Pathogenesis And Virulence Flashcards

1
Q

What are the 5 types of symbiotic relationships

A

Mutualism, amensalism, commenalism, neutralism, parasitism

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2
Q

How is either population effected in a mutualism symbiotic relationship

A

Both populations are benefited

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3
Q

How is either population effected in an amensalism symbiotic relationship

A

One population is harmed and the other is unaffected

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4
Q

How is either population effected in a commensalism symbiotic relationship

A

One benefits the other is unaffected

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5
Q

How is either population effected in a neutralism symbiotic relationship

A

Both are unaffected

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6
Q

How is either population effected in a parasitism symbiotic relationship

A

One benefits and the other is harmed

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7
Q

Define pathogenicity

A

The ability to produce pathologic changes or disease

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8
Q

Define pathogen

A

disease producing microorganism

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9
Q

Define Virulence

A

measure of pathogenicity. Also, involves invasiveness and
pathogenicity

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10
Q

Define toxigenicity

A

ability to produce toxins

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11
Q

What ways do foetus acquire normal flora

A

Mouth and nose populated from birth canal,

  • skin populated by transfer from parents/ doctors
  • intestine and gut flora develops after first meal
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12
Q

What are the differences between primary and opportunity pathogens

A
  • primary causes diseases regardless, whereas opportunistic the disease is caused in compromised hosts
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13
Q

What are the 3 main steps in pathogenic bacteria infection

A

Exposure, adherence, invasion

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14
Q

What does the exposure stage of pathogenic bacteria infection include

A

Direct contact surfer from the environment or vectors

  • main entry point is mucous membranes
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15
Q

What are the 4 main areas of exposure

A

Direct contact
From the environment
From vectors
From fomites (inanimate objects)

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16
Q

What does the adhesion stage of pathogenic bacteria infection include

A

Biofilm formation
- adhesins

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17
Q

What does the invasion stage of pathogenic bacteria infection include

A

Production of lytic substances that alter host tissue

  • penetration of deeper tissues and continued dissemination
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18
Q

What are some main classes of exoenzymes

A

Nucleases, glycohydrolases, phospholipases, proteases

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19
Q

What is the function of glycohydrolases

A

Degrades hyaluronic acid that cements cells together to promote spreading through tissues

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20
Q

What is the function of nucleases

A

Degrades DNA released by dying cells

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21
Q

What is the function of phospholipases

A

Degrades phospholipid bilayer of host cells

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22
Q

What is the function of proteases

A

Degraded collagen in connective tissue to promote spread

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23
Q

What are the main aspects of endotoxins

A

They’re released on bacteria death
- they’re heat stable

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24
Q

What systemic effects are produced by endotoxins

A

Fevers
- intestinal haemorrage
- inflammation
- stimulates the immune system

25
Q

What are the main aspects of exotoxins

A

Soluble
- produced within bacteria ( mainly gram positive)
- may travel away from the site of infection

26
Q

What are the four types ’ of endotoxins

A

AB toxins (tetanus, cholera)

  • site specific (neurotoxins)
  • membrane disrupting (haemolysin)
  • superantigens (staphylococcal enterotoxin)
27
Q

What is the composition difference between endotoxins and exotoxins

A

Endotoxins are lipid A components whereas exotoxins are made of proteins

28
Q

What is the source difference between endotoxins and exotoxins

A

Endotoxins come from gram negative bacteria whereas exotoxins come from primarily gram positive

29
Q

What is the difference in heat stability between endotoxins and exotoxins

A

Endotoxins are heat stable whereas exotoxins are more heat liable

30
Q

What is the difference in the effect on hosts between endotoxins and exotoxins

A

Endotoxins - General systemic symptoms of inflammation and fever

Exotoxins - specific damage to cells dependant upon receptor mediated targeting of cells

31
Q

What is the difference in LD50 between endotoxins and exotoxins

A

. Endotoxins are high whereas exotoxins are low

32
Q

What are the 3 types of pathogen multiplication

A

Local, focal, systemic

33
Q

What is local pathogen multiplication

A
  • small area near entry site
  • extensive tissue damage but still localised
34
Q

What is focal pathogen multiplication

A

Spreads to a secondary location
/ which leads to a secondary infection

35
Q

What is systemic pathogen multiplication

A

Spreads throughout the body

36
Q

What are the main characteristics of diseases

A

signs (objective)
- body temp 98.2f
- heart rate 60-100
- blood pressure 90/60 and 120/80

Symptoms
- subjective
Nausea, loss of appetite

37
Q

What are the main classifications of diseases

A

Infectious
Iatrogenic
Nosocomial
Zoonotic
Non communicable
Non infectious

38
Q

What are the five periods of disease

A

Incubation, prodromal, illness, decline, convalescence

39
Q

Do incubation periods have a variable length

40
Q

What are the features of the incubation period

A

No signs or symptoms
Variable length

41
Q

What are the features of the prodromal period

A
  • Multiplication continues
  • common signs + symptoms
    ( too general to diagnose a specific disease
42
Q

What are the features of the illness period

A
  • Very severe
  • most evident
  • lack of immune response
43
Q

What are the features of the decline period

A
  • decrease in the number of pathogens
  • decrease in signs and symptoms
  • potential to acquire secondary infection
44
Q

What are the features of the convalescence period

A
  • Patient recovers
  • tissue repair leads to normal function
  • length of time depends on damage severity, nature of pathogen, and the site of infection
45
Q

During which periods are infectious diseases contagions

46
Q

What is acute infection

A
  • Symptoms develop quickly
  • brief typically resolves in less than 6 months
47
Q

What is chronic infection

A

Slow onset of symptoms and can worsen over time

  • persists beyond 6 months
48
Q

Which membrane serves as the main portal of entry for pathogens

49
Q

In which disease period does the patient start to get better

A

Convalescence

50
Q

What is the name given to infections/diseases acquired from the hospital

A

Nosocomial

51
Q

What are exotoxins primarily made up of

52
Q

Lipid A is a type of what toxin

A

Endotoxins

53
Q

Tetanus toxin prevents the release of what?

A

Acetylcholine

54
Q

Which toxin lyses red blood cells

A

Haemolysins

55
Q

What is the name of a disease that’s contracted due to a medical procedure

A

Latrogenic

56
Q

What is the measure of pathogenicity

57
Q

What type of infection develops quickly

58
Q

Toxic shock is the most characterised……

A

Superantigen

59
Q

What enzyme breaks down collagen

A

Collagenase