Immune evasion Flashcards

1
Q

What are the two groups of diseases caused by staphylococcus aureus?

A
  1. localized pyogenic or “pus-producing” diseases that are characterized by tissue destruction mediated by hydrolytic enzymes and cytotoxins
  2. diseases mediated by toxins that function as superantigens producing systemic diseases.
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2
Q

Give 5 properties of s.aureus

A
  1. Ability to grow aerobically and anaerobically, over a wide range of temperatures, and in the presence of a high concentration of salt; the latter is important because these bacteria are a common cause of food poisoning.
  2. Polysaccharide capsule that protects the bacteria from phagocytosis
  3. Cell surface proteins (protein A , clumping factor proteins) that mediate adherence of the bacteria to host tissues
  4. Catalase that protects staphylococci from peroxides produced by neutrophils and macrophages
  5. Coagulase converts fibrinogen to insoluble fibrin that forms clots and can protect S. aureus from phagocytosis
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3
Q

What are the 3 types of enzymes released by s.aureus?

A

lipases, nucleases and hyaluronidase

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4
Q

What are the 3 types of toxins released by s.aureus and what do they do?

A

o Enterotoxins (many antigenically distinct) are the heat-stable and acid-resistant toxins responsible for food poisoning

o Exfoliative toxins A and B cause the superficial layers of skin to peel off (scalded skin syndrome)

o Toxic shock syndrome toxin which is a heat- and protease-resistant toxin that mediates multi-organ pathology

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5
Q

Name 4 pyogenic diseases caused by s.aureus

A

Pneuomonia, endocarditis, osteomyelitis, wound infections

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6
Q

Name 3 toxin-mediated diseases caused by s.aureus

A

Food poisoning, scalded skin syndrome, toxic shock syndrome

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7
Q

Name 3 drugs used in oral therapy for s.aureus treatment

A

Trimethoprim-sulfamethoxazole, clinamycin, doxyvycline

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8
Q

What is the drug of choice for intravenous therapy?

A

Vancomycin

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9
Q

How do s.aureus avoid antibody opsonisation? (3 ways)

A
  1. The S.aureus expresses a capsule on its surface helping to hide antigenic structures that can be detected by the innate and adaptive immune components
  2. The s.aureus protein A binds to antibodies via their Fc region instead of their Fab region. This prevents normal opsonisation.
  3. S.aureus secretes protein SSL10 which binds to the Fc region of IgG antibodies preventing the Fc receptors on neutrophils from binding to the same Fc receptors therefore the neutrophils cannot detect IgG on the surface of s.aureus
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10
Q

What are the 5 main antibody opsonisation evasion strategies?

A
  1. Hide antigens
  2. Disrupt functions
  3. Prevent detection
  4. Degrade antibodies
  5. Modify antigenicity
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11
Q

What does s.aureus SCIN protein do?

A

Binds to C3bBb and inhibits the formation of C3 and C5 convertase. This prevents:

  1. C3b deposition on cell surfaces
  2. C3a formation
  3. C5a formation
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12
Q

Explain the classical complement pathway

A

A c1 complex contains one molecule of c1q and 2 molecules of c1r and c1s. The c1 complex can bind to one IgM antibody or 6 IgG antibodies in an immune complex or the c1q can directly bind to a pathogen which activates c1r. C1r is a serine protease and cleaves c1s. The C1r2s2 complex cleaves c4 and c2. C4b and C2b bind to form c3 convertase which cleaves c3 to form c3a and c3b. C3b that binds to the c3 convertase complex forms c5 convertase.

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13
Q

Explain the alternative complement pathway

A

C3b formed by the cleavage of c3 with c3 convertase or the random hydrolysis of c3 due to the breakdown of the internal thioester bond is rapidly inactivated by factor H and factor I.

However when the internal thioester bond reacts with an amino or hydroxyl group on cell surfaces or pathogens, the c3b covalently bound to the cell is now protected from factor H inactivation.

The surface bound C3b then binds to factor B to form C3bB. This complex in the presence of factor D will be cleaved to form C3bBb which is the alternative pathway c3 convertase. This complex is stabilised by the binding of factor P.

The stabilised c3 convertase complex can now cleave much more c3, some of this c3b gets covalently bound to the same pathogen surface as the c3 convertase molecule. The binding of more c3b recruits more factors B, D and P amplifying the cascade. On self cells there will be regulatory proteins preventing the formation of this cascade however pathogens in general do not have these complement regulatory proteins.

If the c3 convertase complex binds to another c3b it forms c5 convertase which cleaves c5 into c5a and c5b.

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14
Q

Explain the lectin pathway

A

Same as classical except MBL protein is used instead of c1q to cleave c4 and c2.

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15
Q

What does s.aureus Efb protein do?

A

Binds to C3d in C3 which changes the shape of the C3 complex preventing the binding of factor B to C3.

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16
Q

What does s.aureus SSL7 protein do?

A

Binds to complement protein 5 preventing its cleavage. This inhibits the formation of the membrane attack complex since C5b is required in its formation.

17
Q

What are the 4 methods s.aureus evades the complement system?

A
  1. Inhibit C3/C5 convertases using SCIN.
  2. Bind to complement factors and prevent their processing (Efb protein)
  3. Cleave complement factors
  4. Acquire host-derived complement regulators e.g. factor H and C4BP.
18
Q

What does C4BP do?

A

Cofactor of factor I and degrades C4b from classical C3 convertases (C4bC2b).

19
Q

What are the 3 types of pathogen recognition receptors?

A
  1. TLR receptors - conserved microbial structures
  2. CLEC receptors - microbial carbohydrates
  3. FPR receptors - formylated peptides
20
Q

How do neutrophils detect opsonised microbes?

A

Through Fc receptors and complement receptors on antibody and complement opsonised microbes respectively.

21
Q

What is the difference between activatory and inhibitory receptors?

A

Activatory enhance immune cell activity.

Inhibitory suppress immune cell activity.

22
Q

How does s.aureus inhibit chemotaxis?

A

The chemotactic receptors C5aR and FPR1 detect C5a and formylated peptides (fMLP) respectively.

CHIPs proteins produced by s.aureus bind to C5aR and FPR1 preventing the binding of their agonists (C5a and formulated peptides).

This means that neutrophils do not migrate to sites of infection and do not become activated through these two receptors.

23
Q

How does s.aureus inhibit phagocytosis?

A

Produces proteins FLIPr and SSL5 which block Fc receptors preventing the detection of IgG opsonised bacteria thus reducing antibody mediated phagocytosis.

24
Q

What are the 3 ways bacteria inhibit phagocytosis?

A
  1. Inhibiting chemotaxis through CHIPs proteins that bind to C5aR and FPR1.
  2. Inhibiting phagocytosis through FLIPr and SSL5 proteins which block Fc receptors.
  3. Killing neutrophils using toxins.
25
Q

What are the 5 ways bacteria evade neutrophils?

A
  1. Inhibit chemotaxis
  2. Inhibit detection of bacteria
  3. Kill neutrophils
  4. Stimulate inhibitory receptors

5 Disrupt intracellular signalling