Lecture 7: Viruses Flashcards

1
Q

characteristics of viruses and bacteria

A

Viruses
◦ Very small: 20 to 300 nanometres
◦ Visible only under electron microscopy
◦ DNA or RNA genome
◦ No cell wall
◦ Lack the normal cellular machinery of living
cells (for example no ribosomes)
◦ Obligate intracellular parasites
◦ Utilise the host’s cellular machinery to
reproduce

Bacteria
◦ Larger: 1000 to 2000 nanometres
◦ Visible under regular light microscopy
◦ DNA genome
◦ Cell wall
◦ Possess the normal cellular machinery of living
cells
◦ Can survive outside a host
◦ Able to replicate independently of the human
host

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2
Q

3 parts of virus

A
  1. Genetic material (DNA or RNA)
  2. protein coat that protects these genes
  3. sometimes, am envelope of lipids that surrounds the protein coat when they are outside of the cell
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3
Q

Describe the genetic material part:
what does it have, purpose

A

Nucleic acid core: At the core of viruses is the genetic material that encodes the transcription of all viral components, mostly proteins (such as enzymes. This is genetic material is either DNA or RNA, never both. It can be single or double stranded

The genetic material is the software program for making copies of the virus

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4
Q

Describe the protein coat part:
what does it have, purpose

A

Surrounding the core is a protective coating made of protein, the capsid. The capsid is rigid and determines the shape of the virus. It is made from repeating protein units called capsomeres

The capsid and its nucleic acid core together form the nucleocapsid

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5
Q

Describe the envelope part:
what does it have, purpose

A

Envelope:
Usually spherical because their envelopes unlike capsids are loose fitting

Envelopes are lipid bilayers that contain phospholipids, cholesterol, proteins. Some of these proteins incoperate carbs and thus are glycoproteins which usually proturde out of envelope as spikes. They attach to host cell surface receptors to allow entry

No envelope are naked viruses

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6
Q

CLASSIFICATION

A

based on
1. type of nucleic acid present
2.single or double stranded
3. presence or absence of envelope

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7
Q

what is the + and - sense strand

A

+ = sense strand = translatable code from 5’ to 3’ direction

  • antisense = translatable in 3’ to 5’
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8
Q

Virus structure: example of the 3 types and example of them

A
  1. Cubic
    Adenovirus (isohedral, 20 sided, protein shell with nucleic acid contained within
  2. Helical
    TM (elongated nucleocapsid rod shaped, capsomeres arranged around a spiral of nucleic acid

3.Complex - Poxvirus

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9
Q

Viral reproduction
why cant they reproduce themselves

A

Unable to reproduce themselves, as they lack the normal
cellular machinery of living cells (for example no ribosomes)

They must infect us and use our cellular machinery to
reproduce

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10
Q

steps of replication

A
  1. Union phase
  2. Penetration phase
    3.transcription phase
    4.Synthesis phase
    5.assembly phase
    6.release phase
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11
Q

Transmission routes types and example

A

Droplets (aerosols); influenza,
corona and rhinoviruses

Faecal oral; norovirus

Animal vectors; dog bites for
Rhabdoviridae (rabies
virus)

Insect vectors;
arboviruses

Bodily fluids;
semen (HIV)
blood (HBV)
saliva (EBV)
breast milk (HCV)

Vertical; mother to child
in utero (HIV)

Fomites (physical
objects)
coronaviruses

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12
Q

what is Viral tropism

A

The ability of a virus to infect a target cell of the host, using a specific receptor to gain entry to the cell

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13
Q

The DISEASE, TARGET, RECEPTOR for…
Epstein Barr (EBV), HIV, influenza, Rhinovirus, Covid

A

Epstein Barr (EBV)
Disease: Infectious mononucleosis Burkett’s lymphoma
Target: B cells
Receptor: Complement C2

Human immunodeficiency (HIV)
Disease: Acquired Immune Deficiency syndrome (AIDS)
Target: T cells and monocytes
Receptor: Cluster of differentiation (CD): CD4

Influenza
Disease: Influenza (flu)
Target: Respiratory epithelium
Receptor: Sialic acid residues

Rhinovirus
Disease: Common cold
Target: Nasal epithelium
Receptor: ICAM

Covid
Disease: Covid-19
Target: Lung epithelium
Receptor: Angiotensin converting enzyme 2
(ACE2)

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14
Q

Immune Response:
Viral versus bacterial infection

A

Viruses
◦ Intracellular infection
◦ Phagocytes cannot “see” the pathogen
inside the host cell
◦ Phagocytosis cannot be used to
eliminate viruses
◦ But virally infected cells can display viral
protein on their cell surface, using MHC
◦ So T cells can “see” them

Bacteria
◦ Most species = extracellular infection
◦ Phagocytes recognize the bacterial
PAMPS using their PRR
◦ Phagocytosis is an effective mechanism
to kill the bacteria

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15
Q

how do Virally infected cells display viral peptides

A

via MHC to cytotoxic T cell TCR

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16
Q

Cell mediated immune response
Virus vs bacteria

A

Viruses
◦ Cell mediated
◦ Natural killer cells bind to infected cells
and degranulate to kill the infected cell
◦ Cytotoxic T cells release chemicals onto
cells infected by virus

Bacteria
◦ Cell mediated
◦ Phagocytosis; macrophages and other
phagocytic cells engulf cells with
bacteria and opsonins on their surface

17
Q

Humoral (antibody mediated) response virus vs bacteria

A

◦ Viruses
◦ Antibody mediated
◦ Neutralisation of virus whilst in circulation.
However, viruses are only in the
circulation as they move from one cell
to another, so antibody neutralisation is
not as effective as with bacteria.
◦ But antibodies can bind to virally
infected cells displaying viral protein on
their cell surface. NK cells can then bind
to the antibody via their Fc receptor.
Antibody dependent cell mediated
cytotoxicity (ADCC) is effective

◦ Bacteria
◦ Antibody mediated
◦ Antibody neutralisation of bacteria whilst
in circulation is an effective immune
response

18
Q

2 Viral detection in labs

A

◦ Antibody detection for evidence of either
infection with (for example HIV, HCV), or
immunity to viruses (for example HBV)

◦ PCR analysis of genes unique to particular
viruses for diagnosis of cu