COMMUNICABLEDISEASES

AQA GCSE Biology · Lessons 1–9
⬇ Student Booklet ⬇ Teacher Booklet

Key Terms — Communicable Diseases

All Terms

01
Health
DefinitionA state of complete physical, mental and social wellbeing.
02
Communicable disease
DefinitionA disease that can spread from person to person (infectious/contagious), caused by a pathogen.
03
Non-communicable disease
DefinitionA disease that cannot spread between people, e.g. asthma, cancer, heart disease. Linked to lifestyle risk factors.
04
Pathogen
DefinitionA microorganism that causes disease: bacteria, viruses, protists and fungi.
05
Droplet infection
DefinitionBreathing in pathogens released into the air when an infected person coughs or sneezes.
06
Non-specific defences
DefinitionDefences that are always present and stop any pathogen entering: skin, nose, trachea (mucus and cilia), stomach acid and tears.
07
Toxin
DefinitionA poison released by bacteria that damages cells and makes you feel ill.
08
Binary fissionTriple only
DefinitionHow bacteria reproduce: the DNA and ribosomes replicate, the cell grows, then it divides into two identical cells.
09
Antibiotic
DefinitionA medicine that kills bacteria inside the body. Antibiotics do not work on viruses.
10
Antiseptic / disinfectant
DefinitionChemicals that kill bacteria outside the body, e.g. on surfaces. Too dangerous to use inside the body.
11
Antibiotic resistance
DefinitionWhen bacteria evolve so an antibiotic no longer kills them. They reproduce quickly and can share plasmids carrying resistance genes.
12
Virus
DefinitionGenetic material (DNA or RNA) inside a protein coat. Acellular, about 100 times smaller than bacteria, and only reproduces inside host cells.
13
HIV / AIDS
DefinitionHIV is a virus that attacks the immune cells. Untreated, it can develop into AIDS, when the immune system is too weak to fight other infections or cancer.
14
Vector
DefinitionAn organism that spreads a disease from one organism to another, e.g. the mosquito for malaria.
15
Protist
DefinitionA unicellular eukaryotic microorganism. A protist causes malaria.
16
Fungicide
DefinitionA chemical spray that kills fungi. It can treat rose black spot, but not a viral disease like TMV.
17
ChlorosisTriple only
DefinitionYellowing of leaves caused by magnesium deficiency, because magnesium is needed to make chlorophyll.
18
Phagocytosis
DefinitionWhen a white blood cell (a phagocyte) engulfs a pathogen and digests it with enzymes.
19
Lymphocyte
DefinitionA white blood cell that produces antibodies and antitoxins.
20
Antigen
DefinitionA protein on the surface of a pathogen that lymphocytes detect.
21
Antibody
DefinitionA protein made by lymphocytes that matches the shape of a specific antigen and binds to it, helping to destroy the pathogen.
22
Antitoxin
DefinitionA substance made by lymphocytes that binds to bacterial toxins and neutralises them.
23
Memory cell
DefinitionA lymphocyte that remembers how to make the antibodies for a specific pathogen, so it can produce them quickly on reinfection.
24
Vaccine
DefinitionA small amount of dead or inactive pathogen (or its antigens) that makes lymphocytes produce antibodies and memory cells without you becoming ill.
25
Primary / secondary response
DefinitionThe primary response to a new pathogen is slow and makes few antibodies. The secondary response, from memory cells, is faster and makes more antibodies.
26
Herd immunity
DefinitionWhen most of a population is vaccinated, so there are not enough infected people to pass the disease on to those who cannot be vaccinated.
27
Monoclonal antibodiesTriple only
DefinitionIdentical antibodies made from a single clone of cells, so they all target one particular antigen.
28
HybridomaTriple only
DefinitionA cell made by combining a lymphocyte with a tumour cell. It can be cloned to make many antibody-producing cells.
29
Painkiller
DefinitionA drug that relieves pain (e.g. aspirin, paracetamol). It treats symptoms but does not kill the pathogen.
30
Toxicity, efficacy, dosage
DefinitionThe three things drug testing checks: is it harmful, does it work, and how much is needed?
31
Placebo
DefinitionA dummy treatment that does not contain the drug.
32
Double-blind trial
DefinitionA trial where neither the doctor nor the patient knows who received the drug or the placebo.
33
Peer review
DefinitionOther scientists check the results before publication, to prevent errors and bias.

Lesson 1 · Communicable Diseases

Do Now

Q1
Name the type of cell a bacterium is.
Model AnswerA prokaryotic cell.
Q2
Name one thing other than disease that can damage health.
Model AnswerDiet or stress.
Q3
An image of a nucleus is 0.8 mm at 450× magnification – what is its real size?
Model Answer0.8450 = 0.00178 mm (about 1.78 µm).

Part 1 · What is a communicable disease?

Read the passage and table, then answer the questions.

Health is a state of complete physical, mental and social wellbeing. Things that damage health include disease, diet and stress. Diseases cause illness and can be communicable or non-communicable.

CommunicableNon-communicable
Can spread from person to person (infectious/contagious)Cannot spread between people
Caused by pathogens – microorganisms that cause disease (bacteria, viruses, protists, fungi)Caused by lifestyle risk factors (diet, alcohol, smoking)
e.g. measles, malaria, influenzae.g. asthma, cancer, heart disease

Questions — What is a communicable disease?

Q1
What are communicable diseases? (1 mark)
Model AnswerDiseases that can spread from person to person (infectious).
Q2
Define 'pathogen'. (1 mark)
Model AnswerA microorganism that causes disease.
Q3
Define 'health'. (2 marks)
Model AnswerA state of complete physical, mental and social wellbeing.
Q4
State three factors that affect health. (3 marks)
Model AnswerDisease, diet and stress.
Q5
Name the four types of pathogen. (2 marks)
Model AnswerBacteria, viruses, protists and fungi.
Q6
Give one example of a communicable disease. (1 mark)
Model AnswerAny one of: measles, malaria, influenza.
Q7
Give one example of a non-communicable disease. (1 mark)
Model AnswerAny one of: asthma, cancer, heart disease.
Q8
An image of a nucleus measures 0.8 mm under a microscope at 450× magnification. Calculate its real size. (2 marks)
Model Answerreal size = imagemagnification = 0.8450 = 0.00178 mm (about 1.78 µm).
Worked Answer — VESSU
V
Variables image size = 0.8 mm · magnification = 450× · real size = ?
E
Equation real size = image sizemagnification
S
Substitute = 0.8450
S
Solve = 0.8450 = 0.00178 mm
U
Units mm (= 1.78 µm)
Answer: 0.00178 mm (about 1.78 µm)

Part 2 · How pathogens spread

Read the passage about spread, then answer the questions.

Pathogens can spread through the air (droplet infection – breathing in pathogens from coughs and sneezes), through water (drinking contaminated water, or contaminated food/poor sanitation), and by direct contact (bodily fluids, e.g. sexual contact or shared needles, or touching surfaces).

Questions — How pathogens spread

Q9
State three ways pathogens can be spread. (3 marks)
Model AnswerThrough the air (droplet infection), through water/food, and by direct contact.
Q10
What is droplet infection? (2 marks)
Model AnswerBreathing in pathogens released into the air when an infected person coughs or sneezes.
Q11
Give an example of spread by direct contact. (1 mark)
Model AnswerAny one of: sexual contact, sharing needles, touching contaminated surfaces.
Q12
How can pathogens spread through water? (2 marks)
Model AnswerBy drinking contaminated water, or through contaminated food and poor sanitation.
Q13
Why is coughing without covering your mouth a problem? (2 marks)
Model AnswerIt releases pathogens into the air as droplets that others can breathe in (droplet infection).

Part 3 · Non-specific defences

Read the passage and look at the diagram, then answer the questions.

The body has non-specific defences that are always there to stop pathogens entering:

  • the skin – a barrier
  • the nose – hairs/cilia trap pathogens
  • the trachea – mucus traps pathogens and cilia move it out
  • the stomach – hydrochloric acid destroys swallowed pathogens
  • tears – chemicals destroy microorganisms
Fig 1.1 — The body's non-specific (always-present) defences.
Fig 1.1 — The body's non-specific (always-present) defences.

Questions — Non-specific defences

Q14
How does the skin act as a defence against pathogens? (1 mark)
Model AnswerIt is a barrier that stops pathogens entering the body.
Q15
How does the trachea defend the body against pathogens? (2 marks)
Model AnswerMucus traps pathogens, and cilia move the mucus out of the trachea.
Q16
How does the stomach defend the body against pathogens? (1 mark)
Model AnswerHydrochloric acid destroys pathogens that are swallowed.
Q17
Why are these called non-specific defences? (2 marks)
Model AnswerThey are always present and protect against any pathogen (not one specific one).
Q18
How do the nose and tears defend against pathogens? (2 marks)
Model AnswerThe nose has hairs/cilia that trap pathogens; tears contain chemicals that destroy microorganisms.
Q19
What traps pathogens in the trachea? (1 mark)
Model AnswerMucus.
Q20
Why does swallowing mucus help protect the body? (1 mark)
Model AnswerThe trapped pathogens are then destroyed by acid in the stomach.

Exam-style questions

Q1
Describe two differences between a bacterial cell and a eukaryotic cell. (2 marks)
Mark SchemeAny two: a bacterial cell has no nucleus (its DNA is a loop in the cytoplasm) and no membrane-bound organelles, and it has plasmids and a cell wall (not made of cellulose); it is also much smaller.
Q2
Figure 1 shows STIs diagnosed in England in 2015 (per 100 000). (4 marks)
Fig 1.2 — STIs diagnosed in England in 2015, per 100 000 of population.
Fig 1.2 — STIs diagnosed in England in 2015, per 100 000 of population.
(a) The female 15-19 population was 1 572 189 – calculate the number diagnosed with an STI.(b) Suggest why the data is given per 100 000 rather than as a number of people.
Mark Scheme(a) population100 000 × rate = 1 572 189100 000 × rate from the figure.(b) So that populations of different sizes can be compared fairly.

Lesson 2 · Bacterial Diseases

Do Now

Q1
How does the skin defend against pathogens?
Model AnswerIt is a barrier that stops pathogens entering.
Q2
How does the trachea defend against pathogens?
Model AnswerMucus traps pathogens and cilia move it out.
Q3
Name the four types of pathogen.
Model AnswerBacteria, viruses, protists and fungi.

Part 1 · How bacteria make us ill

Read the passage and look at the diagram, then answer the questions.

Bacterial pathogens are prokaryotic cells that cause disease by releasing toxins that damage cells, making you feel ill.

Once inside an organism they reproduce rapidly by binary fission (similar to mitosis):Triple only

  • the DNA and ribosomes are replicated
  • the cell grows
  • then it divides into two identical cells (clones)
Fig 2.1 — The structure of a bacterial cell (a prokaryote).
Fig 2.1 — The structure of a bacterial cell (a prokaryote).
Fig 2.2 — Bacteria reproduce rapidly by binary fission.
Fig 2.2 — Bacteria reproduce rapidly by binary fission.Triple only

Questions — How bacteria make us ill

Q1
How do bacteria make you ill? (2 marks)
Model AnswerThey release toxins that damage cells.
Q2
What type of cell is a bacterium? (1 mark)
Model AnswerA prokaryotic cell.
Q3
How quickly can bacteria reproduce? (1 mark)
Model AnswerVery rapidly (under the right conditions).
Q4
Why do bacterial infections often make people feel ill quickly? (1 mark)
Model AnswerBacteria reproduce rapidly, releasing many toxins.
Q5
Triple onlyWhat is binary fission? (2 marks)
Model AnswerThe way bacteria reproduce – the DNA replicates, the cell grows, then it divides into two identical cells.
Q6
Triple onlyWhat are the two cells produced by binary fission? (1 mark)
Model AnswerTwo identical bacteria (clones).
Q7
Triple onlyWhat is replicated before a bacterium divides? (2 marks)
Model AnswerThe DNA and the ribosomes.

Part 2 · Examples of bacterial diseases

Read the table, then answer the questions.

DiseaseSymptoms / spread
Gonorrhoea (STD)Toxins cause thick yellow/green discharge and pain on urinating; can cause infertility. Controlled by antibiotics or barrier contraception (condoms).
Salmonella (food poisoning)Toxins cause fever, abdominal cramps, vomiting and diarrhoea. Prevented by storing/cooking food properly; UK chickens are vaccinated.

Questions — Examples of bacterial diseases

Q8
Which pathogen type causes gonorrhoea? (1 mark)
Model AnswerA bacterium.
Q9
How does gonorrhoea spread? (1 mark)
Model AnswerBy sexual contact (it is a sexually transmitted disease).
Q10
How can the spread of gonorrhoea be controlled? (2 marks)
Model AnswerWith antibiotics, or by using a barrier method of contraception such as a condom.
Q11
Where can salmonella bacteria be found? (1 mark)
Model AnswerIn raw or undercooked food, especially raw chicken.
Q12
How can the spread of salmonella be stopped? (2 marks)
Model AnswerStore raw meat in the fridge, cook food thoroughly, and vaccinate chickens.
Q13
What are the symptoms of salmonella food poisoning? (2 marks)
Model AnswerFever, abdominal cramps, vomiting and diarrhoea.
Q14
What long-term problem can gonorrhoea cause? (1 mark)
Model AnswerInfertility.

Part 3 · Antibiotics

Read the passage about antibiotics, then answer the questions.

Antibiotics kill the bacteria that make us ill and can stop infections spreading. Antiseptics and disinfectants kill bacteria outside the body (e.g. to sterilise surfaces) but are too dangerous to use inside. Antibiotics cannot eradicate bacterial disease because bacteria evolve antibiotic resistance – they reproduce so quickly, and can copy and share plasmids carrying resistance genes. There are now antibiotic-resistant strains of gonorrhoea.

Questions — Antibiotics

Q15
What do antibiotics do? (1 mark)
Model AnswerThey kill the bacteria that make us ill.
Q16
Why can't antiseptics and disinfectants be used inside the body? (2 marks)
Model AnswerThey are too dangerous – they would also kill our own cells.
Q17
Why are bacteria becoming antibiotic resistant so quickly? (2 marks)
Model AnswerThey reproduce very quickly and can copy and share plasmids carrying resistance genes.
Q18
What will scientists have to do about resistant strains? (1 mark)
Model AnswerDevelop new antibiotics.
Q19
Do antibiotics work on viruses? (1 mark)
Model AnswerNo – antibiotics only kill bacteria.
Q20
What is an antiseptic used for? (1 mark)
Model AnswerKilling bacteria outside the body (e.g. on surfaces or skin).
Q21
Name a disease that now has antibiotic-resistant strains. (2 marks)
Model AnswerGonorrhoea.

Exam-style questions

Q1
Bacteria and viruses can reproduce quickly inside the body and make people feel ill. (3 marks)(a) Bacteria and viruses make us feel ill because they produce (antibodies / antitoxins / toxins).(b)(i) Antibiotics are medicines that kill (bacteria / bacteria and viruses / viruses).(iii) What must scientists develop to kill new resistant strains?
Mark Scheme(a) Toxins.(b)(i) Bacteria.(iii) New antibiotics.
Q2
A child has a sore throat. The doctor says the child has a bacterial infection. Explain how the infection makes the child ill. (2 marks)
Mark SchemeThe bacteria reproduce rapidly and release toxins that damage the child's cells, making them feel ill.
Q3
Explain how diseases caused by bacteria are usually treated by doctors. (2 marks)
Mark SchemeWith antibiotics, which kill the bacteria inside the body and stop the infection spreading.
Q4
Food poisoning can be caused by eating food contaminated with Salmonella bacteria. (2 marks)(a) Give one difference between a bacterial cell and an animal cell.(c) Salmonella cases per 100 000 fell from 23.82 (2006) to 12.63 (2014) – describe the trend.
Mark Scheme(a) A bacterial cell has no nucleus (DNA is free in the cytoplasm) / has a cell wall and plasmids.(c) The number of confirmed cases generally decreased between 2006 and 2014.

Lesson 3 · Viral Diseases

Do Now

Q1
Define pathogen.
Model AnswerA microorganism that causes disease.
Q2
Give two examples of bacterial disease.
Model AnswerGonorrhoea and salmonella.
Q3
Why don't antibiotics always work?
Model AnswerBacteria can become antibiotic resistant (and antibiotics don't kill viruses).

Part 1 · What is a virus?

Read the passage and look at the diagram, then answer the questions.

Viruses are not made of cells (they are acellular), so they are not considered living – they cannot reproduce on their own. They are about 100 times smaller than bacteria. A virus is genetic material (DNA or RNA) inside a protein coat. Viruses enter host cells and reproduce rapidly inside them before bursting out and damaging the cell, which makes you feel ill.

Fig 3.1 — A virus reproduces inside a host cell, then new virus particles are released.
Fig 3.1 — A virus reproduces inside a host cell, then new virus particles are released.

Questions — What is a virus?

Q1
How do viruses make us ill? (2 marks)
Model AnswerThey reproduce inside host cells then burst out, damaging the cells.
Q2
What is a virus made of? (2 marks)
Model AnswerGenetic material (DNA or RNA) inside a protein coat.
Q3
Why are viruses not considered living? (2 marks)
Model AnswerThey are not made of cells and cannot reproduce on their own (only inside a host cell).
Q4
How do the sizes of viruses and bacteria compare? (1 mark)
Model AnswerViruses are about 100 times smaller than bacteria.
Q5
What does 'acellular' mean? (1 mark)
Model AnswerNot made of cells.
Q6
Where do viruses reproduce? (1 mark)
Model AnswerInside host cells.
Q7
Why don't antibiotics work on viruses? (1 mark)
Model AnswerViruses reproduce inside our cells, so killing them would mean killing our own cells.

Part 2 · Measles

Read the passage about measles, then answer the questions.

Measles causes a fever and a red skin rash and can be fatal, especially in children. It spreads by droplet infection from coughs and sneezes. To prevent fatalities, young children are vaccinated against it. Someone with measles should be isolated to stop the spread.

Fig 3.2 — The characteristic red skin rash caused by measles.
Fig 3.2 — The characteristic red skin rash caused by measles.

Questions — Measles

Q8
Give two symptoms of measles. (2 marks)
Model AnswerA fever and a red skin rash.
Q9
How does measles spread? (1 mark)
Model AnswerBy droplet infection from coughs and sneezes.
Q10
How is measles prevented? (1 mark)
Model AnswerYoung children are vaccinated against it.
Q11
Why should someone with measles be isolated? (2 marks)
Model AnswerTo stop them spreading the virus to others by droplet infection.
Q12
Why is measles especially dangerous for children? (1 mark)
Model AnswerIt can be fatal in young children.
Q13
What type of pathogen causes measles? (1 mark)
Model AnswerA virus.
Q14
Why does vaccinating children reduce measles deaths? (2 marks)
Model AnswerIt makes them immune, so they do not catch the disease (and cannot spread it).

Part 3 · HIV

Read the passage about HIV, then answer the questions.

HIV (human immunodeficiency virus) causes a flu-like illness.

It spreads by the exchange of body fluids:

  • sexual contact
  • sharing needles
  • from mother to baby through breast milk

If not controlled with antiretroviral medication, HIV attacks the body's immune cells and can develop into AIDS – when the immune system is so weak it cannot fight other infections or cancer.

It can be prevented by:

  • using condoms
  • not sharing needles
  • bottle-feeding babies

Questions — HIV

Q15
Name the pathogen that causes AIDS. (1 mark)
Model AnswerHIV (human immunodeficiency virus).
Q16
How can HIV be spread? (2 marks)
Model AnswerBy exchange of body fluids – sexual contact, sharing needles, or mother to baby through breast milk.
Q17
What does HIV develop into if untreated, and why is that serious? (2 marks)
Model AnswerAIDS – the immune system becomes too weak to fight other infections or cancer.
Q18
How can HIV be controlled? (1 mark)
Model AnswerWith antiretroviral medication.
Q19
Give two ways to prevent the spread of HIV. (2 marks)
Model AnswerAny two of: use condoms, do not share needles, bottle-feed babies.
Q20
What does HIV attack in the body? (1 mark)
Model AnswerThe body's immune cells.
Q21
What are the early symptoms of HIV? (1 mark)
Model AnswerA flu-like illness.

Exam-style questions

Q1
(5 marks)(c) Which of measles, gonorrhoea, AIDS and salmonella are caused by a bacterium, and which by a virus?(d) Give three symptoms of measles.
Mark Scheme(c) Bacterium: gonorrhoea, salmonella. Virus: measles, AIDS.(d) Fever, a red skin rash, and (in serious cases) it can be fatal.
Challenge
In the 1990s some people thought the MMR vaccine caused autism. The graph shows the percentage of children vaccinated with MMR and the number of children who developed autism. Use the graph to explain why the data support the view that there is no link between MMR and autism. (4 marks)
Fig 3.3 — MMR vaccination rate and autism rate over time.
Fig 3.3 — MMR vaccination rate and autism rate over time.
Mark SchemeAutism rates continued to rise even after the MMR vaccine was stopped, so the vaccine cannot be causing the autism; if MMR caused autism, rates should have fallen when it was withdrawn. This shows no link between the two.

Lesson 4 · Vector-Borne Diseases

Do Now

Q1
Name two viral diseases.
Model AnswerMeasles and HIV/AIDS.
Q2
What can HIV develop into, and why is that bad?
Model AnswerAIDS – the immune system becomes too weak to fight other infections or cancer.
Q3
How does a virus make us ill?
Model AnswerIt reproduces inside cells then bursts out, damaging them.

Part 1 · Vectors and malaria

Read the passage and look at the diagram, then answer the questions.

Vector-borne diseases are spread from one organism to another by a vector (e.g. fleas spread bubonic plague; aphids spread plant viruses). Malaria is caused by a protist (a unicellular eukaryotic microorganism). The parasite spends part of its life in mosquitoes and part in humans; by biting humans and drinking their blood, mosquitoes spread the protist – the mosquito is the vector. Infected humans get a high fever and damage to the liver and red blood cells, which the protist destroys as it replicates in them.

Fig 4.1 — Biting insects can carry disease between animals.
Fig 4.1 — Biting insects can carry disease between animals.
Fig 4.2 — The malaria parasite is passed between mosquitoes and humans, infecting the liver and red blood cells.
Fig 4.2 — The malaria parasite is passed between mosquitoes and humans, infecting the liver and red blood cells.

Questions — Vectors and malaria

Q1
Which pathogen causes malaria? (1 mark)
Model AnswerA protist.
Q2
How is malaria spread? (2 marks)
Model AnswerBy mosquitoes (the vector), which pass the protist between humans when they bite and drink blood.
Q3
What is a vector? (2 marks)
Model AnswerAn organism that spreads a disease from one organism to another.
Q4
How does malaria affect the body? (2 marks)
Model AnswerIt causes a high fever and damages the liver and red blood cells.
Q5
State a symptom of malaria. (1 mark)
Model AnswerA high fever (or damage to the liver/red blood cells).
Q6
What is a protist? (1 mark)
Model AnswerA unicellular eukaryotic microorganism.
Q7
What is the vector for malaria? (1 mark)
Model AnswerThe mosquito.

Part 2 · Preventing the spread of malaria

Read the passage about prevention, then answer the questions.

Malaria is widespread in tropical areas and kills around 660 000 people per year. It can be treated with antimalarial drugs, but these are becoming less effective as the protists evolve resistance.

The best strategies target the mosquito vector:

  • using insecticides to kill mosquitoes (or repellent to avoid bites)
  • using mosquito nets to prevent bites
  • preventing mosquitoes breeding by removing standing water (their breeding habitat)

Questions — Preventing the spread of malaria

Q8
What drugs can treat people infected with malaria? (1 mark)
Model AnswerAntimalarial drugs.
Q9
Describe three ways of preventing the spread of malaria. (3 marks)
Model AnswerUse insecticides/repellent to kill or avoid mosquitoes; use mosquito nets to prevent bites; and remove standing water to stop mosquitoes breeding.
Q10
Why are antimalarial drugs becoming less effective? (2 marks)
Model AnswerThe protists are evolving resistance to them.
Q11
Why does removing standing water help prevent malaria? (2 marks)
Model AnswerMosquitoes breed in standing water, so removing it stops them breeding.
Q12
How do mosquito nets help? (2 marks)
Model AnswerThey physically stop mosquitoes from biting people (especially while sleeping).

Part 3 · Evaluating disease data

Read the passage about evaluating data, then answer the questions.

When looking at disease data over time, consider:

  • how and when the data was collected – numbers may be inaccurate, as not all cases or deaths are reported, especially in the past or in less-developed countries
  • do not extrapolate beyond the data shown – you cannot assume patterns you cannot see
  • the sample size – a small sample may be unreliable or not allow a valid conclusion

Questions — Evaluating disease data

Q13
Why might recorded numbers of cases be lower than the true number? (2 marks)
Model AnswerNot all cases are reported or recorded, especially in the past or in less-developed countries.
Q14
Why should you not extrapolate from a graph? (2 marks)
Model AnswerYou cannot assume a pattern continues into regions where there is no data.
Q15
Why is sample size important? (2 marks)
Model AnswerA sample that is too small may be unreliable, so a valid conclusion cannot be drawn.
Q16
Why might a study's conclusion not be valid? (2 marks)
Model AnswerAny of: the sample was too small, the data was incomplete or unreliable, or other factors were not controlled.
Q17
Why is it hard to know the exact number of deaths from a past epidemic? (2 marks)
Model AnswerNot all deaths were recorded, and the exact cause of death could not always be determined.

Exam-style questions

Q1
Pathogens are microorganisms that cause infectious diseases. (5 marks)(a) What type of pathogen causes malaria (bacterium / fungus / protist / virus)?(b) Give two methods used to prevent people catching malaria, with a reason for each.
Mark Scheme(a) Protist.(b) Any two with reasons, e.g. mosquito nets (stop mosquitoes biting), insecticides (kill mosquitoes), removing standing water (stops them breeding).
Q2
Confirmed measles cases in England and Wales fell from 2030 (2012) to 91 (2015). (3 marks)(a) Suggest one reason the actual number might be higher than shown.(b) Calculate the percentage decrease from 2012 to 2015.
Mark Scheme(a) Not all cases were reported/medically confirmed.(b) 2030 − 912030 × 100 = about 95.5% decrease.
Worked Answer — VESSU
V
Variables cases in 2012 = 2030 · cases in 2015 = 91 · percentage decrease = ?
E
Equation % decrease = decreaseoriginal × 100
S
Substitute = 2030 − 912030 × 100
S
Solve = 19392030 × 100 = 95.5
U
Units %
Answer: about 95.5% decrease
Q3
A study found 1.2% of mosquito-net users got malaria vs 40% of non-users. (2 marks)(b) Give one piece of evidence that supports 'nets prevent malaria'.(c) Suggest one reason the newspaper statement may not be valid.
Mark Scheme(b) Far fewer net users (1.2%) got malaria than non-users (40%).(c) Other factors were not controlled, or the sample may not be representative – so it is not 'scientifically proven'.
Q4
In 2014 there was an outbreak of Ebola virus disease (EVD) in Africa. By March 2015 there were an estimated 9 850 deaths worldwide. Suggest why this is an estimate rather than an exact number. (1 mark)
Mark SchemeNot all deaths were reported or recorded (especially in areas without good healthcare), so the true number could not be counted exactly.
Q5
Cholera is a waterborne disease. Figure 1 shows data about cholera from one area of Africa. Using Figure 1, what percentage of cases of cholera reported in 2004 resulted in deaths in 2004? Give your answer to 2 significant figures. (2 marks)
Fig 4.3 — Reported cases and deaths from cholera, 2002-2015.
Fig 4.3 — Reported cases and deaths from cholera, 2002-2015.
Mark SchemeIn 2004: about 90 deaths and about 3400 cases, so 903400 × 100 = about 2.6%.

Lesson 5 · Plant Diseases and Defence

Do Now

Q1
Name three non-specific defences our body has.
Model AnswerAny three of: skin, nose hairs, mucus/cilia in the trachea, stomach acid, tears.
Q2
How do bacteria make us ill?
Model AnswerThey release toxins that damage cells.
Q3
What is a vector? Give an example.
Model AnswerAn organism that spreads disease, e.g. a mosquito.

Part 1 · Plant diseases

Read the table about plant diseases, then answer the questions.

Rose black spot (fungus)Tobacco mosaic virus (virus)
Black spots on leaves; leaves turn yellow and dropA 'mosaic' pattern of discolouration; leaves wrinkle and curl
Black spots block light, reducing photosynthesisDamages chloroplasts, reducing photosynthesis
Reduced growth → can kill the plantReduced growth; also infects tomatoes and peppers
Fig 5.1 — Left: rose black spot (fungus). Right: tobacco mosaic virus on a tomato leaf.
Fig 5.1 — Left: rose black spot (fungus). Right: tobacco mosaic virus on a tomato leaf.

Questions — Plant diseases

Q1
Name a viral disease in plants. (1 mark)
Model AnswerTobacco mosaic virus (TMV).
Q2
Describe the appearance of a plant infected with TMV. (2 marks)
Model AnswerA 'mosaic' pattern of discolouration on the leaves, which can wrinkle and curl.
Q3
Which pathogen causes rose black spot? (1 mark)
Model AnswerA fungus.
Q4
State a symptom of rose black spot. (1 mark)
Model AnswerBlack spots on the leaves (which then turn yellow and drop off).
Q5
How does TMV affect plants? (2 marks)
Model AnswerIt damages the chloroplasts, reducing photosynthesis so the plant grows poorly.
Q6
How does rose black spot reduce plant growth? (2 marks)
Model AnswerThe black spots block light, so less photosynthesis happens and growth is reduced.
Q7
What other plants can TMV infect? (1 mark)
Model AnswerTomatoes, peppers and other closely related species.

Part 2 · Preventing the spread

Read the passage about prevention, then answer the questions.

Plant viruses travel inside the plant through the xylem and phloem and can be spread by insect vectors that feed on the plant, on gardeners' hands/tools, or by infected leaves touching healthy ones.

Viral diseases cannot be cured, so to prevent the spread:

  • kill insect vectors with insecticides
  • disinfect tools and clean hands
  • remove and burn infected plants

Rose black spot spreads by fungal spores carried in air or water and on tools/hands. Unlike viruses, the fungus can be killed with a fungicide spray; also remove and burn infected leaves.

Questions — Preventing the spread

Q8
How can gardeners prevent the spread of TMV? (2 marks)
Model AnswerKill insect vectors with insecticide, disinfect tools and clean hands, and remove and burn infected plants.
Q9
How can gardeners prevent the spread of rose black spot? (2 marks)
Model AnswerSpray with a fungicide, and remove and burn the infected leaves.
Q10
How does TMV spread inside a plant? (1 mark)
Model AnswerThrough the xylem and phloem.
Q11
Why can't a viral plant disease be cured? (1 mark)
Model AnswerViral diseases cannot be cured, so spread must be prevented instead.
Q12
How are rose black spot spores carried between plants? (2 marks)
Model AnswerIn air or water (blown by wind or in raindrops), and on gardeners' tools and hands.
Q13
Why can rose black spot be treated but TMV cannot? (2 marks)
Model AnswerRose black spot is a fungus, which can be killed with a fungicide; TMV is a virus, which cannot be cured.

Part 3 · Plant defences and ion deficiencyTriple only

Read the passage about defences, then answer the questions.

Plants defend themselves with physical barriers (cellulose cell walls, a tough waxy cuticle, and bark), chemical defences (antibacterial chemicals and poisons that deter herbivores), and mechanical defences (thorns, hairy stems/leaves, leaves that droop or curl when touched, and mimicry to look dangerous).

Plants can also be damaged by ion deficiency:

  • magnesium deficiency causes chlorosis – magnesium is needed to make chlorophyll
  • nitrate deficiency causes stunted growth – nitrate is needed for protein synthesis
TypeDefenceHow it works
PhysicalCellulose cell wallStrengthens cells and stops microorganisms invading
PhysicalWaxy cuticleA barrier that stops pathogens entering the leaf
PhysicalBark on treesA hard layer pathogens cannot easily get through
ChemicalAntibacterial chemicalsKill or slow the growth of bacteria
ChemicalPoisonsDeter herbivores, which learn to avoid the plant
MechanicalThornsMake it painful for herbivores to eat the plant
MechanicalHairy stems / leavesDeter insects from landing and laying eggs
MechanicalDrooping / curling leavesMove insects off, or startle animals, when touched
MechanicalMimicryLooking like a dangerous plant (e.g. fake berries) to deter predators

Questions — Plant defences and ion deficiency

Q14
Give two physical defences of plants. (2 marks)
Model AnswerAny two of: cellulose cell walls, a tough waxy cuticle, bark.
Q15
Give one chemical defence of plants. (1 mark)
Model AnswerAntibacterial chemicals or poisons.
Q16
Give two mechanical defences of plants. (2 marks)
Model AnswerAny two of: thorns, hairy stems/leaves, drooping/curling leaves, mimicry.
Q17
What does magnesium deficiency cause, and why? (2 marks)
Model AnswerChlorosis – magnesium is needed to make chlorophyll.
Q18
What does nitrate deficiency cause, and why? (2 marks)
Model AnswerStunted growth – nitrate is needed for protein synthesis.
Q19
What is mimicry as a plant defence? (1 mark)
Model AnswerWhen a plant looks like a dangerous plant to deter herbivores (e.g. fake red berries).

Exam-style questions

Q1
TMV causes leaf discolouration. (5 marks)(a) Suggest how TMV spreads within a plant.(b) Describe how TMV can pass from one plant to another.(c) TMV destroys chloroplasts – explain how this affects the growth of the plant.
Mark Scheme(a) Through the xylem and phloem.(b) By insect vectors, on gardeners' hands/tools, or by infected leaves touching healthy ones.(c) Fewer chloroplasts means less photosynthesis, so less glucose is made for growth, and the plant grows poorly.
Q2
Figure 1 shows a plant cell and the microorganism that causes rose black spot. (7 marks)
Fig 5.2 — A plant cell (0.063 mm) and the rose black spot fungus (0.009 mm). Not to scale.
Fig 5.2 — A plant cell (0.063 mm) and the rose black spot fungus (0.009 mm). Not to scale.
(d) What microorganism causes rose black spot (bacterium / fungus / protist / virus)?(e) Give two ways to prevent its spread to another rose bush.(f) Using Figure 1, calculate how many times longer the plant cell is than the microorganism.(g) The infected rose has yellow leaves and is not growing – explain why.
Mark Scheme(d) Fungus.(e) Remove and burn the spotty leaves; move the diseased bush away (or use a fungicide).(f) 0.0630.009 = 7 times longer.(g) The black spots/yellow leaves reduce photosynthesis, so less glucose is made for growth.
Q3
Two plants in a garden were infected with different diseases. Figure 2 shows a leaf from each plant. (6 marks)
Fig 5.3 — Leaf from a rose bush (left) and a tomato plant (right).
Fig 5.3 — Leaf from a rose bush (left) and a tomato plant (right).
(a) Identify the disease shown on each plant and explain how you decided.(b) Describe one method that would prevent the spread of both diseases.(c) Give one method that would kill the microorganism on the rose bush but not the one on the tomato plant.
Mark Scheme(a) Rose bush: rose black spot (a fungus) – dark/black spots on the leaves. Tomato plant: tobacco mosaic virus – a 'mosaic' pattern of discolouration.(b) Remove and burn the infected leaves (and disinfect tools/wash hands).(c) Spray with a fungicide – this kills the fungus (rose black spot) but not the virus (TMV).
Q4
Triple onlyA gardener is looking at the plants in his greenhouse. (4 marks)(a) Give two ways the gardener could identify the pathogen infecting the plants.(b) Describe the appearance of plants with nitrate deficiency and with magnesium deficiency.
Mark Scheme(a) Any two of: look up the symptoms in a gardening manual/reference, use a testing kit, send a sample to a laboratory, look for the pathogen under a microscope.(b) Nitrate deficiency: stunted growth. Magnesium deficiency: yellow leaves (chlorosis).
Q5
Triple onlyFigure 3 shows part of a deadly nightshade plant. Figure 4 shows part of a gorse plant. (3 marks)
Fig 5.4 — Deadly nightshade, with poisonous berries.
Fig 5.4 — Deadly nightshade, with poisonous berries.
Fig 5.5 — A gorse plant.
Fig 5.5 — A gorse plant.
(a) How will the poisonous berries help the deadly nightshade plant to survive?(b) Which type of defence mechanism are the berries (chemical / mechanical / physical)?(c) Suggest how the gorse plant is adapted to defend itself.
Mark Scheme(a) The poison deters/kills herbivores, so they do not eat the plant.(b) Chemical.(c) It has sharp thorns/spines (a mechanical/physical defence) that stop animals eating it.

Lesson 6 · The Immune System

Do Now

Q1
Define pathogen.
Model AnswerA microorganism that causes disease.
Q2
How do bacteria make you ill?
Model AnswerThey release toxins that damage cells.
Q3
210 million people are infected with malaria each year and half survive – how many survive over 3 years?
Model Answer2102 × 3 = 315 million.

Part 1 · Phagocytosis

Read the passage and look at the diagram, then answer the questions.

If a pathogen gets inside the body, the immune system launches a specific response using white blood cells, which travel in the blood. One way they protect us is phagocytosis: white blood cells called phagocytes have a large lobed nucleus that lets them stretch around bacteria, engulf them and digest them with enzymes. Once a phagocyte has ingested as many pathogens as possible, it dies (dead phagocytes make up mucus/pus).

Fig 6.1 — A phagocyte engulfs and digests a bacterial pathogen.
Fig 6.1 — A phagocyte engulfs and digests a bacterial pathogen.

Questions — Phagocytosis

Q1
What is phagocytosis? (2 marks)
Model AnswerWhen a white blood cell (phagocyte) engulfs a pathogen and digests it with enzymes.
Q2
What is a phagocyte? (1 mark)
Model AnswerA white blood cell that engulfs and digests pathogens.
Q3
How does a phagocyte's nucleus help it? (1 mark)
Model AnswerIts large lobed nucleus lets it stretch around and engulf pathogens.
Q4
What does a phagocyte use to digest pathogens? (1 mark)
Model AnswerEnzymes.
Q5
210 million people get malaria each year and half survive – calculate how many survive over 3 years. (2 marks)
Model Answer2102 × 3 = 105 million x 3 = 315 million survivors.
Worked Answer — VESSU
V
Variables infected per year = 210 million · half survive: 210 / 2 = 105 million · over 3 years = ?
E
Equation survivors = infected2 × number of years
S
Substitute = 105 million x 3
S
Solve = 315 million
U
Units survivors
Answer: 315 million survivors
Q6
Where do white blood cells travel? (1 mark)
Model AnswerAround the body in the bloodstream.
Q7
What happens to a phagocyte after it has ingested pathogens? (2 marks)
Model AnswerIt dies (dead phagocytes make up mucus/pus).

Part 2 · Antibodies

Read the passage and look at the diagram, then answer the questions.

A second, very specific response is carried out by white blood cells called lymphocytes. They detect pathogens by the proteins on their surface called antigens. Lymphocytes produce antibodies – proteins that match the shape of the antigens and bind to them, helping to destroy the pathogen. Some lymphocytes become memory cells, which can produce these antibodies again quickly if you are reinfected with the same pathogen.

Fig 6.2 — Lymphocytes multiply and produce antibodies that lock onto and deactivate pathogens.
Fig 6.2 — Lymphocytes multiply and produce antibodies that lock onto and deactivate pathogens.

Questions — Antibodies

Q8
What are antibodies? (2 marks)
Model AnswerProteins made by lymphocytes that match the shape of antigens and bind to them to help destroy the pathogen.
Q9
What are antigens? (2 marks)
Model AnswerProteins on the surface of a pathogen that lymphocytes detect.
Q10
What is the function of memory cells? (2 marks)
Model AnswerThey can produce the right antibodies again quickly if you are reinfected with the same pathogen.
Q11
Which white blood cells produce antibodies? (1 mark)
Model AnswerLymphocytes.
Q12
Why is the antibody response described as specific? (2 marks)
Model AnswerEach antibody only matches one antigen shape, so it works against one particular pathogen.
Q13
How do lymphocytes detect a pathogen? (1 mark)
Model AnswerBy the antigens (proteins) on its surface.

Part 3 · Antitoxins

Read the passage about antitoxins, then answer the questions.

When bacteria enter the body they produce toxins that damage cells and cause illness. Lymphocytes can also produce antitoxins, which bind to these toxins and prevent them from harming your cells (they neutralise them).

So white blood cells protect us in three ways:

  • phagocytosis – engulfing pathogens
  • producing antibodies
  • producing antitoxins
Fig 6.3 — An antitoxin molecule binds to a bacterial toxin and neutralises it.
Fig 6.3 — An antitoxin molecule binds to a bacterial toxin and neutralises it.

Questions — Antitoxins

Q14
State the three ways white blood cells defend the body. (3 marks)
Model AnswerPhagocytosis (engulfing pathogens), producing antibodies, and producing antitoxins.
Q15
What do antitoxins do? (2 marks)
Model AnswerThey bind to the toxins made by bacteria and neutralise them, so they cannot harm cells.
Q16
Why do bacterial toxins make us ill? (1 mark)
Model AnswerThey damage our cells.
Q17
Which white blood cells produce antitoxins? (1 mark)
Model AnswerLymphocytes.
Q18
How is an antitoxin different from an antibody? (2 marks)
Model AnswerAn antitoxin neutralises a toxin; an antibody binds to a pathogen's antigen to help destroy the pathogen.
Q19
Name the two types of white blood cell mentioned. (1 mark)
Model AnswerPhagocytes and lymphocytes.

Exam-style questions

Q1
Name two types of microbe (microorganism) that cause disease in humans. (2 marks)
Mark SchemeAny two of: bacteria, viruses, protists, fungi.
Q2
Bacteria and viruses can cause communicable diseases. (3 marks)(a) Which structure is found in bacterial cells but not animal cells (cell membrane / mitochondrion / nucleus / plasmid)?(b) Describe how mucus and cilia in the trachea prevent pathogens reaching the lungs.
Mark Scheme(a) Plasmid.(b) Mucus traps the pathogens; cilia sweep the mucus (with the trapped pathogens) up and out of the trachea.
Q3
One way the body protects itself against the entry of pathogens is by producing antimicrobial chemicals. Give two other ways the body stops pathogens entering. (2 marks)
Mark SchemeAny two of: the skin acts as a barrier; nose hairs/cilia and mucus trap pathogens; cilia in the trachea sweep mucus out; stomach acid destroys swallowed pathogens; tears contain chemicals that destroy microorganisms.
Q4
White blood cells produce antibodies. Give two other ways that white blood cells protect us against pathogens. (2 marks)
Mark SchemePhagocytosis (engulfing and digesting pathogens) and producing antitoxins (to neutralise bacterial toxins).
Q5
Hepatitis B is a virus found in body fluids such as blood. (4 marks)
Fig 6.4 — A white blood cell engulfing a group of viruses.
Fig 6.4 — A white blood cell engulfing a group of viruses.
(a)(i) The diagram shows a white blood cell attacking viruses. Describe what happens at the 2nd stage.(a)(ii) What type of chemical is released by some white blood cells to attack viruses?(b) Explain why sharing needles spreads hepatitis B.
Mark Scheme(a)(i) The white blood cell engulfs (surrounds and takes in) the viruses.(a)(ii) Antibodies.(b) The virus is in the blood; sharing needles passes infected blood directly from one person to another.
Q6
Some parts of the body are adapted to reduce the entry of live pathogens. Figure 1 shows the trachea. Explain how the trachea is adapted to reduce the entry of live pathogens. (4 marks)
Fig 6.5 — The position of the trachea.
Fig 6.5 — The position of the trachea.
Mark SchemeThe trachea is lined with cells that make mucus, which traps pathogens (and dust) in the air breathed in; ciliated cells have cilia that sweep the mucus, with the trapped pathogens, up and away from the lungs to be swallowed and destroyed by stomach acid.
Q7
Describe the different ways in which white blood cells protect us from infectious diseases. (4 marks)
Mark SchemePhagocytes engulf and digest pathogens; lymphocytes produce antibodies that bind to antigens to destroy pathogens; lymphocytes produce antitoxins that neutralise bacterial toxins; and memory cells give a faster response on reinfection.

Lesson 7 · Vaccines

Do Now

Q1
Name the two types of white blood cell.
Model AnswerPhagocytes and lymphocytes.
Q2
What do phagocytes do?
Model AnswerThey engulf and digest pathogens.
Q3
What two things can lymphocytes produce?
Model AnswerAntibodies and antitoxins.

Part 1 · What is a vaccine?

Read the passage about vaccines, then answer the questions.

Virus infections cannot be cured – there are no drugs that kill the virus without killing your own infected cells, which is also why antibiotics do not work against viruses (they cannot enter cells). The immune system is the only thing that can fight off a virus. A vaccine contains a small amount of dead or inactive pathogen (or its antigens). This makes the white blood cells (lymphocytes) produce antibodies and become memory cells, without you getting ill – so you become immune.

Fig 7.1 — How a vaccine makes you immune.
Fig 7.1 — How a vaccine makes you immune.

Questions — What is a vaccine?

Q1
What does a vaccine contain? (1 mark)
Model AnswerA small amount of dead or inactive pathogen (or its antigens).
Q2
How does a vaccine make a person immune? (3 marks)
Model AnswerIt makes the lymphocytes produce antibodies and become memory cells, so the body can respond quickly if it meets the real pathogen later.
Q3
Why can't viral infections be cured with drugs? (2 marks)
Model AnswerThe virus is inside our own cells, so killing it would mean killing our cells too.
Q4
Why don't antibiotics work against viruses? (1 mark)
Model AnswerAntibiotics cannot enter cells, where viruses reproduce.
Q5
What is the only thing that can fight off a virus? (1 mark)
Model AnswerThe body's immune system.
Q6
What cells produce the antibodies after vaccination? (1 mark)
Model AnswerLymphocytes (white blood cells).
Q7
Does a vaccine make you ill? (1 mark)
Model AnswerNo – it contains only a small amount of dead or inactive pathogen.

Part 2 · Primary and secondary responses

Read the passage and look at the diagram, then answer the questions.

Vaccines make the body produce memory cells, which remember how to make the antibodies for that specific pathogen. If the person is infected by the same pathogen later, the memory cells make lots of antibodies quickly (a secondary response) to destroy it before it makes the person ill. The first time (the primary response) is slower and makes fewer antibodies. A different pathogen has different antigens, so it would need a new primary response.

Fig 7.2 — The secondary response is faster and larger than the primary.
Fig 7.2 — The secondary response is faster and larger than the primary.

Questions — Primary and secondary responses

Q8
Why is the secondary response faster than the primary response? (2 marks)
Model AnswerMemory cells from the first exposure can make the right antibodies quickly.
Q9
Describe two differences between the secondary and primary response. (2 marks)
Model AnswerThe secondary response is faster and produces more antibodies.
Q10
Why do you need a different vaccine for each disease? (2 marks)
Model AnswerEach pathogen has different antigens, so different specific antibodies (and memory cells) are needed.
Q11
What do memory cells remember? (1 mark)
Model AnswerHow to make the antibodies for that specific pathogen.
Q12
In the secondary response, why doesn't the person get ill? (2 marks)
Model AnswerThe antibodies are made so quickly that the pathogen is destroyed before it can cause illness.
Q13
How does a vaccine help prevent the spread of a virus? (2 marks)
Model AnswerA vaccinated person does not get infected, so they cannot pass the virus on to others.

Part 3 · Herd immunity

Read the passage about herd immunity, then answer the questions.

Not everyone can be vaccinated (e.g. babies and people with immune deficiencies). To protect them, herd immunity is used: vaccinating most of the population means there are not enough infected people to pass the disease on to the vulnerable. Recently, some parents have chosen not to vaccinate their children, with no good evidence for this decision – causing a rise in deaths from once-rare viral diseases like measles.

Fig 7.3 — Herd immunity: if most people are immune, the disease cannot reach the vulnerable.
Fig 7.3 — Herd immunity: if most people are immune, the disease cannot reach the vulnerable.

Questions — Herd immunity

Q14
What is herd immunity? (2 marks)
Model AnswerWhen most of the population is vaccinated, so there are not enough infected people to pass the disease to the vulnerable.
Q15
Why can't everyone be vaccinated? (2 marks)
Model AnswerSome people cannot be, such as babies and people with immune-system deficiencies.
Q16
What is the advantage of vaccinating a large proportion of the population? (1 mark)
Model AnswerIt gives herd immunity, protecting those who cannot be vaccinated.
Q17
What has happened because some parents stopped vaccinating their children? (2 marks)
Model AnswerThere has been a rise in deaths from once-rare viral diseases such as measles.
Q18
How does herd immunity protect a baby who cannot be vaccinated? (2 marks)
Model AnswerIf most people around the baby are immune, the disease cannot spread to reach the baby.
Q19
Why is it important that most of the population is vaccinated? (2 marks)
Model AnswerSo there are not enough infected people for the disease to spread, protecting those who cannot be vaccinated.

Exam-style questions

Q1
Polio is caused by a virus; children are given the polio vaccine. (2 marks)(a)(i) It is hard to kill the polio virus inside the body because it (is not affected by drugs / lives inside cells / produces antitoxins).(iii) The vaccine stimulates white blood cells to produce (antibiotics / antibodies / drugs).
Mark Scheme(a)(i) Lives inside cells.(iii) Antibodies.
Q2
People can be immunised against a pathogen by injecting them with a vaccine. What does a vaccine contain? (1 mark)
Mark SchemeA small amount of dead or inactive pathogen (or its antigens).
Q3
Flu is an infectious disease caused by a virus. Doctors do not prescribe antibiotics to patients with flu. State why. (1 mark)
Mark SchemeAntibiotics only kill bacteria; they have no effect on viruses (so they would not treat the flu).
Q4
People may be immunised against diseases using vaccines. (5 marks)(a)(i) Which part of a vaccine stimulates the body's defence system?(ii) A vaccinated person meets the measles pathogen but does not catch measles – explain why.
Mark Scheme(i) The dead/inactive pathogen (its antigens).(ii) Memory cells from the vaccination recognise the antigens and quickly produce many antibodies, destroying the pathogen before it causes illness.
Q5
Chickenpox is a disease that cannot be treated with antibiotics. (3 marks)(a) What type of pathogen causes chickenpox?(e) If more people were vaccinated, fewer children would get chickenpox. Tick the two correct reasons: (children are less likely to meet someone with the disease / more people will have the correct antibodies / drugs to treat it stop working).
Mark Scheme(a) A virus.(e) Children are less likely to come into contact with someone with the disease; and more people will have the correct antibodies (herd immunity).
Q6
Figure 1 represents the reaction of antibody and antigen for disease X. Using the diagram, suggest why the body's defence against disease X would not be effective against disease Y. (2 marks)
Fig 7.4 — Antibodies binding the antigen of disease X; the antigen of disease Y has a different shape.
Fig 7.4 — Antibodies binding the antigen of disease X; the antigen of disease Y has a different shape.
Mark SchemeThe antibody is a specific shape that fits only the antigen of disease X. Disease Y has a differently shaped antigen, so the disease X antibodies cannot bind to it, and a new primary response (new antibodies) would be needed.
Q7
A child is vaccinated against measles, then infected with measles weeks later. The graph shows the number of measles antibodies in the child's blood from before the vaccination until after the infection. (4 marks)
Fig 7.5 — Measles antibodies in the blood after vaccination and after infection.
Fig 7.5 — Measles antibodies in the blood after vaccination and after infection.
ii) Describe other differences in antibody production after infection compared with after vaccination.iii) Why won't the measles vaccine protect against rubella?
Mark Scheme(ii) After infection the antibodies are produced faster and in greater quantity (secondary response).(iii) Rubella has different antigens, so the measles memory cells/antibodies do not match it.

Lesson 8 · Monoclonal AntibodiesTriple only

Do Now

Q1
What is a lymphocyte?
Model AnswerA white blood cell that makes antibodies.
Q2
What is a vaccine?
Model AnswerA small amount of dead/inactive pathogen that makes you immune.
Q3
What is an antibody?
Model AnswerA protein that binds to a specific antigen.

Part 1 · Producing monoclonal antibodiesTriple only

Read the passage and look at the diagram, then answer the questions.

Monoclonal antibodies (mAbs) are antibodies produced to target one particular cell or chemical, because they are made from a single clone of cells.

They are made in these steps:

  • inject a mouse with the antigen
  • the mouse's immune system makes lymphocytes that produce a specific antibody
  • the lymphocytes are combined with a tumour cell to make a hybridoma
  • the hybridoma is cloned to make many cells that all produce the same antibody
  • the antibodies are collected and purified
Fig 8.1 — Producing monoclonal antibodies.
Fig 8.1 — Producing monoclonal antibodies.

Questions — Producing monoclonal antibodies

Q1
What are monoclonal antibodies? (2 marks)
Model AnswerAntibodies produced from a single clone of cells, so they all target the same particular antigen.
Q2
What is the first step in producing monoclonal antibodies? (1 mark)
Model AnswerInject a mouse with the antigen.
Q3
What is a hybridoma? (2 marks)
Model AnswerA cell made by combining a lymphocyte with a tumour cell.
Q4
Why is the lymphocyte combined with a tumour cell? (2 marks)
Model AnswerThe tumour cell divides rapidly, so the hybridoma can be cloned to make many antibody-producing cells.
Q5
What is done with the hybridoma after it is made? (1 mark)
Model AnswerIt is cloned to make many identical antibody-producing cells.
Q6
Why are the antibodies all the same? (2 marks)
Model AnswerThey come from a single clone of cells, so they are identical and specific to one antigen.
Q7
What is the final step in producing monoclonal antibodies? (1 mark)
Model AnswerThe antibodies are collected and purified.

Part 2 · Uses of monoclonal antibodiesTriple only

Read the table of uses, then answer the questions.

UseHow it works
Pregnancy testsmAbs bind to the HCG hormone in urine – a coloured line appears if pregnant
Measuring substances in bloodmAbs bind to specific chemicals so the amount can be measured (to diagnose disease)
Locating pathogensmAbs with a fluorescent dye bind to antigens and glow, showing where an infection is
Treating cancermAbs carry a toxic drug to cancer cells' antigens, destroying them without harming other cells

Questions — Uses of monoclonal antibodies

Q8
How do monoclonal antibodies work in a pregnancy test? (2 marks)
Model AnswerThey bind to the HCG hormone in urine, producing a coloured line if the person is pregnant.
Q9
How can monoclonal antibodies be used to locate pathogens in the body? (2 marks)
Model AnswerThey are attached to a fluorescent dye and bind to the pathogen's antigens, so they glow under special light, showing where the infection is.
Q10
How can monoclonal antibodies treat cancer? (3 marks)
Model AnswerA toxic drug is attached to the mAb; it binds to antigens on cancer cells and delivers the drug to destroy them, without harming other cells.
Q11
What do monoclonal antibodies bind to in a pregnancy test? (1 mark)
Model AnswerThe HCG hormone.
Q12
Why is using mAbs to treat cancer better than some other treatments? (2 marks)
Model AnswerThey target only the cancer cells, so healthy cells are not harmed.
Q13
How can mAbs help diagnose a disease from a blood sample? (2 marks)
Model AnswerThey bind to a specific chemical/hormone so its amount can be measured.

Part 3 · Evaluating monoclonal antibodiesTriple only

Read the passage about pros and cons, then answer the questions.

Advantages of monoclonal antibodies:

  • they can treat a wide range of diseases
  • they target only the affected cells, so healthy cells are not harmed

Disadvantages:

  • they create more side effects than expected (partly because they are produced using mice)
  • they are not yet as widely used as people first hoped

Questions — Evaluating monoclonal antibodies

Q14
Give two advantages of monoclonal antibodies. (2 marks)
Model AnswerThey can treat a wide range of diseases, and they target only the affected cells (healthy cells are not harmed).
Q15
Give one disadvantage of monoclonal antibodies. (1 mark)
Model AnswerThey cause more side effects than expected (or they are not as widely used as hoped).
Q16
Why might monoclonal antibodies cause side effects? (2 marks)
Model AnswerThey are produced using mouse cells, which can cause unexpected reactions in humans.
Q17
Why is targeting only affected cells an advantage? (2 marks)
Model AnswerHealthy cells are not damaged, so there are fewer harmful effects than with treatments that affect all cells.
Q18
Are monoclonal antibodies used as widely as first hoped? (1 mark)
Model AnswerNo – they are not yet as widely used as expected.
Q19
Suggest why monoclonal antibodies were not adopted as quickly as first hoped. (2 marks)
Model AnswerThey produced more side effects than expected, so their use has been more limited.

Exam-style questionsTriple only

Q1
A drug used to reduce the risk of liver rejection after a transplant contains monoclonal antibodies specific to an antigen on liver cells. The figure shows part of the production process. (8 marks)
Fig 8.2 — Cells used to produce monoclonal antibodies.
Fig 8.2 — Cells used to produce monoclonal antibodies.
(c) Name the three cell types A, B and C in the figure.(d) How is the mouse stimulated to produce cell type A?(e) Explain how the monoclonal antibody stops the patient's white blood cells from attacking the donor liver.(f) Give one use of monoclonal antibodies (not pregnancy tests).
Mark Scheme(c) A = lymphocyte, B = tumour cell, C = hybridoma.(d) By injecting it with the antigen.(e) The monoclonal antibody is specific to the antigen on the donor liver cells; it binds to those antigens and covers them, so the patient's white blood cells cannot recognise and attack the donor cells.(f) Any one of: measuring chemicals in blood/diagnosis, locating pathogens, treating cancer.
Q2
A monoclonal antibody treats pancreatic cancer. Explain how it works. (3 marks)
Mark SchemeThe mAb is specific to antigens on the pancreatic cancer cells; it carries a toxic drug; it binds to the cancer cells and delivers the drug to kill them, without harming healthy cells.
Q3
To make mAbs for RSV, a mouse is injected with the virus. (5 marks)(b) Describe the remaining steps.(c) Describe how injecting the mAb helps treat a patient with RSV.
Mark Scheme(b) The mouse makes lymphocytes that produce a specific antibody; combine a lymphocyte with a tumour cell to make a hybridoma; clone the hybridoma; collect and purify the antibodies.(c) The mAbs bind to antigens on the RSV virus, helping to destroy it / mark it for destruction.

Lesson 9 · Discovering and Developing Drugs

Do Now

Q1
What medicine might we take to stop pain?
Model AnswerA painkiller.
Q2
Triple onlySummarise how monoclonal antibodies are produced.
Model AnswerInject a mouse with antigen, make a hybridoma from a lymphocyte and tumour cell, clone it, then collect the antibodies.
Q3
Triple onlyWhy might a plant with chlorosis not grow well?
Model AnswerWithout chlorophyll it cannot photosynthesise to make glucose for growth.

Part 1 · Where drugs come from

Read the table of drug origins, then answer the questions.

Many drugs originated from plants (which make antibacterial chemicals and toxins to defend themselves) and from microorganisms. Most drugs are now made synthetically in the pharmaceutical industry, but some still start from a natural chemical.

DrugSource and useSource
AspirinFrom willow tree bark – a painkiller, also used to prevent heart attacks/strokes and reduce fever
DigitalisFrom foxgloves – used to treat heart conditions (controls heart rate)
PenicillinFrom Penicillium mould – the first antibiotic, discovered by Alexander Fleming in 1928

Questions — Where drugs come from

Q1
What kind of medicine is aspirin? (1 mark)
Model AnswerA painkiller.
Q2
Which drug originated from willow? (1 mark)
Model AnswerAspirin.
Q3
Which plant did digitalis come from, and what does it treat? (2 marks)
Model AnswerFoxgloves; it treats heart conditions (controls heart rate).
Q4
Who discovered penicillin, and what kind of medicine is it? (2 marks)
Model AnswerAlexander Fleming; it is an antibiotic.
Q5
Where did penicillin originate from? (1 mark)
Model AnswerPenicillium mould.
Q6
Why do plants make antibacterial chemicals and toxins? (2 marks)
Model AnswerTo defend themselves against bacterial pathogens and to deter herbivores from eating them.
Q7
In what year was penicillin discovered? (1 mark)
Model Answer1928.

Part 2 · Painkillers

Read the passage about painkillers, then answer the questions.

Painkillers are drugs that relieve pain – examples include aspirin, paracetamol, ibuprofen and opiates (e.g. morphine and codeine). Painkillers, cough medicines and cold remedies do not cure the disease, because they do not kill the pathogen – they only relieve the symptoms caused by the pathogen (e.g. reducing fever, aches, pains or congestion).

Questions — Painkillers

Q8
What do painkillers do? (1 mark)
Model AnswerThey relieve pain.
Q9
Give an example of a common painkiller. (1 mark)
Model AnswerAny one of: aspirin, paracetamol, ibuprofen, morphine, codeine.
Q10
Why don't painkillers cure infectious diseases? (2 marks)
Model AnswerThey do not kill the pathogen – they only relieve the symptoms.
Q11
What do cough and cold remedies do? (2 marks)
Model AnswerThey relieve symptoms (e.g. congestion), but do not cure the disease.
Q12
Name an opiate painkiller. (1 mark)
Model AnswerMorphine or codeine.
Q13
What is the difference between relieving symptoms and curing a disease? (2 marks)
Model AnswerRelieving symptoms makes you feel better but the pathogen is still there; curing means the pathogen is destroyed.
Q14
Do painkillers treat the cause of an illness or its symptoms? (2 marks)
Model AnswerOnly the symptoms – they do not kill the pathogen causing the illness.

Part 3 · Drug testing

Read the passage and look at the diagram, then answer the questions.

A new drug must be tested before use, and the results peer reviewed (checked by other scientists) before publication to prevent errors and bias.

Testing checks three things:

  • toxicity – is it harmful?
  • efficacy – does it work?
  • dosage – how much is needed?

Pre-clinical testing uses cells and tissues, then animals.

Clinical trials then follow:

  • Phase 1 tests low doses on healthy volunteers, to check for side effects
  • Phase 2 tests on patients with the illness, to check efficacy and dosage

In a double-blind trial some patients get a placebo (no drug) and neither doctor nor patient knows who got which, to check the drug really works.

Fig 9.1 — The stages of testing a new drug.
Fig 9.1 — The stages of testing a new drug.
Fig 9.2 — The phases of clinical trials, from pre-clinical animal studies through to approval.
Fig 9.2 — The phases of clinical trials, from pre-clinical animal studies through to approval.

Questions — Drug testing

Q15
What three things does drug testing check for? (3 marks)
Model AnswerToxicity (is it harmful), efficacy (does it work) and dosage (how much is needed).
Q16
What is the main thing pre-clinical testing checks for? (1 mark)
Model AnswerToxicity (using cells, tissues then animals).
Q17
Why are healthy volunteers used in Phase 1? (1 mark)
Model AnswerIt would be unfair to risk making unhealthy patients worse.
Q18
Define 'placebo'. (1 mark)
Model AnswerA treatment that does not contain the drug (a dummy).
Q19
What is a double-blind trial? (2 marks)
Model AnswerA trial where neither the doctor nor the patient knows who received the real drug or the placebo.
Q20
Why is peer review important? (2 marks)
Model AnswerOther scientists check the results to prevent incorrect conclusions and avoid bias before publication.
Q21
What is the main purpose of Phase 2 testing? (1 mark)
Model AnswerTo test the efficacy and dosage of the drug on patients with the illness.

Exam-style questions

Q1
Where does the drug digitalis, used to slow the heart rate, originate from (bacteria / foxgloves / mould / willow)? (1 mark)
Mark SchemeFoxgloves.
Q2
Scientists developed a new pain-killing drug, drug X. Painkillers do not cure infectious diseases. Why? (1 mark)
Mark SchemePainkillers only relieve the symptoms; they do not kill the pathogen that causes the disease.
Q3
Antibiotics are used to kill some types of pathogen. Alexander Fleming discovered penicillin when a Petri dish of bacteria was contaminated with a fungus. The diagram shows the Petri dish. (4 marks)
Fig 9.3 — Fleming's Petri dish: fewer bacterial colonies grew near the fungus.
Fig 9.3 — Fleming's Petri dish: fewer bacterial colonies grew near the fungus.
(a) Which illness could be treated with an antibiotic (AIDS / measles / salmonella / type 2 diabetes)?(c) The greater the distance from the fungus, the more bacteria grew. Suggest one reason for this.(d) Give two reasons why Fleming's discovery was important.
Mark Scheme(a) Salmonella.(c) The fungus released an antibacterial substance (antibiotic) that spread out and killed nearby bacteria, so fewer grew close to it (less reaches further away).(d) It was the first antibiotic; it has saved many lives by treating bacterial infections.
Q4
Antibiotics were developed in the 1940s and kill bacteria. (3 marks)(b)(i) Which one is an antibiotic (cholesterol / penicillin / thalidomide)?(ii) The use of antibiotics has not reduced the death rate from all diseases to zero. Suggest two reasons why.
Mark Scheme(b)(i) Penicillin.(ii) Any two of: antibiotics do not kill viruses; some bacteria have become antibiotic resistant; many diseases are non-communicable (e.g. heart disease, cancer) and are not caused by bacteria.
Q5
Different antibiotics destroy bacteria in different ways. Some disrupt the cell membrane, some the cell wall, and some stop ribosomes working. (5 marks)(a) Antibiotics that disrupt the cell membrane often cause more side effects in humans than those that disrupt the cell wall. Suggest why.(b) Some antibiotics prevent ribosomes working. Suggest how this damages the bacterium.(c) Some people think governments should pay drug companies to develop new antibiotics. Suggest why.
Mark Scheme(a) Human (animal) cells also have a cell membrane but no cell wall, so a membrane-disrupting antibiotic can damage human cells too.(b) Without working ribosomes the bacterium cannot make proteins/enzymes, so it cannot grow or function and dies.(c) New antibiotics are rarely prescribed (to slow resistance) so companies make little profit, so without funding they will not develop the new antibiotics that are needed to fight resistant bacteria.
Q6
A new drug must be tested before it is sold. (6 marks)(a) What is the main purpose of pre-clinical testing?(b)(i) What is the main purpose of Phase 1 testing? (ii) Why are healthy volunteers used in Phase 1?(c) What is the main purpose of Phase 2/3?(d)(i) What is a placebo? (ii) In a double-blind trial, who knows who received the placebo?
Mark Scheme(a) To test for toxicity (harm).(b)(i) To check for harmful side effects.(ii) So that unhealthy patients are not made worse.(c) To test efficacy and dosage on patients with the illness.(d)(i) A dummy treatment with no drug.(ii) Neither the patients nor the doctors.
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