bioInfectionAndResponse
3.1 Communicable Diseases
Communicable (infectious) diseases are caused by pathogens and spread between individuals or from animals.
3.1.1 Pathogens
Pathogens are microorganisms causing disease. Main types:
Bacteria
Single-celled prokaryotes.
Reproduce rapidly and produce toxins damaging cells.
Examples: Salmonellosis, Gonorrhoea.
Viruses
Smaller than bacteria.
Replicate by invading host cells, causing damage.
Examples: Measles, HIV, Tobacco Mosaic Virus (plants).
Fungi
Eukaryotic (single or multicellular).
Grow on organisms, release spores.
Examples: Athlete's Foot, Rose Black Spot (plants).
Protists
Single-celled eukaryotes.
Often parasitic, transferred by vectors.
Example: Malaria (Plasmodium protist, transmitted by mosquitoes).
3.1.2 Spreading Pathogens
Direct contact: Physical contact with an infected individual.
Droplet infection (airborne): Inhaling pathogens from coughs/sneezes.
Contaminated food/water: Consuming tainted food/water.
Vectors: Organisms (e.g., insects) carrying pathogens between hosts.
3.2 Principles of Disease
3.2.1 Viral Diseases
Measles
Symptoms: Fever, red skin rash.
Spread: Droplet infection.
Prevention: MMR vaccine.
Complications: Pneumonia, encephalitis.
HIV (Human Immunodeficiency Virus)
Symptoms: Initially flu-like, can lead to AIDS.
Spread: Sexual contact, shared needles, mother-to-baby.
Treatment: Antiretroviral drugs control virus, preventing AIDS by attacking immune cells.
Tobacco Mosaic Virus (TMV)
Affects plants.
Symptoms: Mosaic pattern, discolouration, stunted growth.
Effect: Reduces photosynthesis.
3.2.2 Bacterial Diseases
Salmonella
Symptoms: Fever, cramps, vomiting, diarrhoea.
Spread: Contaminated food (e.g., uncooked poultry).
Prevention: Vaccinating poultry, hygienic food prep.
Gonorrhoea
Symptoms: Discharge, painful urination.
Spread: Sexual contact.
Treatment: Antibiotics (resistance growing).
Prevention: Condoms.
3.2.3 Fungal Diseases
Rose Black Spot
Affects rose plants.
Symptoms: Purple/black spots on leaves, yellowing, leaf drop.
Spread: Wind, water.
Treatment: Fungicides, removing affected leaves.
3.2.4 Protist Diseases
Malaria
Symptoms: Recurrent fever, chills, sweating.
Spread: Mosquitoes (vector) transfer Plasmodium protist.
Prevention: Mosquito control, nets, antimalarial drugs.
3.3 Non-Specific Defence Systems
The body's initial barriers:
Skin: Physical barrier; scabs prevent entry.
Nose: Hairs and mucus trap pathogens.
Trachea and Bronchi: Mucus traps pathogens, cilia sweep them up.
Stomach: Hydrochloric acid kills most pathogens in food/drink.
3.4 The Immune System
White blood cells lead the immune response:
Phagocytes: Engulf and digest pathogens (phagocytosis). Non-specific.
Lymphocytes: Specific defence.
Produce antibodies (target specific pathogen antigens/toxins).
Produce antitoxins (neutralise toxins).
Form memory cells after infection for rapid future response (immunity).
3.5 Vaccination
Introduces a harmless pathogen dose (dead, inactive, weakened, or antigens) to stimulate antibody and memory cell production, providing immunity.
Herd immunity: Protects unvaccinated individuals by reducing disease spread when a significant proportion of the population is vaccinated.
3.6 Monoclonal Antibodies
Identical antibodies produced from a single B-lymphocyte clone (hybridoma cells).
Production: Mouse B-lymphocytes (producing specific antibodies) are fused with myeloma (tumour) cells to form hybridoma cells, which divide indefinitely and produce large amounts of the desired antibody.
Uses:
Diagnosis: Pregnancy tests (detect HCG), pathogen detection, blood typing.
Treatment: Targeted drug delivery (e.g., to cancer cells), autoimmune disease treatment, preventing organ rejection.
Research: Identifying specific chemicals/cells.
3.7 Development of Drugs
3.7.1 Antibiotics
Kill bacteria or prevent growth without harming human cells.
Ineffective against viruses.
Antibiotic resistance: Overuse leads to resistance; complete courses and avoid over-prescription.
3.7.2 Painkillers and Other Drugs
Painkillers: Treat symptoms (e.g., aspirin), do not kill pathogens.
Antivirals: Inhibit viral replication (e.g., Tamiflu for influenza, antiretrovirals for HIV).
3.7.3 Drug Discovery and Development
Drugs originate from plants, microorganisms, or chemical synthesis. Examples: Digitalis (foxgloves), Aspirin (willow bark), Penicillin (Penicillium mould).
Rigorous testing for efficacy (effectiveness), toxicity (safety), and dosage:
Preclinical testing: On cells, tissues, and animals.
Clinical trials: On healthy volunteers (low dose) then patients (optimum dose), compared with placebos in double-blind trials.
3.8 Plant Diseases and Defence Responses
3.8.1 Plant Diseases
TMV: Damages chloroplasts, reduces photosynthesis.
Rose Black Spot: Reduces photosynthesis due to leaf drop.
Aphids: Pests feeding on phloem sap, weakening plants.
Ion deficiencies: E.g., nitrates (stunted growth), magnesium (chlorosis).
3.8.2 Plant Defences
Plants have physical, chemical, and mechanical defences:
Physical barriers:
Cell walls: Strong barriers.
Waxy cuticle: Prevents water loss and pathogen entry.
Bark/dead cells: Protective stem layer.
Chemical defences:
Antibacterial chemicals: Deter pathogens/pests.
Poisons: Deter herbivores (e.g., nicotine, digitalis).
Mechanical adaptations:
Thorns/hairs: Deter animals.
Leaves that droop or curl: To dislodge insects.
Mimicry: To trick animals.