Topic 6: Immunity, infection and forensics Flashcards

1
Q

Name the 4 ways of determining time of death of a mammal.

A

Extent of decomposition.
Forensic entomology.
Body temperature.
Degree of muscle contractions.

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2
Q

Describe how Extent of decomposition can be used to determine time of death.

A

Bodies follow same pattern of decay and decomposition.
Enzymes from digestive system from digestive system breakdown surrounding tissue.
Stage of decomposition can estimate time of death.

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3
Q

Describe how Forensic entomology can be used to determine time of death.

A

Each species of insect has specific life cycles.
Determining age of insects enables time of death to be estimated.
Body also acts of site of succession as species occupying it changes so analysis of community also estimates time of death.

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4
Q

Describe how Body temperature can be used to determine time of death.

A

Temperature of body decreases after death as Heat producing metabolic reactions stop.
Only use full up to 24 hours after death as body temp reaches surrounding.
Body position, surrounding conditions like weather will affect heat loss.

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5
Q

Describe how Degree of muscle contraction can be used to determine time of death.

A

After death muscles start to stiffen up as ATP is used up, calcium ions build up in muscles and become fixed in a state of contraction called rigor mortis.
starts 2-4 hours after death and ends around 36 hours after death.

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6
Q

Describe the Polymerase chain reaction.

A

DNA sample, primers, free nucleotides and DNA polymerase solution made.
Mixture is heated to 95 degrees breaking hydrogen bonds.
Mixture is cooled to 55 degrees so primers can bind to strands.
temperature is increased to 70 degrees as that’s when DNA polymerase works copying DNA.
This cycle is repeated many times.

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7
Q

Describe Gel electrophoresis.

A

DNA is cut with Restriction endonuclease enzymes.
Fragments placed in wells in agarose gels fluorescence are added.
Current is passed along gel.
DNA is negative so moves towards Anode.
Bigger fragments move slower as bands appear.

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8
Q

Differences between virus and bacteria.

A

Bacteria don’t require host virus do.
Bacteria only have DNA virus can have either DNA or RNA.
Viruses are significantly smaller than bacteria.
Bacteria have many cell membranes, cell wall, cytoplasm, ribosome plasmids, flagellum and pili viruses have none.

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9
Q

How TB infects humans.

A

First infection may be symptomless. Infected phagocytes ae sealed in tubercles in lungs.
Bacteria lay dormant not destroyed by immune system due to waxy coat.
When immune system becomes weak bacteria becomes active destroying lung tissue.
Can spread to other body parts becoming fatal.

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10
Q

Describe physical barriers to infections.

A

Skin tough physical barrier containing keratin.
Stomach acid and enzymes kills bacteria.
Gut and skin flora, natural bacteria competes with pathogens for food and space.

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11
Q

Name the 4 parts of the Non specific immune response.

A

Inflammation.
Fever.
Lysozyme action.
Phagocytosis.

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12
Q

Describe Inflammation.

A

Histamines released by damaged white blood cells causes vasodilation and permeability of blood vessels.
Increasing antibodies, white blood cells, and plasma going to infected tissue.

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13
Q

Describe Fever.

A

Hypothalamus sets body temp higher, increasing rate of enzyme-controlled reactions. slows rate of bacteria reproduction.
Balance must be struck to not denature own enzymes.

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14
Q

Describe Lysozyme action.

A

Lysozyme is an enzyme found in secretions like tears and mucus that kills bacteria.

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15
Q

Describe Phagocytosis.

A

Process in which Phagocytes engulf pathogens enclosing them in vacuole and exocytosis Lysosomes are entered with it.

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16
Q

Name the two stages of the Hormonal responce.

A

T helper Activation.
Effector stage.

17
Q

Describe T helper activation in the Hormonal responce.

A

Bacterium are engulfed by a Phagocyte, presenting their antigens on the MHC (major histocompatibility complex) becoming an APC ( Antigen presenting cell).
The APC binds to T helper cell with complimentary receptor proteins.
Activating T helper causing it to divide by mitosis.
Forms many activated T helper cells and T memory cells.

18
Q

Describe the Effector stage of the hormonal responce.

A

B cells take on bacteria antigens becoming APC.
APC finds complimentary activated T helper cell and binds to it.
T helper releases cytokines causing B cell to divide by mitosis.
This makes B memory cells and b effector cells.
B effector cells differentiate into Plasma cells.
Plasma cells create antibodies.
T suppressor cells stop response.

19
Q

Name all 5 ways Antibodies destroy pathogens.

A

Agglutination, clumps microbes together phagocytosis easier.
Lysis, burst bacteria membrane.
Opsonisation, mark microbes for easier phagocytosis.
Precipitation, soluble toxins made insoluble.
Neutralisation, neutralises harmful toxins.

20
Q

Describe Natural active immunity.

A

arises from being exposed to an antigen naturally and your body producing antibodies.

21
Q

Describe Natural passive immunity.

A

Is the result of mothers antibodies running through the placenta and being in breast milk.

22
Q

Describe Active artificial immunity.

A

Active artificial immunity is from a vaccination causing a immune system response.

23
Q

Describe passive artificial immunit.

A

Antibodies are injected into your body.

24
Q

Describe Herd immunity.

A

Enough people have been vaccinated that transmission is very unlikely requires around 80-90%.

25
Q

Name the two types of Antibodies.

A

Bactericidal.
Bacteriostatic.

26
Q

Describe Bactericidal antibodies.

A

Kill bacteria by destroying their cell wall causing them to burst (lysis).

27
Q

Describe Bacteriostatic antibodies.

A

Inhibit growth of bacteria by stopping protein synthesis.
Bacteria can’t divide and grow.

28
Q

Describe RNA splicing.

A

Post transcription modification of mRNA.
Enables eukaryotes to produce more proteins than they have genes.

29
Q

Describe the stages of RNA splicing.

A

Transcribed gene creates Pre-mRNA.
All introns and some exons are removed.
remaining genes are joined using spliceosomes.
depending on the order variety of mature functional RNA can be made.

30
Q

Describe Exons.

A

Section of genetic code that codes for proteins.