Med Micro 3 - 1st Line (mucous etc) Flashcards

(25 cards)

1
Q

Mucous membranes

A

Line all body cavities open to the outside. 2 layers: epithelium and connective layer (deeper). Goblet cells secrete mucous.

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2
Q

Lacteal and function

A

A capillary of the lymph system. During an infection, blood vessels get leaky and empty into lacteals. Leads to lymph node unidirectionally

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3
Q

Lymph node

A

Lacteals empty in there. Important in adaptive immunity.

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4
Q

Epithelium of mucous membrane

A

Thin outer layer covering mucous membrane. Living cells. Packed tightly (no crossing for pathogens). Constant shedding and movement (peristalsis). Secrete defensins

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5
Q

Defensins - what are they? Where are they found?

A

Anti-microbial peptides. Found on skin (in sweat), in mucous and neutrophils. Amphipathic.

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6
Q

How are defensins triggered? What is their function?

A

Punch holes in bacterial membrane and cause leakiness; enter cell and disrupt pathways; or promote chemotaxis. Triggered by sugar and PAMPs

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7
Q

Compare skin and mucous membranes

A

Chart

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8
Q

Lacrimal apparatus

A

Makes and drains tears (into nasal cavity, then throat). Contain lysozyme, lactoferrin (binds free iron) and salt.

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9
Q

PAMPs and examples

A

pathogen-associated molecular patterns. ex. LPS and peptidoglycan, lipoteichoic acid, nucleic acids. We have receptors for them on our phagocytes

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10
Q

Interest in defensins

A

Could be used as an antibiotic, and they enhance killing by antibiotics (more can access the cell)

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11
Q

What kind of structure may protect a pathogen against defensins?

A

Capsules, S-layers outside cell, proteases

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12
Q

How do you activate a phagocyte?

A

Cytokines from keratinocytes, PAMPs

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13
Q

Pattern recognition receptors

A

in innate immune cells, identify PAMPs, Some external and some internal ex. TLR and NOD

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14
Q

Toll-like receptors (TLRs)

A

At least 13 types which recognize specific molecules (PAMPs). Identify live and dead bacteria or metabolites. Critical in innate immunity.

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15
Q

What types of cells are most likely going to express TLRs?

A

Dendritic cells, phagocytes

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16
Q

Action of TLRs

A

Binding can result in cytokine production, defensin secretion, phagocytosis and antigen presentation, interferon production, apoptosis

17
Q

Based on some of the virulence factors we’ve discussed so far, what types may help a pathogen avoid TLRs?

A

Signals for internalization of internal pathogens, clotting (cloaking), etc

18
Q

Nucleotide Oligomerization Domain (NOD) Proteins

A

Intracellular receptors for PAMPs. In adaptive immune response (MHC II presentation). Mediate inflammation (chemokine production), apoptosis, and possibly defensins

19
Q

Mutation in NOD

A

Mutation in NOD2 can cause Crohn’s disease (auto-immune disease).

20
Q

Chemokines

A

Involved in chemotaxis. Released by cell to recruit help (important in momement).

21
Q

MHCI and II

A

MHCI are antigen presenting cells resulting from viral infections. MHCII present epitopes after phgocytosis.

22
Q

Epitope

A

A small part of the antigen

23
Q

Antigen types

A

Exogenous, endogenous, auto-antigens. NOT always something foreign.

24
Q

How does microbial antagonism regulate the growth of other bacteria?

A

Based on normal microflora. Finite nutrients (like Fe), defensins (microbes make them too), reduce binding sites, help activate innate immune response, create unfavourable environment (pH)

25
Some of our body’s defenses are used (subverted) by pathogens to provide an avenue for entry. Give examples.
Infect phagocytes which signal chemokines to helper T cells and infects them (HIV); get through lacrimal apparatus to get into the throat (cold); use phagocytosis to get in then escape phagosome.