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OCR A Level Biology A: Pathogens, transmission and the first lines of defence (H420) – Revision Notes

Condensed revision notes and a self-test on pathogens, transmission, first defences, phagocytes and blood smears for OCR A Level Biology A (H420).

Subject
Biology
Level
A LEVELS
Topic
Pathogens, transmission and the first lines of defence
Updated

Aligned to OCR A Level Biology (H420), Version 4.1 (April 2026), for first assessment in 2025. Official specification .

Syllabus page (what it covers and how it is assessed): OCR A Level Biology.

Syllabus points this page covers

H420

  • 4 Biodiversity, evolution and disease (whole topic)

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These revision notes condense OCR A Level Biology A (H420) statements 4.1.1(a) to 4.1.1(e), from the OCR specification Version 4.1 (April 2026), for first assessment in 2025. For full explanations read the study guide, then test yourself with the practice questions. Hub: OCR A Level Biology. Checklist: OCR A Level Biology checklist. Quick check of where you stand: free diagnostics.

4.1.1(a) Pathogen types: learn as pairs

Type Plant disease Animal disease
Bacterium Ring rot (potato) Tuberculosis (TB)
Virus Tobacco Mosaic Virus HIV/AIDS, influenza
Protoctist Potato and tomato late blight Malaria
Fungus Black sigatoka (banana) Athlete’s foot
  • Virus: not a cell, reproduces only inside host cells.
  • Bacterium: prokaryote. Protoctist and fungus: eukaryotes.
  • Binomial names and symptom detail are not required.

4.1.1(b) Transmission

Route Example Detail to state
Vector Malaria; many plant viruses Female mosquito carries the pathogen between hosts; aphids carry plant viruses
Spores Late blight, black sigatoka, athlete’s foot Light; moved by wind, rain splash, floors, towels
Droplets TB, influenza Coughs and sneezes; inhaled
Body fluids HIV Blood, semen, mother to child, shared needles
Contact and tools Tobacco Mosaic Virus, ring rot Sap on hands and tools; infected seed potatoes

Conditions to link in your answer:

  • Climate: warm, wet = mosquito breeding; cool, damp = late blight.
  • Social: overcrowding, poor ventilation, poor sanitation, limited healthcare, travel, trade, monoculture.

Method for a transmission question. (1) Name the route. (2) Say what carries the pathogen. (3) Link to the condition given in the question. (4) Say why that raises the chance of infection.

4.1.1(c) Plant defences

Type Examples How it helps
Chemicals Terpenoids, phenols, alkaloids, defensins, chitinase Kill or inhibit pathogens; chitinase digests fungal chitin
Callose In plasmodesmata and sieve plates, and between wall and membrane Blocks cell-to-cell and phloem movement; strengthens the wall
Lignin and thicker walls Around the site of attack Physical barrier
Hypersensitive response Cells at the site die Pathogen has no living cells to feed on
Stomatal closure Pores shut Fewer bacteria enter
Signalling Salicylic acid Distant cells switch on defences

4.1.1(d) Non-specific defences in animals

Defence Key points
Skin Barrier, sebum, harmless microorganisms compete; no structure detail needed
Mucous membranes Goblet cells make mucus that traps microorganisms; cilia sweep it to the throat; lysozyme in mucus and tears
Expulsive reflexes Cough, sneeze, vomit, diarrhoea
Clotting Platelets release substances; cascade; fibrinogen to fibrin; fibrin mesh traps platelets and cells
Wound repair Scab; cell division at the edges; new tissue
Inflammation Histamine and cytokines; vasodilation; leakier capillaries; phagocytes arrive

Clotting in order: damaged vessel, platelets release substances, cascade, soluble fibrinogen becomes insoluble fibrin, fibrin network traps platelets and red cells, clot. Names of clotting factors are not required.

4.1.1(e)(i) Phagocytes

Neutrophil Macrophage
Nucleus Lobed (2 to 5) Large, kidney-shaped
Lifespan Short Long
Role First responder Antigen-presenting cell

Phagocytosis in six steps.

  1. Cytokines released by infected cells attract and activate phagocytes.
  2. Receptors bind the pathogen; opsonins coat it and make binding easier.
  3. Membrane engulfs the pathogen by endocytosis.
  4. Pathogen sits in a phagosome.
  5. Lysosomes fuse with the phagosome and release enzymes.
  6. Pathogen is digested; an antigen-presenting cell displays its antigens on its surface.

4.1.1(e)(ii) Blood smears and drawing

Cell Identify by
Red blood cell Small, pink, no nucleus
Neutrophil Lobed nucleus, pale granular cytoplasm
Lymphocyte Big round nucleus, thin rim of cytoplasm
Monocyte Largest; kidney-shaped nucleus
Platelet Tiny fragment

Drawing checklist. Sharp pencil. Continuous lines. No shading. Fill the space. Ruled label lines that do not cross. Title, magnification, scale bar.

Magnification. Magnification = image size / actual size. Put both lengths in one unit before dividing (1 mm = 1000 µm). Actual size = image size / magnification. Image size = magnification × actual size.

  • A cell drawn 60 mm across with actual diameter 12 µm: 60 000 / 12 = ×5000.
  • Percentage change = (new - old) / old × 100.

Must-know distinctions

Pair Difference
Pathogen and vector The pathogen causes the disease; the vector only carries it
Fibrinogen and fibrin Fibrinogen is soluble and made first; fibrin is insoluble and forms the mesh
Phagosome and lysosome The phagosome holds the pathogen; the lysosome supplies enzymes
Neutrophil and macrophage Neutrophil is short-lived and acts first; the macrophage lives longer and presents antigens
Chemical defence and callose Chemicals attack the pathogen; callose limits its spread
Magnification and scale bar Magnification is a ratio with no unit; the scale bar shows a real length

Worked reminders

Rate of spread. A lesion grows from 4 mm to 14 mm in 3 days. Rate = (14 - 4) / 3 = 3.3 mm per day. Always give the unit as mm per day.

Differential count. Out of 200 white cells, 124 are neutrophils. Percentage = 124 / 200 × 100 = 62 %. Show the division, then the answer.

Scale bar. A bar 25 mm long is labelled 5 µm. Magnification = 25 000 / 5 = ×5000. A cell that is 60 mm across in the image is then 60 000 / 5000 = 12 µm across.

Model answer shapes

Explain how mucous membranes protect. (1) Goblet cells secrete mucus. (2) Mucus traps pathogens and dust. (3) Cilia beat and move the mucus towards the pharynx. (4) It is swallowed and the pathogens meet acid and enzymes in the stomach.

Describe how a clot forms. (1) Platelets release substances at the damaged vessel. (2) A cascade of reactions follows. (3) Soluble fibrinogen is converted to insoluble fibrin. (4) Fibrin threads form a network that traps platelets and red cells. (5) The clot dries to a scab.

Explain why inflammation helps. (1) Histamine and cytokines are released. (2) Vasodilation brings more blood. (3) Capillaries become more permeable, so fluid and phagocytes pass into the tissue. (4) Phagocytes destroy the pathogen.

Describe how a phagocyte destroys a bacterium. Use the six steps above, in order, using the words chemotaxis, receptors, endocytosis, phagosome, lysosome and enzymes.

Command words in this unit

  • Name or State: one correct term, no explanation.
  • Describe: say what happens, in order.
  • Explain: give the reason as well as the event.
  • Suggest: apply what you know to an unfamiliar situation and justify it.
  • Calculate: show the working, give the unit and keep sensible significant figures.

Last-week checklist

  • Say the pathogen table aloud, disease first, type second.
  • Write one transmission sentence for each disease on the list, naming the carrier and one condition.
  • Sketch a neutrophil and a lymphocyte side by side, label them and add a scale bar.
  • Practise one magnification calculation in both directions: finding magnification, and finding actual size.
  • Rewrite the six phagocytosis steps from memory, using the key terms.

Quick self-test

  1. Name the type of pathogen that causes black sigatoka.
  2. Give two ways that late blight spores are carried between plants.
  3. State what a vector is.
  4. Name the polysaccharide deposited in plasmodesmata after infection and say what it does.
  5. Which protein forms the network in a blood clot?
  6. Describe what cilia do in the airways.
  7. A photomicrograph is at ×6000 and a cell measures 72 mm in it. Calculate the actual diameter in µm.
  8. A cell has an actual diameter of 9 µm. It is drawn at ×2500. Calculate the drawn diameter in mm.
  9. Neutrophils rise from 6.5 to 15.6 (×10⁹ per dm³). Calculate the percentage increase.
  10. Name the structure formed when a phagocyte surrounds a pathogen, and the organelle that fuses with it.
  11. State one role of cytokines in phagocytosis.
  12. Which blood cell has a kidney-shaped nucleus and is the largest white cell in a smear?

Answers

  1. A fungus.
  2. Wind and rain splash (infected tubers carried between fields are another route).
  3. An organism that carries a pathogen from one host to another.
  4. Callose. It blocks plasmodesmata so the pathogen cannot pass from cell to cell, and it strengthens the wall.
  5. Fibrin.
  6. They beat to sweep mucus, with trapped microorganisms, towards the throat.
  7. 72 mm = 72 000 µm. 72 000 / 6000 = 12 µm.
  8. 9 × 2500 = 22 500 µm = 22.5 mm.
  9. (15.6 - 6.5) / 6.5 × 100 = 140 %.
  10. A phagosome; a lysosome.
  11. They attract phagocytes to the infection, or activate them.
  12. The monocyte.

Where marks are usually lost

  • Naming the wrong type for a listed disease, especially late blight (protoctist, not fungus) and malaria.
  • Writing “viruses are living cells” or “bacteria are viruses”.
  • Saying the mosquito “causes” malaria rather than carrying the pathogen.
  • Giving “bad weather” without saying which weather feature helps which stage of spread.
  • Describing callose without saying where it is deposited or what it blocks.
  • Reversing fibrinogen and fibrin.
  • Leaving out units, or mixing mm and µm, in magnification questions.
  • Drawing with shading, overlapping label lines or no title and scale.
  • Stopping phagocytosis at engulfment without the phagosome, lysosomes and enzyme digestion.

Official syllabus

OCR A Level in Biology A (H420), specification Version 4.1 (April 2026), for first assessment in 2025, published by OCR. Statements 4.1.1(a) to 4.1.1(e).

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