Infectious Diseases Flashcards

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1
Q

Define a disease.

A

Ill health/Sickness
Cause reduced effectiveness of functions.
Illness with a set of of symptoms and signs.
Poor physical,mental and social well being.

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2
Q

What is an infectious disease?

A

Diseases caused by pathogens.
Cause harm to health of host
Can be passed from one organism to another i.e. communicable/transmissable.
For example through;
Direct contact
Exchange of fluids
Contamination
Airborne
Vector

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3
Q

What is a pathogen?

A

Pathogens are parasitic disease-causing microorganisms.
pathogens can be prokaryotes/eukaryotes
For example Bacteria (prokaryote), Virus (Not living), proctoctists (eukaryotes), fungi (eukaryotes).

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4
Q

What is a transmission cycle?

A

The passage of a pathogen from one host to another is continually repeated as the pathogen infects new hosts. The way in which a pathogen passes from one host to another is called the transmission cycle.
pathogens:
1. Gain entry to host
2.Colonise host tissue (multiply)
3.Damage host’s tissues
4.Resist host defenses

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5
Q

How can we kill pathogen?

A

We need to break the disease transmission cycle to prevent disease from spreading. Control methods attempt to break transmission cycles by removing the conditions that favor the spread of the pathogen.

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6
Q

What is a protoctist?

A

A protist or protoctist is any eukaryotic organism that is not an animal, land plant, or fungus.

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7
Q

Describe viruses.

A

Non-cellular structure
No plasma membrane, cytoplasm, ribosomes.

Only
1.DNA or RNA
2.Protein coat=capsid
-protective coat
-may have one or two coats
3. Many viruses also have a lipid envelope.
4. Some proteins may be present for e.g. heamagglutin,neuramindiase.

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8
Q

Describe how viruses reproduce.

A

Viruses are all parasitic
Can only reproduce by infecting living cells
Uses protein synthesizing machinery of host cells to replicate.
They:
Virus bind to cell
Incorporate viral DNA/RNA into cell
use host cell’s ribosomes, ER,Golgi to produce viral proteins.
Produce more viruses.

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9
Q

What features are not present in all bacteria?

A

Non-mebrane bound organelles
No nucleus
DNA lies free in cytoplasm in the nuceloid region and is not associated with histone proteins.

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10
Q

What features are present in all bacteria?

A

plasma membrane
cytoplasm
Peptidoglycan cell wall
→ made of chains crossed linked by amino acids
70s ribosomes
Circular DNA
DNA is naked
Not associated with histones

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11
Q

What are the different types of pathogens?

A

Disease → Type of causative agent →Name of causative agent
1.Cholera → Bacteria → Vibrio Cholerae
2. Malaria →Proctoctist →Plasmodium falciparum/P.malariae/P.Vivax/P.ovale
3. HIV/AIDS → (Retro)virus → Human Immunodeficiency virus.
4. Tuberculosis →Bacteria →Mycobacterium tuberculosis/M. bovis
5. Smallpox → Virus →Variola Virus.

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12
Q

Define a disease carrier?

A

A disease carrier (or just a carrier) is a person infected with a pathogen who shows no symptoms, but can be a source of infection in other people (not carrier of an inherited disease). It can be very difficult to trace them as a source of infection.

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13
Q

Give an example of a control measure for infectious diseases.

A

Vaccination is a major control measure for many infectious diseases. Vaccinations work by making us immune to specific pathogens so that they do not live and reproduce within us and do not spread to others, so breaking the transmission cycle.

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14
Q

Define disease eradication?

A

The complete breakage of the transmission cycle of a pathogen so that they are no more cases of the disease caused by the pathogen anywhere in the world.

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15
Q

Give examples of two diseases that have been eradicated.

A

in 1980 WHO declared that small pox had been eradicated and in 2011 rinderpest a severe disease in livestock was eradicated.

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16
Q

Define endemic.

A

A disease that is always in a population.
For example tuberculosis is a disease endemic in the whole human population and Malaria is endemic in tropical and sub-tropical regions such as Africa.

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17
Q

Define epidemic.

A

An epidemic is when there is a sudden increase in the number of people with a disease. For example SARS epidemic in Malaysia.

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18
Q

Define pandemic.

A

A pandemic occurs when there is an increase in the number of cases throughout the continent or across the world . For example covid 19 and HIV/AIDS.

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19
Q

Define incidence.

A

The incidence is the number of people who are diagnosed over a certain period of time, usually a week, month or a year.

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20
Q

Define prevalence.

A

The prevalence of a disease is the number of people who have that disease at any one time.

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21
Q

Define mortality rate.

A

The number of deaths over a particular length of time, usually a year is the mortality rate.

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22
Q

Describe the structure of the causative agent cholera?

A

The causative agent is a bacterium called vibrio cholera. Vibrio cholera is comma shaped, has flagella and is motile.

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23
Q

Describe how cholera is transmitted.

A

Large numbers of vibrio cholera are found in faeces of infected people. Infected person’s faeces/ sewage contaminates food/water.
Houseflies land on faeces and contaminate food/water.
Uninfected person eats contaminated food/water.

Due to absence of proper sanitation-no treatment of faecal waste→poor hygiene and poor living conditions.

Lack of education about transmission.

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24
Q

What is the faecal-oral route?

A

Cholera is transmitted by the faecal-oral route. The faecal-oral route comprises both of water and food borne transmission.

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25
Q

What are the symptoms and effects of cholera?

A
  1. if bacteria is not killed by stomach acid, bacteria reaches the small intestine.
  2. Bacteria secretes choleragen toxin.
  3. Toxin binds to complementary receptor on intestinal epithelial cell and enters via endocytosis.
  4. Disrupts function of intestine epithelium lining.
  5. Loss of chloride and sodium ions (salts) from epithelium cell into intestine.
  6. water potential of intestine decreases, water moves out from blood, down water potential gradient by osmosis through partially permeable membrane.
  7. causes severe diarrhoea + dehydration which can lead to death if not treated.
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26
Q

What are some more symptoms are cholera?

A

Diarrhoea
severe dehydration
Loss of water and salts
Weakness and fatigue
Low Blood Pressure
Weight Loss
Vomitting

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27
Q

How can we diagnose cholera?

A

Dipstick tests of rectal swabs
Identification of vibrio cholera in faecal samples using microscopy.

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28
Q

How can we treat cholera?

A

If people can drink they are given oral rehydration therapy. This involves the use of oral rehydration solution (ORS) that has glucose/salts. We need to ensure that fluid intake=fluid losses in urine and faeces. This helps maintain osmotic balance of blood and tissue fluids. If a person cannot drink they are given the solution intravenously to rehydrate the body.
Almost all treated patients survive.

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29
Q

How can cholera be prevented?

A

Proper sewage treatment to break the transmission cycle.
Chlorinate water to kill bacteria before drinking.
Drink bottled water.
Vaccination only offers short term protection and is no longer recommended.

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30
Q

Describe the global distribution of cholera.

A

Endemic in developing countries for example west and east Africa, Afghanistan, latin America and parts of Asia.
Outbreaks also follow natural disasters or war. For example cholera epidemic during 2010 earthquake in Haiti, 2014-2016 outbreak in Yemen.

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31
Q

Why is it hard to vaccinate against cholera?

A

There are many different strains of vibrio cholera. Each strain that caused a bacteria is more virulent than the last. Adults can be reinfected and have cholera again. This is why it is hard to vaccinate against cholera.

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32
Q

What is the causative organism of malaria in humans?

A

In humans, malaria is caused by plasmodium falciparum (75%), Plasmodium Malariae, Plasmodium Ovale and Plasmodium Vivax (20%).

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33
Q

Describe the structure of the causative agent of malaria.

A

The causative agent is plasmodium- a protoctist (eukaryote), parasite. The appearance changes depending on life cycle stages.
Plasmodium is most motile during initial effective stages.

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34
Q

Define a disease vector.

A

An organism which carries a pathogen from one person to another or from an animal to a human.

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35
Q

What is the disease vector of malaria?

A

Insect Vector=Female Anopheles mosquitoes
Only Female take blood meals to supply eggs with nutrients.
Although blood transfusions, use of unsterile needles, and can pass across placenta from mother can also transmit malaria.

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36
Q

How does the disease vector transmit malaria from infected to uninfected person.

A

Female anopheles mosquito takes a blood meal from infected person and then takes a blood meal from uninfected person.

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37
Q

Describe the life cycle of plasmodium.

A

1.Plasmodium’s gametes fuse, multiplies in and form infective stages in mosquitoes.
2. When mos takes a blood meal, parasite enters host with mos’s anticoagulant and saliva.
3. Infective stages of parasite enter bloodstream and then liver cells.
4. Parasite matures in liver cells, then leaves liver to enter RBC.
5. Parasite multiply in RBCs, causing RBC’s to lyse. (break)
6. Parasites are released and infect other RBC’s.
7. Parasites picked up by another mos in a blood meal.

Remember first: Blood stream, liver than red blood cells.

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38
Q

Describe the symptoms of Malaria.

A

Fever
Anaemia
Nausea
Headaches
Muscle Pain
Shivering
Sweating
Enlarged Spleen

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39
Q

How can we diagnose malaria?

A

Micrscopical analysis of Blood
Dip Stick test for malaria antigens in blood.

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40
Q

When is transmission of malaria most intense?

A

Transmission is more intense in places where the mosquito lifespan is longer (so that the mosquito has time to complete its devolopment inside the mosquito) and where its prefer to bite humans rather than other animals. The long lifespan and strong human biting habit pf the species of anopheles is found in Africa are the main reasons why about 90% of cases are found in africa.

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41
Q

What does transmission of malaria depend upon?

A

Transmission also depends upon climatic conditions that may affect the number and survival of mosquitoes, such as rainfall patterns, temperature and humidity. Transmission may be seasonal with the peak occuring during and just after rainy season.

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42
Q

When can malaria epidemic occur?

A

Malaria epidemics can occur when climate and other conditions suddenly favour transmission in areas where people have little or no immunity to malaria. They can also occur when people with low immunity move into areas with intense malaria transmission.For example when people migrate to find work or to escape poverty, war or natural disasters.

43
Q

What happens if people are continually re-infected with different strains of malaria?

A

If people are continually re-infected by different strands of malaria they become immune. However this only happens if they survive the first five years of life, when mortality from malaria is very high. The immunity lasts only as long as people are in contact with the disease.

44
Q

Why can a malaria epidemic in places where malaria is not an endemic be very serious?

A

The immunity against malaria lasts only as long as people are in contact with the disease. this explains why epidemics in places where malaria is not endemic can be very serious, why malaria is more dangerous in those areas where it only occurs during and after rainy season. This often coincides with the time of maximum agricultural activity, so the disease has a disastrous effect on the economy as people cannot cultivate the land when they are sick.

45
Q

What is recommended before the treatment of malaria?

A

WHO recommends that all cases of suspected malaria are confirmed by using a test that shows the presence of plasmodium before treatment is started. The results of the tests can be available within 30 minutes or less.

46
Q

When are prophylactic drugs taken?

A

Prophylactic drugs are taken before, during and after visiting an area where malaria is an endemic.

47
Q

How can malaria be treated?

A

By anti-malarial drugs such as quinine and chloroquine. Chloroquine is also used as a prophylactic drug ( preventative), stopping an infection occurring if a person is bitten by an infected mosquito. Chloroquine inhibits protein synthesis and prevents the parasite spreading within the body. Another prophylactic proguanile, has the added advantage of inhibiting the sexual reproduction of plasmodium inside the biting mosquito.

48
Q

Define combination therapy.

A

Combination therapy is where multiple drugs are used at the same time and is used to prevent drug resistance.

49
Q

What happens when anti malarial drugs are used widely?

A

Where anti-malarial drugs are used widely, there are strains of drug-resistant plasmodium. The drug is no longer effective against the pathogen. Chloroquine resistance is widespread in parts of South America, South Africa and South East Asia. Newer drugs such as mefloquine are used in some of these areas but mefloquine can have unpleasant side-effects such as restlessness, dizziness, vomiting and disturbed sleep. Resistance to mefloquine has developed in south east Asia.

50
Q

What is the best available treatment available for malaria?

A

Currently the best available treatment particullary for malaria caused by p.falciparum is artemisinin-based combination therapy (ACT). Drugs derived from the plant artimisia annua are used in combination with another drug such as mefloquine.

51
Q

How can we prevent malaria?

A

No vaccine for malaria

  1. Use prophlylactic/preventative drugs.
  2. Reduce number of mosquitoes.
  3. Avoid being bitten by mosquitoes.
52
Q

What is the most effective way to prevent malaria?

A

The most effective way is to kill insect vector and break the transmission cycle. mosquitoes lay eggs in water. larvae hatch and develop in water but breath air by coming to the surface. Oil can be spread over the surfaces of water to make it impossible for mosquitoes larvae and pupae to breath. Marshes can be drained and vegetations cleared to reduce breeding sites for mosquitoes.

53
Q

What are two biological control measures which can be used to kill the insect vector for malaria and break the transmission cycle?

A

Stocking ponds, irrigation and drainage ditches and other permanant bodies of water with fish that feed on mosquito larvae.

Spraying a preparation containing the bacterium bacillus tharingiensis, which kills mosquito larvae but is not toxic to other forms of life.

54
Q

Why is it impossible to eradicate mosquito breeding sites?

A

Mosquitoes will lay their eggs in any small puddle or pool, which makes it impossible to completely eradicate breeding sites, especially in rainy seasons.

55
Q

How can we avoid being bitten by mosquitoes?

A

People should not expose their skin when mosquitoes are most active usually at dusk. Sleep beneath mosquitoes nets treated with long lasting insecticides. Insecticides are sprayed inside homes. This control method is usually effective between three and six months depending on insecticide and surface sprayed. The use of insecticides and nets protects the whole population.

56
Q

Which groups are most at risk from dying from malaria?

A

Young children are most at risk at dying from malaria. pregnant women and young children can be treated with drugs that prevent infections of plasmodium.

57
Q

Describe the structure of the causative organism of HIV?

A

It is RNA virus/retrovirus.
Contains single-stranded RNA as genetic material.
Has protein coat/ capsid made of capsomeres.
Has outer viral envelope made of a lipid bilayer and proteins (mostly derived from host).
Has viral glycoproteins on the outer envelope.
Has 2 enzymes:
1.reverse transcriptase
2. Protease

58
Q

What is the function of reverse transcriptase?

A

Uses RNA as template to produce DNA in host cell.

59
Q

What is the function of Protease?

A

Cleave/process new viral proteins.

60
Q

Describe the life cycle of HIV:

A

1.The viral RNA and reverse transcriptase (RT) enters T helper lymphocytes.
2.RT converts RNA into DNA.
3. The viral DNA is incorporated into the host DNA (in the nucleus of host cell).
4. The cell’s machinery is used to express viral proteins (through transcription and translation).
5. Viral proteins are assembled into many new viruses.

61
Q

How can HIV be transmitted?

A

Through direct exchange of body fluids. There is no vector for HIV and the virus is unable to survive outside of human body.

  1. Semen, vaginal fluids during sexual intercourse.
  2. Blood transmission via infected blood transfusions/contaminated syringes.
  3. Mother to baby transmission across placenta/breast milk.
62
Q

Describe the high risk groups for HIV:

A

High risk groups:
Having multiple sex partners allows virus to spread more widely.
Anal Intercourse increases risk of transmission.
Because less natural lubrication in the rectum, so the rectum, so rectal lining is easily damaged and virus can pass from semen into blood.
and drug users who share needles.

63
Q

Why is it difficult to control the spread of HIV?

A

Slow infection-Virus can stay dormant for years. Virus can incorporate its DNA into host cell and not replicate for a while.

It can change surface proteins to hide from immune system.

64
Q

What are the effects of HIV?

A

HIV infects cells of the immune system, called Helper T lymphocytes.
This destroys helper T cells/ cause their no. to decrease.
Body is unable to defend itself against infection.

65
Q

Define opportunistic infection

A

An infection caused by pathogens that take advantage of a host with a weakened immune system, as may happen in someone with an HIV infection.

66
Q

What are the symptoms of HIV infection?

A

Flu-like symptoms and then symptomless (since virus can stay dormant for years).

Opportunistic infections can occur as a result of compromised immune system.
Collection of opportunistic diseases associated with immunodeficiency caused by HIV=aids.

67
Q

What are some of the opportunistic infections that can occur if someone has AIDS?

A

1.Oral Thrush
2. Pneumonia
3.Cancers like kaposi’s sarcoma
4. Neurodegenerative diseases like dementia.
5. Tuberculosis.
6. Malaria
7. Malnutrition
8. Weight Loss
9.Diarrhoea
10. Fever
11. Sweating

68
Q

Does HIV always progress to aids?

A

HIV does not always progress to AIDS. You can have HIV and if you keep it under control it may not develop to AIDS.

69
Q

What is the treatment for HIV?

A

There is no cure for HIV.

Drug Therapy can only slow down the onset of AIDS.
Zidovudine (similar to the nucleotide base that contains thymine) binds to viral enzyme reverse transcriptase and inhibits it.
Drugs can target viral protease and inhibit it as well.
However, drugs are expensive and have a variety of side effects.

Combination therapy can also be used.
Must follow a strict pattern and timing of medication.
If not followed properly, patients may develop strains of HIV resistant to drugs.

70
Q

How can we prevent HIV?

A

There is no vaccine for HIV.
Use of condoms, femidoms and dental dams.

HIV testing is promoted in high risk groups (e.g. male homosexuals, prostitutes, injecting drug users, sex partners).
Contact tracing: Where the person with HIV traces people he/she has put a risk of infection and that person to be provided a HIV test.
Discourage Needle Sharing
Donated blood is screened for HIV and heat-treated to kill viruses.

71
Q

How can we control mother to child HIV transmission?

A

Both Viral particles and infected lymphocytes are found in breast milk. Mother to child transmission is reduced by treating HIV+ women and their babies with drugs. However HIV+ women in high income countries are advised not to breastfeed their babies because of risk of transmission even if they have a secure supply of drugs. In contrast HIV+ women in low and middle income countries are advised to breastfeed, especially if they have a secure supply of drugs during this period, as the protection provided against other diseases and lack of clean water outweigh risk of transmitting HIV.

72
Q

What are some other problems involved with HIV

A

ٰIn Africa, difficult to reach people for widespread testing in rural area.
Many symptomless carriers
Drugs are expensive and cause many side effects.
pandemic in whole world
Especially high prevalence in Africa.

73
Q

Describe the causative agent of tuberculosis.

A

The causative organism is mycobacterium tuberculosis and mycobacterium Boris.
These are pathogens that live inside human cells, particularly in lungs, which is the first site of infection but the bacteria can be spread throughout the whole body.
M. Tuberculosis causes TB in humans.
M. bovis cause TB in cows, humans and other mammals.

74
Q

How is mycobacterium tuberculosis transmitted?

A

By aerosol infection where pathogen is carried by airborne droplets.

Infected person coughs/sneezes.
Uninfected person breathes in droplets.

75
Q

How is mycobacterium bovis transmitted?

A

Mycobacterium Bovis:
From infected cows/cattle.
Eat Undercooked contaminated meat.
Drink Unpasteurised milk containing bacteria.

76
Q

Where is the site of tuberculosis infection?

A

Site of primary infection=lungs.
Secondary infections in lymph nodes, bones and gut.

77
Q

Define incubation period.

A

This refers to the time period between exposure to a pathogen and the first symptoms appearing in the host.

78
Q

Describe the effects and incubation period of tuberculosis.

A

Tuberculosis is a slow infection, many infections are controlled by immune system and people don’t suffer symptoms, cannot pass on the disease.
The bacteria may be activated after many years when immune system weakened by other infections for e.g HIV.
The incubation period is few weeks to few years.

79
Q

What are the symptoms of tuberculosis?

A

Racking Cough
Coughing Blood
Chest pain
Shortness of breath
Fever
Sweating
Loss Of appetite
Weight Loss

80
Q

How can we diagnose tuberculosis?

A

Chest X-ray
Microscopical examination of sputum (mucus and pus) for bacteria.
Rapid Molecular test detecting presence of DNA from M. tuberculosis.
Long term culture of bacteria.

81
Q

What is the treatment of tuberculosis?

A

When TB is confirmed then patients should be isolated when they are in the most infectious stages (two to four weeks) especially if infected with drug resistant strain of bacterium.

The treatment involves combination therapy and use of multiple antibiotics for example, streptomycin, isoniazid, rifampicin which prevents drug resistance.

the treatment is long for 6-9 months or longer.

DOTS (Direct Observation treatment, short course) make sure patient takes medicine regularly and reduce spread of drug resistance.

82
Q

How can we prevent TB?

A

Bacillus Calmette-Guerin (BCG) vaccine. Derived from M. Bovis.

Isolate patients which are in infectious stages.
Contact tracing and TB screening for early detection to prevent spread,
Cattle tested for TB
Pasteurise milk

83
Q

Why does drug resistance occur?

A

Drug resistance occurs as a result of mutation in the bacterial DNA. Mutation is a random event and occurs with a frequency of about 1 in every 1000 bacteria. If three drugs are used it is reduced to one in a thousand million. if four drugs are used, the chance is reduced to one in a billion.

84
Q

What happens if a person stops treatment of tuberculosis before bacteria is eliminated?

A

The bacteria spread throughout the body, increasing the likelihood that mutations will arise as the bacteria survive for a long time and multiply.

Stopping treatment early means that M. tuberculosis develops resistance to all drugs being being used and makes people more likely to infect others with drug resistance forms of TB.

85
Q

What are the types of drug resistant TB?

A

Multiple-drug resistant strands of TB are resistant forms of TB (MDR-TB) now exist. MDR-TB strains are resistant to at least two main drugs used to treat TB- Isoniazid and rifampicin- which are known as first line drugs. Extensively or extremely drug-resistant TB (XDR-TB) is very dangerous especially for people with HIV.
Treatment for MDR-TB takes longer, is. more expensive. A new drug is called bedaqualline is now available to treat MDR-TB.

86
Q

What is the global distribution of malaria?

A

Endemic all over the world.
Especially high rates in cities due to high migration rate and in overcrowded areas where there is poverty and poor ventilation.
Also more prevenlant where HIV/AIDS is prevalent.

87
Q

Explain the correlation between global distrubutions of AID and TB.

A

Countries where many people have AIDS, also have a high death rate from TB.
Many people who have AIDS die of TB.

This is because TB is an opportunistic infection. People who are HIV+ are more susceptible to TB. Dormant TB is more likely to become active if person is HIV+

88
Q

Define antibiotic.

A

Antibiotics are drugs used, usually derived from microrganisms (such as mold and fungus) to kill/inhibit the growth of bacteria without harming the infected organsim.

89
Q

What are the two different types of antibiotics?

A

Bateriocidal antibiotics-kill bacteria.
Bacteriostatic antibiotics-inhibit bacterial growth.
Prevent spread of bacteria within body.
Harmless to human cells.
Have NO effect on viruses.

90
Q

How do antibiotics work?

A

Inhibit bacterial cell wall synthesis.
Inhibit activity of specific membrane protein/glycoprotein.
Block binding to cells.
Block specific enzyme action.
Inhibit protein syntesis and nucleic acid synthesis.
Target enzymes that bacteria have, but humans dont.

Different antibiotics each have different mechanisms.

91
Q

Describe bacterial cell growth in the absense of penicllin:

A

Bacteiral cell wall is made up of peptidogylcans. When bacteria cells grow, it sectetes autolysins.
Autolysins mae tiny holes to allow the cell wall to stretch.
New peptidoglycans formed.
Peptidase enzyme form cross-links between peptidoglycan chains.
to form cell wall.

92
Q

Describe bacterial cell cycle in the presense of penicillin.

A

Penicillin inhibit peptidase enzyme.
Stops formation of cross-links between peptidoglycan polymers in the cell wall.

Autolysisn make tiny holes to allow the cell wall to stretch.
New peptidoglycans formed but cannot link up.

93
Q

What is the effect of pencillin of bacterial cell growth?

A

As peptidolgycan cannot link up:
Cell Wall is weaker
Cell wall is unable to withstand turgor pressure.
When water moves in by osmis bacteria lyses and dies.
Penicillin is only effective when bacteria is growing.

94
Q

How can we measure the effectiveness of an antibiotic?

A

Diff antibitiocs are effective against diff bacteria.

Antibiotic dics can be placed in a petri dish with growing bacteria. The diameter of the zone of inhibition shows how effective the antibiotic is. The larger the diameter the greater the effectiveness of the antibiotic.

We usually measure in mm not cm.

95
Q

Why do antibiotics not affect viruses?

A

Viruses do not have peptidoglycan cell wall, have protein coat.
They do not have their own metabolism, rely on host cells.
Viruses have no cell structure/very few organelles.
Very few sites for antibiotics to act on.
Viruses live inside host cells, out of reach of antibiotics.

Antivirals exist
Usually target viral glycoproteins on viral envelope.
Prevent binding of virus to host cells.
Inhibit specific viral enzymes.

96
Q

What is antibiotic resistance?

A

When antibiotics are no longer effective against bacteria. Antibiotic resistance can be spread from bacteria to bacteria.

97
Q

Give an example of antibiotic resistance.

A

Many bacteria have penicillinase enzymes which can break down penicillin.
Bacteria become resistant to penicillin.

98
Q

What is antibiotic resistance caused by?

A

Spontaneous/random mutation in bacteria.
Mutation cause change in protein/production of new protein that canot be targetted by antibiotics.

Natural selection enables resistance genes to spread.
Antibiotic is the selection pressure.
Antibiotics only kill bacteria that are non-resitant.

Resistant bacteria survive and reproduce. Antiobiotic resiatnce gene is spread to next gen and other bacteria.

99
Q

Where are antibiotic resistant genes usually found?

A

Antibiotic resiatnt genes are usually found in plasmids.

100
Q

How can bacteria spread antibiotic resistant genes?

A

bacteria can spread antibiotic reistance genes using:
Vertical transmission
Pass plasmids down to daughter cells by binary fission.
Or Horizontal transmission.
pass plasmids to other bacteria by conjugation.

101
Q

How do we speed up antibiotic resistance?

A

Due to patients not completing the course of antibiotics given.
Treatment may not be completed so some susceptible bacteria survives.
Bacteria replicated and have increase chance of mutation/become resistant.

102
Q

What is the consequence of antibiotic resitance?

A

Bacteria can carry several antibiotic reistance genes.
Develop multiple resistance.
become a “super bug”
For example methicillin-resistant staphlyoccus areus (MRSA).
Wounds do not heal and are continually infected by bateria.
Cannot be killed/inhibited by common antibiotics.
Need to controlled by stronger antibiotics.
but we are running out of antibiotics!

103
Q

What is the solution for antibiotic resistance?

A

We need to discover new antibiotics.
We can slightly alter/modify chemical structure of known antibiotics to produce new antibiotic.
But discovery takes time.

the best solution is prevention.
Only use antibiotics when prescribed.
Always finish the course of antibiotics.

104
Q

Syggest why there is a difference in feeding pattern of male and female anopheles mosquitoes.

A

male dont need proteins for egg production.
Males do not have mouthparts for peircing skin.
Adult male only feed on plants.
Blood is toxic to males.
Cant develop presense of humans
Males cannot produce anticoagulant for blood.