FINAL Flashcards

1
Q

Which QS molecule is used by Gram Positive? where are they sensed?

A

AIP, AI-2

TCS, sensed outside

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2
Q

Which QS molecule is used by Gram Negative? where are they sensed?

A

AI-2, AHK, AI-1

inside the cytoplasm because they are membrane diffusable

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3
Q

Endotoxin

A

part of the bacterial pathogen, further characterized by their mode of action

  • LPS, LTA/TA, peptidoglycan, PAMPs
  • weakly antigenic, highly immunogenic (PAMPs)
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4
Q

Exotoxin

A

secreted into the surrounding - types 1,2,3

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5
Q

Type 1 and examples

A

binds to the target cell surface and acts extracellularly (ex.:
superantigen)

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6
Q

Type 2 and examples

A

Type II toxin: binds to target cell surface and acts on the eukaryotic cell membranes (pore-forming toxins, phospholipases)

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7
Q

Type 3 and examples:

A

AB type toxin; binds to the target cell surface, enters the host cells and activates or inactivates intracellular targets.

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8
Q

when are endotoxins released?

A

replication or when the cell lyse

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9
Q

4 clinical stages of septic shock

A
  1. Systemic inflammatory response syndrome (SIRS): fever or hypothermia, high heart rate and high
    respiratory rate.
  2. Sepsis: SIRS + documented septicemia (presence of bacteria in the blood stream).
  3. Severe sepsis: organ dysfunction and low blood pressure. At this stage 70% of patients will die.
  4. Septic shock: low blood pressure despite administration of fluid.
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10
Q

Exotoxin example : nonprotein

A

mycolactone
lipid - good at crossing membranes
-cytotoxic effect, causing necrotization of host cells and has an immunosupressive property
-lesions
-intracellular pathogen, grows in macrophages, and necrotic tissue

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11
Q

Exotoxin example: protein

A

TSST-1

cuase massive activation of T cells and macrophage, massive release of cytokines and causes cytokine storm - shock

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12
Q

exotoxin types and roles : type 2 protein

A
  • kill host cell
  • destroy phagosome and enter the cytoplasm
  • exit the cell

phosophoilpases - PlcA, PlcB in L. monocytogenes destroy the phagosome membrane
pore forming toxins - cause an inrush of water and therefore cell lysis

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13
Q

Explain entry of AB toxins into the cell

A
  • B subunit binds
  • phagosome formation
  • travels to the Golgi
  • high influx of H+
  • disulfide bridge broken
  • A subunit released into the cytoplasm to find target
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14
Q

Diphteria toxin

A
  • causes damage to the mucosa of the throat - forms pseudomembrane
  • Entry: decrease in PH causes a conformational change in B to a pore and A is exposed to the cytoplasm. Reducing conditions reduce the disulfide bond and the A subunit is freed into the cytoplasm to find the target.
  • A subunit : ADP-ribosylation of host cell proteins
  • causes inactivation or change in activity of the protein
  • targets: EF-2: stops protein elongation, G protein: ion disruption, water flows out of the cell
  • antitoxin(purified antibodies against DT) are good vaccines against the disease
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15
Q

what are the targets of the anthrax toxin?

A

andenylate cyclase, zinc dependent protease - leads to cleavage of MAPK - lethality?
AB7 type toxin
A subunites are called EF and LF

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16
Q

what are the benefits to vaccination?

A
  • herd immunity
  • cheaper than treatment
  • protection against bacterial infections for which there is no treatment
  • reduced symptoms
  • prevents infectious disease
  • prevent long-term consequences of the disease
17
Q

4 types of vaccines?

A

whole
conjugate
adjuvant
subunit vaccine

18
Q

whole vaccine

A

Whole, live non-pathogenic organism that provides cross-protective immunity

  • inactivated by heat or chemical
  • not used because too immunogenic ( too many people were getting the disease)
19
Q

subunit vaccine

A

one or more purified proteins, sometimes inactivated, which provide immunity against invariant antigens*
-toxins and surface components

20
Q

conjugated vaccine

A

-protection against capsulated organisms
-Capsular antigens are covalently bound to a protein antigen, which allow the capsular antigens
to be processed and presented on MHC-2 complex, important for antibody-mediated immunity.

21
Q

Adjuvants

A

components of the vaccine that stimulate, modify or augment the immune system activity.