Infection, Immunity and Forensics-notes
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Transcript of Infection, Immunity and Forensics-notes
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A Y O M I D E O L U B U M M O
Infection, Immunity and
Forensics
AYOMIDE OLUBUMMO
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A.O
Explain the nature of the enetic code
!enetic code is the se"uence of #ases on the D$Amolecule, it is read in roups of three #ases calledcodons%
It can #e descri#e as #ein a triplet code& three #asescode for an amino acid%
Deenerate' there is more than one codon for aparticular amino acid%
$on( o)erlappin' each triplet code is discrete andonly read once
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Explain the process of protein synthesis
It is made up of t*o main staes& transcription and translation%
+ranscription occurs in the nucleus
D$A polymerase causes the D$A strands to separate lea)in the#ases exposed%
+he antisense strand acts as a template for the m$A%Free $A nucleotides line up aainst their complementary #ase
pairs%
+he $A nucleotides are -oined toether usin $A polymerase,
in a condensation reaction formin phosphodiester #onds#et*een the nucleotides to form the polynucleotide m$A%
+he m$A strand detaches form the antisense strand and theD$A strands re-oin and recoil%
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Explain the process of protein synthesis
Before the m$A lea)es the nucleus it underoespost transcriptional chanes in *hich the introns.non codin #ases/ are remo)ed%
+he remainin exons are then ordered%
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Explain the process of protein synthesis
Follo*in post transcriptional chanes the m$A lea)es the nucleus and enters thecytoplasm *here it underoes translation%
In the cytoplasm the m$A attached to ri#osome *hich is made up of t*o su#units and ri#osomal $A%
At the start of the m$A molecule is a start codon *hich initiates protein synthesis%
+he ri#osome reads the codons and the t$A molecule *ith the complementaryanticodon to codon #ein read lines up aainst it% Each t$A molecule is attachedto a specific amino acid%
+he ri#osome oes alon the m$A readin the codons and fetchin thecomplementary t$A molecules%
+he anticodon of the t$A lines up aainst the codon of the m$A and hydroen
#onds are formed #et*een the codon and anticodon%As the t$A molecule line up,peptide #onds form #et*een the amino acid%
0hen the ri#osome reads the stop codon *hich is at the end of the m$Amolecule, protein synthesis stops and the polypeptide is released%
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Explain ho* one ene can i)e rise to a num#er of proteins
+his is due to post transcriptional chanes *hich *as mentioneda#o)e%
+he remainin exons can #e arraned into different orders%
+he order of the exons determines the primary structure of the
protein .se"uence of amino acids/+his then determines the secondary and tertiary three
dimensional structure of the protein%
Determines *hat #onds are formed in theses structures, *hether&ionic #ond #et*een side roups
Disulphide& #ond #et*een side roups containin sulphur
1ydroen
+he structure determines the type thus the function of the protein%
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A.O
0hat is D$A profilin used for
D$A profilin is used for identification anddeterminin enetic relationships #et*eenindi)iduals%
+he theory #ehind D$A profilin'E)eryone2s D$A is uni"ue except for identical t*ins
It analyses introns #ecause there are a lare num#erof the them and they are hihly )aria#le .mutations
reularly occur here/%
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0hy can e)idence from D$A profilin #e inconclusi)e
Due to small area of the D$A #ein analysed
+here are many staes of the D$A profile so errorscan arise%
+he D$A sample may #e contaminated%Identical t*ins *ould ha)e identical profile due to
nearly identical D$A%
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1o* is D$A profilin used #y scientist
Used to spot e)olutionary relationships . can spotcommon ancestor/ so is )ery useful in taxonomy%
Used to pre)ent in#reedin in capti)e #reedin
prorammes as in#reedin reduces enetic di)ersity
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1o* can D$A #e amplified
+he sample of D$A can #e amplified usin 34. polymerase chain reaction/%
+he )ial containin& a sample of D$A ta5en from sali)a, free D$Anucleotides, D$A polymerase and D$A primers are placed into the 34machine%
+he mixture is heater to a#out 67 derees, this is done to #rea5 the hydroen
#onds #et*een the D$A strands%+he mixture is then cooled to 88 derees to allo* the D$A primers to anneal
.attach/ to the D$A, to mar5 *here to start replication%
+hen heated to 98 derees to allo* the D$A polymerase to assem#lecomplementary D$A strands usin the D$A nucleotides%
+he cycle of heatin and coolin is repeated approximately :7 times to et alare enouh sample%
D$A polymerase not suita#le in machine as its optimum is a#out :8therefore *ould li5e denature at hih temperatures of machine%
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1o* is el electrophoresis performed
After amplification, the parts of D$A to #e analyses are cut *ithrestriction endonuclease%
+he D$A is stained, and placed in *ell in aar -elly surrounded #y#uffer solution% . the dye usually used is ethium #romide/
An electric current is passed throuh the solution *hich mo)ed theD$A framents *ith the shorter frament mo)in further% .D$Aa#le to mo)e *ith current due to sliht neati)e chare of molecule/%
+he D$A is then )ie*ed under U; liht and seen as #ands%
+he hiher the num#er of matchin #ands the more closely
enetically related the person is%If position of #ands are identical this can #e used to identify suspect%
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A.O
0hat is are the 5ey features of the structure of #acteria
1as flaellum *hich rotates to pro)ide mo)ement to the#acteria%
1as capsule, also 5no*n as slime layer used to 5ill immunecells%
It is a pro5aryote and has a peptidolycan cells *all
4ontains infoldin of cell mem#rane called memosome*hich contains proteins for respiration%
4ontains plasmid *hich are circular pieces of non essentialD$A can #e passed on to host%
4ontains circular Dna
4an ha)e pili, *hich can #e used in replication%
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0hat are 5ey features of )irus
4ontains capsid *hich contains enetic material%
!enetic material can #e D$A or $A .found inretro)iruses, in this case also ha)e re)erse
transcriptase en7 molecules%
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ole of #arriers in protectin the #ody
+here are )arious routes pathoens can ta5e to infect the #ody and these routesha)e #arriers *hich pre)ent entry%
?5in is a physical #arrier it contains 5eratin *hich is hard to penetrate%
3athoens also need antiens to attach to *hich are not present on s5in or #lood%
?5in also secretes se#um *hich has a lo* p1 so creates harsh conditions for
pathoens%?5in has flora *hich are #etter adapted to li)in on s5in therefore outcompete
pathoens
?5in also clots *hen #ro5en to pre)ent entry to pathoens%
Another physical #arrier is the epithelial linin%
It contains ciliated cells *hich s*eep de#ris and mucus that traps the pathoens%
4an also secrete ly
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0hat is 1I;
1uman immunodeficiency )irus%
First staes asymptomatic,
But *hen immune system fails leads to de)elopment
of AID?% .ac"uired immunodefiency syndrome%Death is not #y a )irus #ut #y a secondary infection
that *ouldn@t cause death to someone *ith afunctionin immune system%
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0hat is the series of e)ents that lead to death #y 1I;
!p=>7 molecules attach to cd receptors on the t helper cell%
e)erse transcriptase con)erts $A into D$A, *hich enters the thelper cells%
En
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1o* is 1I; spread
+he )irus cannot sur)i)e out of the #ody for lon%
+herefore it is spread #y direct contact li5e sex orother exchanes of #loodily fluid%
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A.ODescri#e the non specific response of the #ody to infection(Inflammation
3latelets or mast cells in the #lood release histamines
1istamines cause )asodilation and increased permea#ility ofcappliaries% +his leads to increased #lood flo* to infected site,alon *ith the #lood, *hite #lood cells tra)el to the infected
site%Inflammation can also lead to s*ellin, redness and pain
*hich can #e com#ated *ith antihistamines%
Better to ta5e antihistmines in ta#let form not cream, as
cream allo*s application directly to infected site so fasterresponse, has a hiher concentration of the antihistaminesand antihistamines in ta#lets may dissol)e due to stomachacid%
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A.ODescri#e the non specific response of the #ody to infection(lyso
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A.ODescri#e the non specific response of the #ody to infection(interferon
Interferon is a protein released #y infected cells%
+hey act on )irus and inhi#it the action of )irus thusstoppin their spread%
+hey also acti)ate other mechanisms of the nonspecific immune repsonse%
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A.ODescri#e the non specific response of the #ody to infection(phaocytosis
A phaocyte is a type of *hite #lood cell%
It reconises the antien on the pathoen as foreinand enulf it in a phaocytic )acuole%
0ithin the )acuole, the pathoen fuses *ith alysosome *hich contains lyso
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0hat is a + cell
A + cell is a type of *hite #lood cell found in thelymph%
It has antien receptors *hich it uses to #ind to
pathoens *ith a complementary antien%econises and identifies cells as self and nonself%
In the case that it #inds to a non self antien.pathoen/ it is acti)ated underoes mitosis to
differiate into t helper cells, t 5iller cells and tmemory cells
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0hat are the different t cells and *hat do they do
+ helper cell released cyto5ines *hich acti)ates the #effector cells
+ 5iller cells 5ill infected cells
+ memory remem#er the antien allo*in for rapidsecondary response in the case of reinfection% +he tmemory cells are responsi#le for immunity%
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0hat is a # cell
A B cell is a type of *hite #lood cell, that contain ananti#ody on the surface of the cell%
4yto5ines released from the t helper cell acti)ates in
cell and lead to the production of # effector cells.other*ise 5no*n as plasma cells/ *hich o on toproduce anti#odies%
4yto5ines also cause production of # memory cells
*hich also *or5 to heihten secondary response%
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0hat are anti#odies
Anti#odies are proteins produced #y B effector cells%
+hey ha)e :D structure *hich is held toether #ydisulphide #rides% +hey ha)e t*o antien receptors
sites%+hey ha)e a constant reion
+hey also ha)e a )aria#le reion%
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0hat do anti#odies do
+hey cause alutination, they do this #y forminanti#ody(antien complexes *hich case thepathoens to come toether%
Alutination is important as it places the pathoensin one place ma5in it easier to #e enulfed% It alsostops the spread to pathoens%
Also neutralise toxins produced #y pathoens #y
formin toxin(anti#ody complex *hich is enulfed%Bloc5 receptors on pathoen so they cannot #ind to
host cells%
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0hat is immunity
0hen your immune system can ma5e the anti#odiesneed to fiht and 5ill pathoens *hen they infect the
#ody%
It can #e passi)e or acti)e%3assi)e immunity is *hen the anti#odies needed to
fiht the infection is produced #y another oranismand introduce into your #ody%
Acti)e immunity is *hen your immune systemproduces the anti#odies needed to fiht theinfection%
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1o* can you de)elop immunity . passi)e/
3assi)e immunity can #e de)eloped naturally orartificially%
3assi)e natural immunity( *hen the anti#odies are
passed from mother to child throuh #reastmil5%3assi)e artificial immunity( *hen anti#odies are
in-ected into the #ody, this is the case to treattetanus, the tetanus anti#odies act on the tetanus
toxins%
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1o* to de)elop immunity .acti)e/
Acti)e immunity can also #e de)eloped naturally or artificially%Acti)e natural immunity( *hen infected the #ody@s response is slo* #ecause
no memory cells are present, so the #ody has to ma5e numerous t cells *ithdifferent antien receptor until it creates an antien receptor that iscomplementary to the forein antien% +his can ta5e a *hile% +he t helper
cells then #inds to the pathoen and releases cyto5ines to acti)ate # effectorscells and the appropriate anti#ody% +his is the primary response. theresponse *hen infected #y ne* pathoen/% +his response is slo* and onlysmall "uantities of anti#odies are produced%
B memory and t memory cells are also produces so in the case of reinfectionthe secondary response is trier *hich is more rapid and leads to production
of a larer "uantity of anti#odies%Acti)e passi)e immunity( de)eloped #y )accination in *hich you are in-ected
*ith harmless dose of pathoen in order t et your #ody to produce memorycells that *ill allo* for rapid response in the case of reinfesction%
AYOMIDE OLUBUMMO