Health and disease Flashcards

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1
Q

What are communicable diseases?

A

Diseases that can be spread between induviduals

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2
Q

What are non communicable diseases?

A

-Diseases that cannot be transmitted between induviduals
-If you are infected by one disease, you are more susceptible to others

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3
Q

What are pathogens?

A

Organisms such as viruses, protists, bacteria and fungi that cause communicable diseases

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4
Q

A disease caused by Virus (viral):

A

Ebola
-causes haemorrhagic fever
-spread via bodily fluids
-transmission can be reduced by isolating infected induviduals and sterilising any areas where the virus may be present

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5
Q

Name a fungal disease:

A

Chalara Ash Dieback
-symptoms include bark lesions and leaf loss
-fungus is carried through air by wind
-transmission reduced by removing young, infected ash trees and replanting with different species

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6
Q

Name a disease caused by a protist:

A

Malaria
-effects of malaria include damage to red blood cells and liver
-mosquitoes act as vectors - they pass on the protist to humans but don’t get the disease themselves
-mosquito nets and insect repellent can be used to prevent mosquitoes from biting

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7
Q

Name a bacterial disease:

A

Cholera
-Causes diarrhoea
-Spreads through contaminated water sources
-Transmission can be reduced by making sure that people have access to clean water supplies

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8
Q

An example of an STI:

A

HIV
-Human Immunodeficiency Virus - it kills white blood cells, which are really important for immune response
-HIV eventually leads to AIDS, where an infected persons immune system fails
-spread via bodily fluids (e.g blood, semen, vaginal fluids).

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9
Q

What is a virus?

A

-A protein coat around a strand of genetic material
-have to infect host cells in order to reproduce

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10
Q

The lytic pathway (step-by-step)

A

1) Virus attaches itself to a specific host cell and injects its genetic material into the cell
2) The virus uses proteins and enzymes in the host cell to replicate its genetic material and produce the components of new viruses
3) The viral components assemble
4) The host cell lyses, releasing the new viruses, which infect , more cells

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11
Q

The lysogenic pathway

A

1) The genetic material is incorporated into the genome of the host cell
2) The viral genetic material gets replicated along with the host DNA every time the host cell divides - virus is dormant and no new viruses are made
3) Eventually a trigger (e.g the presence of a chemical) causes the viral genetic material to leave the genome and enter the lytic pathway

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12
Q

Example of plants physical defenses:

A

-Most plants and leaves have a waxy cuticle, providing a barrier to stop pathogens/pests.
-Also stops water collecting which reduces the risk of infection by pathogens transferred by water
-Have cell walls made from cellulose

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13
Q

Examples of chemical defenses in plants:

A

-Produce chemicals called antiseptics which kill bacterial and fungal pathogens.
-Produce chemicals to deter pests from feeding on leaves
-These can be used as drugs to treat human disease (e.g Qunine and Aspirin)

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14
Q

Physical barriers to stop pathogens entering the body:

A

-skin act as a barrier to pathogens, if damaged, blood clots quickly seal cuts
-hairs and mucus in nose trap particles that could have pathogens
-cells in trachea and bronchi also produce mucus, trapping pathogens

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15
Q

Chemical barriers to stop pathogens entering the body:

A

-The stomach produces hydrochloric acid, kills most pathogens swallowed
-eyes produce lysozyme in tears, killing bacteria on the surface of the eye.

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16
Q

How does an immune response to a specific pathogen work?

A

1) every pathogen has unique molecules (proteins) on its surface called an antigen

2) when white blood cells come across an antigen on a pathogen, they start to produce antibodies

3) antibodies bind to specifically the new invading pathogen, so can be found by other white blood cells, they won’t lock on to any other pathogens

4) the antibodies are then produced rapidly and flow all around the body to find similar pathogens

17
Q

Why is the first response slow to fighting a pathogen in the body?

A

-as when pathogen first enters the body, there aren’t many B-lymphocytes that can make the specific antibody needed to ‘lock on’ to antigen

18
Q

What are memory lymphocytes?

A

-produced in response to a foreign antigen
-remain in the body for a long time, and ‘remember’ a specific antigen

19
Q

Why are memory lymphocytes so important?

A

-as it ensures the person is now immune
-because their immune system has the ability to respond quickly to a second infection

20
Q

Is the secondary immune response faster/slower? Why?

A

-if the same pathogen enters the body again, there are more cells that will recognise it and produces antibodies
-this secondary immune response is faster and stronger

21
Q

How does immunisation work?

A

-injecting dead or inactive pathogens into the body
-these are antigenic, so your body makes antibodies to help destroy them as well as memory lymphocytes
-so if live pathogens of same type enter body, there will be memory lymphocytes that can cause a fast secondary immune response

22
Q

Advantages of immunisation

A

-Epidemics can be prevented if a large percentage of the population are immunised
-Some diseases (e.g smallpox) have been virtually wiped out by immunisation programmes

23
Q

What is herd immunity?

A

-If a large percentage of a population are immunised against a disease, even those who aren’t immunised are unlikely to catch the disease as there is fewer people to pass it on to you

24
Q

Disadvantages of Immunisation

A
  • Doesn’t always work - sometimes it doesn’t give immunity
  • Sometimes you can have a bad reaction to a vaccine (e.g swelling, or maybe something more serious like a fever or seizures)
25
Q

What are monoclonal antibodies?

A
  • Produced by B-lymphocytes
  • Produced from lots of clones of a single B- lymphocyte, meaning all the antibodies are identical
    -Means they will only target one specific protein antigen
26
Q

How do you make monoclonal antibodies?

A

To get the lymphocyte:
- Inject a mouse with chosen antigen
- Take B-lymphocytes produced by mouse

To get hybridoma:
- Fuse the B-lymphocyte with fast dividing tumour cells from the lab to get hybridoma

This then divides quickly to produce lots of clones that produce the monoclonal antibodies

27
Q

Why are monoclonal antibodies useful?

A

As they will only bind to the molecule that it is programmed to, meaning you can target them at a specific cell or chemical in the body

28
Q

How are monoclonal antibodies used in pregnancy tests?

A
  • The part of the pregnancy test you wee on has antibodies to HCG (hormone produced while being pregnant) with blue beads attached to it
  • The test strip has some more antibodies to the hormone stuck onto it (so they can’t move)

If you’re pregnant and wee on the stick:
- Hormone binds to the antibodies on blue beads
- Urine moves up the stick carrying hormone and beads
- beads and the hormone bind to the antibodies on the strip
-blue beads get stuck on the strip, turning it blue

If you’re not pregnant and wee on the stick:
- The urine moves up the stick carrying the blue beads
- There’s nothing for the blue beads to stick to, so it doesn’t go blue

29
Q

How can monoclonal antibodies be used to find blood clots?

A

-When blood clots, proteins in the blood join together to form a solid mesh
-Monoclonal antibodies have been developed that bind to these specific proteins
-You can attach a radioactive element to these antibodies
-Then, if you inject them into the body and take a picture using a camera that picks up radiation, the picture will have a really bright spot where a blood clot is present

30
Q

How do monoclonal antibodies target cancer cells?

A

-Cancer cells have proteins on their cell membranes that aren’t found on normal body cells
-you can make monoclonal antibodies that will bind to these which can be seen on a special radioactivity detecting camera
-doctors can see exactly what size it is, where it is and if it is spreading

31
Q

How are antibiotics used to treat bacterial infections?

A

-work by inhibiting processes in bacterial cells, but not in host organism
-an example is some antibiotics inhibit the building of bacterial cell walls - this prevents the bacteria from dividing and eventually kills them
-has no effect on the human host

32
Q

Why is it difficult to develop drugs to destroy a virus?

A

-Because viruses use your own body cells to reproduce, making it very difficult to develop drugs that destroy just the virus without killing the body’s cells

33
Q

What is the first stage of developing a new drug?

A

Preclinical Testing:
- Once a drug is discovered, it needs to be developed
- Drugs are first tested on human cells and tissue in the lab
- Next step is to test drug on live animals to test the drug works and to find the best dosage for the drug

34
Q

What is the second stage of developing a drug?

A

Clinical Testing:
- If drug passes the tests on animals, then it’s testes on human volunteers
- Firstly tested on healthy people to ensure no side effects, then is tested on people suffering from the illness
- Patients are randomly put into two groups. One is given the new drug and one is given a sugar pill to test the placebo effect
- Once the drug has finally passed, it will be approved by a medical agency before it can be used to treat patients

35
Q

How do you grow bacteria in a lab?

A

You have to make an agar plate which will form invisible colonies of bacteria on the surface of the jelly:
-Pour hot agar jelly into a Petri dish
-When the jelly is cooled and set, a sterile pipette and spreader can be used to get an even covering of bacteria
-the microorganisms then multiply

36
Q

How do you investigate the effect of substances on bacterial growth?

A