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MICRO-ORGANISMS ……….. and DISEASE. DISEASE IN HUMANS  Types of disease can be categorised in many different ways.  Looking at CAUSE of disease the three.

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Presentation on theme: "MICRO-ORGANISMS ……….. and DISEASE. DISEASE IN HUMANS  Types of disease can be categorised in many different ways.  Looking at CAUSE of disease the three."— Presentation transcript:

1 MICRO-ORGANISMS ……….. and DISEASE

2 DISEASE IN HUMANS  Types of disease can be categorised in many different ways.  Looking at CAUSE of disease the three main groups are:  Biological agents including micro-orgs eg. viruses  Faulty genes (inheritance) eg. CF  Environmental factors eg. Smoking Note: Generally both inherited and environmental diseases are also classed as ‘NON-INFECTIOUS’  If any disease is to be stopped both prevention and cure must be considered……

3 1. Prevention Throughout history, particularly since Victorian times, advancements have been made to deal with disease. Prevention:  Sewerage systems (public health)  Refuse collection  Water purification  Hygiene  Nutrition  Education  Standard of living  Immunisation

4 2. Treatment Throughout history, particularly since WW2, advancements have been made in ways to treat disease. Treatments:  Medical help available to all (NHS)  Anaesthetics  Analgesics  Antiseptics  Antibiotics  Operating techniques eg. Key hole surgery  Development of disease specific treatments eg. chemo and radiotherapy  Genetic engineering

5 Problems continue…… Despite these advance ‘we’ still have major problems with fighting disease.  Antibiotic resistance in bacteria eg.MRSA  Disease caused by social influences: eg.drug abuse, obesity, old age  Viral diseases eg. HIV/AIDS

6 Infectious diseases  Caused by micro-organisms including:  Bacteria (Prokaryotes)  Fungi  Viruses Disease may also be caused by parasitic macro-organisms  The spread of infectious diseases can be (and is) prevented using simple hygiene: Answer Q. e Page 183 (TS bk)

7 Bacteria Bacteria are prokaryotes. These are all single- celled organisms but their cells are very different to the animal and plant cells studied in Year 10:  No cell wall  No distinct nucleus (DNA in long strands and small ‘circles’ or plasmids)  Reproduce by ‘binary fission’  May produce harmful toxins eg. in TETANUS the toxin paralyses the jaw and thoracic muscles eg. Whooping cough, MRSA, pneumonia, septicaemia, cholera, TB

8 Fungi Yeasts, moulds, mushrooms etc were once classified as PLANTS, but now form a separate Kingdom ‘FUNGI’ WHY?......  Do not contain chlorophyll (no photosynthesis) so are…  Heterotrophic feeders, growing directly on ‘food’  Microscopic fungal threads or ‘hyphae’ grow into a ‘mycelium’ (visible mass of hyphae) on the food  Asexual reproduction (spores) eg. Athlete’s foot, thrush (oral, vaginal, systemic)

9 Viruses Viruses are so small that they are only visible using EM. They are considered to be non-living organisms. WHY?  Cannot perform MRS GREN  No cell, just a protein ‘coat’ containing DNA or RNA  Reproduce by taking control of a cell’s DNA eg. common cold, polio, measles, chickenpox, AIDS

10 Parasites  ‘Larger’ organisms (including protoctista) which live on/in a host organism. Note: the host does not benefit in any way from the presence of the parasite eg protoctista: plasmodium (Malaria) worms: tapeworm, toxocara insects: fleas, headlice

11 HIV  Human Immunodeficiency Virus  Contracted by sexual contact or direct transfer of body fluids eg. shared needles of drug users  Infects and destroys the immune system, specifically white blood cells (lymphocytes), preventing the production of antibodies  Body becomes susceptible to invasion from other micro-organisms leading to……..AIDS

12 AIDS  Acquired Immune Deficiency Syndrome  People with HIV eventually die from a collection (syndrome) of diseases that their immune system cannot prevent or fight off eg pneumonia, TB, various cancers

13 Preventing HIV and AIDS  Unless tested a person may be unaware for many years (8+ on average) that they are infected with HIV  During this time they may unknowingly infect others  Precautions should be taken:  fewer sexual partners  safe-sex (condom)  clean needles for drug use/abuse

14 Fighting Disease - Antiseptics  Chemicals used to kill micro-organisms on the SURFACE of the skin  Very useful for pre-surgical cleansing to avoid micro-organisms entering body  Very useful for cleaning surfaces/equipment to be used in surgery  But in some cases can delay healing as may destroy body cells as well as micro- organisms

15 Fighting Disease - Antibiotics  Drugs that kill or slow down the growth of bacteria INSIDE the body (Antibiotics do not affect VIRUSES)  Antibiotics are produced naturally by fungi and plants and were first discovered by Alexander Fleming in 1928. With Chain and Florey the first antibiotic, penicillin, was manufactured for public use  Many strains of bacteria are developing antibiotic RESISTANCE QHow does antibiotic resistance develop?  Infections like MRSA will become more common unless antibiotic resistance is reduced QHow can antibiotic resistance be reduced?

16 Fighting Disease – New Solutions  New antibiotics – expensive and slow and bacteria will soon develop resistance again  Chemically alter existing drugs (antibiotics) – bacteria will soon develop resistance again  Phage technology, using specific viruses to attack and kill bacteria QWhat are the possible advantages and disadvantages of using phage technology

17 Preventing disease - Immunity  Immunity – the means by which the body protects itself from disease  Active Immunity – long lasting immunity acquired as a result of the disease itself or a vaccination against it  Passive Immunity – short lived immunity from introducing antibodies into the body eg for tetanus treatment and through pregnancy and breast feeding

18 Preventing disease - Immunisation Immunisation – where the body is encouraged to make specific antibodies Artificial immunisation uses vaccination HOW DOES IT WORK? 1.A dead or mild form of a pathogen is introduced into the body (often by injection) 2.The body produces specific antibodies in response to the dead/mild form of the pathogen 3.If a virulent form of that pathogen then invades the body the specific antibodies are ready to destroy it Note: Edward Jenner produced the world’s first vaccine against SMALLPOX in 1796 using cowpox virus

19 Artificial Immunisation - Problems  Pathogens may mutate so that antibodies will no longer ‘fit’ to fight the disease eg the common cold  There are very small risks involved in introducing pathogens into the body (even mild or dead ones!) therefore…  Some people chose not to be vaccinated thus increasing the risk of disease spreading (by reducing ‘herd immunity’)  The risks from the disease are much greater than the risks from vaccination

20 Useful pathogens Biological control is the use of living organisms to control pests: - [Predators] - [Parasites] - Disease (pathogens) a pollution-free alternative to using pesticides long lasting and organic pest control eg myxomatosis (myxoma virus) in rabbits Disadvantage– organisms can develop immunity

21 DISEASE IN PLANTS  Plant diseases cause economic problems  Interventions and legislation have been introduced to reduce the problems: Chemical treatments Selectively breeding resistant varieties Crop rotation Change to sowing times Grafting crops onto disease resistant root stock Laws against growing susceptible varieties Laws against transporting infected material  Explain how each of these points may prevent the effect of a disease  Any other suggestions?

22 Example: Potato Blight This disease caused the ‘potato famine’ in Ireland in 1846 resulting in many Irish people moving to America to find work and food  A fungus that attacks potatoes via the leaves  Fungal spores germinate on the leaves and grow into the plant destroying cells  Spores remain in the soil for future crops Current treatments: selectively bred potato varieties resistant to blight fungicides biological control? (organic farming)


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