C3.2 Defense Against Diseases Flashcards

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1
Q

What are pathogens?

A

Disease-causing organisms, and can be directly or indirectly passed from one infected organism to another (eg. virus, bacteria, fungi, prokaryotes, and protozoa)

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2
Q

What are the causes of a disease?

A
  • Genetics
  • Environmental
  • Infection with a pathogen
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3
Q

What are the features of bacteria?

A
  • Prokaryotes lacking a real nucleus and instead have a nucleoid
  • Divide by binary fission (asexual reproduction)
  • Cell walls composed of peptidoglycan
  • Can exist as infectious or non-infectious
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4
Q

What are the features of viruses?

A
  • Not an organism because they lack a nucleus but have DNA or RNA
  • Needs to attach to a host cell to reproduce
  • Cannot be killed by antibiotics
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5
Q

What are features of fungi?

A
  • Eukaryotes with a nucleus and have chitin cell walls
  • Reproduce by producing spores
  • Causes athletes’ foot, skin rashes, vaginal candidiasis allergic reactions (mold spores), ringworm
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6
Q

What are features of protozoan parasites?

A
  • Unicellular eukaryotes, making treatment difficult
  • Often parasitic or symbiotic organisms
  • Can cause malaria, leishmaniosis, giardia, trypanosoma, sleeping sickness, lyme’s disease
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7
Q

What are features of Helminthic parasites?

A
  • Multicellular and eukaryotic
  • Parasitic diseases
  • Can cause Elephantiasis, Schistosomiasis, Toxocariasis, Pinworm, Roundworm or tapeworm infections
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8
Q

Characteristics of innate immune system

A
  • Responds to broad categories of pathogens
  • Timeline: 0 - 12 hours

1st line of defence:
- skin and secretions
- mucous membrane with cilia in respiratory tract (produced by goblet cells)
- saliva, stomach acid

2nd line of defense:
- phagocytes

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9
Q

Characteristics of adaptive immunity

A
  • Responds in a specific way to particular pathogens. This system builds up a memory of pathogens it has encountered, offering more effective protection against common infectious diseases.

– Timeline: 1 - 7 days

– 3rd line of defense:
- T-Lymphocytes
- B-Lymphocytes
- Antibodies
- Memory B-Lymphocytes

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10
Q

What is an example of first line of defense (skin)?

A
  • The outermost layer is a tough layer of dead cells containing large amounts of keratin, acting as a physical barrier to the entry of pathogens
  • Natural microorganism on the skin live in competition for nutrients with harmful pathogens.
  • Sebaceous glands associated with hair follicles
    secrete sebum, which maintains skin moisture and lowers pH. A low pH inhibits growth of bacteria and fungi.
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11
Q

What is an example of first line of defense (mucous membrane)?

A
  • A thinner and softer type of skin. Can be found in areas such as the vagina, the foreskin & head of penis, and airways leading to the lungs
  • The skin in these areas secrete mucus, a sticky solution of glycoproteins
    • traps pathogens or harmful particles which will then be swallowed or expelled
    • contains anti-bacterial enzymes called lysozymes which destroy pathogens.
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12
Q

Outline the process of blood clotting

A
  1. When there is a cut in the skin, platelets aggregate at the site to form a temporary plug and release clotting factors to control bleeding.
  2. The enzyme thrombin is produced which converts soluble fibrinogen dissolved in blood plasma into insoluble fibrin
  3. This forms a mesh of fibres over the damaged area to help trap blood cells.
  4. Platelets aggregate at the area of damage to form a temporary plug and form a solid clot.
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13
Q

What is the second line of defense (phagocytes)?

A
  • A type of white blood cell that squeezes out through pores in the walls of capillaries and moves to sites of infection, engulfing pathogens through endocytosis and digests them using lysosome enzymes.
  • Dendritic cells and macrophages activate an inflammatory response, secreting proteins called cytokines that trigger an influx of defensive cells from the blood.– Macrophages are a type of phagocyte that ingests pathogens and displays antigens from it on its surface to other cells
  • All phagocytes are non-specific, responding to all pathogens
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14
Q

What is the third line of defense (lymphocytes)?

A
  • Circulates in the blood and is contained in lymph nodes
  • Produces antibodies which are large proteins that help destroy pathogens by binding to an complementary antigen
    • makes pathogen more recognizable to phagocytes for easy engulfing
    • prevents viruses from docking to host cells, so they cannot enter the cells
  • Each lymphocyte produces only one type of antibody, hence when a pathogen infects the body for the first time, the lymphocytes that can produce the appropriate antibodies work together to produce antibodies in large quantities to control the pathogen and clear the infection.
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15
Q

Explain the production of antibodies

A
  1. When macrophages ingests pathogens, antigens of the pathogen are displayed on the plasma membrane of the macrophage.
  2. Helper T-lymphocyte cells specific to the antigen of the macrophage will bind to its antigen, becoming activated.
  3. B-lymphocyte cells specific to the antigen is activated by the helper T-lymphocyte cells upon binding to it.
  4. The B-lymphocyte cells divide repeatedly, grow in size and develop an extensive endoplasmic reticulum with many ribosomes attached to it, along with a large Golgi apparatus. This allows a rapid production of antibody-secreting plasma cells.
  5. Antibodies produced by the clone of plasma cells are specific to antigens on the pathogen and help to destroy it
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16
Q

What are antigens?

A

Antigens are mostly glycoproteins that act as recognition molecules and are found on the surface of pathogens, helping the lymphocytes identify them as foreign cells (non-self cells, invading pathogens). This triggers them to produce antibodies with a complementary shape that bind to the antigen. This binding is irreversible.

17
Q

What causes immunity to an infectious disease?

A

Having antibodies against the pathogen or memory cells that allows rapid production of the antibody.

18
Q

How does immunity work?

A

A smaller number of B-cells in the clone that are not activated do not immediately secrete antibodies but remain for a long time after the infection. These B-cells differentiate into memory B-cells that remain inactive unless the same pathogen infects the body again, in which case they are activated and respond rapidly.

19
Q

What is HIV?

A

A retrovirus that uses RNA as its genetic material.

20
Q

How is HIV transmitted?

A
  1. Sex without a condom
  2. Sharing of hypodermic needles by IV drug users
  3. Transfusion of infected blood
  4. Childbirth and breastfeeding
21
Q

How does HIV infect lymphocytes?

A

HIV invades and destroys helper T-cells, resulting in the reduced production of antibodies. This can cause a group of opportunistic infections caused by pathogens to strike when the immune system has weakened. When conditions caused by HIV are combined in a person, they have AIDS.

22
Q

What are antibiotics?

A

Chemicals that block processes occurring in bacteria but not in eukaryotic cells.

23
Q

Why do antibiotics fail to control infection with viruses?

A

Viruses have different metabolic pathways and relies on the host cell’s metabolism to reproduce and spread.

24
Q

How does antibiotic-resistant bacteria evolve? (hint: natural selection)

A

Antibiotics can generally kill bacteria. Some bacteria show variation in antibiotic resistance. This occurs due to random mutation. Resistant bacteria are not killed by antibiotic. They have a selective advantage and will reproduce. Their antibiotic resistance is passed onto their offspring. This causes resistant bacteria to be more common.

25
Q

What are zoonoses?

A

Infectious diseases that can transfer from other species to humans. (eg. rabies and tuberculosis)

26
Q

How do vaccinations work?

A

Vaccines can contain either weakened versions of a pathogen, antigens that allow a pathogen to be recognized by the immune system, or nucleic acids from which antigens can be made. The antigens stimulate a primary immune response, by activation of T-lymphocytes and B-lymphocytes and production of plasma cells and then specific antibodies.

27
Q

Difference between active and passive immunity?

A

Active: immunity due to the production of antibodies by the organism itself after the immune response has been stimulated by a pathogen.

Passive: immunity due to the acquisition of antibodies from another organism (such as colostrum or placenta)

28
Q

What is herd immunity?

A

When the majority of the population is vaccinated, the few who are unvaccinated are protected from the infection.