Viruses Flashcards

(22 cards)

1
Q

define viruses and explain what it means

A

Viruses are obligated intracellular parasites.
.
Meaning:
- By necessity, they can only survive in a living host cell.
- They rely on hijacking host cell machinery to carry out metabolic processes.
.
Why do they need to hijack host cell?
- They require materials like nucleic acids, amino acids, ribosomes, ATP to help them reproduce.
- They are metabolically inert virions in extracellular condiotions.
- they are metabolically active and replicate in intracellular conditions.

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2
Q

Diff types of viruses

A
  1. Bacteriophage
    - Only infect bacteria cells.
    - Includes temperate phages like the lambda phage
    .
  2. Animal virus
    - Infects animal cells only
    EG: influenza, HIV
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3
Q

Can you see viruses under a light or electron microscope?

A

Electron microscope

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4
Q

Struc of viruses and phages

A

Phages:
- Head: viral genome + capsid (icosahedral shaped protein coat) = nucleocapsid
- Phages have linear ds DNA, not RNA
- tail
- tail fibres
.
Influenza:
- Viral membrane
- capsid (protein coat), within the viral membrane
- RNA
- Viral proteins

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5
Q

Roles of viral genome in survival

A
  • Viral genome can be single-stranded/ ds, linear/circular, DNA/ RNA, segmented/ unsegmented
    .
  • Encode both structural and regulatory proteins that aid in survival and replication of virus.
  • Structural protein form viral components like the capsid proteins.
  • Regulatory proteins control gene expression and protein synthesis.
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6
Q

Struc of capsid (present in all viruses)

A

A capsid is:
- a protein coat surrounding the viral genome
- Protein subunits used to form the capsid are called capsomere
- Capsids are usually helical (bananas) or icosahedral (diamond) shaped

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7
Q

Role of envelope in virus survival
(only in envelope viruses, which usually only infect animal cells)

A
  • Envelope is made of phospholipids from the CSM of the host cell,
    .
  • Virus buds off from host cell, taking the phospholipid bilayer with them.
    .
  • Envelope surface contains viral glycoproteins that aid in attachment and adsorption of virus when infecting the next host cell.
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8
Q

State diff enzymes and their roles in viruses

A
  • Viruses contains enzymes that aid in entry and exit to the host cell, and polymerases that aid in gene expression & transcription.
    .
    EGS:
  • Lysozyme is an enzyme in bacteriophages that break down the peptidoglycan bacteria cell wall, resulting in lysis of the host cell.
    .
  • Neuraminidase is an enzyme on the envelope of influenza (animal virus) that aids with its release from the host cell.
    .
  • RNA-dependent RNA polymerase (RNA template, synthesises RNA) like viral replicase influenza.
  • It uses -ve sense RNA as a template to synthesise +ve sense RNA.
  • the +ve sense RNA is used as a template to replicate viral RNA or acts as mRNA to synthesise viral proteins using host cell machinery.
    .
  • RNA dependent DNA polymerase (RNA template, synthesises DNA) like reverse transcriptase in HIV
  • reverse transcribes viral RNA into a complementary ss DNA strand via CBP.
  • the DNA strand is then used as a template to synthesise a complementary DNA strand via CBP.
    .
  • Integrase
  • Catalyses the integration of viral DNA into host chromosome to form a provirus
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9
Q

Different between lysosome and lysozyme

A
  1. Lysosome
    - an organelle that contains hydrolytic enzymes
    - fuses with vesicle to digest food particles taken in via endocytosis
    - Autophagy (digestion of worn out organelles.
    - Autolysis (diff from apoptosis bcuz its uncontrolled and leads to tissue inflammation)
    .
  2. Lysozyme
    - an enzyme found in bacteriophages which breaks down the peptidoglycan bacterial cell wall, resulting in lysis of the host cell.
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10
Q

Reproductive cycle of virus summary

A

APUSAR
.
1. Attachment/ adsorption
2. Penetration and Uncoating
3. Synthesis / Replication
4. Assembly
5. release

APU – How viruses enter
SAR – How viruses reproduce

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11
Q

Describe the Reproductive cycle of a virus

A
  1. Attachment
    - Viral glycoproteins are comp in shape to receptors of the host cell
    - Virus recognises and binds to the host cell receptors to attach to the cell surface of the host cell.
    .
  2. Penetration & Uncoating
    - virus is engulfed into a vesicle
    - Uncoating of capsid to release viral genome into host cell cytoplasm.
    .
  3. Synthesis
    - Virus takes over host cell machinery & raw materials carry out replication and transcription of viral genome, and then viral protein synthesis using host ribosomes.
    - Proteins like capsomere, glycoprotein and enzymes will be synthesised.
    .
  4. Assembly
    - Nucleocapsids are assembled from viral nucleic acids and capsomeres
    - Glycoproteins are embedded into host cell membranes (FOR ENVELOPED VIRUSES ONLY).
    .
  5. Release
    - New viruses lyse the host cell or bud off the membrane to free themselves.
    - New released virions can now infect next host cell.
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12
Q

How do viruses challenge cell theory?

A
  1. Cells are the basic unit of life
    - Viruses lack cell machinery that living cells have.
    - Viruses cannot carry out metabolic processes on their own without a living host cell
    .
  2. All cells arises from pre-existing cells
    - Virions, when in an extracellular environment, are not able to replicate without a host cell.
    .
  3. All living organisms are made of 1 or more cells
    - Viruses are acellular, they do not have protoplasm and organelles.
    - so they cannot carry out metabolic processes w/o host cell
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13
Q

3 Principles of cell theory

A
  1. Cells are the basic unit of life
  2. All cells arises from pre-existing cells
  3. All living organisms are made of 1 or more cells
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14
Q

How do viruses support cell theory?

A
  1. Cells are the basic unit of life
    - have impt genetic info
    - Have the potential to evolve over time & adapt to environment.
    .
  2. All cells arises from pre-existing cells
    - All new viruses come from original viruses.
    - Viruses can replicate when they enter a host cell.
    .
  3. All living organisms are made of 1 or more cells
    - nil
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15
Q

If viruses both support and challenge cell theory, then what are they?

A

Viruses are bets described as infectious particles that are active in intracellularly and inactive in extracellularly

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16
Q

3 Reasons viruses are living things

A
  1. They can regulate metabolic processes
    - such as genome replication, gene expression and protein synthesis.
    .
  2. They can reproduce and synthesise new virions
    .
  3. _they have great genetic diversity _
    - they can rapidly alter their genome as they evolve to better survive in the host cell.
17
Q

2 Reasons viruses are NOT living things

A
  1. They cannot carry out metabolic processes on their own
    .
    They cannot:
    - synthesise proteins
    - grow
    - response to stimuli
    - evolve
    On their own
    ____________________________________
  2. They are accellular
    they lack:
    - a phospholipid membrane
    - membrane organelles
18
Q

What reproductive cycles can temperate phages undergo?

A
  1. lysogenic cycle
    then
  2. lytic cycle
19
Q

Lambda phage reproductive cycle

A
  1. Attachment
    - Tail fibre recognises and binds to receptors on the cell surface of a bacteria cell that has a complemetary 3D conformation.
    .
  2. Penetration
    - Lysozyme from phage hydrolyses bacteria peptidoglycan cell wall.
    - Phage DNA is injected through tail tube and into the cell
    .
  3. Prophage formation (lysogenic)
    - Phage DNA circularises and is integrated at the Prophage insertion site (PIS)
    - Prophage is formed and remains latent
    - Host cell undergoes binary fission
    - subsequent generations of bacteria will have the prophage
    .
  4. Prophage induction
    - occurs upon env trigger (UV, heat, DNA damage)
    - induces the phage to switch to lyric cycle.
    - Lytic genes of phage are now switched on
    - Phage genome will be excised from the host chromosome to stat viral replication and synthesis
    .
  5. Rep and synthesis (lytic)
    - phage hijacks host cell machinery to synthesise phage nuclei acids and proteins
    - Host bacterial chromosome is degraded
    - host DNA polymerases and free deoxyribonucleotides used to replicate phage DNA
    - host RNA polymerases transcribe template phage DNA into mRNA.
    - Host ribosomes, tRNAs and translation factors are used to translate the phage mRNA
    - _Viral proteins and enzymes needed for replication and inhibition of host cell gene expression_ are synthesised.
    .
  6. New phages are assembled
    .
  7. Release
    - Lysozyme hydrolyses the bacteria cell wall
    - cell lyses to release new lambda phages
    -
20
Q

Influenza reproductive cycle (no lysogenic cycle)

21
Q

HIV reproductive cycle

A
  1. Adsorption
    - gp 120 glycoproteins on HIV recognise and bind to CD4 receptors, w a specific 3D conformation that is complementary in shape, on the CSM of T-helper cells.
    - This causes a conformations change in HIV, to expose the gp 41 glycoprotein
    .
  2. Penetration
    - gp 41 bring HIV closer to tbe host cell
    - gp 120 binds to the co-receptor, facilitating fusion of viral envelope with host CSM.
    - Nucleocapsid is released into host cell
    .
  3. Provirus formation
    - Viral SS RNA is reverse transcribed by reverse transcriptase into complementary ss DNA via CBP
    - Viral DNA is used as template by host polymerases to synthesis complementary DNA strand via semi-conservative DNA rep
    - Double stranded viral DNA formed
    - Viral DNA is integrated into host chromosome by integrase
    - Provirus is formed
    - HIV remains in latent phase
    .
  4. Replication and synthesis
    - When host cell is involved in an immune response, it activates the virus,
    - latent phase ends.
    - (Viral genome replication and protein synthesis occurs)
    - Viral DNA is transcribed by host RNA polymerases into RNA
    - Synthesised RNA can act as new viral genome
    - or mRNA to be translated by host ribosomes for synthesis of viral proteins
    .
  5. Assembly
    - viral components like enzymes, capsid, RNA genome etc⁉️⁉️
    - assembled near host cell membrane.
    - gp 120 and 41 glycoproteins embedded into host CSM
    .
  6. Release
    - New HIV virus budsoff from host cell, taking a part of the host’s studded membrane to form its new viral envelope
22
Q

Genome of lambda phage, influenza and HIV viruses