.
    4. Thrombin converts soluble fibrinogen into insoluble fibrin.
    5. Fibrin threads form a mesh that traps erythrocytes: a clot.

    Because each step activates the next, the clot forms rapidly, sealing the skin against pathogens.

  4. TableInnate and adaptive

    Innate systemAdaptive system
    Responds tobroad categories of pathogenspecific pathogens
    Cellsphagocyteslymphocytes
    Over a lifetimedoes not changebuilds up a memory of pathogens met, so it becomes more effective

    The adaptive system recognises antigens: mostly glycoproteins on a pathogen's outer surface. Those on red blood cells can trigger antibody production after a transfusion of the wrong blood group.

  5. LabelA phagocyte at work

    1. pseudopodium
    2. bacterium
    3. lysosome
    4. vesicle
    5. nucleus

    Phagocytes squeeze out of the blood and reach the site of infection by amoeboid movement. They recognise foreign cells, engulf them by endocytosis and digest them with hydrolytic enzymes.

  6. LabelFrom one cell to many

    1. helper T-cell
    2. antigen
    3. plasma cell
    4. memory cell

    Lymphocytes circulate in the blood and also collect in lymph nodes. The body has a vast number of B-cells, each able to make one specific type of antibody. A B-cell is activated only when it binds the molecule it matches and is touched by a lymphocyte activated by that same molecule. It then divides by mitosis into a clone.

  7. GapsA second encounter

    Immunity is the ability to eliminate an infectious disease. It comes from long-lived memory cells: on a second exposure they make the specific antibody faster and in greater amounts. A vaccine contains antigens, or nucleic acid coding for them, so it builds immunity without causing the disease.

  8. GapsInfected by HIV

    HIV passes between people in body fluids: in semen and vaginal fluid during unprotected sex, in blood on shared needles, and from mother to baby during pregnancy or birth, or in breast milk. It infects and kills helper T-cells, so fewer B-cells are activated and fewer antibodies are made. Opportunistic infections take hold: AIDS develops.

  9. GapsAntibiotics

    Antibiotics block processes in bacteria that do not happen in eukaryotic cells, such as building a bacterial cell wall. They cannot control viruses, which have no metabolism of their own and use the host cell's. Each use of an antibiotic selects for resistant bacteria, which survive and multiply, so careful use is needed to slow the rise of multiresistant strains.

  10. TableFrom animals to us

    DiseasePathogenHow it reaches humans
    Tuberculosisbacteriumunpasteurised milk or air breathed out by infected cattle
    Rabiesvirusa bite from an infected mammal, often a dog
    Japanese encephalitisvirusthe bite of a mosquito that fed on infected pigs or birds
    COVID-19virus (SARS-CoV-2)crossed recently from another species; now spreads between people in airborne droplets

    Infectious diseases that pass to humans from other species are zoonoses: they are common, and most newly emerging human diseases start this way.

  11. GapsWhen most are immune

    If a high enough percentage of a population is immune, an infected person rarely meets a susceptible one, so transmission is impeded and an epidemic cannot take hold. This herd immunity also shields people who cannot be vaccinated. Vaccines are rigorously tested: the risk of side effects is very small, but not zero.

  12. TableCOVID-19 by numbers

    WeekNew cases in one townPercentage change on the week before
    11600(first week)
    22400+50 %
    31800−25 %
    41440−20 %

    Percentage change = change ÷ original value × 100. In week 4, 30 in every 100 000 vaccinated people caught it, against 120 in every 100 000 unvaccinated: taken relative to the unvaccinated rate, a percentage difference of 75 %.

  13. Exam diagramSome of the cells and molecules present in a lymph

    1. antigen
    2. B-lymphocyte
    3. T-lymphocyte
    4. plasma cell
    5. antibody