Defence Against Disease

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शिक्षकों के लिए: Defence Against Disease (Biology, HL) के लिए इस्तेमाल के लिए तैयार लेसन स्लाइड्स, रिवीज़न नोट्स — इन्हें अपने लेसन में इस्तेमाल करें, या टॉपिक को एक इंटरैक्टिव क्लास एक्टिविटी की तरह चलाएं जिसे आपके शिक्षार्थी लाइव गेम की तरह खेलें।

लेसन नोट्स

Pathogens and Disease

  • A pathogen is any microorganism that causes disease in another organism.
  • Pathogens include bacteria, fungi, protists, and viruses; all viruses are pathogenic, while not all bacteria, fungi, and protists are.
  • Pathogens cause communicable (infectious) diseases that transfer from a diseased host to a healthy organism.
  • Examples of communicable diseases: tuberculosis, athlete's foot, malaria, cholera.
  • Non-communicable diseases are non-infectious, e.g., cancer, cardiovascular disease, malnutrition.
  • Careful observation of symptoms, incubation times, and transmission mechanisms is crucial to control the spread of disease.

Barriers to Pathogens: Skin and Mucous Membranes

  • The skin and mucous membranes form the primary defence against pathogens.
  • The skin provides a tough physical barrier that prevents pathogen entry; cuts are sealed by blood clots.
  • Sebum from sebaceous glands maintains a low skin pH, inhibiting microorganism growth.
  • Mucous membranes line airways, reproductive areas, and the digestive system, and contain goblet cells that produce mucus.
  • Mucus traps microorganisms and particles, which are swept by cilia to be swallowed and destroyed by stomach acid.
  • Mucus also contains lysozyme enzymes with antibacterial properties.

A cross-section of human skin

A cross-section of human skin

Blood Clotting

  • When the skin is cut, platelets form a temporary plug to stem bleeding.
  • Platelets release clotting factors that trigger a chemical cascade.
  • Clotting factors stimulate release of the enzyme thrombin.
  • Thrombin catalyses conversion of soluble fibrinogen into insoluble fibrin.
  • Fibrin forms a mesh that traps more platelets and blood cells, sealing the wound.
  • Exposure to air hardens the mesh to form a scab.

Composition of human blood

Composition of human blood

The Immune System: Innate vs Adaptive

  • The innate immune system recognises any non-self item (e.g., bacteria, fungi, viruses, pollen) via non-self antigens.
  • Innate responses are non-specific and do not change during an individual's lifetime; phagocytes carry out this response.
  • The adaptive immune system responds to specific non-self antigens and involves antibody production and memory cells.
  • On first exposure, the adaptive response is slow; on second exposure, it is faster and produces more antibodies.
  • Immunological memory develops over a lifetime as exposure to different pathogens occurs.
  • Vaccination uses the adaptive immune system to speed up the response on later exposure.

Lymphocytes and antibodies

Lymphocytes and antibodies

White Blood Cells

  • Phagocytes are white blood cells produced in bone marrow; they remove dead cells and pathogens non-specifically.
  • Phagocytes move by amoeboid movement, engulf pathogens by endocytosis, and digest them using lysosomal enzymes.
  • Lymphocytes are white blood cells involved in specific immune responses; two types: T cells and B cells.
  • T cells mature in the thymus and have T cell receptors specific to particular antigens.
  • T cells are activated when they bind to their specific antigen on an antigen-presenting cell (e.g., macrophage, infected cell).
  • Activated T cells divide by mitosis to form clones with identical receptors.
  • B cells mature in bone marrow and have antibody receptors on their surface; each B cell binds a different antigen.
  • When a B cell binds its specific antigen, it forms an antigen-antibody complex and is activated by T helper cell signalling.

Phagocytosis

Phagocytosis

Adaptive Immune Response

  • Antigens are molecules that trigger an immune response; they are found on cell surface membranes, cancer cells, bacterial cell walls, virus envelopes, and pollen grains.
  • The immune system distinguishes self from non-self based on antigens.
  • Red blood cells have antigens determining blood group: ABO and Rhesus (Rh) markers.
  • Blood type A has N-acetylgalactosamine modification; type B has galactose; type AB has both; type O has neither.
  • Incompatible blood transfusion triggers immune response, causing agglutination (clumping) of red blood cells, which can be fatal.
  • T-helper cells bind to antigens on antigen-presenting cells and become activated.
  • Activated T-helper cells bind to complementary B cells and release signalling proteins to activate them.
  • Activated B cells undergo clonal expansion, producing plasma cells (secrete antibodies) and memory cells (provide immunity).

HIV and AIDS

  • HIV is a retrovirus with RNA and reverse transcriptase; it cannot survive outside the human body.
  • HIV is transmitted by direct exchange of body fluids: sexual intercourse, blood donation, sharing needles, mother to child (placenta, birth, breast milk).
  • HIV infects and attacks T-helper cells, which are key for antibody production.
  • Early infection: antibodies produced against HIV can be detected; individual is HIV positive.
  • Progression: reduced antibody production leads to opportunistic infections; when multiple diseases occur, it is AIDS.
  • Anti-retroviral drugs can slow progression, allowing many HIV-positive individuals to live full lives with normal life expectancies.
  • HIV is the virus; AIDS is the syndrome it causes.

How HIV infects a lymphocyte

How HIV infects a lymphocyte

Antibiotics and Antibiotic Resistance

  • Antibiotics inhibit growth of microorganisms, mostly bacteria, by targeting prokaryotic processes (transcription, translation, DNA replication, ribosome function, cell wall formation).
  • Penicillin is produced by fungi of the genus×Penicillium×and interferes with bacterial cell wall production.
  • Antibiotics are ineffective against viruses because viruses are non-living particles with no metabolism or cell structure.
  • Antibiotic resistance arises from random mutations; resistant bacteria survive treatment and reproduce, passing on resistance alleles.
  • This is evolution by natural selection; overuse of antibiotics exerts selective pressure.
  • MRSA (methicillin-resistant×Staphylococcus aureus×) is resistant to multiple antibiotics.
  • Measures to avoid resistance: avoid antibiotics for non-bacterial infections, maintain hygiene, minimise agricultural use, develop new antibiotics.

How penicillin works

How penicillin works

Zoonoses

  • Zoonotic diseases cross the species barrier from animals to humans.
  • Species specificity may be due to lack of necessary receptors or body temperature differences.
  • Zoonoses are a growing global concern due to close human-animal relationships and potential for pandemics (e.g., COVID-19).
  • Some zoonotic diseases can emerge from animal populations and develop into human-only strains (e.g., HIV).

Vaccines and Immunity

  • A vaccine contains antigens or DNA/RNA coding for antigens, inducing immunity without causing disease.
  • Types: live attenuated (weakened pathogen) and inactivated (killed components or antigens alone).
  • Vaccines are administered by injection or orally; they trigger a primary immune response and produce memory cells.
  • On re-exposure, memory cells produce a faster, stronger secondary response with more antibodies.
  • Herd immunity occurs when a large percentage of the population is vaccinated, protecting unvaccinated individuals.
  • Herd immunity prevents epidemics and pandemics; vaccination programmes can eradicate diseases (e.g., smallpox eradicated in 1980).

How a vaccine produces immunity

How a vaccine produces immunity

Evaluating COVID-19 Data: Skills

  • Percentage difference compares two directly comparable values at the same time: (difference / average) × 100.
  • Percentage change compares values from the same data set at different times: (change / original value) × 100.
  • If original value is larger, change is a percentage decrease; if smaller, a percentage increase.
  • Example: Europe had 18,392 cases in mid-July 2023 vs 1,584 in South-East Asia; percentage difference = 168.3%.
  • Example: Europe had 38,950 cases in mid-June 2023 and 18,392 in mid-July 2023; percentage change = -52.8% (decrease).

स्लाइड्स

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प्रैक्टिस सवाल

फ्री प्रीव्यू — 56 में से 8 सवाल। सभी देखने के लिए साइन अप करें।
  1. 1.Which component of blood has a role in preventing pathogens from entering the body?

    Easy
    • ARed blood cells
    • BBlood plasma
    • CPlatelets
    • DWhite blood cells
  2. 2.What is the principal purpose of sebum secretions onto the surface of the skin?

    Easy
    • ATo prevent microorganisms from sticking to the skin.
    • BTo lower skin pH, which slows down the growth rate of microorganisms.
    • CTo provide a surface texture to the skin that aids the evaporation of sweat.
    • DTo assist in the formation of blood clots as a way of sealing wounds after a cut or graze.
  3. 3.Which phrase best fits into the gap in the following sentence? The shape of antibody molecules gives each one a particular 3-D configuration. This allows each antibody to be ______________ each individual pathogen.

    Easy
    • A...well suited to...
    • B...specific to...
    • C...functional against...
    • D...the same shape as...
  4. 4.Which of the following are considered primary defence against infectious disease?

    Easy
    • ASkin and mucous membranes.
    • BHair and skin.
    • CPhagocytes and fever.
    • DLymphocyte production of antibodies.
  5. 5.Which of these statements correctly describes a lymphocyte?

    Easy
    • AThey have many mitochondria to produce ATP to allow endocytosis of pathogens.
    • BThey have many lysosomes containing hydrolytic enzymes to digest pathogens.
    • CThey provide specific defence against disease-causing organisms.
    • DThey are white blood cells with a lobed nucleus.
  6. 6.What is adaptive immunity?

    Easy
    • ATreating a specific disease through use of antibiotics.
    • BProduction of monoclonal antibodies.
    • CProduction of antibodies by lymphocytes.
    • DEndocytosis of pathogens by phagocytes.
  7. 7.Which of the following is not a contributing factor towards the development of antibiotic resistance in bacteria?

    Easy
    • AStopping a course of antibiotics once symptoms improve.
    • BDevelopment of new antibiotics.
    • CNatural selection which favours mutations in bacteria.
    • DOveruse of antibiotics in agriculture.
  8. 8.When a B-lymphocyte is activated by an antigen, what action is taken?

    Medium
    • AIt engulfs the infected body cell which displays a complementary antigen.
    • BIt secretes signalling proteins that stimulate T-lymphocytes to produce plasma cells.
    • CIt divides repeatedly to form clones of genetically identical plasma cells.
    • DIt attaches to the infected cell displaying the antigen and destroys it.

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