Lecture 10 pt. 2 Flashcards

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1
Q

What is pathogenicity

A

ability of microbe to cause disease

-all or nothing, it either causes or it does not

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2
Q

What is Virulence?

A

Degree or extent of a disease; has different levels

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3
Q

What are Virulence factors?

A

items microbes use to defeat our defenses

-toxicity, aggressiveness, transmission

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4
Q

What is attenuated virulence?

A

still infectious, but weakened and destroyed easily; basis for vaccines

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5
Q

What is the difference between ID50 and LD50

A

ID50– how many cells needed to establish infection 50% of the time
LD50– amount of cells needed to kill 50% of nontreated hosts

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6
Q

What are/is:

  1. Toxins
  2. Toxigenic
  3. Toxemia
A
Toxins= molecules that generate a range of damage to the host
Toxigenic= microbes that can make toxins
Toxemia= when toxins reach the bloodstream
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7
Q

What are the characteristics of endotoxins and where do they come from?

A

Released from gram negative cells (attached to LPS) when they lyse

  • causes fever, chills, body aches, etc.
  • causes septic shock
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8
Q

What are the characteristics of exotoxins and where do they come from?

A

They come from both gram negative and gram positive cells

  • Present from growing bacteria
  • Some have vaccines
  • More dangerous than endotoxin (has a lower LD50)
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9
Q

What is the difference between type I, type II, and type III exotoxin types?

A

Type I-membrane acting; bind host receptor without entering cell and causes signal that alters cell
Type II- membrane damaging; forms pores, removes phosphate head and cell lysis
Type 3- Same as type I

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10
Q

Endotoxins vs Exotoxins

  • What type of bacteria are they found in?
  • When are they made present?
  • Is there a cure?
  • Does the host show signs?
A

Is a lipid / Is a protein
Gram (-) only / Gram (-) and (+)
From dead bacteria / From growing bacteria
No vaccine available / Vaccine available
Host always has a fever / Sometimes host has fever

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11
Q

What is the portal of entry? (1st step to infection)

A
where the pathogen enters host
-largest area is skin, eye, and ears
-Respiratory- most common portal
GI-fecal/oral
Urogenital/placental- STDs, UTI
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12
Q

What is adhesion? (2nd step to infection)

A

Adhere to host tissue Adhesins(1000s of them)

  • nonspecific(hydrophobic) then specific interactions
  • Pathogen mimics something the host cell naturally binds
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13
Q

What are the 4 different means of adhesion?

A
  1. Fimbriae and pili- bind host cell carbohydrates
  2. Sialic acid factor- bind host cell sugar molecule
  3. Heparan binding factor- binds host cell sugar molecule
  4. Fibronectin binding factor- binds host cell protein molecule
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14
Q

What do cells do during the process of invasion (3rd step of infection)?

A
Will either: A) Stay at surface
B)Stay in cell
C)Invade deeper tissue
D)Pass between cells to deeper tissue
-Will obtain nutrients to grow
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15
Q

What are the things that aid in Invasion of the cell?

A

Flagella- used to spread around
Lipases- break down lipids
Proteases- Break down proteins
Siderophores- steal iron from host

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16
Q

How do cells evade host immune system? (4th step of infection)

A
  1. intracellular pathogens- lives inside host cell
  2. latency- lay and wait to attack
  3. masking- coats itself with host molecule
  4. mimicry- pathogen surface resembles host surface
  5. Variation- alter their surface molecules
17
Q

What are the steps of transmission? (5th step of infection)

A

The cell travels through the portal of exit and finds the reservoir (where the cell thrives best) and attaches to a fomite (inanimate object)

18
Q

What are the features of Biosafety level one and BSL2

A

BSL1- no harm to healthy people
(S. epidermidis)
BSL2- Cause disease, but are preventable or treatable (S. aureus)

19
Q

What is the difference between BSL3 and BSL4

A

BSL3 is serious, some treatable, many are airborne (M. tuberculosis)
BSL4- lethal to humans, not treatable, require airtight suits (ebola)

20
Q

What is universal standard precaution(s)?

A

all patients are treated as potentially infectious

  • proper handwashing
  • wear gloves
  • barrier clothing, mask for splash risk
  • Biosharp waste disposal
  • disinfect surfaces
21
Q

How do the toxicity/ LD50 of endotoxins and exotoxins differ?

A
Endotoxins= Low toxicity/ high LD50
Exotoxins= High toxicity/ low LD50
22
Q

Can endotoxins/exotoxins be treated?

A

Endotoxins cannot be treated.

Exotoxins can be treated

23
Q

How do bacterial cells disrupt phagocytosis (disrupt immune cell activity)?

A
  • toxins=destroy immune cell
  • capsule=immune cell can’t engulf
  • Block= fusion of immune cell
  • Escape= break free of immune cell
24
Q

How do bacterial cells suppress immune cells?

A
  • Destroy immune cells
  • Destroy antibodies
  • Disrupt immune signaling