3.1.1 Communicable (infectious) diseases
Pathogens |
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How cause?
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Bacteria |
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Viruses | Live & reproduce rapidly inside cell – cell damage | |
How spread?
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By air |
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By water | Dirty water – cholera | |
Direct contact |
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How prevent?
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What is pandemic? (1)
- A disease affecting ppl in many countries
3.1.2 Viral diseases
Measles
Spread by | Inhalation of droplets from coughs/sneezes |
Symptoms |
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Prevention |
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HIV/AIDs
Spread by |
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Symptoms |
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Treatment | Antiretroviral drugs to control attack |
Prevention |
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Tobacco mosaic virus (TMV)
Spread by | Contact between healthy & infected plants & vectors |
Symptoms | Give distinctive ‘mosaic’ pattern of discoloration on leaves coz viruses destroy cells |
How affect growth of plants? |
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Prevention |
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All viral diseases – no treatment
3.1.3 Bacterial diseases
Salmonella food poisoning
Caused by |
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Spread by | Bacteria ingested in food – disrupt balance of natural gut bacteria |
Symptoms |
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Prevention |
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Gonorrhoea – sexually transmitted disease (STD)
Spread by | Unprotected sexual contact with infected person |
Symptoms |
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Prevention |
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Treatment | Antibiotic penicillin |
3.1.4 Fungal diseases
Rose black spot
Spread | In environment by wind & water |
Symptoms |
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Treatment | Use fungicides |
Prevention | Remove / burn affected leaves / stems |
3.1.5 Protist diseases
Malaria
Spread by | Mosquitos (act as vectors coz they transmit disease) |
Symptoms |
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Treatment | Take antimalarial drugs – kill parasites in blood |
Prevention |
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3.1.6 Human defence systems
Non-specific defence system
Skin |
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Nose | Hair & mucus trap & prevent pathogens entering lungs |
Trachea & bronchi |
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Stomach | Produce HCl – kill pathogens in food |
White blood cell
- Phagocytes (non-specific) & Lymphocytes (specific)
How?
- Ingest pathogens (phagocytes)
Phagocytes move towards, changes shape, attack pathogen, engulfs & digest it with enzymes
2. Produce antibodies (protein) (made by lymphocytes)
- Have complementary shape – specific antibody for specific pathogen
- Allow binding with antigens (foreign microorganisms)
- If same pathogen re-enters body, WBC respond quickly, produce correct antibodies, prevent infection
- 3. Produce antitoxins – counteract toxins
In conclusion – lead to immunity from pathogens
3.1.7 Vaccination
How prevent?
- Contain small amount of dead or inactive forms of pathogen
- Stimulate WBC to respond & produce antibodies quickly specific to pathogen in large quantities to kill pathogen
- Reduce spread of infection – ppl immune
- Prevent illness in an individual
Herd immunity
- Immunising large proportion of population
- Reduce spread of infection / pathogens
MMR vaccine – protects against measles, mumps & rubella
3.1.8 Antibiotics and painkillers
Antibiotics eg penicillin
- Cure bacterial diseases by killing infective bacteria inside body
- Damage bacterial cells – kill bacteria
X kill virus – coz viruses live inside cells & are inaccessible to antibiotic
Overuse – speed up development of resistant strains of bacteria
How bacteria become resistant?
- Mutation
- Some resistant to antibiotics – survive
- Reproduce by binary fission
- Pass gene for resistance of offspring
- Increase population of resistant strain
Why resistant strain spread?
- Ppl not immune to it
- Treatment is not effective
How to reduce resistant strain?
- Reduce use of antibiotics for mild infection
- Patient complete course of antibiotics – kill all bacteria
- Restrict agricultural use of antibiotics
Painkillers eg aspirin, paracetamol
- Treat symptoms
- Don’t kill pathogens
3.1.9 Discovery and development of drugs
Drugs – chemical that affect body chemistry
Discovery – traditionally drug extracted from plants & microorganisms
Plants |
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Microorganism |
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Now, most new drugs are synthesised by chemists in pharmaceutical industry. However, the starting point may still be a chemical extracted from a plant.
Development – testing new drugs
- Pre-clinical trials in lab of new drugs on cells, tissues & live animals
- Test for toxicity, dosage & efficacy
2. Clinical trials – test on healthy volunteers & patients at very low doses
- Monitor for safety & side effects
- If drug is found to be safe, further clinical trials are carried out to find the optimum dose for the drug
3. Double-blind trial
- Placebo & drug is randomly allocated to large no of patients in groups
- Doctors & patients don’t know who has new drug or placebo so
- Data won’t be affected by knowledge
- To verify efficiency & determine correct dose
4. Peer review of data & analysis of result
- Prevent false claims
- Check results are valid, avoid bias
Placebo
- Tablet with no drug / chemical & has no effect
- Used to compare & prove effectiveness of drugs
Placebo effect
- Ppl expect treatment to work so they feel better even though it doesn’t do anything
Why trial is reliable? Large no of ppl
Why stopped early? Sufficient information gained
Why manufacturers don’t take part? They could cheat
Repeat experiment – improve reliability
Why data is unreliable? Ppl lies
Factor similar in volunteers – age & sex