Lecture 3 - ESKAPE Pathogens Flashcards

1
Q

describe gram positive bacteria

A

thick PG layer

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2
Q

describe gram negative bacteria

A

has thin PG layer, outer membrane, and lipoproteins

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3
Q

how can we determine if bacteria is positive or negative in the clinic?

A

gram stain:
- gram positive = purple
- gram negative = colourless

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4
Q

what shape are most gram positive bacteria?

A

cocci

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5
Q

what shape are most gram negative bacteria?

A

rod-shaped

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6
Q

is mycobacterium tuberculosis gram pos or neg?

A

neither!

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7
Q

what stain can we use to determine mycobacterium tuberculosis? why?

A

use acid-fast stain bc has mycolic acids on the cell surface

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8
Q

why is M. tb often misdiagnosed?

A

it is rare and false positives for gram pos are common

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9
Q

how are our immune systems activated by bacteria?

A

surface markers on bacteria activate TLRs

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10
Q

where are TLRs found?

A

mainly innate immune cells like DCs and macrophages

also non-immune cells like fibroblasts and epithelial cells

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11
Q

what do we do when our immune system can’t control bacteria?

A

use antibiotics to clear the infection

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12
Q

where do many antibiotics come from? why?

A

antibiotics often come from other microbes and were originally used to allow for competition in the environment

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13
Q

how do microbes develop resistance via environment?

A

microbes take up helpful genes from other microbes in environment to develop resistance

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14
Q

7 antibiotics that are bacteriocidal

A
  1. B-lactams
  2. aminoglycosides
  3. glycopeptides
  4. ansamycins
  5. quinolones
  6. streptogramins
  7. lipopeptides
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15
Q

5 antibiotics that are bacteriotatic

A
  1. sulfonamides
  2. chloramphenicol
  3. tetracyclines
  4. macrolides
  5. oxazolidinones
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16
Q

what is the only class of antibiotics that works on gram negative only?

A

aminoglycosides

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17
Q

what are the only 3 classes of antibiotics that work on gram positive only?

A
  1. macrolides
  2. lincosamides
  3. glycopeptides
18
Q

how many days is the normal course of antibiotics?

A

7-10 days

19
Q

how long is the normal course of antimycobacterials for M. tb?

A

2 antibiotics for 6 months and 2 additional antibiotics for the first 2 months

20
Q

what antibiotics are used for M. tb infection?

A

isoniazid and rifampicin for 6 months

pyrazinamide and ethambutol for the first 2 months

21
Q

what is the controversy with antibiotic use?

A

ppl say antibiotics affect the microbiota and changes in the microbiota is linked to many diseases so some ppl don’t take antibiotics even when they need them

22
Q

what is dysbiosis?

A

how changes in the microbiota affect the rest of the body and link to disease, etc.

23
Q

4 mechanisms of antibiotic resistance

A
  1. efflux pumps
  2. immunity and bypass
  3. target modification
  4. inactivating enzymes
24
Q

what are the 6 ESKAPE pathogens?

A

E = escherichia
S = staphylococcus
K = klebsiella
A = acinetobacter
P = pseudomonas
E = enterococcus

25
Q

where are do ESKAPE infections occur?

A

nocosomial –> acquire from hospital

26
Q

describe how antibiotic resistance has spread from farming

A
  • livestock given antibiotics to make them bigger
  • we eat the meat and acquire the resistant genes
27
Q

what bacteria is the leading cause of death by infectious diseases in the western world?

A

Staphylococcus aureus

28
Q

is Staphylococcus aureus gram pos or neg?

A

Staphylococcus aureus is gram pos

29
Q

what makes Staphylococcus aureus so dangerous?

A

it has evolved many ways to evade the innate immune system

30
Q

what did people originally believe about Staphylococcus aureus infection? why?

A

originally thought it was extracellular pathogen bc appears as nodules in the kidney

31
Q

is Staphylococcus aureus extracellular?

A

in vitro data has shown that it can survive intracellularly within phagocytic cells like neutrophils and phagocytes (kupffer cells)

then burst to become the extracellular nodes on kidney

32
Q

why does Staphylococcus aureus become nodes in the kidney?

A

Kupffer cells burst when the bacteria builds up and then moves to the kidney to form the nodes

33
Q

why do Kupffer cells take up S. aureus?

A

Kupffer cells are strategically located so they can use special mechanisms to capture bacteria from the high shear forces in the bloodstream

they also uniquely express CRIg

34
Q

what imaging method can be used to detect the bacteria in KCs?

A

intravitral imaging

35
Q

describe the experiment to see if S. aureus is replicating intracellularly

A

stained bacteria with blue dye
- if they replicate, will lose the blue and only see green

found that the bacteria were replicating within KCs

36
Q

is S. aureus actually drug-resistant?

A

no, the drug isn’t able to get to the bacteria bc it is intracellular so the bacteria was surviving

37
Q

what happens if a liposome is used to deliver the drug to S. aureus?

A

the drug can reach S. aureus within the cell

38
Q

what is a pathobiont?

A

symbiont that can promote pathology when specific genetic or environmental conditions in the host are altered

39
Q

why can ESKAPE pathogens not really be considered pathogens?

A

healthy people can have them without disease

40
Q

when do ESKAPE pathogens become pathogenic?

A

in immunosuppressed ppl