11 Viruses Flashcards

(8 cards)

1
Q

Viruses

Definition

A

Obligate intracellular parasites

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2
Q

Viruses

Reasons behind definition

A
  • Can only survive in a living host cell
  • Need to hijack host cell machinery to carry out metabolic processes eg. respiration
    • Do not have raw materials eg. nucleic acids for DNA/ RNA replication; amino acids, ribosomes for protein synthesis & ATP

ie. Metabolically inert virions in extracellular conditions; metabolically active & can reproduce in intracellular conditions

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3
Q

Viruses

Types

A
  • Bacteriophages (typically contains DNA genome)
    • Virulent, lytic: T4
    • Temperate, lysogenic: Lambda
  • Animal (typically contains RNA genome)
    • Enveloped: Influenza
    • Retrovirus: HIV
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4
Q

Viruses

General Structure + Purpose

A
  • Genome: codes for both structural & regulatory proteins [ALL]
    • DNA or RNA
    • ss- or ds-
    • linear or circular
  • Capsid = protein coat of capsomeres: protects Genome [ALL]
    • Helical or icosahedral etc.
  • Envelope = phospholipid bilayer: helps with Attachment & Adsorption during infection of host cell
    • contains Glycoproteins
    • made of host cell cell surface membrane
  • Enzymes: aid entry & exit of host cell/ replication & transcription of viral genome
    • Lysozymes: breakdown of bacterial peptidoglycan cell wall
    • Neuraminadase: aids release of viral progeny
    • RNA-dependent RNA polymerases (eg. viral replicase within Influenza)
    • RNA-dependent DNA polymerases (eg. reverse transcriptase within HIV)
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5
Q

Viruses

General Mechanism

A
  1. Adsorption/ Attachment
    → Recognision & binding of viral glycoproteins to host cell receptors on the cell surface based on complementary 3D conformation
  2. Penetration/ Entry
    → Engulfing of virus (genome) into a vesicle
    → Release of viral genome
  3. Replication & Synthesis
    → Take over of host cell machinery & raw materials for replication & transcription of viral genome, viral protein synthesis
    → Synthesis of capsomeres, glycoproteins, enzymes etc. occur
  4. Assembly
    → Formation of viral nucleocapsides from viral nucleic acids & capsomeres
    → Embedment of glycoprotines into host cell membranes
  5. Release
    → Lysis of host cell in case of phages → death of host cell
    → Budding off from host cell cell surface membrance in case of animal viruses → With ↑ budding, lysis can occur
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6
Q

Bacteriophages

T4 Phage → Stucture

A
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7
Q

Variation within Viruses

Antigenic Drift + Cause

A

1. Lack of proof-reading mechanism in polymerases eg. replicase/ RNA dependent RNA polymerase & reverse transcriptase
2. Single-stranded RNA genome → Lack of backup complementary strand which serves as template for repair

3. ↑ error rates during viral genome replication → spontanous mutations in genomes
4. Δ in genome → Δ in mRNA → Δ in amino acid sequence → Δ in 3D conformation of glycoprotein → Δ in surface antigens
5. Accumulation of mutations within genes coding for surface glycoproteins
6. Surface glycoproteins ie. antigens have a different conformation from previous strains
7. New strain cannot be recognised by antibodies produced during previous infection
8. ↑ ease of infection & spread throughout partially immune population

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8
Q

Variation within Viruses

Antigenic Shift + Cause

Typically applied to Influenza

A

1. Segmented genome of virus enables for major genetic changes of type through reassortment of genome
2. ≥ 2 different strands of a virus/ strains of different viruses infect the same cell simultaneously
3. Viral protein capsids & lipid envelopes removed
4. Genome is exposed & is transcribed into mRNA
5. Host cell packages the 2 different strains such that antigens undergo recombination

6. New combination of viral glycoproteins with different specific 3D conformation
7. Immune system cannot recognise new recombinant strand of virus & do not have antibody protection
8. Further evolution of virus can cause ↑ spread of virus within host cells or virus to jump to a different house

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