Topic 8- L2 - Microbial Pathogenesis Flashcards

1
Q

Infection:

A

Invasion of body by a disease-causing organism (can by asymptomatic, can result in different disease – not same thing as disease)

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2
Q

Disease:

A

Damage or injury to host organism (overt symptoms). Some bacteria cause disease without establishing an infection (toxins)

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3
Q

Pathogen:

A

An organism that causes disease. Pathogenesis: Mechanism that leads to disease

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4
Q

Virulence:

A

Similar to pathogenicity, but often used to describe the severity of the disease (“highly virulent”)

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5
Q

Opportunistic pathogen:

A

Typically non-pathogenic organism that becomes pathogen under certain circumstances (e.g. immunocompromised host, access to an open wound)

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6
Q

Inflammation –

A

body’s immune response to infection or injury - important

part of how we clear infections

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7
Q

Excessive inflammation can have effects from

A

mild to life-threatening.

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8
Q

Immunocompromised individuals with weakened immune response are

A

subject to greater risk of infection, more difficulty clearing infections

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9
Q

Major steps in infection / microbial diseases

A

Adherence, colonization, invasion, spread

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10
Q

For adherence, microbes target specific cell or tissue types such as

A

Receptors (e.g glycoprotein or glycolipids) on the surface, providing a foothold for invasion

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11
Q

Many types/categorizations of adherence factors:

A

Pili, fimbriae, adhesins, surface proteins, capsules.

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12
Q

Mucous membranes:

A

Tightly packed epithelial cell layers covered with a mucous layer. Important protective layer

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13
Q

Mucous membranes line common body access points

A

(airways, oral cavity, GI tract) and are common places where infections initiated

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14
Q

Invasion:

A

ability of pathogen to enter host cells and/or tissues. Penetrate beyond where microbes (microbiota) normally reside

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15
Q

Colonization:

A

Expanding population – Planktonic or Biofilm

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16
Q

Spread:

A

Moving beyond site of initial infection. Uncontrolled Systemic spread (via bloodstream) often results in very serious infections/disease

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17
Q

An example of an invasion strategy by a pathogen.

A

S. pyogenes secretes an enzyme called hyaluronidase that degrades hyaluronic acid, a polysaccharide that acts as “cement” to connect some types of host cells. This enzyme can disrupt epithelial layer to facilitate invasion.

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18
Q

Virulence factor:

A

Molecules (typically proteins) produced by a pathogen that contribute to its ability to cause disease

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19
Q

Nutrient acquisition:

A

E.g. siderophores, secreted molecules that capture iron from the environment

20
Q

Immune resistance:

A

Factors that help pathogen survive immune defenses (e.g. resistance to reactive oxygen species)

21
Q

Immune evasion/disruption:

A

Factors that hide microbe from immune system or that disrupt function of immune system

22
Q

Extracellular enzymes, protein secretion systems/effectors &
toxins :

A

damage host cells and/or manipulate host cell biology

23
Q

Many ways that pathogens evade the immune system:

A
  • Hide inside cells (intracellular pathogens)
  • Produce a capsule that hides surface antigens (preventing immune detection) & can inhibit uptake and destruction by immune cells
  • hide or modify other antigens.
  • disrupt immune function/kill immune cells (including toxins, secreted enzymes, secretion systems…)
24
Q

hide or modify other antigens.

E.g.

A

pathogen associated molecular patterns (PA M P s ) such as LPS detected by immune system – trigger immune response

25
Q

Secreted (or surface) enzymes can promote virulence in different ways:

A
  • Provide free up nutrients
  • Damage host cells
  • Inactivate immune cell mechanisms
  • Disrupt barriers to enable pathogen invasion/spread
26
Q

Examples of secreted enzyme virulence factors that operate by affecting blood clotting. S. aureus secretes

A

coagulase, which induces clots to prevent immune detection. S. pyogenes secretes streptokinase, which dissolves clots, enabling this pathogen to spread

27
Q

What type of secretion system used by pathogens

A

Type III secretion systems

T3SS

28
Q

T3SS effectors proteins have very specific targets

A

(often a specific protein) in host cell. Manipulate host cell biology in their favour

29
Q

Different effectors often have

A

complementary activities

30
Q

Exotoxins (“toxins”) are secreted

A

protein toxins. Similar to bacteriocins
but target host. Amongst the most important virulence factors.

(Not made by all pathogens, other make many)

31
Q

Example of a bacterial toxin: ⍺-toxin from Staphylococcusaureus toxin proteins

A

polymerize in host cell membrane to form a pore. This can have a range of effects, from cell lysis to signaling changes. This toxin has a major effect on the virulence of S. aureus strains.

32
Q

AB-type toxins has two subunits

A
  • A subunit exerts biological effect

- B subunit(s) bind host cell receptor (usually glycoprotein/glycolipid) to mediate uptake

33
Q

A subunits generally modify or degrade a

A

specific molecule (or set of very similar molecules) – typically a host cell protein.

34
Q

AB-type toxin example: Botulinum toxin

A
produced by Clostridium botulinum. 
Rarely infects (adult) humans. However - grows/produces toxin on foods we consume
35
Q

Botulinum toxin

AB-type toxin. B subunit targets

A

toxin to motor neurons

36
Q

Botulinum toxin

AB-type toxin. A subunit is a

A

protease that cleaves specific SNARE proteins that are required by these cells to release the neurotransmitter acetylcholine.

37
Q

Absence of acetylcholine

release leads to

A

muscle paralysis

38
Q

toxoids / toxins

A

Inactivated toxins as vaccines

39
Q

Because toxins efficiently, manipulate

human biology in targeted way – can also be used to

A

treat non-bacterial disease

40
Q

Botox (botulinum toxin) best example of toxins used for treatment – used to treat range of diseases like

A

(migraines, cerebral palsy, painful muscle spasms)…in addition to “bunny lines”

41
Q

Toxins vs. secretion systems

A
  • An important difference between
    toxins & secretion systems is that toxins can diffuse and spread to distant cells/tissues.
  • Toxins often (not Secretion system effector proteins always) more potent, lone wolves. Effectors (often) more nuanced, work together.
42
Q

Yersinia pestis(plague)

A
  • Gram-negative Proteobacterium
  • Primarily a pathogen of rodents. Carried by a disease vector – fleas. Fleas spread disease between rodents.
  • spread form person to person (via lice)
43
Q

Three forms of plague – all caused by same bacterium:

A
  • Bubonic plague (infection of lymph nodes)
  • Pneumonic plague (infection of lungs)
  • Septicemic plague (bloodstream - rare)
44
Q

Yersinia pestis - virulence due to ability to

A

survive/subvert the immune system.

Access infection site (lymph nodes, lungs, blood) & colonize/grow.

45
Q

Main virulence factors for Yersinia pestis include:

A
  • T3SS injects many different effector proteins into immune cells to inactivate immune functions
  • An abundant fimbrial protein that acts as a capsule
  • F1 capsule through to inhibit uptake of Y. pestis by immune system & detection of surface antigens