Chapter 1 - V Flashcards

1
Q

Virus

A

chemical complexes of RNA or DNA protected by protein

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2
Q

What are viruses

A

Viruses are tiny non-living agents

all viruses have genetic information surrounded by a protein coat

some also contain external structure and an envelope pf phospholipids

They are obligate intracellular parasites - require host to reproduce

Each type of virus infects a specific unicellular species or type of cell in multicellular - need the right virus receptor

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3
Q

What are viruses

A

Viruses are not cells
They cannot synthesize their own ATP, aa, or nucleotides

They cannot synthesize protein on their own

  • they lack the ability to extract energy from molecules to build nucleic acids
  • they lack ribosomes
  • they have an extracellular state (inert) and intracellular state (replicating)
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4
Q

Viruses vs cells

A

cells are always dsDNA, virus can be DNA or RNA, ss or ds

viruses don’t have plasma membrane (maybe envelope)

Virus can’t carry out translation independently like normal cells. Requires ATP and nucleotide from the host cell

virus also can’t do translation without a host cell

Viruses don’t have metabolic capabilities. Cells have extensive ATP synthesis, oxidation of reduced C. aa and nucleotide biosynthesis

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5
Q

What percentage of your genomes has its origins in virus sequence?

A

50%

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6
Q

Central dogma of molecular biology

A

Usually cells DNA –> RNA –> protein

however viruses can mix these steps up eg.

RNA - DNA - RNA - Protein

RNA - RNA - protein

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7
Q

Diversity of viruses

A

Even though viruses are very simple, they are still very diverse group

structure can be:

  • Naked - non enveloped
  • enveloped
  • complex capsid

Viral genetic material can be ssDNA/RNA, dsDNA/RNA
- their genes can be wither circular or linear

  • Circular dsRNA does not exist
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8
Q

Diversity of viruses

A

Viruses vary in type of host cell that they can infect

  • species specific
  • cell/tissue specific

They can infect more than one species/cell type
- just need the right cell receptors on the host

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9
Q

Diversity of viruses: Example

A

Infects only Humans

  • poliovirus
  • HIV
  • Smallpox

Infects humans and other animals

  • Influenza
  • Rabies
  • Covid
  • Ebola
  • Measles
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10
Q

Replicating strategies: lytic and lysogenic cycle

A
  • Where genomes are replicated in the infected cell

Replication cycle: lytic, persistent, latent)

one or more rounds of mRNA expression

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11
Q

Virus structure

A
  • virus fall into 2 categories: naked or enveloped

In naked virus, the genome is enclosed by only a capsid-protein shell

The capsid is made of multiple copies of protein subunits called capsomeres
- it could be made from one type of protein or several different proteins

Nucleic capsid - when nucleic acid binds to capsid

A capsomere might bind tightly to a structure on a host or they maybe attachment proteins that protect the outside of the capsid (eg spike proteins)

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12
Q

Enveloped Viruses

A

have lipid bilayer surrounding their capsid
- lipid bilayer can be derived from the host cell plasma membrane or any other membrane (eg Golgi, ER)

Some enveloped viruses have a matrix later protein just below the enveloped
- eg gp41/120 Hemogluttinate etc

Enveloped glycoproteins are acquired for attachment to host cell

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13
Q

Why do some viruses have envelopes and some don’t

A

Relates to virus replication cycle

Enveloped: virus buds out through the membrane and acquires envelope without killing the host cell immediately

  • Virus replication occurs for long periods of time
  • when it leaves the host cell contents are not released into the bloodstream (cuz enveloped)

Naked: cell lyses, all progeny is released at once - cell is dead
- as leave cell, all contents are released to the extracellular environment

Sometimes viruses have complex structure - possess a capsid that is not helical but icosahedral and may have other structures like protein tail or complex outer wall

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14
Q

What is more stable, naked or enveloped

A

Naked virus is more stable in environment

The envelope may dry out and tear from result of virus structure
- since the attachment protein the virus uses to bind to host cell are in the enveloped - if the envelope is lost, it virus becomes non infectious

cleaning agents like detergent can disrupt envelope - naked viruses are notoriously stable. Poliovirus can persist in chlorinated swimming pool water

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15
Q

Why do we study viruses

A

They cause disease n humans, wild animals, crops

if understand virus, we can develop a protocol to limit the spread

Enzyme RT and RNases enable pharmaceutical companies to manufacture human products in bacteria or yeast cell

Can also impact society:

  • loss of productivity - economics
  • allocation of resources - medical facilities, research monies
  • closure of public venues, hospitals, schools, airports
  • Chaine in social behaviouirs
  • Change in policy and education
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16
Q

We can use viruses for

A

Antimicrobial therapy
- bacteriophages to treat patient with bacterial infections and used as antiseptics and disinfectant

Gene therapy - use viruses as a delivery system to deliver a wild type copy of gene to cell type that is carrying a mutated copt of the gene

Treatment of cancer

  • viruses genetically modified t be used as anti-cancer agents
  • these viruses can replicate in cancer cells but not healthy cells
17
Q

where do viruses that infect hymans come from

A

Unclear where they come from but:

All new viruses strain evolve from poxivirus that infected rodents
- H1N1 came from bird and swine flu viruses

Virus jumping
- different viruses use different ways to jump species

Eg

  • fecal-oral route
  • inhalation
  • get cut and enter through wound
  • consumption eg meat
18
Q

Virus Evolution

A

2 evolutional pathways

Co-evolution with host:

  • infect one species only
  • Advantage for virus: prosperous host = prosperus virus
  • disadvantage for the virus if host becomes extinct
  • one example is ebola virus

Infection of multiple host species:

  • advantage if one host is compromised, the virus can replicate into another
  • disadvantage - cannot optimize for any one situation
  • eg rabies, influenza
19
Q

Fitness in co-evolution

A

If mutation is not good for virus, it might lose its ability to infect cell which is needed to replicate more virus

  • if mutation is neutral, no obvious effect on virus
  • Beneficial virus - more virulent, ability to infect new host or infect host more efficiently

However, highly virulent viruses kills its host too soon
- if it is too slow, host immune system will kill it

therefore virus and host tend to co-evolve towards a symbiotic relationship

20
Q

Example of virus co-evolution

A
  • Rabbit were introduced into Austratlia and there reproduce real fast damaging crops and vegetation
  • myxoma virus was deliberately introduced to control rabbit population - spread through mosquito binds
  • worked a few months but virus mutated
  • rabbits resistant and virus deceased in virulence
21
Q

SARS- CoC- 2

A

Coronavirus are an enveloped virus with a helical capsid and a single stranded RNA genome