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microbiology - viruses, prions and viroids

front 1

define virus

back 1

PARTICLES, that are infectious agents and are obligate intracellular paracites because they need a host cell to replicate

front 2

viruses are ____ specific.

back 2

host cell. (very strict and eukaryotic cell viruses cannot affect prokaryoticand vice versa. only exception is rabies

front 3

what two structural components do all viruses have and describe them.

back 3

1.nucleic acid core/genome- either DNA or RNA genetic material that can be used to classify viruses
2.capsid-protein cote that surrounds nucleic acid core

front 4

what two other structural components can be found in viruses and describe them.

back 4

1.envelope- membrane like structure that surrounds capsid. they sometime steal the membrane from their host cell but they do not function as such
2. spikes-made of glycoprotien and are associated with enveloped viruses. function as attachment to host cell

front 5

what is so special about pox viruses

back 5

they are the largest and pretty much self sufficient. size matters .they have multilayered capsids and make own envelope

front 6

describe the shapes found in viruses

back 6

1.icosahedral/ spherical
2.helical

front 7

what is icosahedral/ spherical

back 7

polyhedron with about 20 equilateral triangular faces. shape of a capsid

front 8

what is helical

back 8

cylindrical-tube-like structure

front 9

what is an enveloped viruses shape

back 9

usually spherical however shape of capsid underneath can vary

front 10

what is a viron

back 10

fully assembed virus particle ; extracelluar form of virus

front 11

define nucleocapsid

back 11

genome and capsid

front 12

what is an enveloped virus?

back 12

a virus with an envelope

front 13

what is a naked capsid virus?

back 13

not surrounded by an envelope

front 14

bacteriophage, phage, φ

back 14

viruses that affect prokaryotic cells( means bacteria eating)

front 15

how do viral replication and cell replication differ

back 15

cell replication=1 to 2
viral replication= 1 to many

front 16

viral cultivation- live animals advantages and disadvantages

back 16

advantages-monkeys are close to human,s some viruses wont replicate unless in live animal, good for when we want to see effect on entire animal
disadvantages-very expensive, pediree (not working with genetially identical) and dont know genentic composition, with monkeys they come from other parts of the world and they can be different. also ethics is a factor

front 17

organ culture-(whole organ or part of organ) advantages and disadvantages

back 17

adv. they will be like they would be in the animal. you can control / maintain to a certain extent. dis- sacrifice animal, expensive and most organs dont cooperate

front 18

embryonated eggs- what is used and advantages and disadvantages

back 18

fertalized eggs typically chicken eggs. 1st type of test outside original viral place
adv. - cheap, different tissues in egg, viral propigation .
disadv- innoculating egg is not easy. cant’ see what is going on

front 19

tissue/ cell culture- what happens and what are the two types and explain them and their advantages and disadvantages

back 19

take cells (animal cells typically sticky) place in glass or plastic container. cells attach to bottom. then baith cells with some kind of medium
two types:
continuous cell lines
primary cell lines

front 20

what are continuous cell lines and what are their advantages and disadvantages

back 20

can be transferred indefinitely take growing cells in fresh container and medium and they will continue to grow) adv. passed indefinitely . disadvantage- tend not to be normal cells, eg. cancers. often form monolayer but these don’t

front 21

what are primary cell lines and their advantages and disadantages?

back 21

cells that come directly from host- adv. normal cells disadv- transfered indefinitely

front 22

what makes infecting plants so hard?

back 22

the barrier is plant cell wall because viruses can’t get inside by on their own and do so via storm damage insect damage, disease damage and things like that. once affect, spread quickly! shead in seeds

front 23

three ways plants are infected

back 23

-whole plant cultures
-plant cell protoplast
-plant tissue culture

front 24

how is a whole plant culture infected?

back 24

rub stem and leaves with virus and abrasive material

front 25

how is a plant cell protoplast able to be infected

back 25

plants w/o cell wall

front 26

why are plant tissue cultures advantages

back 26

adc- cheaper and replicate faster and get more. genetically engineer

front 27

what is a viral assay ?

back 27

methods used “enumerate” viruses

front 28

what are the two types of viral assays?

back 28

1.hemagglutination assay
2.plaque assay

front 29

when and where is hemagglutination assay useful and what do they do?

back 29

for animal viruses useful only w/ viruses w/ hemagglutininc causes red blood cells to clump together (you have to have something to hold them together)

front 30

what are the steps for hemagglutination assay

back 30

1.serially dilute viruses suspended in wells of microtiter plate
2.add same concentration of sheep red blood cells to each well
3.look for hemagg. ( if occured virus particle allows rbs to connect to another virus well and look like they are holding hands. if not occurred all break apart and there is a red dot at the bottom. titer=reciprocal of greatest dil. of virus that allows for hemagg. disadvantage is you cannot cannot compare titer of different viruses. used to monitor viral loads

front 31

what are plaque assays?

back 31

for bacterophage that lyce host cells.

front 32

what are the steps for plaque assay

back 32

serially dilute in suspended mix each solution to generate bacteria lawn incculate and count number of plaquest in bacteria. lawn and multiply diltion factor . disadvantage is that you can under estimate

front 33

what are the 2 major types of viral replication?

back 33

-productive response
-non productive response

front 34

what are the other types of replication

back 34

-non- integrative lysogeny
-persistent or chronic viral infections
-latent virus infection

front 35

what is productive response

back 35

when virus successfully infects host cell, begins to replicate and continue to, proglenine are produced and released from cell. length varies

front 36

what is non productive response

back 36

sucessfully inects ,begins to replicate but replication stops. host cell still infected but virus will not kill cell

front 37

what is non- integrative lysogeny

back 37

virual DNA does not integrate but stays in cytoplasm

front 38

what is persistent or chronic viral infections

back 38

slow productive response. infect host cells and begin replicating but it takes a long time (examples-1. hepatitis b. virus - not food born, blood born, and sexually transmitted. sometimes never goes away 2-mesles virus (rubeola) incubation period ~ 1 month. 2- epstein - barr virus (herpes virus) . causes mono )

front 39

what are latent virus infections

back 39

infects then goes dorment but may begin replicating again.( ex. herpes simplex virus type I and II.type 1-> cold sores/ fever blisters. type-> genital herpes infected for life . 2->varicella -> zoster virus - chicken pox and shingles)

front 40

what cycle does productive response go through? what do productive responses with bacteriophages do?

back 40

lytic cycle
. they lice cells open they kill them but not necessarily lice them

front 41

step 1 of the lytic cycle and describe?

back 41

adsorption- host range is defined.. very specific pairing of host and virus. if it does not pair correctly, virus will not affect. virons (use fibers) attach proteins specifically interact with host cell receptor. cell walls are typically receptors (pili, flagella) for animals glycoprotiens

front 42

step 2 of the lytic cycle and describe

back 42

penetration and uncoating- virus gets into cell and viral genome is released. occur simultaneously for bacteriophage(s) φ-> inject genome (usually all that enters) some φ-> genome inserted into bacteria cell wall for all phage the only thing that enters is genome. animal virus-. (endocytosis) membrane fusion event. fusion of envelope with some membrane of the cell via fusion protien and nuclieocapsid is entered. fusion proteins remain at surface and due to bumping cells fuse to each other. uncoating step varies

front 43

step 3 of the lytic cycle and describe

back 43

replication (synthesis)- varies from virus to virus . always occur during “eclipse phase” - time in viral replication when virus has been taken apart. does not always start here. for φ starts at penetration. (stepwise and sequential)
early functions: early mRNA ->early proteins (nucleiaces: shut down factory; polymerase)
late functions:late mRNA-> late proteins (caped proteins , spike proteins etc)

front 44

step 4 of the lytic cycle

back 44

assembly (stepwise and sequential) maturation genome is replicated, build capsid, genome is stuffed, other parts are added if needed some viruses have to get an envelope

front 45

step 5 of the lytic cycle

back 45

release- getting bacteria out of host cell
φ late proteins endolysin
animal vir-> varies considerably some have to just sit and wait. some acquire envelope s they leave or exocytosis.

front 46

what cycle does nonproductive response go though

back 46

lysogeny λ . everything goes a planned until replication stops λ jumps into bact chromosome

front 47

step 1 of lysogeny

back 47

absorption- λ example-e. coli virus

front 48

step 2 of lysogeny

back 48

penetration and uncoating

front 49

step 3 of lysogeny

back 49

replication begins

front 50

step 4 of lysogeny

back 50

if lysogeny occurs-> integration. λ DNA plants itself inside e. coli chromosomes. λ DNA is replicated along with bacteria chromosome indefinitely

front 51

step 5 of lysogeny

back 51

induction- lytic cycle (activity repressor) was keeping it off

front 52

step 6 of lysogeny

back 52

replication continues

front 53

step 7 of lysogeny

back 53

assembly of virus particles

front 54

step 8 of lysogeny

back 54

release of virus particles

front 55

what happens when replication begins in the lysogenic cycle

back 55

early protiens called λ repressor is made λ repressor blocks lytic cycle . when in effect w. coli , has two options- go productive ( lytic cycle ) or non-productive (lysogenic cycle) if enough repressor is made->lysogeny occurs

front 56

what determines is lysogeny or the lytic cycle occurs

back 56

if the cell is healthy or not

front 57

when does induction occur and what happens?

back 57

naturally occurs due to nutrient limitation and damaged DNA
in lab-> induction of lytic cycle w/ agents that damage DNA
as a result of DNA Damage bac. cell produces a protease. it cleaves (a different) repressor of a DNA repair system an it turns on
bact protease also cleaves λ repressor
lytic cycle is turned on

front 58

what are virulent or lytic viruses and what is an example?

back 58

only capable of entering productive response. ex. -> cold viruses (rino-virus)

front 59

what are temperate viruses?

back 59

capable of entering non-productive response

front 60

what is a lysogen

back 60

bacterial cell infected (dormantly) w/ φ; have medical significance

front 61

why is it hard to treat viruses? why cant you use antibiotics?

back 61

because of intamacy with its host cell. you cant use antibiotics because they target certain things.

front 62

what are used to treat viruses

back 62

antivirals

front 63

what is amantadine used for?

back 63

revents influenza A by blocking penetration and uncoating steps

front 64

what is adenine arabinoside and what is it used for?

back 64

nucleotide mimic. herpes virus

front 65

what is acyclovir used for?

back 65

to block herpes virus DNA polymerase since they have it and humans don't and used for shingles

front 66

what is Azidothymidine (AZT) and why does it work?

back 66

used for HIV . works because HIV is a retrovirus

front 67

what is a retrovirus? and what makes it occur

back 67

due to reverse transcriptase which AZT targets

front 68

what is interferon (cytosine)

back 68

chemicals produced by cells

front 69

where and when is interferion produced

back 69

produced by mammals . it is an immunoregulatory molecule
produced in response to double stranded RNA (some viruses have it), endotoxins (LPS) ,some viruses and other antigenic stimuli (something that can turn on a viral response)
function against viruses: cells virually infected prod. interferon whic triggers other cells to produce antiviral molecule * esp RNA viruses because they replicate in cytoplasm

front 70

why is interferon produced

back 70

in response to double stranded RNA which is found in some virues, endotoxins (LPS), some viruses and other antigenic stimuli

front 71

what is the relationship between interferon and viruses?

back 71

interferon functions against viruses . the cells virually infect produce interferon which triggers other cells to produce antiviral molecule *especially RNA viruses becaue they replicate in cytoplasm

front 72

Is interferon host specific? are they virus specific?

back 72

they are host specific but not virus specific

front 73

what does cancer mean

back 73

uncontrolled cell growth; cell cycle is no longer properly regulated

front 74

what is a tumor

back 74

a lump or mass of cells growing out of control

front 75

what is a benign tumor?

back 75

a noncancerous , non-spreading tumor

front 76

what is a malignant tumor

back 76

a cancerous tumor and cells are spreading (metastasis)

front 77

what are three cause of cancers?

back 77

-mutagenic agent
-carinogenic agents
-viruses

front 78

what is a mutagenic agent?

back 78

induce mutations above spontaneous mutations and lead to cancerous conditions

front 79

what is a carsinogenic agent?

back 79

potential to cause cancerous conditions

front 80

what type of viruses usually cause cancer?

back 80

DNA viruses and long term viruses

front 81

what is a transforming agent virus?

back 81

tell cells to divide and induce S phase and is very dangerous

front 82

how is papillomavirus (HPV) transmitted and what are they

back 82

sexually and they are benign warts which lead to cervial cancer

front 83

what is the herpes virus I?

back 83

fever blisters that lead to lip or mouth cancer

front 84

what is the herpes virus II?

back 84

genital herpes that lead to cervical and penile cancer

front 85

what is kinds of viruses do EBV lead to?

back 85

mono which leads to hodgkins disease and burkett's lymphoma

front 86

what is burkett's lymphoma and where is it found

back 86

which is usually found in tropical parts of the world . it is usually a tumor in the jaw but is very treatable

front 87

what is the human herpes virus and when does it usually infect

back 87

a feaver and a rash that is very prevalent and usually infects in childhood

front 88

what is kaposis sarcoma

back 88

cancer of vascular epithelial tissue

front 89

what is the risk of hepadna viruses

back 89

risk of liver cancer

front 90

what are RNA viruses

back 90

some retroviruses and HTLV i and HTLV II ( human tull lymphotropnic virus and some are associated with leukemia

front 91

what is a viroid

back 91

piece of circular RNA

front 92

what is the host of Viroids

back 92

plant patogen.

front 93

what is the smallest known infectious agent

back 93

plant cell nucleus

front 94

what is the mode of infection for viroids

back 94

it blocks mRNA splicing

front 95

what is the definition if a prion

back 95

pieces of proteins ( a proteinaceous infectious particles

front 96

what are the host for prions

back 96

mammals

front 97

what is the mode of infections for prions

back 97

(coded for by host) they are misfolded protien and presence of one can cause others to misfold (we think) and causes tangles and kills them (most are not mutants

front 98

what is a example of a disease that is caused by prions

back 98

krutz-jacob disease (KJD)