Corner stone seminar 3: Resisting resistance Flashcards

1
Q

How can we reduce bacterial infection without antibiotics?

A

Reducing transmission through sanitation and vaccination

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2
Q

What limited access to antibiotics around the world?

A

health inequalities

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3
Q

In rich countries what are most infectious diseases?

A

healthcare infections

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4
Q

What healthcare things come with infection risk?

A
  1. transplants
  2. complex operations
  3. Orthopaedic implants
  4. chemotherapy
  5. broad spectrum treatments
  6. catheters
  7. things that dampen the immune system like aging and premature babies
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5
Q

Where do most infectious diseases come from?

A

bacteria that are already on/in the body waiting to get in a sterile site or for a comprised immune system

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6
Q

Why don’t we know the true burden of antibiotic resistance?

A

Most countries don’t have it as a priority as they have bigger problems so it is hard to quantify the problem

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7
Q

What are the 2 main mechanisms of antibiotic resistance?

A
  1. reduced permeability and efflux
  2. enzymatic degradation of the antibiotic
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8
Q

How does antibiotic resistance transmit through bacterial populations?

A
  1. Many of the enzymes are pre-evolved so they are on mobile genetic elements
  2. Bacteria are very old and have encountered most antibiotics before so have had the time to develop resistance
  3. Pass the resistance through the populations on mobile genetic elements
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9
Q

How is antibiotic-resistant bacteria transmitted between people?

A
  1. mostly as commensals until immunocompromised
  2. families share bacteria between themselves and their dogs
  3. dogs encounter many bacteria in the environment and bring them into contact with people
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10
Q

Why did development of antibiotics stall in the 80s?

A
  1. the original ones were too successful and there was no real need for more for a few years
  2. people stopped researching as it looked like it wasn’t needed
  3. this created a vacuum of research when resistance was rising and a lot of expertise was separated or gone
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11
Q

What was the BristolBridge project?

A
  1. throw money at people and try to find something that works
  2. an interdisciplinary international research
  3. funding research and one health studies in other countries like Thailand
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12
Q

How is Antibiotic susceptibility testing currently done?

A
  1. phenotypic testing
  2. limited by growth rates
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13
Q

How did an interdisciplinary approach lead to the development of new AST that is now on clinical trials?

A
  1. An observation that bacteria could vibrate like particles and that we could use it to detect if the bacteria were still alive
  2. Use physicists to use light waves to detect this vibration
  3. resistant bacteria would live and keep moving
  4. we would know within minutes if the bacteria was resistant
  5. use engineers to make this machine
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14
Q

What are One Health studies?

A

A research approach the recognises the human health is closely linked to animal health and the environment

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15
Q

Why is raw feeding dogs bad for antibiotic resistance?

A

they pick up more resistant bacteria and pass them onto the people they live with

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16
Q

Why is antibiotic resistance in farming such a problem?

A

because we eat the animals

17
Q

What can controlling agricultural use of antibiotics do?

A

reduce the resistance in the infection but not the rate of infection itself

18
Q

What is CTX-M?

A

a type of resistance that is very important

19
Q

What causes CTX-M resistance on farms?

A

dry cow therapy that stops mums from getting infections when feeding calves.
The colostrum ends up coated with antibiotics and then the only bacteria that can colonise the calves are resistant to cefquinome.

20
Q

How was CTX-M resistance reduced?

A
  1. Cannot use dry cow therapy to get the red tractor accreditation
  2. resistance was massively decreased
21
Q

What are the 2 types of ß-lactamases?

A
  1. serine ß-lactamase
  2. metallo ß-lactamase
22
Q

What are the differences between the 2 types of ß-lactamase?

A

they work very differently so you cannot design 1 inhibitor for both of them.
Serine ß-lactamases are mostly used

23
Q

What bacteria did Prof. Avison discover?

A

Stenotrophomonas maltophilia

24
Q

What makes Stenotrophomonas maltophilia resistance hard to treat?

A

It has both types of ß-lactamase enzymes

25
Q

What is AVIBACTAM?

A

an serine ß-lactamase inhibitor

26
Q

How can AVIBACTAM be used to combat Stenotrophomonas maltophilia’s resistance?

A

Used in combination therapy with other antibodies can greatly improve treatment outcomes