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

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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
Q

Some of our body’s defenses are used (subverted) by pathogens to provide an avenue for entry. Give examples.

A

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.