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?

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
where are do ESKAPE infections occur?
nocosomial --> acquire from hospital
26
describe how antibiotic resistance has spread from farming
- livestock given antibiotics to make them bigger - we eat the meat and acquire the resistant genes
27
what bacteria is the leading cause of death by infectious diseases in the western world?
Staphylococcus aureus
28
is Staphylococcus aureus gram pos or neg?
Staphylococcus aureus is gram pos
29
what makes Staphylococcus aureus so dangerous?
it has evolved many ways to evade the innate immune system
30
what did people originally believe about Staphylococcus aureus infection? why?
originally thought it was extracellular pathogen bc appears as nodules in the kidney
31
is Staphylococcus aureus extracellular?
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
why does Staphylococcus aureus become nodes in the kidney?
Kupffer cells burst when the bacteria builds up and then moves to the kidney to form the nodes
33
why do Kupffer cells take up S. aureus?
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
what imaging method can be used to detect the bacteria in KCs?
intravitral imaging
35
describe the experiment to see if S. aureus is replicating intracellularly
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
is S. aureus actually drug-resistant?
no, the drug isn't able to get to the bacteria bc it is intracellular so the bacteria was surviving
37
what happens if a liposome is used to deliver the drug to S. aureus?
the drug can reach S. aureus within the cell
38
what is a pathobiont?
symbiont that can promote pathology when specific genetic or environmental conditions in the host are altered
39
why can ESKAPE pathogens not really be considered pathogens?
healthy people can have them without disease
40
when do ESKAPE pathogens become pathogenic?
in immunosuppressed ppl