Mechanisms of Viral Infection Flashcards

1
Q

How can some bacteria evade complement?

A

Bacteria can resist complement:
LPS and capsules = failure to trigger complement as complement cannot bind
Negative binding: coat self with IgA that doesn’t fix complement, factor H sequestration + blockage of C3b binding
Block/expel MAC: capsule prevent C3b receptor access, C5a proteases prevent it forming

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2
Q

How do staphs and meningoccoccus evade the immune system?

A

Staphs produce leukocidins which prevent opsonisation and thus efficient phagocytosis
Also produce protein A (binds Fc portion of IgG, preventing opsonisation)

Meningococcus and Hib block contact w immune cells using capsules

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3
Q

Give other examples of ways in which intracellular pathogens which evade the immune system
mTB, listeria and salmonella, Shigella

A

Intracellular pathogens e.g. mTB, listeria and salmonella can survive inside macrophages: Promote own safe uptake- mediated by CR3 and mannose lectin receptors
Shigella injects molecules which preps cell for invasion
Listeria escapes phagosome-lysosome to cytoplasm
Resist oxidative killing by producing catalases/ peroxidases
Controls Ag presentation: Stops CTLs and cell activation

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4
Q

How can certain microbes mess with Ab binding?

A

Production of Fc receptors by microbes = antibodies bind the wrong way = not opsonised properly
Staphs, Streps, HSV, VZV, CMV

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5
Q

How can certain microbes cause antigen concealment?

A

Concealment of antigen by:
1. hiding inside cells and not get recognised
2. Infecting privileged sites where hay little migration of leukocytes, eg eyes
3. Block MHC presentation, by messing w TAP eg Herpes
4. Surface uptake of host molecules: eg CMV takes up host b2microglobulin and incorporates it into their own cell surface to avoid detection

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6
Q

Give the 3 other ways in which microbes can evade the adaptive!!! immune system

A

Immunosuppression
e.g. by decreasing MHC, receptors, apoptosis, cytokine switch, IgA proteases

Antigenic variation- mutations can avoid immunity in the community

Persistence/latency/reactivation

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7
Q

Describe the pathogenic mechanisms of Strep Pneumo

What does it cause, how is it transmitted, what does it release?

A

Gram + causes pneumonia, otitis media and meningitis
Transmitted via aerosol, enters nasopharynx and colonises
Release adhesins to bind surface molecules
Release sIgA proteases to break down IgA

Endothelial cell damage–> pneumonia, bacteria can access blood = bacteraemia-> Septicaemia and meningitis

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8
Q

How does strep pnemonia evade lung defences?

A

Inhaled in lungs and evades lung defences by:
-sIgA proteases
-Capsules which prevent phagocytosis
-Pneumolysin (toxin causes lysis of epithelial surfaces)
-Teichoic acids= bad inflammation

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9
Q

What are 4 ways in which VIRUSES can evade the immune system?

A
  • Latency: VZV, herpes simplex
  • Decreases MHC expression: Cytomegalovirus (CMV)
  • Decrease Ag presentation/cause concealment by binding to TAP Eg= herpes simplex
  • Mutation of epitopes: HIV can mutate its epitopes to escape neutralizing Abs or to avoid recognition by CD8+ T cells
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10
Q

Describe Persistence as an immune evasion strategy using VZV

A
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11
Q

What is antigenic diversity? Give an example

A

Antigenic Diversity/ polymorphisms: genetically stable and alternative forms of Ags in a population of microbes
e.g. serotypes of Strep.pneumoniae

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12
Q

What is antigenic variation?

A

Antigenic Variation: Pathogens can change their surface Ags to evade the host’s immune system. They can switch between different Ag forms w/in a specific clone or its progeny.

Phase Variation: Microbes can reversibly switch Ag expression at a low frequency. This ON/OFF Ag system allows them to evade the immune response during infection or spread through a community.

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13
Q

What are the symptoms of gonorrhoea?
Describe how Neisseria Gonorrhoea has antigenic variation

A

Gram neg coccus causes inflammatory, myogenic infection
Symptoms: dysuria, redness, pain on urination, destruction mucosa
Neisseria Gonorrhoea has v variable structures + can undergo phase and antigenic variation.
This confuses/avoids immune responses.

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