Ch. 10 Flashcards

1
Q

Why can an organism in one host be a pathogen in another?

A

speculate it is because of disruption in the balance of normal microbiota and host factors

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2
Q

immune system recognizes our normal microbiota, but in some cases….

A

our immune system mounts a defense against our normal microbiota

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3
Q

examples of normal microbiota that can be also be opportunistic pathogens

A

Group B streptococci infections (doesn’t affect mother but affects baby). E. coli in the appendix that enters abdominal cavity, and weakened immune system allows yeast infections

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4
Q

tropism

A

capability of a virus to infect a distinct group of cells in the host. can limit spread of infection in some cases

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5
Q

Does tropism stay the same?

A

no it can change. 60-80% of new infectious diseases in humans emerged bc of expanded tropism. Ex: HIV, Covid

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6
Q

pathogenicity

A

ability of a microbe to cause a disease. all or nothing, so pathogen or not

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7
Q

virulence

A

degree or extent of disease a pathogen causes

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8
Q

what is virulence determined by?

A

microbe, host, and evolves over time

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9
Q

virulence factors

A

ways a pathogen is able to overcome host defenses like pathogen toxicity, transmission factors

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10
Q

attenuated pathogen

A

a weakened, less vigorous virus. can be used to make vaccines that can stimulate an immune response

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11
Q

why is virulence evolving?

A

because it changes in response to host factors as well as environmental factors.

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12
Q

Infectious does-50 (ID50)

A
  • # of cells or virions in the case of viruses that are needed to establish an infxn in 50% of all exposed susceptible hosts
  • more infectious = a lower ID50
  • highly infectious does not mean more dangerous
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13
Q

lethal-dose 50 (LD50)

A

amount of toxin that’s needed to kill 50% of affected hosts that are not treated

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14
Q

LD50 and ID50 can change based on what?

A

species affected, human immune fitness, route of exposure (inhaled, injected, airborne)

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15
Q

toxins

A

small amount of molecules that generate a range of adverse effects. can cause tissue damage, suppress immune responses, etc

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16
Q

toxigenic

A

microbes that make toxins

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17
Q

toxemia

A

when toxins get in the bloodstream and spread throughout the body

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18
Q

endotoxins

A

can enter from localized or systemic infections. lipid portion, toxic to us and animals, released when gram-negative bacteria divide or die. if present in sufficient quantities, endotoxins causes septic shock.

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19
Q

the immune system and/or antibiotics kill gram-negative pathogens, which causes…

A

endotoxemia: endotoxins getting in the bloodstream

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20
Q

exotoxins can be what?

A

gram pos or gram neg

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21
Q

exotoxins are often classified into three main families based on their mode of action. what are they?

A
  • type 1: membrane acting extracellular toxins. bind but don’t enter the cell (staph and strep)
  • type 2: membrane damaging toxins. disrupt or destabilize the cell membrane. cell lyses (hemolysins)
  • type 3: intracellular toxins. enter the cell to exert their effects (Pertussis)
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22
Q

toxicity level of endotoxins

A

lower (relatively high LD50)

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23
Q

toxicity level of exotoxins

A

higher (many have a low LD50)

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24
Q

5 steps to infection

A
  1. Enter the host
  2. Adhere to host tissues
  3. Invade tissues and obtain nutrients
  4. Replicate while warding off immune defenses
  5. Transmit to a new host
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25
Q

1) enter the host

A
  • portal of entry: any site that a pathogen uses to enter the host. mucous membranes = most common
  • some pathogens have more than 1 portal of entry
  • portal of entry = often mode of transmission
  • site where disease develops (not necessarily the only or main site affected)
26
Q

integumentary system

A

blocks most microbes from entering the body. consists of skin, hair, nails, and associated glans

27
Q

ocular

A

conjuctiva: enters thru eyes = pink eye

28
Q

parenteral

A

enter thru bloodstream, subcutaneous tissues, muscles usually by injections

29
Q

most common portal of entry

A

respiratory system. coughs and sneezes = travel through droplets in the air. doesn’t necessarily cause respiratory infections

30
Q

digestive-system pathogens

A

frequently have fecal-oral transmission. invade mucosal surfaces of the GI tract

31
Q

urogenital

A

sexually transmitted pathogens. enter through the mucosal lining of the vagina/cervix or urethra in men

32
Q

transplacental entry

A

vertical transfer of pathogens. mother to baby

33
Q
  1. adhering to host tissues
A
  • Adhesins: virulence factors used to stick to host cells in a specific or nonspecific manner
  • Bacterial adhesins include: cell wall components, capsules, fimbriae, pili
34
Q

quorum sensing

A

a communication mechanism between bacteria that allows specific processes to be controlled, such as biofilm formation, virulence factor expression

35
Q
  1. pathogen must invade tissues and obtain nutrients
A
  • Once adhered the pathogen may remain on cell surfaces, reside inside the cell, or invade deeper by passing through or between cells.
  • bacteria produce siderophores that snatch iron
  • extracellular enzymes: break down nutrients in the local environment and allows pathogens to scavenge nutrients as they damage host tissues
36
Q

invasins

A
  • allow pathogens to invade host tissues. ex: flagella, collagenases, neuraminidases, coagulases, kinases
  • local acting factors
  • usually membrane associated or secreted enzymes
37
Q

mechanism of action for invasins

A

break down host tissue, form blood clots, allow to replicate, induce host to take up the pathogen, motile

38
Q

pili and fimbriae are binding factors that are examples of ____, which are virulence factors that allow pathogens to _______ to host tissues

A

adhesins, adhere/stick

39
Q

In contrast, flagella and collagenases tend to act as ______ which help pathogens spread deeper into host tissues

40
Q

pathogens generate cytopathic effects which…

A

damage host cells.
- cytocidal: own cells will die
- noncytocidal: damaged not death

41
Q

Viral pathogens generate cytopathic effects when they:

A
  • invade host cells
  • release toxins that can damage cell
  • obtaining nutrients
42
Q

oncogenic pathogen

A

own host cell that turns to cancer

43
Q
  1. pathogen must evade host immune defenses so it can replicate
A

most pathogens don’t make it this far but can either hide or undermine immune system

44
Q

hide - intracellular pathogens

A

spend a majority of their time inside host cells. Ex: viruses

45
Q

hide - latency

A

quietly exist inside a host. usually causes persistent or recurrent disease

46
Q

hide - antigenic masking

A

pathogen may conceal antigenic features

47
Q

hide - mimicry

A

emulating host molecules

48
Q

hide - variation

A

periodically altering the surface molecules. immune system doesn’t recognize bc the previous virus changed

49
Q

undermining the host immune system

A

immune suppression. pathogens suppress immune function by targeting immune cells, making protases, interfere with transcription of interleukins, interfere with molecular makeup

50
Q
  1. pathogen must be transmitted to a new host to repeat the cycle
A

Symptoms can facilitate transmission to others
Itchiness🡪 scratching bacteria under nails
Coughing/Sneezing 🡪 droplets in the air that spread
Diarrhea 🡪 secretions, frequent bowel movements

51
Q

portal of exit

A

route used for exit. often the portal of entry

52
Q

maintaining a reservoir (source of infxn)

A

environmental, organism, fomite

53
Q

biosafety levels are based on what?

A

level of infectivity, extent of disease caused and mortality rate, mode of transmission, availability of treatment and preventions

54
Q

BSL-1 agents

A

very well characterized. rarely cause disease
ex: E.coli

55
Q

BSL-2 agents

A

cause disease, not airborne agents, treatable, preventable, vaccines available
Ex: influenza, staph, herpes

56
Q

BSL-2 plus

A

dangerous, incurable, no vaccines
Ex: HIV

57
Q

BSL-3 agents

A

some are treatable and can be transmitted through the air. serious or lethal human diseases
Ex: mycobacterium tuberculosis, certain influenza strains

58
Q

BSL-4 agents

A

no cure, most dangerous, lethal in humans. dangerous and “exotic” pathogens
Ex: ebola

59
Q

standard precautions used with all patients

A

hand hygiene, gloves if risk of exposure to wounds, bodily fluids, or mucous membranes, barrier gowns and face shields when splash risk, disinfection

60
Q

transmission precautions - contact precautions

A

wound/skin infection, resistant infection, infectious diarrhea
- limit patient transport
- special attention to hand washing
- gloves at all times
- gown at all times
- single patient use equipment
Examples: MRSA, Gram negative antibiotic resistant bacteria, and C. difficile

61
Q

transmission precautions - droplet precautions

A

most respiratory infections, influenza, pertussis
- limit patient transport
- procedural mask at all times

62
Q

transmission precautions - airborne precautions

A

tuberculosis, rubeola (measles), varicella (chickenpox)
- limit patient transport
- N95 or comparable respirator
- Place patient in Airborne infection isolation room (AIIR) facility