block D Flashcards

(30 cards)

1
Q

what was viruses initially discovered as? and by whom?

A

Adolf mayer and Dmitri ivanowsky in 1892 defined it as filterable agents that required living cells for propogation and had distinct characteristics from bacteria, coined ‘virus’ in 1898 by martinus beijerinck

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2
Q

what is the definition of a virus and the name of its feild of study

A

a genetic element that cannot replicate independently of a living host cell.

study of viruses is called ‘virology’

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3
Q

what is a virion, its purpose, and its makeup

A

a complete virus particle that exists outside host cell

facilitates transmission from one host cell to another

contains nucleic acid genome surrounded by protein coat (and sometimes an envelope)

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4
Q

what is tropism in releation to viruses

A

the ability of a specific virus to infect and replicate within particular cell types, tissues or host species

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5
Q

what are the culturing differences between bacteriophages, animal viruses, and plant viruses?

A

bacterial viruses are the easiest to grow and are model systems for virology

animal viruses can be cultivated in tissue, cell cultures, eggs or animal models

plant viruses are typically most difficult to study due to requiring growth of whole plant (some are as easy to culture as animal viruses but mostly its harder)

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6
Q

what are the 6 modern methods for studying and identifying viruses

A

-Electron microscopy (advanced imaging)

-molecular methods:
*PCR
*Genome sequncing/metagenomic sequncing
*comparative genomics

-antigenic and serological tests:
*antigen detection
*serological tests

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7
Q

why are viruses absent from the tree of life?

A

the tree of life is based on relatedness of ribosomal RNA (rRNA) sequnces, viruses lack ribosomes. they rely on a host cell for their life cycle and all metabolic intermedietes and protein synthesis

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8
Q

what are the structural components of a virus (and the virion outside a host cell)

A

a complete viral particle is known as a virion, able to protect the viral genome outside a host cell aswell as contributing to cell attachment.

-all virions have a nucleocapsid consisting of capsid, a protein shell around the viral genome made of CAPSOMERES and the genome, viral nucleic acids

-some virions contain virus specific enzymes with roles in viral infections and genome replication

-virions can be naked or enveloped with the evelope laye derived from host cell membrane, viral glycoprotiens embedded in envelope can act as receptor binding molecules for infection of host cells

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9
Q

what is the size range of mammalian viruses

A

~0.02-1 micrometer

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10
Q

what do the ‘giant’ viruses (1micrometer) infect

A

infect amoebae and other protozoans

has genome larger then some bacteria

ebola is a big fella being more worm lookin then virus looking

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11
Q

what are the physical properties of virions

A

highly symmetrical structures:
-helical symmetry = rod shaped viruses
-icosahedral symmetry = spherical viruses
-complex symmetry = mixed structure

helical symmetry has the virion length determined by nucleic acid length and its width determined by capsomere size and packing

icosahedral symmetry is a highly efficent packaging structure with capsomeres forming triangular faces, symmetrically arranged with 20 faces and 12 vertices

complex symmetry has components with both icosahedral and helical symmetry, with tailed bacteriophages being the most structurally complex virions (the classic D20 on a stick with legs virus)

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12
Q

what are VALs

A

virion associated lysins (VALs) occur in bacteriophages

depolymerases and lytic enzymes degrade bacterial cell structures such as polysaccharide capsids and the peptidoglycan layer

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13
Q

what are nucleic acid polymerases

A

occur in RNA viruses
polymerase is a structural component of virion
required for infection and replication in host cells

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14
Q

what are NAs?

A

Neuraminidases (NAs) occur in influenza viruses

NAs are enzymes that cleave glycosidic bonds targeting glycoprotiens and glycolipids (connective tissue)

required for liberation of new virion particles from host cells (breaks open cell to spread virions)

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15
Q

what are viral genomes made of

A

very varied, can be double stranded, single stranded.
can be DNA or RNA.

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16
Q

what is the baltimore classification of viruses

A

genomic classification devised by american viroligist david baltimore based on the relationship between the viral genome and its mRNA, splitting viruses into 7 classes:
-class 1 and 7: dsDNA + or -
-class 2: ssDNA + charge
-class 3: dsRNA + or -
-class 4: ssRNA+ charge
-class 5: ssRNA - charge
-class 6: ssRNA + retrovirus

single stranded genomes have polarity

17
Q

what is the disease based classification of viruses and the 5 types it speaks on

A

another form of classification based on route of harm. sometimes similar diseases can result from completely un-genetically-related viruses though

-respiratory viruses: often aquired by inhalation of droplets and replicated in repiratory tract e.g influenza

-enteric viruses: replicate in gut and cause gastric infections, aqured by ingestion of faecal-contaminated material e.g poliovirus

-arboviruses: infect insects that ingest vertebrate blood, replicate in tissue of insect and transmit to vertebrate host, eg flaviviruses

-hepatitis viruses: all viruses that cause liver disease eg hepadnaviruses

-sexually transmitted viruses eg herpes simplex (HSV), HIV

18
Q

what is viral tropism and its 3 subtypes?

A

the range of hosts, tissues or cells that a virus can infect and replicate within

-cellular tropism: the ability of a virus to replicate in a particular cell type

-tissue tropism: the ability of a virus to replicate within a particular tissue

-host tropism: ability of a virus to replicate in particular host species

19
Q

how is viral tropism determined

A

by a combination of host cell susceptibility and permissiveness

-succeptibility is the ability to express the correct receptors to enable viral entry

-permissiveness is the ability to support a complete viral multiplication cycle

similar viruses can have different tropisms tho, like HSV-1 and HSV-2 with ine spread by oral contact causing mouth sores and the other spread b sexual contact causing genital herpes

20
Q

what are the 6 major stages of replication for most viruses?

A

1- recogniton and attachment
2-penetration
3-uncoating
4-synthesis
5-assembly
6-release

21
Q

what are the key differences in replication cycles of viruses that infect eukaryotic cells vs those infecting prokaryotic cells

A

1-viral components entering cell: in prokaryotes only nucleic acid enters the host cell, in eukaryotes the entire virion enters host cell

2-site of replication: prokaryotes lack nuclei so all viral replication occurs in cytoplasm, in eukaryotes most viruses replicate in cell nucleus

3-site of assembly: in prokaryotes the cytoplasm is the site of assembly, while in eukaryotes some viroplasms (viral membrane bound factories) form to increase efficency of virion assembly

22
Q

what is the 1st step of viral replication in depth?

A

to initiate infection, virions must bind to specific host cell receptors, these receptors often have vital functions unrelated to viral infection, presence/absence of receptors determines tropism.

viral attatchment proteins include the capsid, proteins extending out the capsid, and glycoproteins

23
Q

what is steps 2 and 3 of viral replication in depth

A

once attached virion particle can be taken up into cell via 2 methods depending on if virus is enveloped or naked

-fusion with cytoplasmic membrane (eneloped virus, entire viral capsid may enter or just nucleic acid, eg HIV)
-endocytosis (enveloped and naked viruses)

viral nucleic acid then must be released into cell cytoplasm to be translated and replicated (uncoating) through 2 methods:
-via a pore in cell or endosomal membrane (only in viropexis used by viruses such as influenza A and poliovirus)
-via endosomal fusion of virion and endosomal membrane

24
Q

describe step 4 of viral replication in depth along with the 4 nucleic acid polymerases associated with genome replication

A

viral genome replication

viruses use host components for their reproduction, however many encode their own nucleic acid polymerases:

-DNA dependant RNA polymerase (DdRp) copies DNA making RNA, present in all organisms

-DNA dependent DNA polymerase (DdDp) copies DNA to make DNA, present in all organisms

-RNA dependent RNA polymerase (RdRp) copies RNA to make RNA, helps in RNA virus replication, olny present in viruses

-RNA dependent DNA polymerase (RdDp) copies RNA to make DNA serving as reverse transcriptase present only in viruses

translation of viral mRNA depends on host cell functions with eukaryotic ribosomes only recogising plus sense mRNA, menaing all viruses must translate their genome into plus sense mRNA for translation of viral proteins (purpose of RNA dependent RNA polymerase)

viruses prefer preferential translation of mRNA, many viruses are post-translationaly modified such as hepatitis C and ebola virus

25
what is preferential translation
the hijacking of host cell amchinery favoring viral mRNA over host mRNA while suppressing host protein synthesis (host shutoff)
26
what are the properties of replication on DNA viruses
the smaller the genome, the more dependent on host resources the virus is many DNA viruses promote cell growth transcription occurs in host cell nucleus except for poxviruses as regulated interactions between DNA binding proteins and regions of viral genome with regulatory regions similar to host cell's early genes are transcribed first; non-structural proteins, often with roles in genome replication like RdRp genome replication incited by early genes initiates transcription of late genes (mostly structural proteins) DNA-replication is semi conservitive (1 strand is original one is copied)
27
what are the properties of RNA virus replication
mostly similar to DNA viruses except: -genome replication is reliant on viral encoded RNA-dependent RNA polymerase. -double stranded replicative intermediate is ALWAYS formed, acting as a template molecule for synthesis of complementary strand -replication often occurs in host cell cytoplasm -RNA polymerases do not proof read as well as DNA polymerase making RNA viruses more prone to mutation
28
describe step 5 of virus replication in detail
viral assembly: viral capsid forms around nucleic acid, consisting of 2 steps; capsid assembly and packaging (the placing of viral genome inside capsid) most capsids self-assemble spontaneously helical viral capsids assemble around viral genome (often during replication) mediated by interaction between capsid proteins and nucleic acid icosahedral viral capsids either: -assemble around viral genome -assemble as empty pro-capsids using scaffolding proteins with subsequent genome packaging
29
describe step 6 (final step) of viral replication in detail
release: final step requiring newly assembled particles (virions) to be released from cell by 3 main methods: -cell lysis where cell is destroyed allowing virions out thorugh many holes -exocytosis where virions are packaged inside vesticles and released from cell via membrane fusion -budding (only in enveloped viruses) where free viral capsid in cytoplasm is enclosed in cell membrane lipid layer and buds off
30
what are common infection outcomes associated with animal viruses?
most animal virus infections end with cell lysis -some viruses can establish persistent or chronic infection such as hepatitis C virus -latent infections can occur where virus enters cell but does not replicate eg HSV and varicella-zoster virus (chickenpox) -a small number of viruses are known to be oncogenic and can transform normal cells to cancerous cells such as human papilloma virus (hpv) abortive infections are when viral replication is blocked during infection process resulting in no new virions or disease symptoms