bio - communicable & non communicable diseases Flashcards

1
Q

Pathogen

A

microorganisms that cause infectious diseases
relies on their host to provide the conditions they need to grow and reproduce

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2
Q

Bacteria

A

Not all bacteria is bad
some are pathogens & cause diseases
Can be spread by: ingesting contaminated food, preparing food in unhygienic conditions, sexual contact
Antibiotics are becoming useless against bacteria as bacteria learns how to beat them by sharing their plasmids

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3
Q

Viruses

A

Very small pathogens - not living cells
has a strand of genetic material inside a protein coat - this replicates inside host cells to make new viruses

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4
Q

Plant defence responses

A

Physical - barriers e.g., Tough waxy cuticle around upper leaf, layer of dead cells around stem, cell wall
Mechanical thorns & hairs – prevents insects
Chemical - use of chemicals to attract or repel certain animals/organisms

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5
Q

Protists

A

Single celled eukaryotic microorganisms

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6
Q

Smoking

A

Chemical Carcinogens in cigarettes increase the chance of lung cancer.
Damages lining of arteries leading to atheroma build-up and a heart attack + stroke.
COPD - Chronic Obstructor Pulmonary Disease as smoking destroys many alveoli, so airways become inflamed & mucus builds up → patient become breathless.

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7
Q

Alcohol

A

Damages liver
yellow eyes
drowsiness
vomiting blood
alcoholic hepatitis
cirrhosis of the liver
alcoholism increases. treatment costs from the NHS

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8
Q

Diet

A

Bad diet leads to type 2 diabetes
Balanced diet + lack of highly processed foods → less chance of cardiovascular diseases or type 2 diabetes
Obesity leads to high blood pressure & build deposits up of fatty deposits leading to cardiovascular disease

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9
Q

Smoking (leads to)

A

Lung disease, cancer
Low birth weight & premature birth

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10
Q

Alcohol (leads to)

A

Liver & brain damage
Abnormal foetal brain development

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11
Q

Obesity (leads to)

A

Type 2 diabetes

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12
Q

Poor diet, smoking & no exercise (leads to)

A

Cardiovascular disease

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13
Q

Carcinogens & radiation (leads to)

A

Cancer

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14
Q

Health

A

state of physical and mental well-being

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15
Q

Measles

A

Type - Virus
cause - Droplet infection
Symptoms - Itching, fever
Cure - Vaccination

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16
Q

HIV

A

Type - Virus
cause - direct contact bodily fluids
Symptoms - AIDS, weak immune system
Cure - antiretroviral drugs prevent virus from replicating

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17
Q

Salmonella

A

Type - Bacteria
cause - food and contaminated utensils
Symptoms - stomach aches, vomiting, diarrhoea
Cure -Vaccinating animals / hygienic food prep

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18
Q

Gorrhoea

A

Type - Bacteria
cause - unprotected sex
Symptoms - pain in urinating, discharge from genitals
Cure - Barrier contraception, antibiotics

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19
Q

Tobacco mosaic Virus (TMV)

A

Type - Virus
cause - Get through wounds in the plant
Symptoms -Reduced photosynthesis, discoloured leaves, stunted growth
Cure - removing infected part of plant

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20
Q

Aphid infection

A

Type - Virus
cause - aphids greenflies are vectors
Symptoms - Stunted growth, yellow leaves
Cure - Insecticides & Natural predators of vector e.g. ladybird

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21
Q

Rose Blackspot

A

Type - fungus
cause - Spores
Symptoms - black slash purple spots on upper surface of leaves
Cure - Burning infected areas in an enclosed chamber

22
Q

Malaria

A

Type - protists
cause - mosquitoes are vectors for malaria
Symptoms - Recurrent fever, cough, muscle pains, headaches, sweats and chills
Cure - Vaccination, Mosquito Nets and repellent

23
Q

read me

A

The Immune System is designed to protect us from viruses and bacteria but can also respond to Allergens such as pollen or dust.
The body usually identifies allergens as harmful as soon as they enter the sinuses. The immune system responds by producing antibodies to fight off the allergen. Although the immune system produces antibodies in relatively small quantities the first time it encounters an allergen, subsequent exposures result in a specific immune response.
With repeated exposure, the body produces large amounts of the antibody greater to that allergen and stimulates mast cells in the respiratory system to release histamine, a chemical responsible for traditional allergic symptoms such as a runny nose, coughing, itchy eyes, and sneezing. This same chemical is responsible for other allergic reactions in the skin that result in itches and some inflammation.
By releasing histamine and manufacturing allergic Symptoms the body has created a process to expel the allergen out of the body. Runny noses, coughing, and sneezing all help rid the body of the presumably harmful allergen.

24
Q

Cancer

A

when abnormal cells divide in an uncontrolled way

25
Q

Benign tumour

A

Stays and grows in one place

26
Q

malignant tumour

A

grows into other tissues and metastasize

27
Q

how cancer happens

A
28
Q

How is malaria transmitted

A
29
Q

lifecycle of mosquitos

A
30
Q

methods of controlling mosquito (malaria’s vector) lifecycle

A

1) Draining stagnant pools of water - gives the raft of eggs / larva / pupa no stagnant water to live in so they die
2) Spraying pools of water with insecticides - It chemically kills the raft of eggs / larva / pupa
3) Spraying pools of water with oil - prevents pupa from breathing air & reduces O2 content of water so Larva & raft of eggs die

31
Q

First line of defence against pathogens in humans

A
  • mucus in mouth, nose, and trachea traps pathogens
  • trachea and bronchus are lined with cilia, which “waft” mucus back up to the throat to be swallowed
  • urine is antimicrobial and kills pathogens.
  • scabs form a protective barrier to stop bacteria entering.
  • tears are antimicrobial.
  • hairs in nose to trap larger particles.
  • skin is a tough barrier, with a dead outer layer of cells that microorganisms can’t penetrate, glands secrete antimicrobial oils.
  • stomach is full of hydrochloric acid which kills microorganisms.
  • Ear wax, eye lashes
32
Q

Second line of defence against pathogens in humans

A

The second line of defence is also non-specific. It involves a type of white blood cell called phagocytes. They are attracted to any area of your body in which an infection is present. Then, they engulf the pathogen through phagocytosis.

33
Q

Phagocytosis

A

Phagocytes engulf pathogens by phagocytosis. by then the pathogen is engulfed and enclosed in a vacuum and digestive enzymes are secreted. the enzyme kills and digests the pathogen.

34
Q

antigen

A

a specific shaped protein on the surface of each pathogen. They are specific to the pathogen.

35
Q

Lymphocytes - antibodies

A

Lymphocytes are white blood cells. Lymphocytes recognise only one type of antigen and binds to it once it comes into close proximity. They can also produce antibodies specific in shape to the antigens of that pathogen. It takes multiple days to find the correct shape, in which time illness is felt. So, they release the antibodies into the blood. These antibodies are going to bind to the antigens of that pathogen causing the pathogens to clump together making it more vulnerable to phagocytosis & the antibodies will kill the pathogens.

36
Q

Memory Lymphocytes

A

After the infection and the pathogens have died, the memory lymphocytes and antibodies remain in the blood. What happens if you’ve got a secondary infection of the same, pathogen, your memory lymphocytes will very quickly produce correct antibodies which will bind to the pathogens, as no time needs to be wasted finding the correct lymphocyte.

37
Q

Lymphocytes - antitoxins

A

Lymphocytes also make antitoxins which bind to any toxins the pathogen makes, neutralising it. Toxins are what make you feel sick.

38
Q

specific antibodies shape

A

Just like enzymes the antibody binds to specific antigens because the shape of the antigen is complementary to the shape of the antigen binding site.

39
Q

How does a vaccination work?

A

A vaccine is a small quantity of a dead or inactive pathogen. it still possesses the same antigens as a normal pathogen so that the body develops memory lymphocyte cells that’s recognise the active pathogen too.

40
Q

immune response to disease exposure

A

1) After exposure, lots of different lymphocytes attempt to make antibodies that recognise antigens on the pathogen.
2) once an antibody binds correctly, the lymphocyte differentiates to make plasma cells and memory cells.
3) The plasma cells produce antibodies and help the phagocytes fight off the infection.
4) once the pathogen is defeated, the plasma cells die but the memory cells remain.
5) Reinfection is instantly recognised by memory cells which quickly produce lots of plasma cells.

41
Q

how are monoclonal antibodies made

A

1) Inject mouse with chosen antigen that you want to produce antibodies for

2) The mouse’s lymphocytes are now going to produce specific antibodies for that antigen.

3) Remove the lymphocytes from the mouse. This lymphocyte produces the antibodies that you want to make the monoclonal antibodies from. So even though this lymphocyte can produce antibodies, it can’t divide.

4) Fuse the lymphocyte with a cancer cell (a tumour cell). The tumour cell can’t produce antibodies, but it can divide incredibly rapidly by mitosis. This forms a hybridoma which can divide incredibly rapidly producing many monoclonal antibodies, which are all specific to the same antigen.

42
Q

3 uses of monoclonal antibodies

A

Diagnosis – eg pregnancy tests/ covid tests
Research - to locate or identify specific molecules in cells
Treatment – eg cancer treatment, binding to cells and carrying a radioactive or toxic substance

43
Q

use of monoclonal antibodies in pregnanacy tests

test stick and if pregnant

A

monoclonal antibodies are used in pregnancy tests. A hormone called HCG (human chorionic gonadotropin ) is found in the urine of women only when they are pregnant. Pregnancy testing sticks use monoclonal antibodies to detect this hormone.
Here’s how they work:

The test stick
The bit of the stick you wee on has some antibodies to the hormone, with blue beads attached. The test strip (the bit of the stick that turns blue if you’re pregnant) has some more antibodies to the hormone stuck onto it (so that they can’t move).

If you’re pregnant
If you’re pregnant and you wee on the stick, the hormone binds to the antibodies on the blue beads. The urine moves up the stick, carrying the hormone and the beads. The beads and hormone bind to the antibodies on the strip. So the blue beads get stuck on the strip, turning it blue.

44
Q

role of monoclonal antibodies in cancer treatment

A

chemotherapy drugs kill all cells, but particularly fast-growing cells like cancer cells. This unfortunately includes other cells like hair, skin and intestinal cells resulting in hair loss, cracked skin and digestive problems. However, mAbs targets cancer cells while leaving healthy cells unaffected and they also target the toxic drugs to specific places in the body reducing the number of accidental cell deaths.
e.g. herceptin stops breast cancer cell growth

45
Q

role of monoclonal antibodies in treating a disease

A

Treating diseases
Different cells in the body have different antigens on their cell surface. So you can make monoclonal antibodies that will bind to specific cells in the body (e.g. just liver cells). Cancer cells have antigens on their cell membranes that aren’t found on normal body cells. They’re called tumour markers. In the lab, you can make monoclonal antibodies that will bind to these tumour markers.
An anti-cancer drug can be attached to these monoclonal antibodies. This might be a radioactive substance, a toxic drug or a chemical which stops cancer cells growing and dividing. The antibodies are given to the patient through a drip. The antibodies target specific cells (the cancer cells) because they only bind to the tumour markers. The drug kills the cancer cells but doesn’t kill any normal body cells near the tumour.

46
Q

phases of drug research

A

Preclinical - Tested on cells then on engineered mice. Does it work? how much? side effects?
Clinical - phase one - tested on a small no. of healthy male volunteers – safety?
Clinical - phase two - tested on a small number of patients - Does it work? how much?
Clinical - phase three - large scale trials - does it work for all? getting the dose right.
Clinical - phase four - distribution and scalability - despite drug being available it is still monitored and checked for long term effects

47
Q

Single blind trial

A

patients don’t know who’s getting the placebo but doctors do.

48
Q

double-blind trial

A

neither patients nor doctors know you who is getting the placebo and who isn’t. only drug company knows.

49
Q

use of monoclonal antibodies in pregnanacy tests

if not pregnant

A

If you’re not pregnant and you wee on the stick, the urine still moves up the stick, carrying the blue bead But ove’s thing to stick the blue beads onto the test strip, so it doesn’t go blue,

Control window
Pregnancy tests also have a control window. This shows the person using the test whether the test has worked conecth. The control window contains antibodies to the antibodies that are attached to the blue beads. This means that once the blue beads reach the control window, the antibodies attached to them will bind to the antibodies stuck to the control window. The control window should go blue both when a pregnancy test is positive as well as negative. If it doesn’t, it means the test has not worked.

50
Q

use of monoclonal antibodies in research

A

Using monoclonal antibodies in research
Monoclonal antibodies can be used to locate specific molecules on a cell or in a tissue. First, monoclonal antibodies are made that will bind to the specific molecules you’re looking for. The antibodies are then bound to a fluorescent dye. If the molecules are present in the sample you’re analysing, the monoclonal antibodies will attach to them, and they can be detected using the dye.

51
Q

problems with monoclonal antibodies

A

However, monoclonal antibodies do cause more side effects than were originally expected, e.g. they can cause fever, vomiting and low blood pressure. When they were first developed, scientists thought that because they targeted a very specific cell or molecule, they wouldn’t create a lot of side effects, but in some cases the unpleasant side effects outweigh the benefits of the treatment. This means that they are not as widely used as treatments as scientists had originally thought they might be.