The human micro biome Flashcards

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1
Q

gut microbiota is now considered a

A

vital organ

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2
Q

microbiota

A

the microorganisms that typically inhabit a specific environment

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3
Q

microbiome

A

the totality of microbes, their genomes and environmental interactions in a defined environment e.g. the gut of a human

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4
Q

dysbiosis

A

microbial imbalance on or within the body

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5
Q

colonisation resistance

A

crowds out pathogens

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6
Q

how many microbial cels to human cells

A

x10

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7
Q

how many bacterial cells

A

10^14

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8
Q

example of co-evolution

A

e.g. effect of absence of H.pylori

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9
Q

diversity of the micro biome allows

A

the natural system to have the potential to cope with change and stress without further artificial intervention e.g. antibiotic treatment

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10
Q

role of micro biome (4)

A

1) immune system regulation
2) improves intestinal functions
3) gut brain links in communication
4) important to us as a liver- because of metabolites produced in the gut

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11
Q

immune system regulation and microbiome

A

removes toxins and carcinogens- crowds out pathogen- colonisation resistance

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12
Q

when does microbial succession of the micro biome occur

A

from birth to later years- critical inoculation in infancy/birth

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13
Q

consequence son disappearing human microbiota: clean water

A

reduced faecal transmission

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14
Q

consequence son disappearing human microbiota: increase in caesarean sections

A

reduced vaginal transmission

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15
Q

consequence son disappearing human microbiota: reduced breastfeeding

A

reduced cutaneous transmission and a changed immunological environment

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16
Q

consequence son disappearing human microbiota: Increased used of antibiotics

A

selection for a changing composition

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17
Q

consequence son disappearing human microbiota: smaller families

A

reduced early life transmission

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18
Q

reasons we couldnt live without microbiota

A

they synthesise many vitamins, that alone we couldn’t produce

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19
Q

human micro biome includes

A

a huge microbial diversity that is yet to be described

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20
Q

human micro biome is regarded as

A

less complex than soil and other environmental microbiomes

21
Q

HMP

A

human micro biome project

22
Q

main aim of HMP

A

a strategy to understand the microbial components of the human genetic and metabolic landscape, and how they contribute to normal physiology and predisposition to disease- Turnbaugh et al

23
Q

HMP is

A

worldwide- US, Europe and Asia

24
Q

what enables characterisation of whole microbial communities: genres, proteins and metabolic products

A

highly parallel DNA sequences combined with high-throughput mass spectrometer

25
Q

what questions need to be asked when determining if humans share a core microbiome

A
  • how is the micro biome acquired and transmitted?

- how similar are micro biomes between members of a family, or members of a community?

26
Q

what questions need to be asked when looking at how micro biomes correlate with human health

A
  • how stable is the micro biome?
  • how do genetics, diets and socioeconomic background influence the composition of the micro biome?
  • can variation be systemically studied?
27
Q

why do new technological and bioinformatic tools need to be developed to support HMP

A
  • data generated is vast

- reproducible and representativesamplng for body sites

28
Q

micro biome analysis uses

A

16S rRNA sequencing

29
Q

16S rRNA

A

a component of 30S subunit of prokaryotic ribosomes- contains highly conserved and highly variable regions- used to identify and distinguish between taxonomic groups

30
Q

how many nucleotides is 16S rRNA

A

1,500

31
Q

metagenome sequencing

A

whole genome shotgun sequencing of the micro biome. identify the repertoire of functions and pathway present within the microbiome-

32
Q

what is essential for the defining of the microbiome

A

figuring out what microbiota do

33
Q

how many reference genomes isolated form the human body do HMP plan to sequence

A

3000

34
Q

predicted that many organism will be previouslt

A

unreported

35
Q

most genomes will only be sequenced to

A

a high quality draft stage

36
Q

what is a high quality draft stage

A

sufficient info for an assessment of gene content but with some knowledge (FUN- function unknown genes)

37
Q

why are sequencing technologies largely restricted

A

due to relatively small classes of microbe that can be cultured
-therefore improved culture methods needed

38
Q

VBNC

A

viable non-culturable

39
Q

in the absence of culture

A

genome sequencing must be performed

40
Q

considerations when planning HMP

A
  • normal micorbiome must be defined, before impact on disease can be assessed
  • relatedness of individuals being studied
  • demographic of participants
  • ethical, legal and logistical barriers
41
Q

condition: Psoriasis

A

skin

42
Q

Crohns disease

A

gut

43
Q

ulcerative colitis

A

gut

44
Q

bacterial vaginosis

A

vaginal

45
Q

sexual-transmitted infections

A

uretheral

46
Q

obesity

A

gut

47
Q

acne

A

skin

48
Q

febrile illnesses in childtren

A

‘virile’- blood, GI, respiratory