Milk Flashcards

(40 cards)

1
Q

Complex glycans

A

Human milk oligosaccharides (HMOs)

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2
Q

Who breaks down HMOs?

A

Bifidobacterium (In MOM)

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3
Q

HMOs allow

A

Mitigation of harmful bacteria with growth of beneficial

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4
Q

Abundance of HMOs

A

Third most abundant component in human milk and more than protein

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5
Q

HMOs

A

Indigestible that serve as metabolic substrate for beneficial bacteria and commensals

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6
Q

Variations in HMOs

A

Concentration: Lactation stage (colostrum vs mature milk) and Type: Genetics of mother

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7
Q

Colostrum vs Mature milk HMO numbers

A

20-25g/L vs 5-15g/L

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8
Q

Number of HMOs identified in human milk

A

> 200

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9
Q

HMOs are ___ because ___

A

Prebiotics because they are indigestible and make their way to the gut without modification

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10
Q

Benefits of HMOs

A

1) Grow beneficial bacteria
2) Modulate intestinal epithelial cell responses
3) Prevent pathogens in epithelium (antimicrobial and antibiofilm activity)

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11
Q

Genetics of HMOs

A

Goes along with mom’s blood group + depends on type of glucosyltransferase expressed

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12
Q

HMOs can have _____ units

A

15 disaccharide units with different isomeric forms

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13
Q

Number of HMOs that are neutral

A

75%

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14
Q

Culturing of human milk have found

A

Staph (aureus and epidermidis), Strep salvarius, Lactobacillus, and Bifidobacterium

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15
Q

9 Core Genera of Milk

A

Staphylococcus, Strep, Sphingomonas, Serratia, Pseudomonas, Propionibacterium, Ralstornia, Corynebacterium, Bradyrhizobiaceae

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16
Q

Core Genera in milk %

A

95%

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17
Q

Number of bacteria BF babies consume a day

18
Q

Enteromammary Pathway

A

Bacteria from human gut travels to the mammary gland to mold epi cells, immune cells, and bacteria itself

19
Q

HMM unique to

20
Q

HMM influenced by

A

Mother’s skin (Staph and Corynebacterium), Enteromammary pathway, backflow from baby

21
Q

Sources of baby microbiomes

A

delievery –> HMM

22
Q

Two core genera in HMM

A

Staph and Strep

23
Q

NEC

A

Most common GI disease in pre-term infants and most common cause of death but incompletely understood

24
Q

% of low birth weight babies that develop NEC

25
Mortality of NEC
10-30%
26
Risk factors of NEC
Formula + acid supplement medications + Longterm antibiotics
27
How human milk protects from NEC
Down-regulates pro-inflammatory genes + SCFA production to lower pH and O2 to suppress pathogens and support barrier maturation and function
28
DHM
Mimicking MOM that is usually a complex mix of different samples of MOM
29
Limitations of DHM
No microbiome and inactivation of components due to pasteurisation and varies + no specific gestational age or nutritional needs of infant considered
30
Downfall of DHM (3)
Lack microbiota so more vulnerable to infection + reduced Ig, lactoferrin, cytokines, growth factors + harder to digest and absorb nutrients
31
Human milk banks all over
US and Australia with Japan and Norway having pasteurisation free options
32
Mimicking MOM new option
Mix donor and MOM and incubate over time (3 or 10% MOM)
33
MOM + DHM -->
No change in alpha diversity, but significant difference in members (50% restoration to famiies in MOM)
34
Frozen MOM + DHM
No difference in repopulation from immediate processing
35
MOM + DHM vs MOM
Metabolic analysis similar + similar IL8 in cell lines (safe)
36
HMO structures
Lactose elongated by 1,3 or 1,6 linked lactobiose or N-acetyl glucosamine
37
3 Types of HMOs
Fructose at end (35-50%), N-acetylglucosamine at end (42-55%), or Salic acid at end (12-14%)
38
Neutral VS Acidic HMOs
Sialic acid is acidic and fructose or N-acetylglucosamine neutral (75%)
39
Bioactives (5)
Ig, HMOs, WBC, AMPs, miRNAs
40
MOM benefits
Complete and personal nutrition, Enhances immune development, gut colonisation, pathogen protection, less GI disease