Lecture 7: Infectious Diseases Flashcards

(34 cards)

1
Q

What causes infection

A

bacteria, viruses, fungi, protozoa, prions

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2
Q

what are the steps of infection

A

Chronologic sequence of events
Portal of entry
Regulated by virulence factors

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3
Q

are most infectious agents targeting specific cells or organs

A

yes

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4
Q

How does the infectious agent get into the body

A

Mucosae (respiratory, alimentary, lower urinary, reproductive, ear/eye)
Subcutaneous tissues

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5
Q

what are the bodies cells that help to stop infectious agents initial multiplication

A

Macrophage, lymphocytes, dendritic cells

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6
Q

where does the infectious agent go after initial multiplication

A

Then local (submucosa, subcutis), regional (lymph node), systemic spread

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7
Q

what does the mucus protective layer of the body do

A

Prevents direct adherence
Blocks/traps organisms
Can facilitate action of phagocytes
Delivers antigens to local lymphoid tissue
Keeps antimicrobial substances and atb close to mucosa

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8
Q

what can cause changes in goblet cell function and chemical composition of mucus that can lower protection

A
Dehydration
Shipping
Humidity
Ventilation
Weather changes
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9
Q

how have microorganisms evolved to take advantage of our mucus protective layer

A

Source of food (carbohydrates, peptides)
If able to colonize inner mucus: prevents expulsion
Can specifically adhere to molecules in mucus
Microbial mucolysis ability is virulence factor

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10
Q

how do you ingest an infectious agent

A

via infectious fomites

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11
Q

where is the thickest layer of mucus protective layer

A

in the colon

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12
Q

where is the thinnest layer of the mucus protective layer

A

in the jejunum

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13
Q

what is located in the protective mucosal fluids

A

gastric acid, lyzozymes

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14
Q

describe inhaling a fomite

A

Nostrils  Nasal turbinates, pharynx or lower airways
Depends on size, shape, weight
Virus > prions > bacteria > fungi > Protozoa
BUT mostly inhaled with fomites!
Air turbulence in turbinates increases deposition

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15
Q

describe the mucuciliary apparatus

A
Biphasic mucus layer
Tip of cilia in gel
Nasal cavity & sinus:
Moves downward
Conductive respiratory:
Moves upward
Ultimately swallowed
Injury to epithelial cells (influenza, rhino) can disrupt and cause secondary bacterial infections
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16
Q

describe infectious agent cutaneous penetration

A

Via abrasions, scratches, bite wounds, insect bite
Limited range of host targets
but limited defenses

17
Q

describe the pathogenicity of the infectious agents

A
Regulated by virulence factors
In bacterial genes
Their expression permits bacteria to 
Colonize mucosae, 
Infect cells,
Grow and replicate,
Cause cell death
18
Q

what infectious agents have good motility

19
Q

what infectious agents can digest the mucus layer

20
Q

describe colonization of an infectious agent

A
Adhesion of sufficient amount of bacteria
Via:
Fimbria/Pilus
Adhesion molecules
Needs to be faster than cell renewal
21
Q

describe spreading of an infectious agent

A

Spreading
Destruction of collagen, tight junctions between cells
Provides safe spot for bacteria

22
Q

describe the toxins released by infectious agents

A

Exotoxins (gram +), endotoxins (gram -) (LPS: lipopolysaccharide)
Damages cells and extra-cellular matrix
Kills cells via cytolysis or activation of complement

23
Q

since Viruses are unable to produce energy and contain a limited number of enzymes what are they considered

A

obligate intracellular parasites

24
Q

how have viruses evolved

A

Have evolved to target specific cells in animals to sustain theirs needs
Not as many virulence factor
not as complex as bacteria.

25
describe permissive viral target cells
Allows for viral replication
26
describe non permissive viral target cells
no replication – used as reservoir | Can become permissive (ex with cell maturation or activation)
27
describe step 1 of the viral replication cycle
1. Attachement and Entry Determines which organs are infected Viruses bind to normally expressed receptors
28
describe step 2 of the viral replication cycle
2. Replication stage How much of the cell is hijacked Organelles, genome, other How much cell dysfunction, cell death
29
describe step 3 of the viral replication cycle
3. Shedding How the virus exits determines cell’s fate If cell killed or lysed  causes more severe disease
30
describe parvovirus viral replication
Infects intestinal crypt epithelial cells Receptors on basolateral surface So coming in from circulation, not directly from intestine M-cell  Peyer’s patch  circulation Not most direct; prevents contact with protective mechanism, tight junctions
31
how do non-enveloped viruses attach to cells
They attach to host cells using a protein coat (viral coat, capsid, capsomeres) Usually kill infected cells to release newly formed virus.
32
how do enveloped viruses attach to cells
They attach to host cells using a viral envelope | Usually do not kill infected cells to release newly formed virus.
33
what are the innate host cell defences against viruses
Inflammation | Interferon
34
what are the host cell mediated immunity against viruses
NK and cytotoxic T cells | Antibodies important only for subsequent infections