Dental Plaque Flashcards

1
Q

What are the early colonisers in dental plaque?

A

S. mitis group (S. mitis, S. sanguis, S. oralis)

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2
Q

What is the timeframe of plaque maturation?

A
  • After 7 days strep still dominant

- After 14 days only 15% strep, anaerobic rods and filaments dominate

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3
Q

What are cryptitopes?

A

Hidden binding sites that bacteria can attach to after it is exposed (e.g. after enzyme action removes component to expose binding site)

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4
Q

What bacterial species is the main co-aggregator?

A

Fusobacterium nucleatum

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5
Q

What linkages for EPS are soluble and insoluble? Why do bacteria use both? Give an example for each.

A

a1-6 = soluble (Glucans - used to form water channels)

a1-3 or a1-4 = insoluble (Mutan - resists being washed away)

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6
Q

What are THREE beneficial and THREE antagonistic microbial interactions in biofilm.

A

Beneficial

  • Enzyme complementation
  • Food web (ie. feed off each others byproducts)
  • Co-aggregation

Antagonistic

  • Nutrient competition
  • pH extremes
  • Bacteriocins
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7
Q

What are the FIVE Koch’s Postulates for plaque derived diseases?

A
  1. Microbe should be present in sufficient numbers to initiate disease
  2. Microbe should cause increased levels of specific antibodies
  3. Microbe should possess suitable virulence factors
  4. A pure culture should be able to cause the disease in a suitable animal model
  5. Elimination of the microbe should result in clinical improvement
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8
Q

What bacteria are prevalent in early demin lesions? Which bacteria comes later, and why?

A
  • S. mutans and A. naeslundii

- Lactobacilli come later (poor attachment to tooth surface)

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9
Q

Why is S. mutans much better at attaching to tooth structure vs. Lactobacilli?

A

S. mutans has three different kinds of extracellular Glucosyltranserase (GTF) which produce glucans to aid in attachment.

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10
Q

How is S. mutans aciduric and acidogenic?

A
  • Aciduric because it has high level of membrane bound ATPase activity with optimal pH lower than others
  • Acidogenic because it shuts off PTS system and uses homofermentation in high nutrient conditions (producing the strong lactic acid)
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11
Q

What are FOUR important pathogenic determinants of bacteria and THREE less important ones.

A

Important

  • GTF (attachment/colonisation)
  • IPS production (intracellular glycogen)
  • Lactate dehydrogenase (lactic acid production)
  • Aciduricity (withstand lower pH)

Less important
- Fructosyltransferase (fructan - extracellular food)
- Antigen I/II (attachment)
- PTS (sugar transport in low sugar condns “teaspoon”)
NOTE: Multiple sugar TS more important “shovel”

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12
Q

What are THREE important ways in which fluoride is antagonistic against S. mutans?

A
  • Inhibit glycolysis (inhibit enolase)
  • Acidifies internal pH
  • Reduces IPS synthesis
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13
Q

What is one unique way xylitol antagonises S. mutans?

A

S. mutans engages in a futile cycle with xylitol, spending ATP to bring it in only to realise it cannot use it, so it spends ATP pumping it out, but then takes it in again with ATP.

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14
Q

Describe the changes in microbiology from health to gingivitis.

A

Streptococci -> Actinomyces naeslundii/israelii (non-bleeding stage) -> black pigmented anaerobes like p.gingivalis (bleeding stage)

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15
Q

True or false: Nutrient supply to bacteria increases during gingivitis.

A

True, increased GCF flowrate provides bacteria with more nutrients.

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16
Q

What are FOUR host biological features that may result in damage during periodontitis.

A
  • More immune complexes (type III hypersensitivity)
  • More complement (type II hypersensitivity)
  • Prostaglandins (osteoclast activity)
  • Macrophages (RoS)
17
Q

What is the acronym for bacterial pathogenicity?

A

AGED (Attachment, Growth, Evasion, Damage)

18
Q

Why might the red complex be particularly relevant in periodontitis?

A
  • They produce a range of proteases.
19
Q

Give an example of AGED from P. gingivalis.

A

Attachment - has fimbrae
Growth - produces haemolysin (breaks down RBCs for iron)
Evasion - produces capsule
Damage - proteases (degrade collagen and host protease inhibitors)

20
Q

What bacteria do we mainly see subgingivally in periodontal lesions and why?

A

Usually gram -ve anaerobes that are asaccharolytic.

- This is because GCF provides lots of protein.

21
Q

Explain the pyramid diagram of bacteria in periodontal disease.

A

The top is the red complex (late colonisers), but they cannot exist with the lower tiers being there first (early and secondary colonisers).

22
Q

Which THREE viruses may be implicated in aggressive periodontal disease?

A
  • EBV
  • HSV
  • Cytomegalovirus
23
Q

What are FOUR features of the microbiology seen in apical periodontitis?

A
  • Restricted group of species (average 6 species)
  • Mostly anaerobic
  • Both gram +ve and -ve
  • Fastidious nutritional requirements (pulp is rich in nutrients)
24
Q

What are THREE mechanisms of action for:

  • Flouride
  • Xylitol
  • CHX
A
Fluoride
- Inhibit enolase (glycolysis)
- Reduce IPS (energy for acid prodn)
- Reduce EPS (plaque less sticky)
Xylitol
- Futile cycle (inhibit PTS system)
- Decrease aciduricity
- Decrease adherence
CHX
- Decrease adherence
- inhibit PEP-PTS
- interfere with ATPase (aciduricity)
- Detergent effect (damages membrane)