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when was the tobacco mosiac disease transfer from plant-to-plant (virus discovery)
1886
when was it known that the causative agent of tobacco mosaic disease could pass through the pores of a filter (virus discovery)
1892
when was the tobacco mosaic virus purified, enabling the study of its structure using electron microscopy (virus discovery)
1935
why were viruses initially distinguished from other infectious agents because theyre….
small and obligate intracellular (needs a host cell) microbes
how do we now distinguish viruses from cellular lifeforms based on their structure
single type of nucleic acid (DNA or RNA)
protein coat
multiply within host cells using host machinery
responsible for synthesis of structures that transfer viral nucleic acid to other cells
what is host range/ tropism
the spectrum of host cells a virus can infect
all organisms are susceptible
some viruses infect different species than other viruses
only infect certain tissues/ cells
what is the host range primarily determined by
the ability of the virus to attach to the host cell and reproduce
what does attachment involve for the host range
viral proteins and a receptor on the host cell
how does viral size vary
most are way smaller than or the same size as bacteria
giant viruses are..
susceptible to smaller viruses (virophages)
what is a virion
complete, fully developed, infectious viral particle, found outside a host cell- made of nucleic acid surrounded by a protein coat
what are differences of virus genome’s
DNA or RNA
singe-stranded or double-stranded
circular or linear
segmented or non-segmented
what is a capsid
protein coat that surrounds a virus’s genome- present in all viruses
what is an evelope
lipid layer that covers the capsid - not in all
what are characteristics of an evelope
formed from plasma membrane when virus exits host cell
spike proteins on outside
what are the viral structures
helical
polyhedral
complex
helical structure
nucleic acid within a hollow, cylindral capsid
polyhedral structure
many-sided, often icosahedral (20 triangular faces)
complex structure
lacks symmetry (ex: bacteriophage)
what is a bacteriophage
virus that infects bacteria
forms plaques
what are plaques
zones of bacterial cell lysis
infects the cell to replicate and lyses the cell to further infect other cells
culturing animal viruses
sometimes only able to in living animals
what are other ways viruses can be grown
embryonated eggs and cell cultures
cell culture for viruses
plant/ animal cell grown in media in the lab and cell lines
primary cell lines
derived from tissue, survive only a few gens
continuous cell lines
derived from cancerous cells (immortal)
ex: HeLa cells
why have bacteriophages been studied
its a model of virus replication
some phage undergo what kind of life cycle
lytic, which converts bacterial cell to make more phages (lysis)
what the lytic life cycle
attachment
penetration
biosynthesis
maturation
release
lytic- what is the attachment stage (first)
phage attaches by the tail fibers to a receptor of the bacterial cell
lytic- what is the penetration stage (second)
dna is injected into the bacterial cell
lytic- what is the biosynthesis stage (third)
production of phage dna and proteins
lytic- what is the maturation stage (fourth)
assembly of phage particles
lytic- what is the release stage (fifth)
phage lyse the bacterial cell and release into the environment
what is the lysogenic life cycle
phage genome integrates into bacterial genome to prophage and is passed down as the bacterial cell vertically divides
how do some phages choose between lytic and lysogenic cycles
temperate phage- depends on the signal based on the bacteria
animal- what is the attachment (1) stage
virus binds to receptor on host cell
animal- what is the entry (2) stage
virus enters into host cell through injection, receptor-mediated endocytosis, fusion (enveloped virus)
animal- what is the uncoating stage (3)
loss of capsid, releases nucleic acid into host cell
animal- what is the biosynthesis stage (4)
production of nucleic acid and proteins- depends on baltimore classification
animal- what is the maturation stage (5)
nucleic acid and capsid proteins assemble
animal- what is the release stage (6)
leaves the host cell by rupture or budding (enveloped virsuses)
what is budding in release of animal viruses
pushes against the membrane- membrane breaks and makes the envelope
how do dna genome viruses replicate
dna polymerase
how do rna genome viruses replicate
rna-dependent rna polymerase
what does the structure of the viral genome impact the performance of …
transcription
the manner by which viruses synthesize mRNA is the basis of the baltimore classification system…
dna vs rna genome
ds vs ss genome
(+) vs (-) sense genome
what are some rna viruses considered
retroviruses
what is the meaning of a retrovirus
rna genome but they convert their genome into a dna version to integrate into the host cell genome
what enzyme does the retrovirus use
rna-dependent dna polymerase
what does rna-dependent dna polymerase do
reads rna and synthesizes dna
what is meant by latent virus
virus can lay dormant in a host for an extended period of time- doesnt cause symptoms
what are examples of latent viruses
herpes simplexvirus (cold sores)
varicella virus (chicken pox, shingles)
what is meant by chronic/ persistent infections
gradually increases over time (HIV)
what are prions
misfolded proteins that induce misfolding of host proteins
characteristics of prions
doesnt contain dna/ rna
initiates a chain reaction
affects brain/ neurological function
when was prion first discovered
1982 from disease in sheep called scrapie
how does amplification of prions occur
conversion- convert an existing protein into the prion form
where are PrPC located
membrane of cells in the brain
what are normal host protein PrpC
C for cellular and primarily alpha helices
what is the prion form PrpSc
Sc for scrapie and formation of beta pleated sheets
what happens when PrpC comes into contact with PrpSc
PrpC is converted into PrpSc (chain rxn)
what do PrpSc proteins form when aggregated
amyloids
what happens when amyloids accumulate in infected tissue
causes damage and cell death
how can prions be sporadic
spontaneous conversion of PrpC to PrpSC
how can prions be acquired
ingestion of prions from infected animals
why are prion diagnosis challenging
long incubation period before symptoms show and need analysis of brain tissue
why are there no treatments available
prion structure is too simple
cant target naturally existing proteins
not easily degraded
how do you prevent prion
ban animal-product feeds
control imported animal products from foreign countries
careful removal of nervous system tissue by slaughterhouses
how do you decontaminate prions
incineration