topic 6 Flashcards

1
Q

state the role of micro organisms in breaking down organic matter and releasing carbon compounds into the atmosphere

A

micro organism such as bacteria and fungi are an important part of the carbon cycle
when plants and animals die, microorganism inside and on them will secrete enzymes that decompose dead organic matter into smaller molecules that they can respire
when micro organisms respire these small molecules, methane and CO2 are released
this then recycles CARBON back into the atmosphere

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

how can body temperature be used to determine the time of death

A

body temperature usually ranged between 67
as soon as an individual dies their body temperature starts to cool due to the absence of heat producing reactions
the environmental conditions need to be noted
the cooling of the body follows a sigmoid curve
body temperature is taken via the rectum or abdominal stab with a LONG thermometer
however the body temperature cn be affected by many factors such as

body size 
body position 
clothing 
air movement 
humidity 
temperature of the surroundings
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

how can rigorous mortis be used to determine the time of death

A

after death the muscle cells become starved of oxygen and oxygen dependant reactions stop
respiration in the cells becomes aerobic and produces lactic acid
the ph of the cell falls inhibiting the enzymes and therefore inhibiting aerobic respiration
the ATP needed for muscle contraction is no longer produced
and therefore actin and myosin become fixed ( they no longer slide over each other - sliding ligament theory)

smalle msucles stiffen faster than larger muscles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what occurs straight after death

A

autolysis - the cells and tissue begin to break down by the body’s enzymes and bacteria
putrefaction - this is when the skin begins to turn greenish due to the formation of sulfhaemoglobin
the micro organisms decompose tissues and organs, this produces gases such as methane which causes the body to bloat
the skin begins to blister and fall off
the tissues begin to liquefy and seep out into the areas around the body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

how can forensic entomology be used to determine the time of death

A

the presence of insects allow forensic entomologists to make an estimate on how much time it has been since death
record the location and condition of the body and then take some sample of the insects found on near or under the body.
making sure to nite when and when each insect was foun
the temperature of the air, ground, body and maggot mass are measured in order that the rate of maggot development can be determined
some of the maggots will be taken back to the lab, where they will be fed and allowed to complete their development
this is useful for species identification and establishing when they pupate

for example blow flies
blow flies will find the body on the time of death
they will then lay their eggs a few days after death
it then goes through EGG, LARVA ( MAGGOT), THEN PUPATE
if a maggot is found on the body it is then back to the lab and fed till it finished its life course and then it is calculated from there ehrn the egg was laid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

explain how the stages of succession can be used to determine the time of death

A

immediately after the time of death the conditions in the dead body are favourable for bacteria
as the bacteria decompose tissue, the conditions in the dead body become more favourable for flies and their large
when the large feed on a dead body, they ,are the conditions form favourable for beetles
as a dead body dries out the conditions become less favourable for flies and the beetles remain and decompose the dry tissue
after this it is no longer favourable for any organism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what are the non specific responses to infection

A

interferon
phagocytosis
inflammation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what are the steps of phagocytosis

A

a phagocyte recognises the antigen on a pathogen
the cytoplasm of the phagocyte moves round the pathogen engulfing it
the pathogen is now contained in the phagocytic vacuole in the cytoplasm of the phagocyte
a lysosome ( an organelle which contains digestive enzymes lysozymes) fuses with the phagocytic vacuolee
the lysozyme then break down the pathogen
the phagocyte then presents the pathogen’s antigens ( it becomes an antigen presenting cell)
this will then initiate the specific response to infection

macrophages can also act as phagocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what is interferon used for

A

when cells are infected with VIRUSES they produce the PROTEIN interferon
interferon is Iseo to prevent viruses from spreading to uninfected cells
this is done through
preventing viral replication, by inhibiting the production of viral proteins
they activate the cells involved in the specific immune response to kill infected cells
they activate other mechanism of non specific response for example they promote inflammation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what is the process of inflammation

A
  • the immune system cells recognise foreign antigens on the surface of the pathogen and release histamine that trigger inflammation
  • histamine cause vasodilation ( widening of blood vessels) of the arterioles increasing blood flow of the capillaries to the site of the infection
  • it also increases the permeability of the capillaries this allows white blood cells and antibodies leak from the blood to the tissue, causing them to be attacked by the white blood cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

outline the specific response to infection

A
  • the macrophage becomes antigen presenting
  • they bind to the t helper cells
  • this activates the t helper cells which causes them do dived by mitosis
  • the activated t helper cells then bind to the antigen presenting cells
  • the results in the release of cytokines
  • this causes colonial expansion of the B cells as well as the activation of t killer cells
  • the B cells will then differentiate into b memory and b effector cells
  • through further differentiation they will differentiate into plasma cells
  • the plasma cells will produce antibodies
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

describe the structure of antibodies

A

antibodies are made from 4 polypeptide chain; two heavy chains and two light chains
each of these chains has a variable region and a constant region
the variable regions of the antibody form the antigen binding sight
the shape of the variable regions are complimentary to a particular antigen, the variable region differs between antibodies
the hinge region allows flexibility when the antibody binds to the antigen
the constant region allow binding to the receptors on the phagocytes and macrophages (this region is the same for all antibodies)
disulphide bridges hold the polypeptide chains together

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

how to antibodies help to clear infections

A
  1. agglutinating pathogen - the pathogens are clumped together to make phagocytosis easier
  2. opsonisation - the pathogens are marked for phagocytosis
  3. neutralisation - neutralisation of harmful toxins
  4. lysis - breaking down of bacterial cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

describe the structure of a virus

A

viruses are non living, which contain either DNA or RNA (they can either be single or double stranded) enclosed in a capsid. it is sometimes covered in a lipid envelope ( from the cell membrane - phospholipid bi layer of the host cell)

in the HIV virus they have the same structure but they contain REVERSE TRANSCRIPTASE and DNA INTERGRASE

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

describe the structure of bacteria

A

the Dan of bacteria exists in the cytoplasm, it can also exist as plasmids
they contain ribosomes
they have a cell wall
and they have a plasma membrane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

how does the his virus invade the t helper cells

A

the HIV virus has the GP120 glycoprotein on the surface
this binds to the CD4 receptors on the t helper cells
the envelope surrounding the virus fuses with the t helper cells membrane
enabling the viral RNA to enter the cell

17
Q

how does the HIV virus hijack protein synthesis

A

the HIV virus uses the enzyme REVERSE TRANSCRIPTASE is sued to make a complimentary strand of DNA from the viral RNA template
then from this DNA intergrase will insert the viral DNA into the human DNA
transcription and translation will take place to produce viral proteins
this then is used to form new viruses
the new virus bud out of the T cell, taking some of the host cell’s membrane and forming an envelope and killing the host cells
the infected t helper cells are also killed by t killer cells
this means there will be a reduction in the amount of t helper cells
so less can release cytokines
and less t killer cells are activated and no colonial expansion of B cells
and therefore no antibodies are produced to kill the virus

18
Q

how does mycobacterium tuberculosis cause tb

A
  • the bacteria is engulfed by a phagocyte
  • the bacteria can survive and replicate inside the phagocyte
  • usually the immune system seals the infected phagocyte in tubercles (which are in the lungs)
  • when sealed inside the tubercles the bacteria becomes dormant and there are no symptoms
  • the dormant bacteria is then later reactivated this suavely occurs when the immune system is weakened
19
Q

what are the physical barrier to infection

A

stomach acid - has hydrochloric acid and enzymes which kill bacteria

gut and skin flora - the gut and skin flora are bacteria which out compete the pathogens for resources such as food

skin - has a tough physical barrier of keratin

20
Q

how does the HIV virus evade being killed - evolutionary race

A

the HIV kills the t helper cells that it infects
this reduced the overall number of t helper cells in the body therefore reducing the chance of the HIV being killed ( due to not cytokines so no t killer cells and no B cells and therefore no antibodies)
the HIV virus has a high rate of mutation in the gene that codes for their antigen
this can change the structure of the antigen and form new strains of the virus
this means that the b memory cells will not be able to recognise the new antigen
so it has to undergo the primary specific response to infection

21
Q

how does the mycobacterium tuberculosis evade being killed - evolutionary race

A

it has a thick way cell wall that enables ti to not be broken down by the hydrolytic enzymes produced by the macrophage
there is variation amount every population of mycobacterium tuberculosis and those that have the thickest waxy coverings survive and those with the thinner coverings are broken down
the tb bacteria has also learnt to survive inside the macrophage and therefore remain protected as the macrophage has self antigens and therefore will not recognise it as foreign
unless the host cells enzymes can evolve to produce more effective enzymes to digest the waxy coat of the bacteria
the bacteria will remain dormant inside the macrophage

22
Q

what are all the types of immunity

A

natural active immunity - catching the disease and getting the antibodies for it
artificial active immunity - getting vaccinated

natural passive immunity - when a child may become immune from the antibodies it gets from the placenta and breast milk
artificial passive immunity - when you are injected with antibodies

23
Q

how do vaccination help an individual to develop immunity

A

a vaccination is a weak or attenuated form of the pathogen that is able to cause an immune response but weak enough not to cause illness
this cause the primary response to infection
this then produces the be memory cells the remain in the blood for longer
if an individual is infected with the virus again, then they will only undergo the secondary response
which produces a larger volume of antibodies and is much faster

24
Q

how do antibiotics work in order to kill bacteria

A
  • inhibiting the synthesis of the peptidoglycan cell membrane - this causes osmotic lysis which makes the cell burst
  • disrupting the cell membrane
  • inhibiting the synths of nucleic acid
  • inhibiting the bacteria enzymes
25
Q

how do bacterias develop antibiotic resistance

A
  1. spontaneous mutations, which will then be passed in to all the bacteria during binary fission and therefore developing a resistance
  2. conjugation - a bacteria may have the gene for antibiotic resistance and this will be passed on through cell to cell recognition or through a sexual reproduction
26
Q

why is there an antibiotic resistance

A
  • over use of antibiotics
  • animals may feed on antibiotics
  • GP will prescribe antibiotics unnecessarily or for viral infections
  • the use of broad spectrum antibiotics
27
Q

what are the treatments for HIV

A
  1. reverse transcriptase inhibitors - it inhibits the enzyme reverse transcriptase, so the viral RNA can not be converted into viral DNA, therefore viral DNA can not be integrated into the host cell DNA and new viral proteins can not be produced
  2. protease inhibitors - they inhibit the protease enzymes that are used to hydrolyse larger proteins into smaller polypeptide used in the maufactor of viral proteins
  3. inergrase inhibitors - they prevent viral DNA from integrating into the hots cell DNA therefore preventing transcription and translation and the production of viral proteins