AS Lecture 11 - Microbiome of the gut Flashcards

1
Q

What is microbiota?

A

Qualitative and quantitative information about the different microbes present in a system – so who is there and how abundant.

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2
Q

What is the microbiome?

A

Functions that these microbiota have, e.g. bile metabolism – their gene catalogue

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3
Q

What is metagenomics?

A

Either “gain-of-function” or DNA based approach to create gene catalogues, used to define the microbiome.

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4
Q

What is metataxonomics?

A

Creation of 16S rRNA gene inventories, used to define the microbiota

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5
Q

What is metabonomics?

A

Catalogue of the metabolites in a sample (metabolomics in a tissue or isolate)

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6
Q

How does metataxonomics work?

A

Take a sample (faecal) > DNA/RNA extracted from all microbes in sample > PCR SSU rRNA or any house keeping gene detected by illumina MiSeq and analysed

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7
Q

What can be found out in a metataxonomics analysis?

A

Popn/Community dynamics, diversity indices, microbial biomarkers, DNA=diversity, RNA=metabolic activity, robust/strong bioinformatic support, 20-50£ per sample

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8
Q

How much of the stool is microbial biomass?

A

50-55% of stool sample - 50-250g

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9
Q

How much of the microbial biomass is contained in the large intestine?

A

1-2kg

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10
Q

What are the different concentrations of microbial biomass in each part of the GIT (stomach, duodenum, small intestine, colon)?

A
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11
Q

What do the microbes do as an asset to the host?

A

Defence - bacterial antagonism Priming of mucosal immunity - IBD is thought to be autoimmune to the gut flora Peristalsis Metabolism of dietary carcinogens Synthesis of B and K vitamins Epithelial nutrients (e.g. SCFAs - butyrate) Conversion of prodrugs Utilisation of indigestible (CH2O)n

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12
Q

What do the microbes do as a liability to the host?

A

Procarcinogens -> carcinogens (hydrogen sulphide) Overgrowth syndromes (C. Difficile infections) Opportunism - Translocation Essential ingredient for IBD **Utilisation of indigestible (CH2O)n – obesity Role in insulin resistance and non-alcoholic fatty liver disease.** ** controversial topics

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13
Q

How many different types of microorganisms colonise the gut?

A

Viruses (1200), eukaryotes (very few in humans, but murine systems show large fungal diversity), bacteria (>1000 species in total but 160 species per person)

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14
Q

What should humans be thought of as?

A

Superorganisms, with it’s own genome contributing to the familiar and extended genome - predominantly bacterial

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15
Q

What is the specificity of the microbiome?

A

It is host specific and can be changed by diet, drugs, pregnancy and surgery Family and pets share a common bacterial popn, more similar than with some random person

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16
Q

Which diseases have very strong association for microbiota’s role? I.e. Which diseases are thought to have microbes as a cause?

A

Asthma, eczema, diabetes, obesity, Non-alcoholic fatty liver disease, depression, heart disease, colon cancer, inflammatory bowel disease

17
Q

How does absence of a microbiome impact the host?

A

Inestinal, exocrine, vascular, endocrine, infection, immunity, epithelia, morphology, metabolism, nutritional, hepatic

18
Q

How is bacterial colonisation predicted?

A

It is inevitable, not pre-ordained or the same for every individual - predictable at phylum level but contains degree of randomness

19
Q

How can bacterial colonisation be influenced in first year of life?

A

By antibiotics

20
Q

What are the ecological interactions between members of different species?

A
21
Q

What does amensalism involve?

A

One organism growing and in doing so inadvertently damages another, but it is not evolved to do so – collateral damage.

22
Q

What is the problem with inflammatory bowel disease?

A

It is a multi-factorial disease and involves environmental factors but no pathogen has been identified

23
Q

Which diseases don’t occur in sterile rodent models?

A

Colocrectal cancer, breast cancer, metabolic syndrome and diabetes

24
Q

Is there a connection between the gut microbiota and the host?

A

The microbiota aren’t isolated, they are interconnected

25
Q

What are the 2 types of omic approaches to microbiome investigation?

A

Bottom up - start from DNA -> metabolite [metataxonomics and metagenomics] Top down - metabolite -> DNA [metabolomics, metabonomics]

26
Q

What is a positive point of metataxonomics?

A

There is no need to cultivate any bacteria, it is just analysing DNA

27
Q

Are people born sterile?

A

12-18 months is when you are colonised and a community is established - if born vaginally you have Lactobacilli, if born from C section then staph aureus will be present Some people are born sterile but bacteria have been found in the placenta and in the mucus plug in the baby’s rectum

28
Q

How is the gut biome resilient?

A

It stays the same over a long time, with not much change occurring, unless antibiotics or surgery or diet change Even if antibiotics given, then when they are stopped, after a couple of weeks it will return to ‘normal’ colony type

29
Q

What is another problem of microbes in the gut?

A

They can break down some drugs, so can respond differently to the drug which could cause big issues when treating different patients

30
Q

What is mutualism?

A

Good for the host and the microbiome

31
Q

What is commensalism?

A

Probiotic microbes which don’t reproduce in the host

32
Q

What is metataxonomics?

A

Checking what microbes are there and their abundance

33
Q

What is metagenomics?

A

What are the microbes are doing

34
Q

What is metabonomics and metabolonics?

A

Metabonomics - metabolites from many sources Metabolonics - metabolites from one source

35
Q

What are the main 2 phyli in the gut biome?

A

Firmicutes, Bacteroidetes and actinobacteria

36
Q

How is metabonomics/ metabolomics investigated?

A

Sample (faeces, urine, blood), tested with H1 NMR and LC-MS which is analysed

37
Q

What can be the result of a metabonomics/ metabolomics?

A

Metabolic profiles, biomarkers, metabotypes

38
Q

What are bacterial proteases important for?

A

They are known to be the communicators between host genes, env and microbiome (so are affected by each as well) They are also a potential virulence factor in colorectal cancer and IBD - so can compromise tight junction integrity

39
Q

What happens if you are at either end of the microbiome spectrum?

A