Topic 6 - Disease and Forensics Flashcards
(129 cards)
What is the name of the glycoprotein on HIV?
gp120
What does gp120 bind to?
A cd4 receptor on a T helper cells(lymphocytes)
Why is unbroken skin a barrier to HIV?
Keratin in skin surface forms a hard, impenetrable, physical barrier.
What is an enzyme’s structure?
An enzyme is a globular protein.
It has an active site and charged R groups on outside of molecules - specifically hydrophilic on the outside.
How could HIV drugs work?
- HIV drugs would prevent viral replication so T helper cells will not be burst by virus particles leaving the cell.
- Inhibition of reverse transcriptase so DNA could not be made from viral RNA.
- Inhibition of integrase by drugs so viral DNA cannot integrate into host DNA.
HIV genetic material?
RNA
Linear nucleic acid
No plasmids
Mycobacterium tuberculosis genetic material?
DNA
Circular nucleic acid
Plasmids
How do macrophages act as APCs?
Macrophages present antigens to T helper cells. The macrophage binds to T helper cell by CD4 receptors on T cell and by MHC (major histocompatibility complex) on macrophages.
T helper lymphocyte decrease: the effect on other blood components? (In HIV)
B cells are not activated meaning fewer antibodies. T killer cells increase.
Change in CD4 T-lymphocytes during HIV and decrease after HIV infection.
Gp120 in virus binds with CD4 receptors in surface membrane of lymphocyte. Viral RNA enters the lymphocyte and is used to produce viral DNA by action of reverse transcriptase to form new viruses. Lymphocyte is destroyed when new viruses bud out of cell.
Changes in number of CD4 T-lymphocytes during first six weeks after infection with HIV.
Numbers decrease.
Small decrease in first week and between 4-6 weeks.
Large decrease between weeks 2 to 3.
Credit use of manipulated figures.
TB vs. Hosts in an evolutionary race
Affecting APC affecting T cell helper cells
Mutation has occurred in the DNA
There is a change in antigen of bacteria. Memory T cells will not recognise the new antigen. Another primary immune response is needed. E.g. New antigen needs to be presented to the T helper cells to activate another population of T helper cells. Phagocytes/ macrophages unable to recognise, engulf, and destroy bacteria. Antigen presentation is not possible.
Why antibody B not present after infection?
If antibodies will only be present if antigen is present, antigen H is not present in vaccine. Vaccination failed to stimulate immune response.
Organism in a pond
Surrounded by fast-growing trees
Allele frequency
Mutant allele increases, normal decreases
Reproductive success of mutant/non-photosynthetic individuals.
As trees develop, pond will be more shaded. Less light means less photosynthesis is possible. Photosynthetic individuals die and non-photosynthetic survive to pass on allele by using organic compounds - more in nutrients in pond.
Phagocytosis and lysozyme in APCs(macrophages)
Bacteria have to be taken into macrophages.
Fusion of phagosome with lysosome.
Phagosome are broken down by enzymes. (E.g protease - not lysozyme as mentioned in stem of question)
Part of the pathogen has to be on membrane of macrophage.
Type of immunity that results in production of antibody after infection?
Natural active immunity
Secondary immune response
On infection - second exposure - memory cells are activated, cloned, and stimulated. B me merit cells differentiate into plasma cells. In secondary response, antibodies are released from plasma cells.
Antibody A after vaccination vs. After infection
Levels of antibody rise sooner, faster and higher, after infection
The name of the enzyme used in the process to amplify DNA sample
Polymerase
The process that could be used to separate DNA fragments to create DNA profiles
Electrophoresis
Which suspect based on DNA profiles?
Suspect which matches all of the trends I’m the sample.
DNA profiling assumes every individual’s DNA is unique apart from identical twins.
DNA profiling analyses the introns (non-coding blocks) (short tandem repeats)
Non-coding DNA is hypervariable large
Larger number of introns
Many combinations at each locus.
DNA profiling evidence not absolutely conclusive.
DNA profiling has several different stages
Contamination can arise at any stage
Only a few sequences ( a small portion) of DNA is analysed. Possibility of two identical profiles from unrelated individuals. Identical twins or closely related individuals may also show same profile.
Suggest how DNA profiling could be useful to scientist who examine fossils of animals and plants.
Comparisons can be made between DNA from fossils and other organisms to find genetic relationships (how closely related) and therefore can be used opinion taxonomy/classification. These comparisons can also be used to understand evolutionary lines and to determining common ancestor.
Comment on reliability of data. No indication of no. Rats used No data pints No error bars in graph No indication of variability No statistical evidence No indication of experimental details, control variables. Or control group. Mean
A comment cannot be made
Caution should be taken in interpreting results.
Mean has been used so there must have been some repeats