MFD11 Diseases as an imbalance of microbes Flashcards

Aim * To describe how changes in the microbiota are associated with human diseases. Content * Revisiting Koch’s postulates * Bacterial identification. * Changes in the human microbiome in disease * The gut microbiome * The oral microbiome * The ecological plaque hypothesis for oral disease

You may prefer our related Brainscape-certified flashcards:
1
Q

Give an example of a common condition caused by dysbiosis of microbial community in the gut:

A

Irritable bowel disease (IBD)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What laboratory tool is used to test koch’s postulate 1 (The suspected pathogen must be present in all cases of the diseases and absent from healthy animales)

A

microscopy and staining

samples taken from a diseased animal and a healthy animal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What laboratory tool is used to test koch’s postulate 2
(The suspected pathogen must be grown in pure culture (after being isolated from diseased host))
2) What would be observed?

A

laboratory cultures: This involves streaking agar plate with sample from diseased animal,
2) then you will observe colonies of suspected pathogen.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What laboratory tool is used to test koch’s postulate 3
(the suspected pathogen from the pure culture must cause the disease in a healthy animal
2) What would be observed?

A

Experimental animals :
inoculate a healthy, susceptible laboratory animal,
2)observe inoculated animal becomes diseased

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What laboratory tool is used to test koch’s postulate 4

the pathogen must be reisolated from the new host and shown to be the same as the originally inoculated pathogen

A

Laboratory reisolation and culture:
remove a blood or tissue sampla and observe by microscopy, the culture,
2) Observe:
Pure culture is the same organism as before

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

RECAP: what are the 4 koch’s postulates:

A
  • The organism must be present in all cases of disease, and not present in healthy individuals
  • The organism must be isolated in pure culture
  • The isolated organism must cause disease in a suitable animal
  • The organism must be re-isolated from infected animal
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Give 3/5 resasons why Koch’s postulate cannot be applied:

A
  • If the bacteria cannot be grown in culture
  • If no infecting organism can be detected
  • If no suitable animal model is available
  • If more than one species of bacterium is involved
  • If it is the level rather than just the presence of the infecting bacterium that is important
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

1) what does OUT stand for?
2) What is it?
3) What does it let you observe?

A

1) oxonomic taxanomic unit, basically
2) means species,
3) only lets you look at bacteria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What extra reading would you take if you wanted to see viruses present as well when doing DNA sequencing?

A

shotgun reading

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Why are we able now to collect data on complex microbial populations?

A

1) Advances in DNA sequencing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What gene is sequenced in targeted microbiome analysis for bacteria?
2) Why?

A

1) 16S rRNA gene

2) Conserved area

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What does metagenomics involve ?

A

sequencing all DNA

present in a sample, then using bioinformatics

to predict the source/function of the DNA

sequences

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Depending on __1__ you sample in the __2__ there is big differences in what organisms are present.

A

1) where

2) body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

1) how many species are present in the gut microbiome?

2) Are there differences in the no. of species between people?

A

1) lots and lots , one of the most diverse areas in the body
over 300
2) yes, more difference than in oral microbial communities

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What type of gut microbiota are essential for development of a healthy immune system?

A

commensal gut microbiota

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are the differences in the microbiota between individuals associated with:

A
  • Obesity
  • Colorectal cancer
  • Inflammatory bowel disease
  • Many systemic conditions (though links are often less clear cut).
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is New-onset Paediatric Crohn’s Disease?

HINT: mention what occurs due to bacterial dysbiosis

A

Is a type of inflammatory bowel disease, the microbiome dysbiosis leads to a drop in bacterial populations with similar metabolic reactions thus genes are missing that are required fro certain metabolic pathways.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

How many people are affected by Crohn’s disease and ulcerative colitis?

A

over 3.6 million (incidence is on the rise)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What factors are involved in development of Inflammatory bowel disease?

A

Host genetics play a key role, but <50% concordance between monozygotic twins. Therefore, not just about host genetics.
Gut microbiome is gaining increasing attention and what environmental factors effect that

20
Q

What conditions are encompassed by inflammatory bowel disease (IBD)?

A

Crohn’s disease and ulcerative colitis

21
Q

what environmental factors effect gut micriobiome (thus amy cause IBD)

A

genetics, birth route, lattitude, hygiene, stress, diet/nutrition, drugs (antibiotics)

22
Q

Define perturbation:

A

deviation of a process from regular path

23
Q

What 3 effects does a healthy gut micobiome have on the body (complex and stable)?

A

1) protect against pathogens
2) train/stimulate immune function
3) supply nutrients, energy, vitamins and SCFA (short-chain fatty acids)

24
Q

What 5 effects does a unhealthy gut micobiome have on the body (disease state)?

A

1) Inflammation (more local than systemic)
2) ocidative stress
3) increase in gram-negative bacteria (REMEBER disease can be the right organisms at the wrong levels as well as the wrong organisms)
4) infection (opportunistic/pathogenic)
5) altered metabolite production

25
Q

What are the 2 methods employed to target the microbiome and treat dysbiosis?

A

1) Careful selection of antibiotics to minimise unwanted shifts in the microbiota
2) Repopulation of the gut with healthy bacteria

26
Q

Give 3 examples of Repopulation of the gut with healthy bacteria to treat microbiome dysbiosis:

A

1) Prebiotics (You rely on the healthy bacteria being there still and you feed them)
2) Probiotics (live yogurts, full of good bacteria- atm not regulated yogurt companies just feed you bacteria you don’t even know if it will reach the gut)
3) Faecal microbiota transplantation (encouraging results for relapsing C. diff. infection but not so clear for IBD).= microbiome restored (sometimes)

27
Q

Give an example of careful selection of antibiotics to minimise unwanted shifts in the microbiota to treat microbiome dysbiosis:

A

E.g. avoid repeated use of a single antibiotic

28
Q

2 Major dental plaque-related diseases:

A
  • Dental caries

* Periodontitis.

29
Q

What is the Specific plaque hypothesis

A

diseases are caused by a single microorganism.

30
Q

What is the Non-specific plaque hypothesis:

A

diseases are caused by the amount of plaque.

31
Q

What is the Ecological plaque hypothesis:

A

disease is caused by
interactions of specific microorganisms with the
microbial community

32
Q

What bacteria is elevated in caries and though to cause it?

A

S.Mutans

33
Q

Why does demineralisarion occur?

minus the chemistry side- don’t forget critical pH an dissolution values

A

1) a stress e.g. acid production
2) pH lowered ( acidic)
3) ecological shift bacterial population changes (more S.mutans, Lactobacillusspp. scardovia wiggsiae)
4) demineralisation occur

34
Q

Describe the progression to cavitiation of teeth (surface errosion):

A

1) health
2) subsurface demineralisation
3) White spot lesion (still reversible)
4) cavitation (not reversible)

35
Q

In the Extended Caries Ecological Plaque Hypothesis, what bacteria are present in the dynamic stability stage ( net mineral gain, lesion regression/arrest):

A

dominance of non-MS actinomyces

36
Q

What is actinomyces?

2) What does it do with streptococci in the oral cavity?

A

1) a genus of the Actinobacteria class of bacteria. They are all gram-positive.
2) form a fundamental component of the indigenous microbiota, being among initial colonizers in polymicrobial biofilms. They can adhere
to surfaces such as on teeth and to co-aggregate with other bacteria.

37
Q

In the Extended Caries Ecological Plaque Hypothesis, what bacteria are present in the acidogenic stage ( roughly no mineral gain or loss):

A

“low -pH” non-MS and Actinomyces

38
Q

In the Extended Caries Ecological Plaque Hypothesis, what bacteria are present in the acidoduric stage ( net mineral loss):

A

increase in MS and non-mutans aciduric bacteria

39
Q

What are the 3 stages in the extended caries ecological plaque hypothesis? (from good to bad)

A

1) dynamic stability stage
2) acidogenic stage
3) Aciduric stage

40
Q

What is the keystone pathogen idea in periodontitis development?

A

The idea there is a key pathogen driving caries however it doesn’t ever have a high population.

41
Q

What is the suggested hypothesis of how P,gingivalis is a keystone pathogen?

A

1) It produces ginigpain
2) gingipain binds to TLR of immune cells
3) resulting in inflammation and impaired leukocyte killing
4) allowing without changes in its population to manipulate the populations of microbiota
5) Inflammation also causes complement-dependent and bone loss

42
Q

What is the polymicrobial synergy and dysbiosis (PSD) model of periodontal disease

A

Periodontitis is initiated by a synergistic and dysbiotic microbiota, within which different members, or specific gene combinations thereof, fulfil distinct roles that converge to shape and stabilize a disease-provoking microbiota.

43
Q

What possible roles will polymicrobial synergy play in the polymicrobial synergy and dysbiosis (PSD) model of periodontal disease:
(DO NOT NEED TO MEMORISE JUST comprehend what the role of ps is in disease progression)

A

it arises due to
interspecies interactions within the cariogenic community and interactions include:
1) one organism providing a substratum for the attachment and colonization of another,
2) nutritional cross feeding, and the co-ordinated metabolism of complex substrates
3) physical interactions & diffusible soluble factors could modulate virulence gene expression

44
Q

Does polymicrobial synergy only occur in cariogenic communties?
2) In cariogenic communties which populations of bacterai are involved>

A

1) Synergistic interactions also occur in the healthy state but between commensal bacteria.
2) In cariogenic communities, synergistic interactions occur between acidogenic and aciduric bacteria during the different stages of biofilm development and acidification,

45
Q

Define:

acidogenic bacteria

A

Producers of acid from fermentable carbohydrates, found in dental biofilm (q.v.); may be related to caries development.

46
Q

Define:

aciduric bacteria

A

The aciduric group of bacteria consists of those micro-organisms that are able to live and multiply in degrees of acidity unfavorable for the development of most microbes.